阅读说明：本技术 杂环化合物和含有该杂环化合物的有害节肢动物防除组合物 (Heterocyclic compound and harmful arthropod control composition containing same ) 是由 田代真之 田中绫香 中嶋祐二 于 2020-02-18 设计创作，主要内容包括：本发明提供对有害节肢动物具有优异的防除效果的式(I)表示的化合物或其氮氧化物、以及含有该化合物的有害节肢动物防除组合物和施用该化合物的有害节肢动物的防除方法。[式中,Q表示Q1所示的基团或者Q2所示的基团,Z表示氧原子等,A～(2)、A～(3)和A～(6)表示氮原子等,A～(4)表示CR～(1a)等,A～(5)表示氮原子等,A～(7)表示NR～(6g)等,G～(1)、G～(2)、G～(3)和G～(4)表示氮原子等,R～(1a)表示被选自氰基和卤素原子中的1个以上取代基取代的C1－C6链式烃基等,R～(2)表示可以被1个以上卤素原子取代的C1－C6烷基等,而且,n表示0、1或者2。](The present invention provides a compound represented by formula (I) or a nitrogen oxide thereof having an excellent controlling effect on harmful arthropods, a harmful arthropod controlling composition containing the compound, and a method for controlling harmful arthropods to which the compound is applied. [ wherein Q represents a group represented by Q1 or a group represented by Q2, Z represents an oxygen atom or the like, A 2 、A 3 And A 6 Represents a nitrogen atom or the like, A 4 Represents CR 1a Etc. A 5 Represents a nitrogen atom or the like, A 7 Represents NR 6g Etc. G 1 、G 2 、G 3 And G 4 Represents a nitrogen atom or the like, R 1a Represents a C1-C6 chain hydrocarbon group substituted with 1 or more substituents selected from a cyano group and a halogen atom, or the like, R 2 Represents a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, etc., and n represents 0, 1 or 2.])

1. A compound represented by the formula (I) or a nitrogen oxide thereof,

in the formula (I), the compound is shown in the specification,

R²represents C1-C6 alkyl, cyclopropyl or cyclopropylmethyl which may be substituted by 1 or more halogen atoms,

n represents 0, 1 or 2,

G¹represents a nitrogen atom or CR^3a，

G²Represents a nitrogen atom or CR^3b，

G³Represents a nitrogen atom or CR^3c，

G⁴Represents a nitrogen atom or CR^3d，

R^3a、R^3b、R^3cAnd R^3dEach of which is the same OR different and represents a C1-C6 chain hydrocarbon group which may be substituted by 1 OR more substituents selected from group B, a C3-C7 cycloalkyl group which may be substituted by 1 OR more substituents selected from group E, a phenyl group which may be substituted by 1 OR more substituents selected from group H, a five-OR six-membered aromatic heterocyclic group which may be substituted by 1 OR more substituents selected from group H, OR ¹²、NR¹¹R¹²、NR^11aR^12a、NR²⁴NR¹¹R¹²、NR²⁴OR¹¹、NR¹¹C(O)R¹³、NR²⁴NR¹¹C(O)R¹³、NR¹¹C(O)OR¹⁴、NR²⁴NR¹¹C(O)OR¹⁴、NR¹¹C(O)NR³¹R³²、NR²⁴NR¹¹C(O)NR³¹R³²、N＝CHNR³¹R³²、N＝S(O)_pR¹⁵R¹⁶、C(O)R¹³、C(O)OR¹⁷、C(O)NR³¹R³²、C(O)NR¹¹S(O)₂R²³、CR³⁰＝NOR¹⁷、NR¹¹CR²⁴＝NOR¹⁷、S(O)_mR²³Cyano groups, nitro groups, hydrogen atoms, or halogensThe number of atoms,

p represents a number of 0 or 1,

m represents 0, 1 or 2,

R³⁰represents a C1-C6 chain hydrocarbon group which may be substituted by 1 OR more halogen atoms, a halogen atom, OR³⁵、NR³⁶R³⁷Or a hydrogen atom,

R³⁵represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms,

R¹⁷represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a phenyl group which may be substituted by 1 or more substituents selected from the group D, or a hydrogen atom,

R¹¹、R²⁴、R³⁶and R³⁷Each of which is the same or different and represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, or a hydrogen atom,

R¹²represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more substituents selected from group F, a C3-C7 cycloalkyl group which may be substituted by 1 or more substituents selected from group J, a C3-C7 cycloalkenyl group which may be substituted by 1 or more substituents selected from group J, a phenyl group which may be substituted by 1 or more substituents selected from group D, a six-membered aromatic heterocyclic group which may be substituted by 1 or more substituents selected from group D, a hydrogen atom, or S (O)₂R²³，

R²³Represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, or a phenyl group which may be substituted by 1 or more substituents selected from the group D,

R^11aAnd R^12aTogether with the nitrogen atom to which they are bonded represent a three-to seven-membered non-aromatic heterocyclic group which may be substituted by 1 or more substituents selected from group E,

R¹³represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted by 1 or more halogen atoms, (C3-C6 cycloalkyl) C1-C3 alkyl group which may be substituted by 1 or more halogen atoms, a phenyl group which may be substituted by 1 or more substituents selected from group D, a penta-substituent which may be substituted by 1 or more substituents selected from group DA hetero-or hexa-membered aromatic heterocyclic group, or a hydrogen atom,

R¹⁴represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted by 1 or more halogen atoms, (C3-C6 cycloalkyl) C1-C3 alkyl group which may be substituted by 1 or more halogen atoms, or a phenyl C1-C3 alkyl group, wherein the phenyl moiety in the phenyl C1-C3 alkyl group may be substituted by 1 or more substituents selected from group D,

R¹⁵and R¹⁶Each of which is the same or different and represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms,

R³¹represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms, or a hydrogen atom,

R³²represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more substituents selected from the group F, a C3-C7 cycloalkyl group which may be substituted by 1 or more substituents selected from the group J, S (O) ₂R²³Or a hydrogen atom,

q represents a group represented by Q1 or a group represented by Q2,

z represents an oxygen atom or a sulfur atom,

A²represents a nitrogen atom or CR^6b，

A³Represents a nitrogen atom or CR^6c，

A⁶Represents a nitrogen atom or CR^6f，

A⁷Represents NR^6g、CR^6hR⁶ⁱOr an oxygen atom, or a salt thereof,

A⁴and A⁵Combination of (A) represents⁴Is CR^1aAnd A is⁵Is a nitrogen atom or CR^6eOr represents A⁴Is a nitrogen atom or CR^6dAnd A is⁵Is CR^1bIn the combination of (a) and (b),

R^1aand R^1bAre respectively the same or different and representC1-C6 chain hydrocarbon group substituted with 1 or more substituents selected from cyano group and halogen atom, C3-C4 cycloalkyl group which may be substituted with 1 or more substituents selected from cyano group and halogen atom, SR⁸、S(O)R⁸、S(O)₂R⁸、OR⁸Or OS (O)₂R⁸，

R⁸Represents a C1-C6 chain hydrocarbon group substituted with 1 or more substituents selected from cyano groups and halogen atoms, or a C3-C4 cycloalkyl group which may be substituted with 1 or more substituents selected from cyano groups and halogen atoms,

R^6b、R^6hand R⁶ⁱEach of which is the same or different and represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted with 1 or more halogen atoms, a halogen atom, or a hydrogen atom,

R^6c、R^6d、R^6eand R^6fEach of which may be the same or different, represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted by 1 or more halogen atoms, a C1-C6 alkoxy group which may be substituted by 1 or more halogen atoms, NR ²⁵R²⁶、C(O)R⁷、C(O)OR⁷、C(O)NR¹⁹R²⁰、NR²⁵C(O)R¹⁸、NR²⁵C(O)OR¹⁸、NR²⁵C(O)NR¹⁹R²⁰A cyano group, a halogen atom, or a hydrogen atom,

R^6grepresents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, or a hydrogen atom,

R¹⁹and R²⁵Each of which is the same or different and represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, or a hydrogen atom,

R²⁶represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more substituents selected from group L, a C3-C7 cycloalkyl group which may be substituted by 1 or more substituents selected from group M, a C3-C7 cycloalkenyl group which may be substituted by 1 or more substituents selected from group M, a phenyl group which may be substituted by 1 or more substituents selected from group KA six-membered aromatic heterocyclic group substituted with 1 or more substituents, a hydrogen atom, or S (O)₂R²⁷，

R²⁷Represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted with 1 or more halogen atoms, or a phenyl group which may be substituted with 1 or more substituents selected from the group K,

R⁷、R¹⁸and R²⁰Each of which is the same or different and represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more substituents selected from the group L, a C3-C7 cycloalkyl group which may be substituted with 1 or more substituents selected from the group M, or a hydrogen atom,

Group B: a group consisting of C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, C1-C6 alkylthio group which may be substituted with 1 or more halogen atoms, C1-C6 alkylsulfinyl group which may be substituted with 1 or more halogen atoms, C1-C6 alkylsulfonyl group which may be substituted with 1 or more halogen atoms, C3-C6 cycloalkyl group which may be substituted with 1 or more halogen atoms, cyano group, hydroxyl group and halogen atom,

group C: a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, and a halogen atom,

group D: by a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a hydroxyl group, a C1-C6 alkoxy group which may be substituted by 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted by 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted by 1 or more halogen atoms, a mercapto group, a C1-C6 alkylthio group which may be substituted by 1 or more halogen atoms, a C1-C6 alkylsulfinyl group which may be substituted by 1 or more halogen atoms, a C1-C6 alkylsulfonyl group which may be substituted by 1 or more halogen atoms, an amino group, an NHR ²¹、NR²¹R²²、C(O)R²¹、OC(O)R²¹、C(O)OR²¹Cyano groups, nitro groups and halogen atoms,

R²¹and R²²Each of which is the same or different and represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms,

group E: a group consisting of C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, oxo group, hydroxy group, cyano group and nitro group,

group F: by C1-C6 alkoxy which may be substituted by 1 or more halogen atoms, phenyl which may be substituted by 1 or more substituents selected from the group D, a five-or six-membered aromatic heterocyclic group which may be substituted by 1 or more substituents selected from the group D, C3-C7 cycloalkyl which may be substituted by 1 or more halogen atoms, a three-to seven-membered non-aromatic heterocyclic group which may be substituted by 1 or more substituents selected from the group C, amino, NHR²¹、NR²¹R²²A halogen atom and a cyano group,

group H: by C1-C6 alkyl which may be substituted by 1 OR more halogen atoms, a five-OR six-membered aromatic heterocyclic group which may be substituted by 1 OR more substituents selected from the group D, OR ¹⁰、NR⁹R¹⁰、C(O)R¹⁰、C(O)NR⁹R¹⁰、OC(O)R⁹、OC(O)OR⁹、NR¹⁰C(O)R⁹、NR¹⁰C(O)OR⁹、C(O)OR¹⁰Halogen atom, nitro group, cyano group and amino group,

R⁹represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms, or a C3-C6 cycloalkyl group which may be substituted by 1 or more halogen atoms,

R¹⁰represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms, a C3-C6 cycloalkyl group which may be substituted by 1 or more halogen atoms, or a hydrogen atom,

group J: a group consisting of a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, a halogen atom and a cyano group,

group K: a C1-C6 catenated hydrocarbon group which may be substituted with 1 or more halogen atoms, a C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylthio group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylsulfinyl group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylsulfonyl group which may be substituted with 1 or more halogen atoms, a C3-C6 cycloalkyl group which may be substituted with 1 or more halogen atoms, a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, a di (C1-C4 alkyl) amino group which may be substituted with 1 or more halogen atoms, a C2-C6 alkylcarbonyl group which may be substituted with 1 or more halogen atoms, an alkoxycarbonyl group which may be substituted with 1 or more halogen atoms, a C2 to 865 alkoxycarbonyl group which may be substituted with 1 or more halogen atoms, a C6327 alkoxycarbonyl group, C2-C6 alkoxycarbonyloxy which may be substituted with 1 or more halogen atoms, aminocarbonyl, (C1-C6 alkyl) aminocarbonyl which may be substituted with 1 or more halogen atoms, [ di (C1-C4 alkyl) amino ] carbonyl which may be substituted with 1 or more halogen atoms, (C2-C6 alkoxycarbonyl) amino which may be substituted with 1 or more halogen atoms, (C2-C6 alkoxycarbonyl) (C1-C6 alkyl) amino which may be substituted with 1 or more halogen atoms, cyano, amino, nitro, hydroxyl and halogen atoms,

Group L: a group consisting of C3-C6 cycloalkyl which may be substituted with 1 or more halogen atoms, phenyl which may be substituted with 1 or more substituents selected from the group K, a five-or six-membered aromatic heterocyclic group which may be substituted with 1 or more substituents selected from the group K, C1-C6 alkoxy which may be substituted with 1 or more halogen atoms, C1-C6 alkyl which may be substituted with 1 or more halogen atoms, di (C1-C4 alkyl) amino which may be substituted with 1 or more halogen atoms, cyano, amino, nitro, hydroxyl and halogen atoms,

group M: a group consisting of C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, C2-C6 alkoxycarbonyl group which may be substituted with 1 or more halogen atoms, amino group, cyano group and halogen atom.

2. A compound or its nitroxide according to claim 1, wherein Q is a group represented by Q1.

3. A compound or its nitroxide according to claim 1, wherein Q is a group represented by Q2.

4. A compound or its nitroxide according to any one of claims 1-3, wherein R^3a、R^3b、R^3cAnd R^3dEach, which may be the same OR different, is C1-C6 alkyl, C2-C6 alkenyl, C3-C7 cycloalkyl, phenyl, pyridyl, pyrimidyl, OR ¹²、CR³⁰＝NOR¹⁷A hydrogen atom or a halogen atom, wherein the C1-C6 alkyl group, the C2-C6 alkenyl group and the C3-C7 cycloalkyl group may be substituted with 1 or more substituents selected from a halogen atom and a cyano group, and the phenyl group, the pyridyl group and the pyrimidinyl group may be substituted with 1 or more substituents selected from group J.

5. A compound or its nitroxide according to any one of claims 1 to 4, wherein G¹Is a nitrogen atom or CH, G²Is CR^3b，G³Is CR^3c，G⁴Is a nitrogen atom or CH, R^3bAnd R^3cEach, which may be the same OR different, is C1-C6 alkyl, C2-C6 alkenyl, C3-C7 cycloalkyl, OR¹²A hydrogen atom or a halogen atom, wherein the C1-C6 alkyl group, the C2-C6 alkenyl group and the C3-C7 cycloalkyl group may be substituted with 1 or more substituents selected from a halogen atom and a cyano group.

6. A compound or its nitroxide according to any one of claims 1-5, wherein G¹Is CH, G²Is CR^3b，G³Is CR^3c，G⁴Is CH, R^3bAnd R^3cEach of which is the same or different and is a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms or a hydrogen atom.

7. A compound or its nitroxide according to any one of claims 1-6, wherein R^1aAnd R^1bEach of which is the same or different, a C1-C6 alkyl group which may be substituted with 1 or more substituents selected from a cyano group and a halogen atom, or a cyclopropyl group which may be substituted with 1 or more substituents selected from a cyano group and a halogen atom.

8. A compound or its nitroxide according to any one of claims 1 to 7, wherein R²Is ethyl.

9. A compound or its nitroxide according to any one of claims 1 to 8, wherein Z is an oxygen atom.

10. A harmful arthropod control composition containing the compound according to any one of claims 1 to 9 or a nitrogen oxide thereof.

11. A composition comprising 1 or more members selected from the group consisting of group (a), group (b), group (c) and group (d), and the compound according to any one of claims 1 to 9 or a nitrogen oxide thereof,

group (a): a group consisting of an insecticidal active ingredient, an acaricidal active ingredient and a nematicidal active ingredient;

group (b): a bactericidal active ingredient;

group (c): plant growth regulating ingredients;

group (d): avoiding the ingredients.

12. A method for controlling a harmful arthropod, which comprises applying an effective amount of the compound according to any one of claims 1 to 9 or a nitrogen oxide thereof, or an effective amount of the composition according to claim 11 to a harmful arthropod or a habitat of a harmful arthropod.

13. A seed or vegetative propagation organ holding an effective amount of a compound according to any one of claims 1 to 9 or a nitrogen oxide thereof, or an effective amount of a composition according to claim 11.

Technical Field

The present patent application claims priority and benefit of the paris convention based on japanese patent application 2019-027139 (application No. 2/19/2019) and japanese patent application 2019-117010 (application No. 6/25/2019), the entire contents of which are hereby incorporated by reference into the present specification.

The present invention relates to a heterocyclic compound and a harmful arthropod control composition containing the heterocyclic compound.

Background

Hitherto, various compounds have been studied for the purpose of controlling harmful arthropods. For example, patent document 1 describes that a certain compound has a pest control effect.

Documents of the prior art

Patent document

Patent document 1: international publication No. 2016/129684

Disclosure of Invention

The present invention addresses the problem of providing a compound having excellent control efficacy against harmful arthropods.

The present inventors have conducted studies to find out a compound having an excellent controlling effect against harmful arthropods, and as a result, have found that a compound represented by the following formula (I) and the like have an excellent controlling effect against harmful arthropods.

Namely, the present invention is as follows.

[1] A compound represented by the formula (I) (hereinafter, referred to as the compound N of the present invention) or a nitrogen oxide thereof (hereinafter, a compound represented by the formula (I) or a nitrogen oxide thereof is referred to as the compound of the present invention).

[ in the formula,

R²represents C1-C6 alkyl, cyclopropyl or cyclopropylmethyl which may be substituted by 1 or more halogen atoms,

n represents 0, 1 or 2,

G¹represents a nitrogen atom or CR^3a，

G²Represents a nitrogen atom or CR ^3b，

G³Represents a nitrogen atom or CR^3c，

G⁴Represents a nitrogen atom or CR^3d，

R^3a、R^3b、R^3cAnd R^3dRespectively, the same OR different, represent a C1-C6 chain hydrocarbon group which may be substituted by 1 OR more substituents selected from group B, a C3-C7 cycloalkyl group which may be substituted by 1 OR more substituents selected from group E, a phenyl group which may be substituted by 1 OR more substituents selected from group H, a five-OR six-membered aromatic heterocyclic group which may be substituted by 1 OR more substituents selected from group H, OR¹²、NR¹¹R¹²、NR^11aR^12a、NR²⁴NR¹¹R¹²、NR²⁴OR¹¹、NR¹¹C(O)R¹³、NR²⁴NR¹¹C(O)R¹³、NR¹¹C(O)OR¹⁴、NR²⁴NR¹¹C(O)OR¹⁴、NR¹¹C(O)NR³¹R³²、NR²⁴NR¹¹C(O)NR³¹R³²、N＝CHNR³¹R³²、N＝S(O)_pR¹⁵R¹⁶、C(O)R¹³、C(O)OR¹⁷、C(O)NR³¹R³²、C(O)NR¹¹S(O)₂R²³、CR³⁰＝NOR¹⁷、NR¹¹CR²⁴＝NOR¹⁷、S(O)_mR²³Cyano group, nitro group, hydrogen atom or halogen atom,

p represents a number of 0 or 1,

m represents 0, 1 or 2,

R³⁰represents a C1-C6 chain hydrocarbon group which may be substituted by 1 OR more halogen atoms, a halogen atom, OR³⁵、NR³⁶R³⁷Or a hydrogen atom,

R³⁵represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms,

R¹⁷represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a phenyl group which may be substituted by 1 or more substituents selected from the group D, or a hydrogen atom,

R¹¹、R²⁴、R³⁶and R³⁷Respectively, the same or different, represent a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, or a hydrogen atom,

R¹²represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more substituents selected from group F, a C3-C7 cycloalkyl group which may be substituted by 1 or more substituents selected from group J, a C3-C7 cycloalkenyl group which may be substituted by 1 or more substituents selected from group J, a phenyl group which may be substituted by 1 or more substituents selected from group D A six-membered aromatic heterocyclic group of (A), a hydrogen atom, or S (O)₂R²³，

R²³Represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, or a phenyl group which may be substituted by 1 or more substituents selected from the group D,

R^11aand R^12aTogether with the nitrogen atom to which they are bonded represent a three-to seven-membered non-aromatic heterocyclic group which may be substituted by 1 or more substituents selected from group E,

R¹³represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted with 1 or more halogen atoms, (C3-C6 cycloalkyl) C1-C3 alkyl group which may be substituted with 1 or more halogen atoms, a phenyl group which may be substituted with 1 or more substituents selected from group D, a five-or six-membered aromatic heterocyclic group which may be substituted with 1 or more substituents selected from group D, or a hydrogen atom,

R¹⁴represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted by 1 or more halogen atoms, (C3-C6 cycloalkyl) C1-C3 alkyl group which may be substituted by 1 or more halogen atoms, or phenyl C1-C3 alkyl { the phenyl moiety in the phenyl C1-C3 alkyl group may be substituted by 1 or more substituents selected from the group D },

R¹⁵and R¹⁶Each of which is the same or different and represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms,

R³¹Represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms, or a hydrogen atom,

R³²represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more substituents selected from the group F, a C3-C7 cycloalkyl group which may be substituted by 1 or more substituents selected from the group J, S (O)₂R²³Or a hydrogen atom,

q represents a group represented by Q1 or a group represented by Q2,

z represents an oxygen atom or a sulfur atom,

A²represents a nitrogen atom or CR^6b，

A³Represents a nitrogen atom or CR^6c，

A⁶Represents a nitrogen atom or CR^6f，

A⁷Represents NR^6g、CR^6hR⁶ⁱOr an oxygen atom, or a mixture of oxygen atoms,

A⁴and A⁵Combination of (A) represents⁴Is CR^1aAnd A is⁵Is a nitrogen atom or CR^6eA combination of (1); or A⁴Is a nitrogen atom or CR^6dAnd A is⁵Is CR^1bIn the combination of (a) and (b),

R^1aand R^1bRespectively, the same or different, represents a C1-C6 chain hydrocarbon group substituted with 1 or more substituents selected from a cyano group and a halogen atom, a C3-C4 cycloalkyl group which may be substituted with 1 or more substituents selected from a cyano group and a halogen atom, an SR⁸、S(O)R⁸、S(O)₂R⁸、OR⁸Or OS (O)₂R⁸，

R⁸Represents a C1-C6 chain hydrocarbon group substituted with 1 or more substituents selected from cyano groups and halogen atoms, or a C3-C4 cycloalkyl group which may be substituted with 1 or more substituents selected from cyano groups and halogen atoms,

R^6b、R^6hand R⁶ⁱRespectively, the same or different, represent a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted with 1 or more halogen atoms, a halogen atom, or a hydrogen atom,

R^6c、R^6d、R^6eAnd R^6fRespectively, the same or different, represent a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted by 1 or more halogen atoms, a C1-C6 alkoxy group which may be substituted by 1 or more halogen atoms, NR²⁵R²⁶、C(O)R⁷、C(O)OR⁷、C(O)NR¹⁹R²⁰、NR²⁵C(O)R¹⁸、NR²⁵C(O)OR¹⁸、NR²⁵C(O)NR¹⁹R²⁰A cyano group, a halogen atom, or a hydrogen atom,

R^6grepresents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, or a hydrogen atom,

R¹⁹and R²⁵Respectively, the same or different, represent a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, or a hydrogen atom,

R²⁶represents a C1-C6 chain hydrocarbon group which may be substituted by 1 or more substituents selected from group L, a C3-C7 cycloalkyl group which may be substituted by 1 or more substituents selected from group M, a C3-C7 cycloalkenyl group which may be substituted by 1 or more substituents selected from group M, a phenyl group which may be substituted by 1 or more substituents selected from group K, a six-membered aromatic heterocyclic group which may be substituted by 1 or more substituents selected from group K, a hydrogen atom, or S (O)₂R²⁷，

R²⁷Represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C3-C7 cycloalkyl group which may be substituted with 1 or more halogen atoms, or a phenyl group which may be substituted with 1 or more substituents selected from the group K,

R⁷、R¹⁸And R²⁰Each of which is the same or different, represents a C1-C6 chain hydrocarbon group which may be substituted with 1 or more substituents selected from group L, a C3-C7 cycloalkyl group which may be substituted with 1 or more substituents selected from group M, or a hydrogen atom.

Group B: a group consisting of a C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylthio group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylsulfinyl group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylsulfonyl group which may be substituted with 1 or more halogen atoms, a C3-C6 cycloalkyl group which may be substituted with 1 or more halogen atoms, a cyano group, a hydroxyl group and a halogen atom.

Group C: a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, and a halogen atom.

Group D: by a C1-C6 chain hydrocarbon group which may be substituted by 1 or more halogen atoms, a hydroxyl group, a C1-C6 alkoxy group which may be substituted by 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted by 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted by 1 or more halogen atoms, a mercapto group, a C1-C6 alkylthio group which may be substituted by 1 or more halogen atoms, a C1-C6 alkylsulfinyl group which may be substituted by 1 or more halogen atoms, a C1-C6 alkylsulfonyl group which may be substituted by 1 or more halogen atoms, an amino group, an NHR ²¹、NR²¹R²²、C(O)R²¹、OC(O)R²¹、C(O)OR²¹Cyano groups, nitro groups and halogen atoms.

R²¹And R²²Each of which is the same or different and represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms.

Group E: a C1-C6 chain hydrocarbon group which may be substituted with 1 or more halogen atoms, a C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, a halogen atom, an oxo group, a hydroxyl group, a cyano group, and a nitro group.

Group F: by C1-C6 alkoxy which may be substituted by 1 or more halogen atoms, phenyl which may be substituted by 1 or more substituents selected from the group D, a five-or six-membered aromatic heterocyclic group which may be substituted by 1 or more substituents selected from the group D, C3-C7 cycloalkyl which may be substituted by 1 or more halogen atoms, a three-to seven-membered non-aromatic heterocyclic group which may be substituted by 1 or more substituents selected from the group C, amino, NHR²¹、NR²¹R²²Halogen atom and cyano group.

Group H: from C1-C6 alkyl which may be substituted by more than 1 halogen atom, may be substituted byA five-OR six-membered aromatic heterocyclic group substituted with 1 OR more substituents selected from group D, OR ¹⁰、NR⁹R¹⁰、C(O)R¹⁰、C(O)NR⁹R¹⁰、OC(O)R⁹、OC(O)OR⁹、NR¹⁰C(O)R⁹、NR¹⁰C(O)OR⁹、C(O)OR¹⁰Halogen atom, nitro group, cyano group and amino group.

R⁹Represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms, or a C3-C6 cycloalkyl group which may be substituted by 1 or more halogen atoms,

R¹⁰represents a C1-C6 alkyl group which may be substituted by 1 or more halogen atoms, a C3-C6 cycloalkyl group which may be substituted by 1 or more halogen atoms, or a hydrogen atom.

Group J: a group consisting of a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, a halogen atom and a cyano group.

Group K: a C1-C6 catenated hydrocarbon group which may be substituted with 1 or more halogen atoms, a C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkenyloxy group which may be substituted with 1 or more halogen atoms, a C3-C6 alkynyloxy group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylthio group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylsulfinyl group which may be substituted with 1 or more halogen atoms, a C1-C6 alkylsulfonyl group which may be substituted with 1 or more halogen atoms, a C3-C6 cycloalkyl group which may be substituted with 1 or more halogen atoms, a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, a di (C1-C4 alkyl) amino group which may be substituted with 1 or more halogen atoms, a C2-C6 alkylcarbonyl group which may be substituted with 1 or more halogen atoms, an alkoxycarbonyl group which may be substituted with 1 or more halogen atoms, a C2 to 865 alkoxycarbonyl group which may be substituted with 1 or more halogen atoms, a C6327 alkoxycarbonyl group, C2-C6 alkoxycarbonyloxy which may be substituted with 1 or more halogen atoms, aminocarbonyl, (C1-C6 alkyl) aminocarbonyl which may be substituted with 1 or more halogen atoms, [ di (C1-C4 alkyl) amino ] carbonyl which may be substituted with 1 or more halogen atoms, (C2-C6 alkoxycarbonyl) amino which may be substituted with 1 or more halogen atoms, (C2-C6 alkoxycarbonyl) (C1-C6 alkyl) amino which may be substituted with 1 or more halogen atoms, cyano, amino, nitro, hydroxyl and halogen atoms.

Group L: a group consisting of C3-C6 cycloalkyl which may be substituted with 1 or more halogen atoms, phenyl which may be substituted with 1 or more substituents selected from the group K, a five-or six-membered aromatic heterocyclic group which may be substituted with 1 or more substituents selected from the group K, C1-C6 alkoxy which may be substituted with 1 or more halogen atoms, C1-C6 alkyl which may be substituted with 1 or more halogen atoms, di (C1-C4 alkyl) amino which may be substituted with 1 or more halogen atoms, cyano, amino, nitro, hydroxyl and halogen atoms.

Group M: a group consisting of C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, C1-C6 alkoxy group which may be substituted with 1 or more halogen atoms, C2-C6 alkoxycarbonyl group which may be substituted with 1 or more halogen atoms, amino group, cyano group and halogen atom. ]

[2] The compound according to [1] or a nitroxide thereof, wherein Q is a group represented by Q1.

[3] The compound according to [1] or a nitroxide thereof, wherein Q is a group represented by Q2.

[4]According to [1]～[3]The compound of any one of (1) or a nitroxide thereof, wherein R^3a、R^3b、R^3cAnd R^3dRespectively, the same OR different, C1-C6 alkyl group, C2-C6 alkenyl group, C3-C7 cycloalkyl { the C1-C6 alkyl group, the C2-C6 alkenyl group and the C3-C7 cycloalkyl group may be substituted with 1 OR more substituents selected from a halogen atom and a cyano group }, phenyl group, pyridyl group, pyrimidyl group { the phenyl group, the pyridyl group and the pyrimidyl group may be substituted with 1 OR more substituents selected from group J }, OR ¹²、CR³⁰＝NOR¹⁷Hydrogen atom or halogen atom.

[5]According to [1]～[4]The compound of any one of (1) or an oxynitride thereof, wherein G is¹Is a nitrogen atom or CH, G²Is CR^3b，G³Is CR^3c，G⁴Is a nitrogen atom or CH, R^3bAnd R^3cRespectively, the same or different, is C1-C6 alkyl, C2-C6 alkenyl, C3-C7 cycloalkyl { the C1-C6 alkyl group,The C2-C6 alkenyl group and the C3-C7 cycloalkyl group may be substituted by 1 OR more substituents selected from a halogen atom and a cyano group }, OR¹²Hydrogen atom or halogen atom.

[6]According to [1]～[5]The compound of any one of (1) or an oxynitride thereof, wherein G is¹Is CH, G²Is CR^3b，G³Is CR^3c，G⁴Is CH, R^3bAnd R^3cRespectively, the same or different, is a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms or a hydrogen atom.

[7]According to [1]～[6]The compound of any one of (1) or a nitroxide thereof, wherein R^1aAnd R^1bAre each the same or different and are a C1-C6 alkyl group which may be substituted by 1 or more substituents selected from the group consisting of a cyano group and a halogen atom, or a cyclopropyl group which may be substituted by 1 or more substituents selected from the group consisting of a cyano group and a halogen atom.

[8]According to [1]～[7]The compound of any one of (1) or a nitroxide thereof, wherein R²Is ethyl.

[9] The compound or its oxynitride according to any one of [1] to [8], wherein Z is an oxygen atom.

[10] A harmful arthropod control composition comprising the compound according to any one of [1] to [9] or a nitrogen oxide thereof.

[11] A composition comprising 1 or more members selected from the group consisting of group (a), group (b), group (c) and group (d), and a compound described in any one of [1] to [9] or a nitrogen oxide thereof (hereinafter, referred to as the composition of the present invention):

group (a): a group consisting of an insecticidal active ingredient, an acaricidal active ingredient and a nematicidal active ingredient;

group (b): a bactericidal active ingredient;

group (c): plant growth regulating ingredients;

group (d): avoiding the ingredients.

[12] A method for controlling a harmful arthropod, which comprises applying an effective amount of the compound according to any one of [1] to [9] or a nitrogen oxide thereof, or an effective amount of the composition according to [11] to a harmful arthropod or a locus where a harmful arthropod inhabits.

[13] A seed or a vegetative propagation organ, which retains an effective amount of the compound according to any one of [1] to [9] or its nitrogen oxide, or an effective amount of the composition according to [11 ].

According to the present invention, harmful arthropods can be controlled.

Detailed Description

The substituents in the present invention are explained.

The halogen atom represents a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.

When the substituent is substituted with 2 or more halogen atoms or substituents, these halogen atoms or substituents may be the same or different from each other.

The expression "CX-CY" in the present specification means that the number of carbon atoms is X to Y. For example, the expression "C1-C6" means that the number of carbon atoms is 1 to 6.

Chain hydrocarbyl refers to alkyl, alkenyl or alkynyl.

Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, a 1, 1-dimethylpropyl group, a 1, 2-dimethylpropyl group, a 1-ethylpropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, and a hexyl group.

Examples of the alkenyl group include a vinyl group, a 1-propenyl group, a 2-propenyl group, a 1-methyl-1-propenyl group, a 1-methyl-2-propenyl group, a 1, 2-dimethyl-1-propenyl group, a 1-ethyl-2-propenyl group, a 3-butenyl group, a 4-pentenyl group and a 5-hexenyl group.

Examples of the alkynyl group include an ethynyl group, a 1-propynyl group, a 2-propynyl group, a 1-methyl-2-propynyl group, a 1, 1-dimethyl-2-propynyl group, a 1-ethyl-2-propynyl group, a 2-butynyl group, a 4-pentynyl group and a 5-hexynyl group.

Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, a tert-butoxy group, a pentyloxy group, and a hexyloxy group.

Examples of the alkenyloxy group include a 2-propenyloxy group, a 2-butenyloxy group and a 5-hexenyloxy group.

Examples of the alkynyloxy group include a 2-propynyloxy group, a 2-butynyloxy group and a 5-hexynyloxy group.

Examples of the fluoroalkyl group include a trifluoromethyl group, a 2,2, 2-trifluoroethyl group, a pentafluoroethyl group, a 2,2,3,3, 3-pentafluoropropyl group, a 1,1, 1-trifluoropropan-2-yl group, and a heptafluoropropyl group.

Examples of the cycloalkyl group include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl.

Examples of the cycloalkenyl group include a cyclopropenyl group, a cyclobutenyl group, a cyclopentenyl group, a cyclohexenyl group and a cycloheptenyl group.

The three-to seven-membered non-aromatic heterocyclic group represents an aziridine ring, an azetidine ring, a pyrrolidine ring, an imidazoline ring, an imidazolidine ring, a piperidine ring, a tetrahydropyrimidine ring, a hexahydropyrimidine ring, a piperazine ring, an azepane ring, a heterocyclic ring, and a method for producing a compound, and a,Oxazolidine ring, isoOxazolidine ring, 1, 3-A oxazinane ring, a morpholine ring, a 1, 4-oxazepane ring, a thiazolidine ring, an isothiazolidine ring, a 1, 3-thiazine ring, a thiomorpholine ring or a 1, 4-thiazepane ring.

Examples of the three-to seven-membered non-aromatic heterocyclic group which may be substituted by 1 or more substituents selected from group E include the following groups.

The five-membered or six-membered aromatic heterocyclic group means a five-membered aromatic heterocyclic group or a six-membered aromatic heterocyclic group. The five-membered aromatic heterocyclic group is pyrrolyl, furyl, thienyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl, pyrazolyl, etc,Azolyl radical, isoOxazolyl, thiazolyl, isothiazolyl,Oxadiazolyl or thiadiazolyl. The six-membered aromatic heterocyclic group means a pyridyl group, a pyridazinyl group, a pyrimidinyl group, a pyrazinyl group, a triazinyl group or a tetrazinyl group.

(C3-C6 cycloalkyl) C1-C3 alkyl which may be substituted by 1 or more halogen atoms includes, for example, cyclopropylmethyl, (2-fluorocyclopropyl) methyl, cyclopropylfluoromethyl and (2-fluorocyclopropyl) fluoromethyl.

Phenyl C1-C3 alkyl { the phenyl moiety of the phenyl C1-C3 alkyl can be substituted with 1 or more substituents selected from group D }, examples include benzyl, 2-fluorobenzyl, 4-chlorobenzyl, 4- (trifluoromethyl) benzyl and 2- [ 4- (trifluoromethyl) phenyl ] ethyl.

Alkylthio, alkylsulfinyl and alkylsulfonyl are taken to mean radicals having S (O)_zAlkyl groups of the moieties indicated.

As the alkylthio group in which z is 0, for example, methylthio, ethylthio, propylthio and isopropylthio are mentioned.

As the alkylsulfinyl group where z is 1, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl and isopropylsulfinyl are mentioned.

As the alkylsulfonyl group wherein z is 2, for example, methylsulfonyl group, ethylsulfonyl group, propylsulfonyl group and isopropylsulfonyl group are mentioned.

Examples of the nitroxide of the compound represented by formula (I) include compounds represented by the following formula.

[ in the formula, R⁴⁰Represents any substitution selected from the group HWherein x represents 0, 1, 2, 3 or 4, y represents 0, 1, 2 or 3, and the other symbols represent the same meanings as described above.]

The compounds of the present invention may sometimes exist in more than one stereoisomer. Examples of the stereoisomers include enantiomers, diastereomers, geometric isomers and the like. The compounds of the present invention include individual stereoisomers and mixtures of stereoisomers in any ratio.

The compounds of the present invention sometimes form acid addition salts. Examples of the acid for forming an acid addition salt include inorganic acids such as hydrogen chloride, phosphoric acid, and sulfuric acid, and organic acids such as acetic acid, trifluoroacetic acid, benzoic acid, and p-toluenesulfonic acid. Acid addition salts are obtained by mixing the compounds of the present invention with an acid.

Examples of the compound N of the present invention include the following compounds.

[ mode 1 ] of]Compounds of the invention N is R^3a、R^3b、R^3cAnd R^3dAre respectively the same OR different and are C1-C6 alkyl, C2-C6 alkenyl, C3-C7 cycloalkyl { the C1-C6 alkyl, the C2-C6 alkenyl and the C3-C7 cycloalkyl may be substituted with 1 OR more substituents selected from halogen atoms and cyano }, phenyl, pyridyl, pyrimidyl { the phenyl, the pyridyl and the pyrimidyl may be substituted with 1 OR more substituents selected from group J }, OR ¹²、CR³⁰＝NOR¹⁷A hydrogen atom or a halogen atom.

[ mode 2 ] of]Compounds of the invention N is R^3a、R^3b、R^3cAnd R^3dAnd are each the same or different and a C1-C6 alkyl group, a C2-C6 alkenyl group, a C3-C7 cycloalkyl group { the C1-C6 alkyl group, the C2-C6 alkenyl group and the C3-C7 cycloalkyl group may be substituted with 1 or more halogen atoms }, a hydrogen atom or a halogen atom.

[ mode 3 ] of]The compound according to mode 2, wherein G¹Is a nitrogen atom or CH, G²Is CR^3b、G³Is CR^3c、G⁴Is a nitrogen atom or CH.

[ means 4 ]]The compound according to mode 2, wherein G¹Is CH, G²Is CR^3b、G³Is CR^3c、G⁴Is CH.

[ means 5 ]]Compounds of the invention N is G¹Is CH, G²Is CR^3b、G³Is CR^3c、G⁴Is CH, R^3bAnd R^3cAnd each is the same or different and is a C1-C6 alkyl group which may be substituted with 1 or more halogen atoms, or a hydrogen atom.

[ means 6 ]]Compounds of the invention N is G¹、G³And G⁴Is CH, G²Is CCF₃The compound of (1).

[ means 7 ]]The compound according to mode 2, wherein G¹Is a nitrogen atom, G²Is CR^3b，G³Is CR^3c，G⁴Is CH.

[ means 8 ]]The compound according to mode 2, wherein G¹Is CH, G²Is CR^3b，G³Is CR^3c，G⁴Is a nitrogen atom.

[ means 9 ]]Compounds of the invention N is R²A compound which is a C1-C6 alkyl group.

[ means 10)]Compounds of the invention N is R²A compound which is ethyl.

[ means 11]A compound according to mode 1, wherein R²Is C1-C6 alkyl.

[ means 12)]A compound according to mode 2, wherein R²Is C1-C6 alkyl.

[ means 13]A compound according to mode 3, wherein R²Is C1-C6 alkyl.

[ means 14)]A compound according to mode 4, wherein R²Is C1-C6 alkyl.

[ means 15)]A compound according to mode 5, wherein R²Is C1-C6 alkyl.

[ means 16]A compound according to mode 6, wherein R²Is C1-C6 alkyl.

[ means 17]A compound according to mode 7, wherein R²Is C1-C6 alkyl.

[ means 18)]The compound according to mode 8, wherein，R²Is C1-C6 alkyl.

[ means 19]A compound according to mode 1, wherein R²Is ethyl.

[ means 20]A compound according to mode 2, wherein R²Is ethyl.

[ means 21]A compound according to mode 3, wherein R²Is ethyl.

[ means 22]A compound according to mode 4, wherein R²Is ethyl.

[ means 23]A compound according to mode 5, wherein R²Is ethyl.

[ means 24]A compound according to mode 6, wherein R²Is ethyl.

[ means 25]A compound according to mode 7, wherein R²Is ethyl.

[ means 26)]A compound according to mode 8, wherein R ²Is ethyl.

[ mode 27] the compound N of the present invention is a compound wherein Q is a group represented by Q1.

[ mode 28] the compound N of the present invention is a compound wherein Q is a group represented by Q2.

[ mode 29] A compound according to mode 1, wherein Q is a group represented by Q1.

[ mode 30] A compound according to mode 2, wherein Q is a group represented by Q1.

[ mode 31] A compound according to mode 3, wherein Q is a group represented by Q1.

[ mode 32] A compound according to mode 4, wherein Q is a group represented by Q1.

[ mode 33] A compound according to mode 5, wherein Q is a group represented by Q1.

[ mode 34] A compound according to mode 6, wherein Q is a group represented by Q1.

[ mode 35] A compound according to mode 7, wherein Q is a group represented by Q1.

[ mode 36] A compound according to mode 8, wherein Q is a group represented by Q1.

[ mode 37] A compound according to mode 9, wherein Q is a group represented by Q1.

[ mode 38] A compound according to mode 10, wherein Q is a group represented by Q1.

[ mode 39] A compound according to mode 11, wherein Q is a group represented by Q1.

[ mode 40] A compound according to mode 12, wherein Q is a group represented by Q1.

[ mode 41] A compound according to mode 13, wherein Q is a group represented by Q1.

[ mode 42] A compound according to mode 14, wherein Q is a group represented by Q1.

[ mode 43] A compound according to mode 15, wherein Q is a group represented by Q1.

[ mode 44] A compound according to mode 16, wherein Q is a group represented by Q1.

[ mode 45] A compound according to mode 17, wherein Q is a group represented by Q1.

[ mode 46] A compound according to mode 18, wherein Q is a group represented by Q1.

[ mode 47] A compound according to mode 19, wherein Q is a group represented by Q1.

[ mode 48] A compound according to mode 20, wherein Q is a group represented by Q1.

Mode 49 a compound according to mode 21, wherein Q is a group represented by Q1.

[ mode 50] A compound according to mode 22, wherein Q is a group represented by Q1.

[ mode 51] A compound according to mode 23, wherein Q is a group represented by Q1.

[ mode 52] A compound according to mode 24, wherein Q is a group represented by Q1.

[ mode 53] A compound according to mode 25, wherein Q is a group represented by Q1.

[ mode 54] A compound according to mode 26, wherein Q is a group represented by Q1.

[ mode 55] A compound according to mode 1, wherein Q is a group represented by Q2.

[ mode 56] A compound according to mode 2, wherein Q is a group represented by Q2.

[ mode 57] A compound according to mode 3, wherein Q is a group represented by Q2.

[ mode 58] A compound according to mode 4, wherein Q is a group represented by Q2.

[ mode 59] A compound according to mode 5, wherein Q is a group represented by Q2.

[ mode 60] A compound according to mode 6, wherein Q is a group represented by Q2.

[ mode 61] A compound according to mode 7, wherein Q is a group represented by Q2.

[ mode 62] A compound according to mode 8, wherein Q is a group represented by Q2.

[ mode 63] A compound according to mode 9, wherein Q is a group represented by Q2.

[ mode 64] A compound according to mode 10, wherein Q is a group represented by Q2.

[ mode 65] A compound according to mode 11, wherein Q is a group represented by Q2.

[ mode 66] A compound according to mode 12, wherein Q is a group represented by Q2.

[ mode 67] A compound according to mode 13, wherein Q is a group represented by Q2.

[ mode 68] A compound according to mode 14, wherein Q is a group represented by Q2.

[ mode 69] A compound according to mode 15, wherein Q is a group represented by Q2.

[ mode 70] A compound according to mode 16, wherein Q is a group represented by Q2.

[ mode 71] A compound according to mode 17, wherein Q is a group represented by Q2.

[ mode 72] A compound according to mode 18, wherein Q is a group represented by Q2.

[ mode 73] A compound according to mode 19, wherein Q is a group represented by Q2.

[ mode 74] A compound according to mode 20, wherein Q is a group represented by Q2.

[ mode 75] A compound according to mode 21, wherein Q is a group represented by Q2.

[ mode 76] A compound according to mode 22, wherein Q is a group represented by Q2.

[ mode 77] A compound according to mode 23, wherein Q is a group represented by Q2.

[ mode 78] A compound according to mode 24, wherein Q is a group represented by Q2.

[ mode 79] A compound according to mode 25, wherein Q is a group represented by Q2.

[ mode 80] A compound according to mode 26, wherein Q is a group represented by Q2.

[ means 81 ]]The compound according to any one of modes 1 to 80 or the compound N of the present invention, wherein R^1aAnd R^1bAre each the same or different and is a C1-C6 alkyl group substituted with 1 or more substituents selected from a halogen atom and a cyano group; or cyclopropyl which may be substituted by 1 or more substituents selected from cyano and halogen atoms, A²Is a nitrogen atom or CH, A⁷Is NR^6g，R^6c、R^6d、R^6eAnd R^6fAre each the same or different and are a halogen atom or a hydrogen atom.

[ means 82]A compound according to mode 81 wherein R^6gIs methyl.

[ means 83]A compound according to mode 81 wherein A⁴Is a nitrogen atom or CR^6d，A⁵Is CR^1b，A⁶Is CR^6f。

[ means 84)]A compound according to mode 82, wherein A⁴Is a nitrogen atom or CR^6d，A⁵Is CR^1b，A⁶Is CR^6f。

[ means 85 ]]The compound according to any one of modes 1 to 80 or the compound N of the present invention, wherein R^1aAnd R^1bC1-C6 alkyl groups which are the same or different and are substituted with 1 or more substituents selected from a halogen atom and a cyano group, respectively; or cyclopropyl which may be substituted by 1 or more substituents selected from cyano and halogen atoms, A²Is a nitrogen atom, A⁷Is NR^6g，R^6c、R^6d、R^6eAnd R^6fAre each the same or different and are a halogen atom or a hydrogen atom.

[ means 86]A compound according to mode 85, wherein R^6gIs methyl.

[ means 87]The compound according to any one of modes 1 to 80 or the compound N of the present invention, wherein R^1aAnd R^1bAre each identical or different and are C1-C3 fluoroalkyl, A²Is a nitrogen atom or CH, A⁷Is NR^6g，R^6c、R^6d、R^6eAnd R^6fIs a hydrogen atom and Z is an oxygen atom.

[ means 88]A compound according to mode 87 wherein R^6gIs methyl.

[ means 89 ]]A compound according to mode 87 wherein A⁴Is a nitrogen atom or CR^6d，A⁵Is CR^1b，A⁶Is CR ^6f。

[ means 90 ]]A compound according to mode 88, wherein A⁴Is a nitrogen atom or CR^6d，A⁵Is CR^1b，A⁶Is CR^6f。

[ means 91 ]]The compound according to any one of modes 1 to 80 or the compound N of the present invention, wherein R^1aAnd R^1bAre each identical or different and are C1-C3 fluoroalkyl, A²Is a nitrogen atom or CH, A⁴Is a nitrogen atom or CR^6d，A⁵Is CR^1b，A⁶Is CR^6f，A⁷Is NR^6g，R^6c、R^6d、R^6eAnd R^6fIs a hydrogen atom and Z is an oxygen atom.

[ means 92)]A compound according to mode 91, wherein R^6gIs methyl.

[ means 93 ]]The compound according to any one of modes 1 to 80 or the compound N of the present invention, wherein R^1aAnd R^1bAre each identical or different and are C1-C3 fluoroalkyl, A²Is a nitrogen atom, A⁷Is NCH₃，R^6c、R^6d、R^6eAnd R^6fIs a hydrogen atom and Z is an oxygen atom.

[ means 94]A compound according to mode 93 wherein A³And A⁴Is a nitrogen atom, A⁵Is CR^1b，A⁶Is CH.

[ means 95 ]]A compound according to mode 93 wherein A³Is a nitrogen atom, A⁵Is CR^1b，A⁴And A⁶Is CH.

[ means 96]A compound according to mode 93 wherein A⁴Is a nitrogen atom, A⁵Is CR^1b，A³And A⁶Is CH.

[ means 97 ]]A compound according to mode 93 wherein A⁵Is CR^1b，A³、A⁴And A⁶Is CH.

[ means A1]Compounds of the invention N is R²Is ethyl, G¹And G⁴Is CH, G²Is CR^3b、G³Is CR^3c、R^3bAnd R^3cRespectively the same OR different and is a C1-C3 chain hydrocarbon group which may be substituted by 1 OR more halogen atoms, a cyclopropyl group, a phenyl group which may be substituted by 1 OR more halogen atoms, OR ¹²A halogen atom or a hydrogen atom, R¹²Is a C1-C3 alkyl group which may be substituted by 1 or more halogen atoms or a hydrogen atom, Z is an oxygen atom, A is⁶Is CH, R^1aAnd R^1bRespectively identical or different and is C1-C3 alkyl substituted by more than 1 halogen atom or SR⁸，R⁸Is a C1-C3 alkyl group substituted with 1 or more halogen atoms.

[ mode A2] A compound according to mode A1, wherein n is 2 and Q is a group represented by Q1.

[ mode A3] A compound according to mode A1, wherein n is 2 and Q is a group represented by Q2.

[ means A4]A compound according to mode A2, wherein A²Is a nitrogen atom, A³And A⁶Is CH.

[ means A5]A compound according to mode A4, wherein A⁴Is a nitrogen atom or CH, A⁵Is CR^1b。

[ means A6]According toCompounds of mode A1 to A5, wherein R^1a、R^1bAnd R⁸Is trifluoromethyl.

[ means A7]The compound according to any one of modes A1 to A5, wherein R is¹²Is C1-C3 alkyl.

[ means A8]A compound according to mode A7, wherein R^1a、R^1bAnd R⁸Is trifluoromethyl.

[ means A9]A compound according to mode A3, wherein A³Is a nitrogen atom, A⁷Is NCH₃，A⁴Is CH, A⁵Is CR^1b。

[ means A10]A compound according to mode A9, wherein R^1bIs trifluoromethyl.

[ means A11]A compound according to mode A10, wherein R ¹²Is C1-C3 alkyl.

Next, a method for producing the compound of the present invention will be described.

Production method 1

The compound represented by the formula (I-b) (hereinafter, referred to as the compound (I-b)) or the compound represented by the formula (I-c) (hereinafter, referred to as the compound (I-c)) can be produced by reacting the compound represented by the formula (I-a) (hereinafter, referred to as the compound (I-a)) with an oxidizing agent.

[ in the formula, the symbols represent the same meanings as described above. ]

First, a method for producing compound (I-b) from compound (I-a) is described.

The reaction is usually carried out in a solvent. Examples of the solvent include halogenated hydrocarbons (hereinafter, referred to as halogenated hydrocarbons) such as dichloromethane and chloroform; nitriles such as acetonitrile (hereinafter referred to as "nitriles"); alcohols such as methanol and ethanol (hereinafter referred to as alcohols); acetic acid; water; and mixtures of 2 or more thereof.

Examples of the oxidizing agent include sodium periodate, m-chloroperoxybenzoic acid (hereinafter, referred to as mCPBA), and hydrogen peroxide.

When hydrogen peroxide is used as the oxidizing agent, a base or a catalyst may be used as needed.

Sodium carbonate may be mentioned as the base. When a base is used in the reaction, the base is usually used in a proportion of 0.01 to 1 mol based on 1 mol of the compound (I-a).

As the catalyst, for example, tungstic acid and sodium tungstate can be cited. When a catalyst is used in the reaction, the catalyst is usually used in an amount of 0.01 to 0.5 mol based on 1 mol of the compound (I-a).

In the reaction, the oxidizing agent is usually used in a proportion of 1 to 1.2 mol based on 1 mol of the compound (I-a).

The reaction temperature is usually in the range of-20 to 80 ℃. The reaction time is usually in the range of 0.1 to 12 hours.

After completion of the reaction, water is added to the reaction mixture, extraction is performed with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (e.g., sodium sulfite, sodium thiosulfate) and an aqueous solution of a base (e.g., sodium hydrogencarbonate) as necessary, whereby the compound (I-b) can be obtained.

Next, a process for producing compound (I-c) from compound (I-b) will be described.

The reaction is usually carried out in a solvent. Examples of the solvent include halogenated hydrocarbons, nitriles, alcohols, acetic acid, water, and a mixture of 2 or more of these.

Examples of the oxidizing agent include mCPBA and hydrogen peroxide.

When hydrogen peroxide is used as the oxidizing agent, a base or a catalyst may be used as needed.

Sodium carbonate may be mentioned as the base. When a base is used in the reaction, the base is usually used in a proportion of 0.01 to 1 mol based on 1 mol of the compound (I-b).

As the catalyst, for example, sodium tungstate is exemplified. When a catalyst is used in the reaction, the catalyst is usually used in an amount of 0.01 to 0.5 mol based on 1 mol of the compound (I-b).

In the reaction, the oxidizing agent is usually used in a proportion of 1 to 2 moles based on 1 mole of the compound (I-b).

The reaction temperature is usually in the range of-20 to 120 ℃. The reaction time is usually in the range of 0.1 to 12 hours.

After completion of the reaction, water is added to the reaction mixture, extraction is performed with an organic solvent, and the organic layer is washed with an aqueous solution of a reducing agent (e.g., sodium sulfite, sodium thiosulfate) and an aqueous solution of a base (e.g., sodium hydrogencarbonate) as necessary. The organic layer was dried and concentrated to obtain compound (I-c).

Further, the compound (I-c) can be produced by reacting the compound (I-a) with an oxidizing agent in a one-step reaction (one-pot method).

The reaction is usually carried out by a method for producing the compound (I-c) from the compound (I-b) using an oxidizing agent in a proportion of 2 to 5 moles relative to 1 mole of the compound (I-a).

Production method 2

The compound represented by the formula (II-1S) (hereinafter, referred to as the compound (II-1S)) can be produced by reacting the compound represented by the formula (II-1O) (hereinafter, referred to as the compound (II-1O)) with a sulfurizing agent.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction is carried out in a solvent or in the absence of a solvent. Examples of the solvent include ethers such as tetrahydrofuran and methyl t-butyl ether (hereinafter, referred to as ethers); halogenated hydrocarbons; aromatic hydrocarbons (hereinafter, referred to as aromatic hydrocarbons) such as toluene and xylene; nitriles; nitrogen-containing aromatic compounds such as pyridine, picoline, lutidine and quinoline; and mixtures of 2 or more thereof.

Examples of the vulcanizing agent include diphosphorus pentasulfide, Lawson's reagent (2, 4-bis (4-methoxyphenyl) -1, 3-dithia-2, 4-diphosphetane-2, 4-disulfide), and the like.

In the reaction, the sulfiding agent is usually used in a proportion of 1 to 3 moles based on 1 mole of the compound (II-1O).

The reaction temperature is usually in the range of 0 ℃ to 200 ℃. The reaction time is usually in the range of 1 to 24 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby the compound (II-1S) can be obtained.

Production method 3

The compound represented by the formula (II-2S) (hereinafter referred to as the compound (II-2S)) can be produced by reacting a compound represented by the formula (II-2O) (hereinafter referred to as the compound (II-2O)) with a sulfurizing agent.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction can be carried out according to production method 2.

Production method 4

The compound (II-1O) can be produced by reacting a compound represented by the formula (M-1) (hereinafter, referred to as the compound (M-1)) with a compound represented by the formula (M-2) (hereinafter, referred to as the compound (M-2)) in the presence of a base.

[ in the formula, X^bRepresents a leaving group such as a fluorine atom, a chlorine atom, a bromine atom, an iodine atom or the like, and the other symbols represent the same meanings as described above.]

The reaction is usually carried out in a solvent. Examples of the solvent include ethers; aromatic hydrocarbons; nitriles; aprotic polar solvents (hereinafter referred to as aprotic polar solvents) such as dimethylformamide (hereinafter referred to as DMF), N-methylpyrrolidone (hereinafter referred to as NMP), and dimethylsulfoxide (hereinafter referred to as DMSO); and mixtures of 2 or more thereof.

Examples of the base include organic bases (hereinafter, referred to as organic bases) such as triethylamine, diisopropylethylamine, pyridine, and 4- (dimethylamino) pyridine; alkali metal carbonates such as sodium carbonate and potassium carbonate (hereinafter referred to as alkali metal carbonates); and alkali metal hydrides such as sodium hydride (hereinafter, referred to as alkali metal hydrides).

The reaction may be carried out using a metal catalyst as required. Examples of the metal catalyst include copper catalysts such as copper (I) iodide, copper (I) bromide, copper (I) chloride, copper (I) oxide, copper (I) trifluoromethanesulfonate, copper (I) tetraacetonitrile hexafluorophosphate, and copper (I) 2-thiophenecarboxylate; nickel catalysts such as bis (cyclooctadiene) nickel (0) and nickel chloride (II); palladium (II) acetate, tetrakis (triphenylphosphine) palladium (0), tris (dibenzylideneacetone) dipalladium (II) and the like. When the metal catalyst is used in the reaction, the metal catalyst is usually used in a proportion of 0.01 to 0.5 mol based on 1 mol of the compound (M-1).

The reaction can also be carried out using a ligand as required. Examples of the ligand include triphenylphosphine, 4, 5-bis (diphenylphosphino) -9, 9-dimethylxanthene (hereinafter, referred to as Xantphos), 2 ' -bis (diphenylphosphino) -1, 1 ' -binaphthyl, 1 ' -bis (diphenylphosphino) ferrocene, 2-dicyclohexylphosphino-2 ', 4 ', 6 ' -triisopropylbiphenyl, 2-dicyclohexylphosphino-2 ', 6 ' -dimethoxybiphenyl, 1, 2-bis (diphenylphosphino) ethane, 2 ' -bipyridine, 2-aminoethanol, 8-hydroxyquinoline, 1, 10-phenanthroline, trans-1, 2-cyclohexanediamine, trans-N, N ' -dimethylcyclohexane-1, 2-diamine, N ' -dimethylethylenediamine, and the like. When a ligand is used in the reaction, the ligand is usually used in an amount of 0.01 to 0.5 mol based on 1 mol of the compound (M-1).

In the reaction, the compound (M-2) is usually used in an amount of 0.8 to 1.2 mol and the base is usually used in an amount of 1 to 3 mol based on 1 mol of the compound (M-1).

The reaction temperature is usually in the range of-20 ℃ to 150 ℃. The reaction time is usually in the range of 0.5 to 24 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby the compound (II-1O) can be obtained.

Production method 5

The compound (II-2O) can be produced by reacting a compound represented by the formula (M-3) (hereinafter, referred to as the compound (M-3)) with the compound (M-2) in the presence of a base.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction can be carried out according to production method 4 using compound (M-3) in place of compound (M-1).

Production method 6

The compound (II-1O) can be produced by reacting a compound represented by the formula (M-4) (hereinafter, referred to as the compound (M-4)) with a carbonylating agent.

[ in the formula, A⁸Represents NH or CHR^6bThe other symbols represent the same meanings as described above.]

The reaction is carried out in a solvent or in the absence of a solvent. Examples of the solvent include ethers; aromatic hydrocarbons; halogenated hydrocarbons; esters such as ethyl acetate (hereinafter, referred to as esters); nitriles; an aprotic polar solvent; and mixtures of 2 or more thereof.

Examples of the carbonylating agent include 1,1 '-carbonyldiimidazole and 1, 1' -carbonylbis (1,2, 4-triazole).

In the reaction, the carbonylating agent is usually used in a proportion of 1 to 3 moles based on 1 mole of the compound (M-4).

The reaction temperature is usually in the range of 0 to 150 ℃. The reaction time is usually in the range of 0.1 to 24 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby the compound (II-1O) can be obtained.

Production Process 7

The compound represented by the formula (II-3O) (hereinafter referred to as the compound (II-3O)) can be produced by reacting the compound represented by the formula (M-5) (hereinafter referred to as the compound (M-5)) with the compound represented by the formula (M-6) (hereinafter referred to as the compound (M-6)) in the presence of a base.

[ in the formula, R⁵⁰Represents a C1-C6 alkyl group, X^cRepresents a fluorine atom, a chlorine atom or a bromine atom, and the other symbols represent the same meanings as described above.]

The reaction is usually carried out in a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, halogenated hydrocarbons, esters, nitriles, aprotic polar solvents, alcohols, water, and a mixture of 2 or more thereof.

Examples of the base include organic bases, alkali metal carbonates, and alkali metal hydrides.

In the reaction, the compound (M-6) is usually used in an amount of 1 to 2 mol and the base is usually used in an amount of 1 to 5 mol based on 1 mol of the compound (M-5).

The reaction temperature is usually in the range of 0 to 150 ℃. The reaction time is usually in the range of 0.1 to 24 hours.

After the reaction is completed, the compound (II-3O) can be obtained by performing post-treatment operations such as addition of water to the reaction mixture, extraction with an organic solvent, drying of the organic layer, and concentration.

The compound (M-5) is a commercially available compound, or can be produced by a known method.

Production method 8

The compound represented by the formula (II-4O) (hereinafter referred to as the compound (II-4O)) can be produced by reacting the compound represented by the formula (M-7) (hereinafter referred to as the compound (M-7)) with a condensing agent.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction is usually carried out in a solvent or in the absence of a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, halogenated hydrocarbons, esters, nitriles, aprotic polar solvents, and mixtures of 2 or more thereof.

Examples of the condensing agent include a mixture of 2 or more of an azodiester such as triphenylphosphine and diethyl azodicarboxylate.

In the reaction, triphenylphosphine is usually used in an amount of 1 to 5 mol, and an azodiester is usually used in an amount of 1 to 5 mol, based on 1 mol of the compound (M-7).

The reaction temperature is usually in the range of 0 to 150 ℃. The reaction time is usually in the range of 0.1 to 24 hours.

After the reaction is completed, the compound (II-4O) can be obtained by performing post-treatment operations such as addition of water to the reaction mixture, extraction with an organic solvent, drying of the organic layer, and concentration.

Manufacturing method 9

The compound represented by the formula (II-1 n0) (hereinafter referred to as compound (II-1 n0)) can be produced according to the following scheme.

[ in the formula, X^dRepresents a chlorine atom, a bromine atom or an iodine atom, and the other symbols represent the same meanings as described above.]

First, a method for producing a compound represented by the formula (M-9) (hereinafter, referred to as compound (M-9)) is described.

Compound (M-9) can be produced by production method 4 using a compound represented by formula (M-8) (hereinafter, referred to as compound (M-8)) in place of compound (M-2).

Next, a method for producing a compound represented by the formula (M-10) (hereinafter, referred to as compound (M-10)) is described.

Compound (M-10) can be produced by reacting compound (M-9) with a halogenating agent.

The reaction is usually carried out in a solvent. Examples of the solvent include alcohols, nitriles, ethers, aromatic hydrocarbons, aprotic polar solvents, halogenated hydrocarbons, water and a mixture of 2 or more thereof.

Examples of the halogenating agent include chlorine, bromine, iodine, N-chlorosuccinimide, N-bromosuccinimide, N-iodosuccinimide and the like.

In the reaction, the halogenating agent is usually used in a proportion of 1 to 20 mol based on 1 mol of the compound (M-9).

The reaction temperature is usually in the range of-20 ℃ to 200 ℃. The reaction time is usually in the range of 0.1 to 72 hours.

After the reaction is completed, a post-treatment operation such as addition of water to the reaction mixture, extraction with an organic solvent, drying of the organic layer, concentration and the like is carried out, whereby the compound (M-10) can be obtained.

Next, a process for producing compound (II-1 n0) from compound (M-9) will be described.

Compound (II-1 n0) can be produced by reacting compound (M-9), a compound represented by formula (R-1) (hereinafter, referred to as compound (R-1)), and a halogenating agent.

The reaction is usually carried out in a solvent. Examples of the solvent include alcohols, nitriles, ethers, aromatic hydrocarbons, aprotic polar solvents, halogenated hydrocarbons, water and a mixture of 2 or more thereof.

Examples of the halogenating agent include chlorine, bromine, iodine, N-chlorosuccinimide, N-bromosuccinimide, N-iodosuccinimide and the like.

In the reaction, the compound (R-1) is used in an amount of usually 1 to 20 mol and the halogenating agent is used in an amount of usually 1 to 20 mol based on 1 mol of the compound (M-9).

The reaction temperature is usually in the range of-20 ℃ to 200 ℃. The reaction time is usually in the range of 0.1 to 72 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby compound (II-1 n0) can be obtained.

The compound (R-1) is a commercially available compound or can be produced by a known method.

Next, a process for producing compound (II-1 n0) from compound (M-10) will be described.

Compound (II-1 n0) can also be produced by reacting compound (M-10) with compound (R-1) in the presence of a metal catalyst and a base.

The reaction is usually carried out in a solvent. Examples of the solvent include alcohols, nitriles, ethers, aromatic hydrocarbons, aprotic polar solvents, water and a mixture of 2 or more thereof.

Examples of the metal catalyst include palladium catalysts such as tetrakis (triphenylphosphine) palladium (0), 1' -bis (diphenylphosphino) ferrocene dichloropalladium (II), tris (dibenzylideneacetone) dipalladium (0), and palladium (II) acetate; nickel catalysts such as bis (cyclooctadiene) nickel (0) and nickel chloride (II); and copper catalysts such as copper (I) iodide and copper (I) chloride.

Examples of the base include alkali metal hydrides, alkali metal carbonates, and organic bases.

Ligands may also be used in the reaction. Examples of the ligand include triphenylphosphine, xanthphos, 2 ' -bis (diphenylphosphino) -1, 1 ' -binaphthyl, 1 ' -bis (diphenylphosphino) ferrocene, 2-dicyclohexylphosphino-2 ', 4 ', 6 ' -triisopropylbiphenyl, 2-dicyclohexylphosphino-2 ', 6 ' -dimethoxybiphenyl, 1, 2-bis (diphenylphosphino) ethane, 2 ' -bipyridyl, 2-aminoethanol, 8-hydroxyquinoline, and 1, 10-phenanthroline. When a ligand is used in the reaction, the ligand is usually used in an amount of 0.01 to 1 mol based on 1 mol of the compound (M-10).

In the reaction, the compound (R-1) is usually used in an amount of 1 to 20 mol, the metal catalyst is usually used in an amount of 0.01 to 0.5 mol, and the base is usually used in an amount of 0.1 to 5 mol, based on 1 mol of the compound (M-10).

The reaction temperature is usually in the range of-20 ℃ to 200 ℃. The reaction time is usually in the range of 0.1 to 72 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby compound (II-1 n0) can be obtained.

Manufacturing method 10

The compound represented by the formula (II-2 n0) (hereinafter referred to as compound (II-2 n0)) can be produced according to the following scheme.

[ in the formula, the symbols represent the same meanings as described above. ]

The compound represented by formula (M-11) (hereinafter, referred to as compound (M-11)) can be produced by production method 4 using compound (M-3) in place of compound (M-1) and compound (M-8) in place of compound (M-2).

The compound represented by formula (M-12) (hereinafter referred to as compound (M-12)) can be produced by using compound (M-11) in place of compound (M-9) and following the procedure of production method 9 for producing compound (M-10) from compound (M-9).

Compound (II-2 n0) can be produced from compound (M-9) by the method for producing compound (II-1 n0) from compound (M-9) according to production method 9, using compound (M-11) in place of compound (M-9).

Further, compound (II-2 n0) can be produced by the method for producing compound (II-1 n0) from compound (M-10) according to production method 9, using compound (M-12) in place of compound (M-10).

Production method 11

The nitrogen oxide of the compound represented by the formula (I) can be produced by reacting the compound represented by the formula (I) with an oxidizing agent. The reaction can be carried out, for example, according to the method described in production Process 1, U.S. patent application publication No. 2018/0009778, or International publication No. 2016/121970.

The following describes a method for producing the intermediate.

Reference production method 1

The compound represented by the formula (M-1A) (hereinafter, referred to as the compound (M-1A)) and the compound represented by the formula (M-1B) (hereinafter, referred to as the compound (M-1B)) can be produced according to the following schemes.

[ in the formula, the symbols represent the same meanings as described above. ]

The compound represented by the formula (M-14) (hereinafter referred to as the compound (M-14)) can be produced by reacting a compound represented by the formula (M-13) (hereinafter referred to as the compound (M-13)) with hydrazine.

The reaction is usually carried out in a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, nitriles, aprotic polar solvents, alcohols, water, and a mixture of 2 or more thereof.

In the reaction, a base may be used as required. Examples of the base include alkali metal carbonates, alkali metal hydrides, and organic bases. When a base is used in the reaction, the base is usually used in a proportion of 1 to 3 moles based on 1 mole of the compound (M-13).

In the reaction, hydrazine is usually used in a proportion of 1 to 3 moles based on 1 mole of the compound (M-13).

The reaction temperature is usually in the range of 0 ℃ to 150 ℃. The reaction time is usually in the range of 0.5 to 24 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby the compound (M-14) can be obtained.

Compound (M-1A) can be produced by production method 6 using compound (M-14) in place of compound (M-4).

Compound (M-1B) can be produced by production method 6 using compound (M-15) in place of compound (M-4).

The compound (M-13) and the compound (M-15) are commercially available compounds, or can be produced by a known method.

Reference manufacturing method 2

The compound represented by the formula (M-3A) (hereinafter referred to as the compound (M-3A)) can be produced by reacting the compound represented by the formula (M-16) (hereinafter referred to as the compound (M-16)) with the compound represented by the formula (R-2) (hereinafter referred to as the compound (R-2)).

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction is usually carried out in a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, nitriles, aprotic polar solvents, alcohols, water, and a mixture of 2 or more thereof.

In the reaction, a base may be used as required. Examples of the base include alkali metal carbonates, alkali metal hydrides, and organic bases. When a base is used in the reaction, the base is usually used in a proportion of 1 to 3 moles based on 1 mole of the compound (M-16).

In the reaction, the compound (R-2) is usually used in an amount of 1 to 3 moles based on 1 mole of the compound (M-16).

The reaction temperature is usually in the range of 0 ℃ to 150 ℃. The reaction time is usually in the range of 0.5 to 24 hours.

After the reaction is completed, the compound (M-3A) can be obtained by performing post-treatment operations such as addition of water to the reaction mixture, extraction with an organic solvent, drying of the organic layer, and concentration.

The compound (M-16) and the compound (R-2) are commercially available compounds, or can be produced by a known method.

Reference production method 3

The compound represented by the formula (M-3B) (hereinafter referred to as the compound (M-3B)) can be produced by subjecting the compound represented by the formula (M-17) (hereinafter referred to as the compound (M-17)) to intramolecular condensation.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction is usually carried out in a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, halogenated hydrocarbons, esters, nitriles, aprotic polar solvents, water, and a mixture of 2 or more thereof.

Acids or bases may be used in the reaction. Examples of the acid include sulfonic acids such as p-toluenesulfonic acid; carboxylic acids such as acetic acid; and polyphosphoric acid. Examples of the base include organic bases, alkali metal carbonates, and alkali metal hydrides. In the reaction, the acid is usually used in an amount of 0.1 to 2 mol in the case of using an acid and the base is usually used in an amount of 1 to 5 mol in the case of using a base, based on 1 mol of the compound (M-17).

The reaction temperature is usually in the range of 0 to 150 ℃. The reaction time is usually in the range of 0.1 to 24 hours.

After the reaction is completed, the compound (M-3B) can be obtained by performing post-treatment operations such as addition of water to the reaction mixture, extraction with an organic solvent, drying of the organic layer, and concentration.

The compound (M-17) is a commercially available compound or can be produced by a known method.

Reference manufacturing method 4

The compound (M-4) can be produced by reacting a compound represented by the formula (M-18) (hereinafter, referred to as the compound (M-18)) with the compound (M-2).

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction is usually carried out in a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, nitriles, aprotic polar solvents, alcohols, water, and a mixture of 2 or more thereof.

In the reaction, a base may be used as required. Examples of the base include alkali metal carbonates, alkali metal hydrides, and organic bases. When a base is used in the reaction, the base is usually used in a proportion of 1 to 3 moles based on 1 mole of the compound (M-18).

In the reaction, the compound (M-2) is usually used in a proportion of 0.8 to 1.2 mol based on 1 mol of the compound (M-18).

The reaction temperature is usually in the range of 0 ℃ to 150 ℃. The reaction time is usually in the range of 0.5 to 24 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby the compound (M-4) can be obtained.

The compound (M-18) is a commercially available compound or can be produced by a known method.

Reference manufacturing method 5

The compound (M-6) can be produced by reacting the compound (M-2) with the compound (R-2).

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction is usually carried out in a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, nitriles, aprotic polar solvents, alcohols, water, and a mixture of 2 or more thereof.

In the reaction, a base may be used as required. Examples of the base include alkali metal carbonates, alkali metal hydrides, and organic bases. When a base is used in the reaction, the base is usually used in a proportion of 1 to 5 moles based on 1 mole of the compound (M-2).

In the reaction, the compound (R-2) is usually used in a proportion of 1 to 5 moles based on 1 mole of the compound (M-2).

The reaction temperature is usually in the range of 0 ℃ to 150 ℃. The reaction time is usually in the range of 0.5 to 24 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby the compound (M-6) can be obtained.

Reference manufacturing method 6

The compound (M-7) can be produced by reacting a compound represented by the formula (M-19) (hereinafter, referred to as the compound (M-19)) with a compound represented by the formula (M-20) (hereinafter, referred to as the compound (M-20)).

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction can be carried out, for example, by the method described in Tetrahedron Letters,41,2295,2000.

The compound (M-19) is a commercially available compound, or can be produced by a known method.

Reference manufacturing method 7

The compound (M-20) can be produced by reacting the compound (M-2) with hydroxylamine.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction is usually carried out in a solvent. Examples of the solvent include ethers, aromatic hydrocarbons, nitriles, aprotic polar solvents, alcohols, water, and a mixture of 2 or more thereof.

In the reaction, a base may be used as required. Examples of the base include alkali metal carbonates, alkali metal hydrides, and organic bases. When a base is used in the reaction, the base is usually used in a proportion of 1 to 5 moles based on 1 mole of the compound (M-2).

In the reaction, hydroxylamine is usually used in a proportion of 1 to 5 mol based on 1 mol of the compound (M-2).

The reaction temperature is usually in the range of 0 ℃ to 150 ℃. The reaction time is usually in the range of 0.5 to 24 hours.

After the reaction is completed, the reaction mixture is subjected to a post-treatment operation such as addition of water, extraction with an organic solvent, drying of the organic layer, and concentration, whereby the compound (M-20) can be obtained.

Reference manufacturing method 8

The compound represented by the formula (M-2-b) or the compound represented by the formula (M-2-c) can be produced by reacting the compound represented by the formula (M-2-a) with an oxidizing agent, or the compound represented by the formula (M-2-c) can be produced by reacting the compound represented by the formula (M-2-b) with an oxidizing agent.

[ in the formula, the symbols represent the same meanings as described above. ]

These reactions can be carried out based on production method 1.

Reference manufacturing method 9

The compound represented by the formula (M-2-d) (hereinafter, referred to as the compound (M-2-d)) can be produced according to the following scheme.

[ in the formula, R⁵²Represents a hydrogen atom, a methyl group or an ethyl group, X^aRepresents a chlorine atom or a bromine atom, and the other symbols represent the same meanings as described above.]

The compound represented by the formula (M-22) (hereinafter referred to as the compound (M-22)) can be produced by reacting the compound represented by the formula (M-21) (hereinafter referred to as the compound (M-21)) with the compound represented by the formula (R-3) (hereinafter referred to as the compound (R-3)).

The reaction is usually carried out in a solvent. Examples of the solvent include aromatic hydrocarbons, alcohols, nitriles, and a mixture of 2 or more of these.

In the reaction, the compound (M-21) is usually used in an amount of 1 to 10 moles based on 1 mole of the compound (R-3).

The reaction temperature is usually in the range of 0 ℃ to 200 ℃. The reaction time is usually in the range of 0.1 to 48 times.

After the reaction is completed, the compound (M-22) can be obtained by performing a usual post-treatment operation.

The compound (R-3) and the compound (M-21) are commercially available compounds, or can be produced by a known method.

The compound represented by the formula (M-23) (hereinafter referred to as the compound (M-23)) can be produced by reacting the compound (M-22) with the compound represented by the formula (R-4) (hereinafter referred to as the compound (R-4)).

The reaction is usually carried out in a solvent. Examples of the solvent include aromatic hydrocarbons, nitriles, and a mixture of 2 or more of these.

In the reaction, the compound (R-4) is usually used in an amount of 1 to 10 moles based on 1 mole of the compound (M-22).

The reaction temperature is usually in the range of 60 ℃ to 120 ℃. The reaction time is usually in the range of 0.1 to 48 times.

After the reaction is completed, the compound (M-23) can be obtained by performing a usual post-treatment operation.

The compound (R-4) is a commercially available compound, or can be produced by a known method.

The compound represented by formula (M-24) (hereinafter, referred to as compound (M-24)) can be produced by reacting compound (M-23) with N-iodosuccinimide. The reaction can be carried out according to the method for producing the compound (M-10) from the compound (M-9) of production method 9.

Compound (M-2-d) can be produced by reacting compound (M-23) or compound (M-24) with compound (R-1). These reactions can be carried out according to the method for producing compound (II-1 n0) from compound (M-9) or compound (M-10) of production method 9.

Reference manufacturing method 10

The compound represented by the formula (M-2-f) can be produced by reacting a compound represented by the formula (M-2-e) (hereinafter, referred to as the compound (M-2-e)) with silver fluoride in the presence of a metal catalyst.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction can be carried out, for example, according to the method described in Journal of the American Chemical Society,2014,136,3792.

Reference manufacturing method 11

The compound represented by the formula (M-2-g) can be produced by reacting the compound (M-2-e) with sodium iodide in the presence of a metal catalyst.

[ in the formula, the symbols represent the same meanings as described above. ]

The reaction can be carried out, for example, according to the method described in Journal of the American Chemical Society,2002,124,14844.

The compound of the present invention may be used in combination or mixture with 1 or more components (hereinafter, referred to as the present component) selected from the following groups (a), (b), (c) and (d).

The above-mentioned mixing or combination means that the compound of the present invention and the present component are used simultaneously, separately or with a time lag.

When the compound of the present invention is used together with the present component, the compound of the present invention and the present component may be contained in separate preparations or may be contained in 1 preparation.

One aspect of the present invention is a composition containing 1 or more components selected from the group consisting of group (a), group (b), group (c) and group (d), and the compound of the present invention (hereinafter, referred to as composition a).

Group (a) is a compound consisting of an acetylcholinesterase inhibitor (e.g., a carbamate-based insecticide, an organophosphate-based insecticide), a GABA-agonistic chloride channel antagonist (e.g., a phenylpyrazole-based insecticide), a sodium channel modulator (e.g., a pyrethroid-based insecticide), a nicotinic acetylcholine receptor antagonistic modulator (e.g., a neonicotinoid-based insecticide), a nicotinic acetylcholine receptor allosteric modulator, a glutamate-stimulated chloride channel allosteric modulator (e.g., a macrolide-based insecticide), a juvenile hormone analog, a multi-site inhibitor, a chord organ TRPV channel modulator, a mite growth inhibitor, a microbially derived insect intestinal membrane disruptor, a mitochondrial ATP biosynthetic enzyme inhibitor, an oxidative phosphorylation uncoupler, a nicotinic acetylcholine receptor channel blocker (e.g., a nereistoxin-based insecticide), a chitin synthesis inhibitor, Desquamation inhibitors, ecdysone receptor agonists, octopamine receptor agonists, mitochondrial electron transport system complex i.ii.iii.iv inhibitors, voltage-dependent sodium channel blockers, acetyl CoA carboxylase inhibitors, ryanodine receptor modulators (e.g. diamide-based insecticides), chordal organ modulators, microbial insecticides, and other insecticidal, acaricidal and nematicidal active ingredients. These are described in the classification of IRAC-based mechanisms of action.

Group (b) is a group consisting of nucleic acid synthesis inhibitors (e.g., phenylamide-based bactericides, acylamino acid-based bactericides), cell division and cytoskeleton inhibitors (e.g., MBC bactericides), respiration inhibitors (e.g., QoI bactericides, QiI bactericides), amino acid synthesis and protein synthesis inhibitors (e.g., anilinopyridine-based bactericides), signal transduction inhibitors, lipid synthesis and membrane synthesis inhibitors, sterol biosynthesis inhibitors (e.g., DMI bactericides such as the triazole series), cell wall synthesis inhibitors, melanin synthesis inhibitors, plant defense inducers, multi-site contact active bactericides, microbial bactericides, and other bactericidal active ingredients. These are described in the classification based on the mechanism of action of FRAC.

Group (c) is a group of plant growth regulating ingredients comprising mycorrhizal fungi and rhizobia.

The group (d) is a group of repellent ingredients.

Examples of combinations of the present components and the compounds of the present invention are described below. For example, cotton boll-carb (alanycarb) + SX represents a combination of cotton boll-carb (alanycarb) and SX.

The abbreviation of SX indicates 1 compound of the present invention selected from any one of the compound groups SX1 to SX1630 described in examples. The present components described below are all known components, and can be obtained from commercially available preparations or can be produced by known methods. When the component is a microorganism, it can also be obtained from a strain preservation organization. Note that numerals in parentheses denote CAS RNs (registered trademark).

Combinations of the present components of the above group (a) with the compounds of the present invention:

avermectin (abamectin) + SX, acephate (acephate) + SX, acequinocyl (aceponochyl) + SX, acetamiprid) + SX, acetoprolide (aceprolide) + SX, fluthrin (acrinathrin) + SX, acenaparou (acrinophyr) + SX, alfonophyr SX, alfadoxol (afidophyn) + SX, alfurasodium (aflavolatoner) + SX, alanycarb) + SX, aldicarb) + SX, allethrin (allethrin) + SX, alpha-cypermethrin (SX), alpha-thiodan (alpha-endosulfan) + aluminum phosphide (metalphosphine) + SX, alpha-cypermethrin, SX-cypermethrin) + SX, SX-cypermethrin, SX-carbazepine (SX, SX-carbazepine (SX, fenthion) + (SX, guazatine, azathion, triazophos) + (fenthion, triazophos) + (azathion) +, azathion, triazophos) + (SX, azathion) + (SX, and azathion, azathion) + (azathion, and azathion (azathion) + (sodium chloride, and sodium chloride, sodium (sodium chloride) + (sodium, sodium chloride) +,Bendiocarb (benfuracarb) + SX, transfluthrin (benfluthrin) + SX, benfuracarb (bensultap) + SX, bensultap (SX), benzoxate (benzoximate) + SX, Benzpyrimoxan (benzpyrimoxan) + SX, beta-cyfluthrin (beta-cyfluthrin) + SX, beta-cypermethrin (beta-cypermethrin) + SX, bifenazate (bifenazate) + SX, bifenthrin (bifenthrin) + SX, bioallethrin (bioallethrin) + SX, bioresmethrin (bioresmethrin) + SX, bistrifluoromethrin Urea (bistrifluron) + SX, borax (borax) + SX, boric acid (boric acid) + SX, bromoxynil-benzamide (brofenlanilide) + SX, bromopropylate (brozophylate) + SX, hexythiazox (buprofefazine) + SX, chlorfenthiuron (budocarbamimide) + SX, butoxycarb (butoxycarb) + SX, cadusafos) + SX, calcium phosphate (calcei phos) + SX, carbaryl) + SX, carbofuran (SX) + SX, carbothiocarb (carbosulfan) + SX, thiocarb hydrochloride (tep chloride) + (carbonyl chloride) + SX, chlorfenapyr) + (carbonyl chloride) + SX, chlorfenapyr (carbonyl) + SX, chlorfenapyr) + (SX, chlorfenapyr) + (SX, chlorfenapyr) +, SX) + (SX) + (SX, chlorfenapyr) +, SX, chlorfenapyr (SX) + (SX, chlorfenapyr) +, chlorfenapyr, SX) + (SX, chlorfenapyr) +, chlorfenapyr (SX) +, SX) + (SX) +, chlorfenapyr, 4, chlorfenapyr) + (SX, chlorfenapyr (SX) +, SX, chlorfenapyr (SX) + (SX) +, 4, chlorfenapyr) + (SX, chlorfenapyr, 4, chlorfenapyr (SX, chlorfenapyr (SX, chlorfenapyr (SX) + (SX) +, chlorfenapyr, SX) +, 4, chlorfenapyr (SX, chlorfenapyr, 4, SX, 4, chlorfenapyr) +, SX) +, chlorfenapyr) + (SX) +, SX, 4, chlorfenapyr, 4, SX, chlorfenapyr, 4, chlorfenapyr, 4, SX, 4, S) + (SX, chlorfenapyr, 4, SX, S) + (SX, chlorfenapyr SX, S) + (SX, S) + (SX, S) + (SX (SX, S) +, S) + (SX, S) + (SX, tetrachlordiazine (clofentezine) + SX, clothianidin (clothianidin) + SX, concanavalin A) + SX, coumaphos (coumaphos) + SX, cryolite (cryolite) + SX, cyanophos (cycloprophos) + SX, cyantraniliprole (cyantraniliprole) + SX, cycloprothimide (cydoniole) + SX, cycloprothimide (cyromopropron) + SX, cycloprothidin (cyoxprid) + SX, cyenopyramid (cyromazine) + SX, cyfluthrin (cyfluthrin) + SX, cyfluthrin (cyhalothrin) + SX, cyhalothrin (SX), cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin (SX, cyhalothrin, SX, cyhalothrin) + SX, cyhalothrin, SX, cyhalothrin) + SX, cyhalothrin (SX, cyhalothrin, SX, cyhalothrin) + SX, cyhalothrin, SX, cyhalothrin (SX, cyhalothrin, SX, cyhalothrin) + SX, cyhalothrin, SX, cyhalothrin (SX, cyhalothrin (SX, cyhalothrin (SX, diclomethazole + SX, diclomezotiz + SX, dicofol + SX, dicrotophos (dicrotophos) + SX, flutenzine (diflovidazin) + SX, diflubenzuron (diflubenzuron) + SX, permethrin (dimefluthrin) + SX, dimethoate) + SX, methoprene (dimethox) + SX, methoprene (dimethofos) + SX, dipyropropyridaz + SX, dinotefuran (dinotefuran) + SX, disodium octaborate (disodenium octoborate) + SX, disulfoton (disulfox) + SX, DNOC (2-methyl-4, 6-dinitrophenol) + SX, doramectin (doramectin) + SX, doxazotin) + SX, diclofenthion + SX Dried leaves of Dryopteris filix-mas) + SX, emamectin benzoate (emamectin-benzoate) + SX, enynthrin (empenthrin) + SX, endosulfan (endosulfan) + SX, EPN (O-ethyl O- (4-nitrophenyl) phenyl thiophosphate) + SX, epsilon-metofluthrin (epsilon-metofluthrin) + SX, epsilon-cyfluthrin (epsilon-metofluthrin) + SX, S-fenvalerate (esfenvalerate) + SX, ethiofencarb (ethiofencarb) + SX, ethion + ethion nitrile (ethion) + SX, ethoprophos (ethoprophos), ethoprophos (ethoprophos, ether) + extract of dryopterin, extract of SX, thion, S-methoprene, SX) + SX, S-methoprene, SX, S-methoprene, SX, S-, Herba Chenopodii extract (exfracts or complexed blend of Chenopodium ambrosoides) + SX, Artemisia chrysanthemi extract (extract of tanium vulgare) + SX, Urtica dioica extract (extract of Urtica dioica) + SX, Ginkgo biloba mistletoe extract (extract of Viscum album) + SX, famshur (famshur) + SX, fenamiphos (fenamiphos) + SX, fenazaquin (fenazaquin) + SX, fenbutatin oxide (fenbutatin oxide) + SX, fenitrothion (fentrothion) + SX, fenobucarb (fenbucarb) + SX, fenoxycarb (fenxycarb) + SX, fenpropathrin, fenflurazophos (fenflurazone) + SX, fenpyrazofenoxafen) + SX, fenpyrafluthrin (fenpyrazofen) + SX, fenpyraflufen) + SX, fenflurazophos (fenflurazone) + SX, fenflurazone, fenflurazophos (SX, fenflurazocarb, fenflurazone) + SX, fenflurazone, fenflurazocarb SX, fenflurazocarb SX, fenflurazocarb, fenflurazon) + SX, fenflurazon, SX, fenflurazocarb, fenflurazon, fenflurazocarb SX, fenflurazon, fenflurazocarb, SX, fenflurazocarb SX, fenflurazon, fenflurazocarb SX, fenflurazon, fenflurazocarb, fenflurazon, SX, fenflurazon, SX, fenflurazon, SX, fenflurazon, SX, fenflurazon, SX, fenflurazon, Flucythrinate) + SX, fluensulfone (flunsulfone) + SX, trifluorethofenprox (flufenoprox) + SX, flufenoxuron (flufenoxuron) + SX, fipronil (flufiprole) + SX, flumethrin (flumethrin) + SX, flupyradifurone (flupyradifurone) + SX, flupirimin (flupyrronin) + SX, fluralanin (fluralane) + SX, fluvalinate) + SX, flutriallate SX, flutriafol (fluvalinate) + SX, flutriafol (flutriallate) + SX Azole amide (fluxamide) + SX, varroate (formanate) + SX, fosthiazate (fosthiazate) + SX, praethrin (furamethrin) + SX, furacarb (furathiocarb) + SX, gamma-cyhalothrin (gamma-cyhalothrin) + SX, glutamine synthetase-omega/kappa HXTX-Hv1a peptide (GS-omega/kappa TX-Hv1a peptide) + SX benzoxim (halofenprox) + SX, chlorfenapyr (halofenozide) + SX, dexheptafluthrin (heptafluthrin) + SX, heptylphosphos) + SX, hexaflumuron (SX, flufenozide) +, hexythrothizox, beta-acid salt (tacohydrazone of beta-phosphonohydrazone) + SX, beta-acetylthifenthiuron (SX), hexaflumethrin (SX, phosphoethyl acetate) + SX, phosphoethyl salicylate (SX, phosphoethyl acetate) + SX, thiofenapyrethrin (SX, thiofenapyr (SX, thiofenamidopropyl) + SX, thiofenamidothiofenamidopropyl) + SX, oxathifenprox (SX, phosphocarb (SX, thiofenamidothiofenamate) + (SX, phosphocarb (SX, phenacyl) +, phenacyl) and thiofenamidothiofenamidothiofenamidopropyl) + (SX, thifenthifenprox (SX, thifenprox, SX, thifenprox, SX, thifenprox, SX, thifenprox, SX, thifenprox, SX, thifenthifenthifenthifenprox, SX, thifenprox, SX, thifenprox, thifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthiuron (SX, thifenthiuron (SX, S SX, X is differentTriazophos (isoxathion) + SX, ivermectin) + SX, kadethrin (kadethrin) + SX, kappa-tefluthrin (kappa-tefluthrin) + SX, kappa-bifenthrin (kappa-bifenthrin) + SX, alanobitin (kinoprene) + SX, lambda-cyhalothrin (lambda-cyhalothrin) + SX, lepimectin (lepimectin) + SX, lime sulphur (lime sulflur) + SX, lotilanide (lotilaner) + SX, lufenuron) + SX, machine oil (chiroine oil) + SX, malathion (malathion) + SX, triazophos (carfenbathrin) +, methomyl) +, methomylohydrocarb (SX), methomyl (SX, methomyl (SX), methomyl (methomyl) + SX, methomyl (methomyl ) + (SX, methomyl, methomylohmmethyl, methomyl) + (SX, methomyl, methomylohydrocarb) +, SX, methomylohmmethyl (methomylohmmethyl, SX, methomylohmyl) +, methomyl, methomylohol) +, SX, methomylohmethmylohr) +, SX, methomylohr, SX, Methyl bromide (methyl bromide) + SX, metofluthrin (methofluthrin) + SX, metolcarb) + SX, Methoxadone (methoxazone) + SX, mevinphos (mevinphos) + SX, milbemectin) + SX, milbemycin oxime (milbemycin oxime) + SX, and monofluthrin (momflulothrin) + SXPhosphorus monocrotophos (monocrotophos) + SX, moxidectin (moxidectin) + SX, naled) + SX, Melia azedarach oil (neem oil) + SX, nicotine (nicotine) + SX, nicotine-sulfate) + SX, nitenpyram (nitenpyram) + SX, novaluron (novaluron) + SX, noviflumuron (noviflumuron) + SX, quinoa (oil of the society of chemigum ammoniacticum) + SX, omethoate) + SX, oxamyl (oxamate) + SX, oxamyl (oxamyl) + SX, oxazosulfenyl (trade name, ALLESTM) + SX, phosphorus absorbent (oxydemethothion) + SX, methothion (SX, methothion) + SX, methothion (methothion) + SX, methothion) + SX, methothion (phenothion) + SX, methothion) + SX, methothion, methosulfide, Pirimicarb (pirimicarb) + SX, pyrithion (pirimiphos-methyl) + SX, potassium cyanide (potassiumcyanide) + SX, prallethrin (prallethrin) + SX, profenofos (profenofos) + SX, proffluthrin (profluthrin) + SX, propargite (profungite) + SX, pyriproxyfen (propathromazine) + SX, propoxur (proplururon) + SX, propylene glycol alginate (propylene glycol alginate) + SX, prothioconazole) + SX, pyrithion (prothiofos) + SX, pyriproxyfen (pyrithion) + SX, pyrithion (pyridalyl) + SX, pyribenzoxim (SX, pyrithion (pyridalyl) + SX, pyridalyl) + SX, pyridalyl (SX, pyridalyl) + SX, pyridalyl (pyridalyl) + SX, pyridalyl (pyridalyl) + SX, pyridalyl) +, pyridalyl) +, SX, S, pyridalyl, S, SX, S, Ryanodine (ryanodine) + SX, saleanner + SX, selamectin (selamectin) + SX, sigma-cypermethrin (sigma-cypermethrin) + SX, silafluofen (silafluofen) + SX, sodium borate (sodium borate) + SX, sodium metaborate) + SX, spinetoram) + SX, spinosad (spinosad) + SX, spirodiclofen (spirodiclofen) + SX, spiromesifen (spiromesifen) + SX, spiroperimidine + SX, spirotetramat SX) + SX, flubenamide (sulfenamide) + SX, sulfopyrad) + SX, sulfotep (sulfofluramide) + SX, sulflur (sulfur) + SX, sulflur SX (sulflur) Luoride) + SX, tartrazine (tartar emitic) + SX, T-fluvalinate (tau-fluvalinate) + SX, tebufenozide) + SX, tebufenpyrad (tebufenpyrd) + SX, butylpyrimidinophos (tebuformfos) + SX, teflubenzuron (teflubenzuron) + SX, tefluthrin (tefluthrin) + SX, temephos) + SX, terbufos (terbufos) + SX, terpene components extracted from catnip of the extrusions of biochemical reactions, Brandiname: tetrachlorous blend QRD 460) + SX, chlorfenapyr (tetrachlvinphos) + SX, tetradifuron sulfone (tetradifon) + SX, tetramethrin (tetramethrin) + SX, tetradifluthrin (tetracethrin) + SX, cyantraniliprole (tetrachloprole) + SX, theta-cypermethrin (theta-cymethrin) + SX, thiacloprid (thiacloprid) + SX, thiamethoxam (thiocyclam) + SX, thiodicarb (thiodicarb) + SX, thiodicarb (thiofenox) + SX, thiothifenphos (thon) + SX, dimethifenthifenthifenthiuron (thon) + SX, thiodicarb) + SX, thiofenthifenthifenthifenthifenthifenthiuron (SX), thiodicarb) + SX, thifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthiuron (SX, thifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenuron) + SX, thifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenuron (SX) + SX, thifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthifenthi, Aphidicolin (vamidothion) + SX, Quassia amara extract (wood extract of Quassia amara) + SX, XMC (3, 5-dimethylphenyl N-methylcarbamate) + SX, carboximidazol (xylcarb) + SX, zeta-cypermethrin) + SX, zinc phosphide (zinc phosphonide) + SX, N- [ 3-chloro-1- (pyridin-3-yl) -1H-pyrazol-4-yl ]-N-ethyl-3- (3,3, 3-trifluoropropanesulphinyl) propanamide (1477923-37-7) + SX, 4- [ 5- (3, 5-dichlorophenyl) -5- (trifluoromethyl) -4, 5-dihydro-1, 2-Azol-3-yl]-2-methyl-N- (1-oxothiabut-3-yl) benzamide (1241050-20-3) + SX, 3-methoxy-N- (5- { 5- (trifluoromethyl) -5- [ 3- (trifluoromethyl) phenyl]-4, 5-dihydro-1, 2-Oxazol-3-yl } indan-1-yl) propanamide (1118626-57-5) + SX, N- [ 2-bromo-6-chloro-4- (1,1,1,2,3,3, 3-heptafluoropropan-2-yl) phenyl]-3- { ethyl [ (pyridin-4-yl) carbonyl group]Amino } -2-methoxybenzamide (1429513-53-0) + SX, N- [ 2-bromo-6-chloro-4- (1,1,1,2,3,3, 3-heptafluoropropan-2-yl) phenyl]-3- [ ethyl (4-cyanobenzoyl) amino]-2-methoxybenzamide (1609007-65-9) + SX, N- [ 2-bromo-6-difluoromethoxy-4- (1,1,1,2,3,3, 3-heptafluoropropan-2-yl) phenyl]-3- { methyl [ (pyridin-4-yl) carbonyl group]Amino } -2-methoxybenzamide (1630969-78-6) + SX, 1- { 2-fluoro-4-methyl-5- [ (2,2, 2-trifluoroethyl) sulfinyl]Phenyl } -3- (trifluoromethyl) -1H-1, 2, 4-triazol-5-amine (885026-50-6) + SX, protein Cry1Ab (BT crop protein Cry1Ab) + SX for BT crops, protein Cry1Ac (BT crop protein Cry1Ac) + SX for BT crops, protein Cry1Fa (BT crop protein Cry1Fa) + SX for BT crops, protein Cry1A.105(BT crop protein Cry1A.105) + SX, protein Cry2Ab (BT crop protein Cry 2) + SX for BT crops, protein Vip3A (BT crop protein Vip3A) + SX for BT crops, protein A (BT crop protein Cry3 Cry A) Cry3Ab 31 Ab 19, protein BX 3 BX 19/Cry 19) for BT crops, protein Cry 19 BX 11 SX, protein Cry 19 Ab 28 Ab 19 (BT crop protein BX, BT crop protein BX 3, SX 3 BX 3, SX 3 BX 11-28, SX, protein Cry 11 A.31B 11B 0001-11B, BX, SX, BX, Bx, SX, Bx, SX 3, Bx, By 3, Bx, By 3, By 12, Bx, By 12, By 3, Bx, By 3, By 12, By 3, Bx, By 3, By 11, By 12, By 3, By 3, By 3, By, SX, By 3, By 3, By, SX, By 3, SX, By 3, By 3, By, SX, By, SX, By, SX, velvet bean looper nuclear polyhedrosis virus (Anticarsia gemmatalis mNPV) + SX, alfalfa silverleaf looper nuclear polyhedrosis virus (Autographa californica mNPV) + SX, apple cabbage looper granulosis virus V15(Cydia pomonella GV strain V15) + SX, apple cabbage looper granulosis virus V22(Cydia pomonella GV 22) + SX, apple heterospolla pleiothis pomonella granulosis virus (Cryptophyllobia leucotreta GV) + SX, apple heterosporum granulosis virus (Cryptophyllobia leucotreta GV) + SX, masson pine moth cytoplasmic polyhedrosis virus (Dendrolimus puncatus cydopsis virus) + SX, cotton bollworm nuclear polyhedrosis virus BV-0003 strain (Helicographa argea NPV strain BV-3) + SX, Spodoptera nucifera polyhedrosis virus (Helicoverpa zea NPV) + SX, gypsymoth nucleopolyhedrovirus (Lymantria dispar NPV) + SX, cabbage looper nucleopolyhedrovirus (Mamestra brassica NPV) + SX, Pennychia xylostella nucleopolyhedrovirus (Mamestra flagellata NPV) + SX, Pennychia xylostella nucleopolyhedrovirus (Mamestra contugrata NPV) + SX, Pinus nigra nucleopolyhedrovirus (Neodrion abortus NPV) + SX, Pinus piniperi nucleopolyhedrovirus (Neodrio pectinifera NPV) + SX, Pinus piniperus (Neodurospora NPV) + SX, Spodoptera SX, Spodopteria litura heterospodoptera SX, Spodoptera SX, Spodoptera NPV) + SX, Spodoptera Spirovirus (Spodoptera NPV) + SX, Spodoptera SX, Spirovirus (Spodoptera NPV, Spodoptera Spiro SX, Spodoptera Spiro SX, Spodoptera Spiro Spirovirus (Spiro SX, Spodoptera Spiro Spirovirus (Spiro Spodoptera Spiro NPV, Spiro Spodoptera Spiro SX, Spiro Spodoptera Spiro SX, Spiro Spodoptera Spiro SX, Spiro, Arthrobotrys digitata (Arthrobotrys dactyloides) + SX, Bacillus firmus GB-126 strain (Bacillus firmus strain GB-126) + SX, Bacillus firmus I-1582 strain (Bacillus firmus strain I-1582) + SX, Bacillus megaterium (Bacillus megaterium) + 371), Bacillus AQ175 strain (Bacillus sp. strain AQ175) + SX, Bacillus AQ177 strain (Bacillus sp. strain AQ177) + SX, Bacillus aquaticum 178 (Bacillus sp. strain AQ178) + SX, Bacillus sphaericus 2362(Bacillus sphaericus strain 2362) + SX, Bacillus sphaericus AB174us strain (Bacillus sphaericus strain TS 3) + SX, Bacillus sphaericus strain SX 3632, Bacillus sphaericus 3632 strain SX, Bacillus sphaericus 3632, Bacillus sphaericus strain SX, Bacillus strain SX #3, Bacillus sphaericus strain SX #3, Bacillus sphaericus strain SX, Bacillus sphaericus strain SX #3, Bacillus strain SX 3, Bacillus sphaericus strain SX #3, Bacillus sphaericus strain SX #3, Bacillus strain SX #3, Bacillus strain SX 3, Bacillus sphaericus strain SX, Bacillus strain SX #3, Bacillus strain SX # 2, Bacillus sphaericus strain SX # 2, Bacillus strain SX, Bacillus sphaericus strain SX #3, Bacillus sphaericus strain SX # 2, Bacillus strain SX #3, Bacillus strain SX strain Sx strain SX # 2, Bacillus strain SX #3, Bacillus strain SX # 2, Bacillus strain SX # S strain SX # 2, Bacillus strain SX, Bacillus strain Sx strain SX # 2, Bacillus strain SX, Bacillus strain Sx strain, Bacillus thuringiensis subsp.Aizawai strain ABTS-1857 strain (Bacillus thuringiensis subsp.Aizawai strain ABTS-1857) + SX, Bacillus thuringiensis subsp.Aizawai strain AM65-52 strain (Bacillus thuringiensis subsp.Aizawai strain AM65-52) + SX, Bacillus thuringiensis subsp.Aizawai strain GC-91 strain (Bacillus thuringiensis subsp.Aizawai strain GC-91) + SX, and Bacillus thuringiensis subsp.Aizawai strain Serotype H-7 strain (Bacillus thuringiensis subsp.Aizawai strain H-SX) 7) (ii) SX, Bacillus thuringiensis subspecies ABTS351 strain (Bacillus thuringiensis subssp. Kurstaki strain ABTS351) + SX, Bacillus thuringiensis subspecies BMP123 strain (Bacillus thuringiensis subspecies Kurstaki BMP123) + SX, Bacillus thuringiensis subspecies EG234 strain (Bacillus thuringiensis subspecies EG7841) + SX, Bacillus thuringiensis subspecies EVB 7841 strain SX, Bacillus thuringiensis subspecies SKB sp. Kurstaki SP 19 strain (Bacillus thuringiensis subspecies SX) SX, Bacillus thuringiensis subspecies SX H19 strain (Bacillus thuringiensis SX) SX, Bacillus thuringiensis subspecies SX, Bacillus Sucus sp.8531 strain SX + SX, Bacillus thuringiensis SX H3 strain (Bacillus thuringiensis subspecies SX) SX, Bacillus thuringiensis SX 19 strain (Bacillus thuringiensis SX) SX H.85S sp.19 strain, Bacillus thuringiensis SX, Bacillus Sucus sp.85S sp., Bacillus thuringiensis subsp SA-11 strain (Bacillus thuringiensis subsp. Kurstaki strain SA-11) + SX, Bacillus thuringiensis subsp. SA-12 strain (Bacillus thuringiensis subsp. SX SA-12) + SX, Bacillus thuringiensis subsp. T.Tenebriosis strain NB176 (Bacillus thuringiensis subsp. Tenebriosis strain NB176) + SX, Bacillus thuringiensis subsp. Thiensistis MPPL002 strain (Bacillus thuringiensis subsp. Thiensistis SX), Bacillus thuringiensis subsp. SX + SX, Bacillus thuringiensis subsp. SX-12 strain (Bacillus thuringiensis subsp. SX + SX, Bacillus thuringiensis subsp. SX, Bacillus thuringiensis SX, Bacillus thuringiensis subsp. SX, SX 24, Bacillus thuringiensis subsp. Suaedius, SX, Bacillus thuringiensis subsp. Suaedius, SX.sp. sp. sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp.sp., Bacillus thuringiensis var. israelensis strain BMP144) + SX, Bacillus thuringiensis serotype H-14 strain (Bacillus thuringiensis var. israelensis serotype H-14) + SX, and Bacillus thuringiensis var. japonensis strain s strain buibiui) + SX, Bacillus thuringiensis variant M-7 strain (Bacillus thuringiensis var. san diego strain M-7) + SX, Bacillus thuringiensis variant 7216 strain (Bacillus thuringiensis var.7216) + SX, Bacillus thuringiensis var. aestivi) + SX, Bacillus thuringiensis variant (Bacillus thuringiensis var. aestivi) + SX, Bacillus thuringiensis T36 strain (Bacillus thuringiensis var. T36) + SX, Bacillus sphaericus ANT 03 strain (Beauveria bassiana strain ANT-03) + SX, Beauveria bassiana ATCC74040 strain (Beaubayania bassiana strain ATCC74040) + SX, Bacillus sphaericus strain SX, Beauveria bassiana strain (Beauveria) SX-12) + SX, Beauveria SX, Beaubergenia bassiana ATCC 7432, Bacillus sphaericus strain (Beaubergiana) 4, SX-SX, SX-K # 11, B strain (Beaubergenia bassiana, B bergenia bassiana) +, The strains Mortierella Minnesiensis (Hirsutella Minnesotensis) + SX, Hirsutella rossica (Hirsutella rhodosiliensis) + SX, Mucor tsugakii (Hirsutella thomsonii) + SX, Streptomyces giganteus (Lagenidium giganteum) + SX, Verticillium lecanii strain KV01 (Lecanicillium lecanii straim KV01) + SX, Verticillium lecanii DAOM198499 conidium (Lecanicillium lecanii conium SX) SX, Verticillium lecanii strain DAOM198499 SX, Verticillium lecanii strain SX, Verticillium SX 216596, Methylopsis SX, Plasmodium lecanii strain SX, Plasmodium chrysosporium SX strain SX, Methylophilum chrysosporium SX, Methylophilum SX strain SX, Methylophilum chrysosporium SX, Methylophilus SX SX, Methylophilus Sphaeformis SX 3976, Methylophilus Sp strain SX 52 (Methylophilus SpA 39251, Methylophilus SpA Sp, SpA Sp, Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA Sp SpA, Paecilomyces tenuipes strain T1 (Paecilomyces tenuipes strain T1) + SX, Paenibacillus japonicus (Paenibacillus popilliae) + SX, Pasteurella sp Pn1 strain (Pasteuria nishizawa strain Pn1) + SX, Pasteurella invaginalis SX, Pasteurella multocida SX, Pasteurella usgae) + SX, Pesteurella thoynei + SX, and Serratia entomophila (Serratia entomomo) phila) + SX, Verticillium chlamydosporium (Verticillium chlamydosporium) + SX, Verticillium lecanii strain NCIM1312) + SX.

Combinations of the present components of the above group (b) with the compounds of the present invention:

the compound is prepared from the components of acid benzene-S-methyl (acetylsalicylic-S-methyl) + SX, aldimorph + SX, ametoctradin (ametoctradin) + SX, aminopyrifen + SX, amizopyr (SX), amisulbrom (amisulbactam) + SX, dichlofluanid (anilazine) + SX, azaconazole (azaconazol) + SX, azoxystrobin (azoxystrobin) + SX, basic copper sulfate (basic coppersulfate) + SX, benalaxyl (benalaxyl-M) + SX, benalaxyl (benodanil) + SX, benoxanid SX, benomyl) + SX, benoxanil, fenthifenthizamide (phenyl) + SX, fenpyrad (fenpyrazamide) + SX, fenpyrazamide) + -S, fenpyrazamide) + (bromarozole) + SX, brome (SX, bromarozole) + SX, brome (SX, fenpyrazamide) + SX, fenpyrazamide (fenpyrazamide) + SX, fenpyrazamide) + -S) + (bromarofen) + SX, fenpyrazamide (brom-S) + SX, fenpyrazamide (bromarofen) + SX, fenpyrazamide (brom SX, fenpyrad) + SX, fenpyrazamide (brom SX, fenpyrad, fenpyrazamide SX, fenpyrazamide (bromarol) + SX, fenpyrazamide) + SX, fenpyrad (brom SX, fenpyrad (bromarol) + -S) + SX, fenpyrad (brom SX, fenpyrad) + SX, fenpyrad, fenpyr SX, fenpyrad (brom SX, fenpyr SX, fenpyr-S) + SX, fenpyr-S) + SX, fenpyr SX, bromuconazole (bromouconazole) + SX bupirimate (bupirimate) + SX, captan (captafol) + SX, captan (captan) + SX, carbendazim (carbendazim) + SX, carboxin (carboxin) + SX, cyprodinamide (carpropamid) + SX, chlorfenapyr (chinomethionat) + SX, chitin) + SX, chlorotoluene (chloroneb) + SX, chlorothalonil (chlorothalonil) + SX, ethyclidine) + SX, clethochlochlorrin B + SX, copper (II) acetate) + SX, copper (II) hydroxide (chloride) hydrate, cycobalamin (chloride) + SX, cyazoxanamide (SX), cyazoamide (SX, cyazomethicillin) + (SX, cyazofamide (SX) +, cyazoxanamide (SX, cyazofamide) +, cyazoxanamide (SX, cyazoxanamide) +, cyazoxanamide (SX, cyazoamide (SX, cyazoxanamide) + SX, cyazomethicilli (SX, cyazomethine) +, cyazomethicillin (SX, cyazomethine) +, SX, cyazomethicillin (SX, cyazomethine (SX, cyazomethicillin) +, SX, cyazomethicillin (SX, cyazomethicillin) + (cyazomethine) + (SX, cyazomethicillin (cyazomethicillin) + (cyazomethicillin, SX, cyazomethicillin (cyazomethicillin, SX, cyazomethicillin (cyazomethicillin, SX, Pyridazone (dimethomozine) + SX, niclosamide (dicloran) + SX, diethofencarb (diethofencarb) + SX, difenoconazole (difenoconazole) + SX, diflumetorim (diflumetorim) + SX, dimethachlone (dimethaclone) + SX, dimethiophenol (dimethiol) + SX, dimethomorph (dimethomorph) ) + SX, dimoxystrobin (dimoxcarbazone) + SX, diniconazole (diniconazole) + SX, diniconazole M (diniconazole-M) + SX, dinocap (dinocap) + SX, dipotassium hydrogen phosphite (dipotassium hydrogen phosphate) + SX, dipyrromethenon + SX, dithianon (dithianon) + SX, diethylenetriamine copper complex (II) (doxycyanotonic acid bisstyryl ether copolymer (II) salt) + SX, dodemorph SX, dodemodin (doxorhexyne) + SX, doxorzine (SX), dicofoxadifenon + SX, dicoform SX, doxazoxystrobin, doxazone extract (SX), doxazosin + SX, doxazoxystrobin + SX, doxazosin + SX, doxazoxystrobin + SX, doxazosin + SX, doxazoxystrobin + SX, doxazophos extract (SX, doxazoxystrobin) +, doxazoxystrobin + SX, doxazon + SX, doxazophos extract (SX, doxazoxystrobin + SX, doxazon extract (SX, doxazophos extract (SX, doxazoxystrobin + SX, doxazon extract (SX, doxazophos extract (SX, doxazoxystrobin + SX, doxazon extract (SX, doxazon + SX, doxazophos extract (SX, doxazoxystrobin + SX, doxazophos extract (SX, doxazon + SX, doxazoxystrobin + SX, doxazocarb extract (SX, doxazoxystrobin + SX, doxazocarb extract (SX, doxazon extract (SX, doxazoxystrobin + SX, doxazon + SX, doxazocarb extract (SX, doxazoxystrobin + SX, doxazocarb extract (SX, doxazon extract (SX, doxazocarb extract (SX, doxazon + SX, doxazocarb extract (SX, doxazoxystrobin + SX, doxazon + SX, doxazocarb extract, doxazoxystrobin + SX, doxazocarb extract (SX, doxazoxystrobin + SX, doxazon + SX, doxazocarb extract (SX, doxazon + SX, doxazocarb extract (SX, doxazocarb, doxazo, Herba Equiseti Arvinsis extract (extract of Equisetum arvense) + SX, herba Ecliptae extract (extract of Tropaeolum majus) + SX, and herba Equiseti Arvinsis,Fenpyroxadone (famoxadone) + SX, fenamidone (fenamidone) + SX, fenaminostrobin (fenaminostrobin) + SX, fenarimol (fenarimol) + SX, fenbuconazole (fenbuconazole) + SX, methylflutolamide (fenfuram) + SX, fenhexamid (fenhexamid) + SX, cyanamide (fenoxanil) + SX, fenpiclonil) + SX, fenproxamide + SX, fenpropadine (fenpropidin) + SX, fenpropimorph (fenpropimorph) + SX, fenpyrazone SX, fenpyrazamide (fenpyrazoxazole) SX, fenpyrazamide (fenpyrazamide) + SX, fenpyrazone SX, fenpyraclostrobin (fenpyrazone SX) + SX, fenpyraclostrobin (fenpyraclostrobin) + SX, fenpyraclostrobin (SX), fenpyraclostrobin (fenpyraclostrobin) + (SX, fenflurazone (SX), fenflurazone (fenflurazone) + SX, fenflurazole) + SX, fenflurazone (fenflurazone) + SX, fenflurazofluoride) + SX, fenflurazone (fenflurazone, fenflurazone fluoride, fenflurazone) + SX, fenflurazone fluoride, fenflurazone, SX, fenflurazone fluoride, SX, fenflurazone fluoride, fenflurazone, SX, fenflurazone fluoride, SX, fenflurazone fluoride, SX, fenflurazone fluoride, SX fluoride, SX fluoride, fenflurazone fluoride, SX fluoride, fenflurazofluoride, fenflurazone fluoride, SX, fenflurazofluoride, fenflurazone fluoride, SX, fenflurazofluoride, SX, fenflurazone fluoride, SX, fenflurazofluoride, SX fluoride, fenflurazofluoride, SX, fenflurazone fluoride, SX fluoride, fenflurazone fluoride, fenflurazofluoride, SX fluoride, fenflurazofluoride, fenflurazone, SX fluoride, fenflurazone fluoride, SX fluoride, fenflurazone fluoride, SX, Furbenconazole (fluolimide) + SX, fluoxaprilin + SX, fluoxastrobin) + SX, fluquinconazole (fluquinconazole) + SX, flusilazole (flusilazole) + SX, flusulfamide (fluusulfamide) + SX, fluthiacetonitrile (fluthianil) + SX, flutolanil (flutolanil) + SX, flutriafol (flutriafol) + SX, fluxapyroxad) + SX, folpet) + SX, fosetyl-aluminum + SX, fuberidazole) + SX, furalaxyl (furalaxyl) + SX, furametpyr) + SX, guazatine (guazatine) + SX, hexaconazole (hexaconazole) + SX, fluxapyroxad, fluxad, and mixtures thereof,Morelin (hymexazole) + SX, imazalil (imazalil) + SX, imibenconazole (emidazole) + SX, iminoctadine (iminoctadine) + SX, iminoctadine triacetate (iminoctadine triacetate) + SX, dipyridafluxam + SX, iodopropynyl butylcarbamate (iodocarb) + SX, iprazole (iprazozole) + SX, iprodione (SX), iprodione (iprifluoraflifluoride) + SX, flufenoquin + SX, iprobenfos (iprobenfenfon) + SX, iprodione (iprodione) SX, iprodione (SX), iprodione (iprodione) + SX, iprodione (iprovalicarb) + SX, iprodione (iprodione), iprodione (SX), iprodione (SX, iprodione) + SX, iprodione, SX, iprodione (SX, iprodione, SX, iprodione (SX, iprodione, SX, iprodione) +, SX, iprodione, SX, iprodione, SX, maneb) + SX, flufenoxaprop-p-ethyl (mefenthiflunazole) + SX, mepanipyrim) + SX, mefenoxam (mepanil) + SX, meptyldinocap (meptyldinocap) + SX, metalaxyl-M) + SX, metazol) + SX, metconazole) + SX, sulfocarb (methasulfocarb) + SX, metiram) + SX, metominostrobin (metominostrobin) + SX, metrafenone) + SX, metoclopramide (metofenone) + SX, metoclopramide) +, metoclopramide) + SX, and S, metoclopramide) + SX, mineral oil (minostrobin, metoclopramide) +, SX, metoclopramide) + SX, SX, metoclopramide (SX, metoclopramide) +, metoclopramide) + SX, metoclopramide) +, SX, metoclopramide) +, Oxadixyl (oxadixyl) + SX, fluorothiazolePyrithylone (oxathiapirolin) + SX, oxine-copper + SX,Oxolinic acid (oxolinic acid) + SX,Imidazole (oxpoconazole) + SX,Imidazole fumarate (oxyponazole fumarate) + SX, carboxin (oxyproxacin) + SX, oxytetracycline (oxytetracycline) + SX, pefurazoate (pefurazoate) + SX, penconazole (penconazole) + SX, pencycuron (pencycuron) + SX, fluxafen (penflufen) + SX, penthiopyrad (penthiopyrad) + SX, phenalene (phenamacacril) + SX, phosphorous acid (phoruousacid) + SX, phthalide (phtalamide) + SX, fenthizamide (picarb) SX, picoxystrobin (picoxystrobin) + SX, fludioxonil (piperazox) + SX, pyridalyl SX, propineb (propamocarb) + SX, propamocarb (SX), prophosphocarb (SX), propamocarb (SX, propamocarb) + SX, propamocarb SX, prophyrdoxyccarb (SX, prophyroxide) + SX, prophyroxide, prophyr, Prothioconazole (prothioconazole) + SX, pyrazoylhydroxylamine (pyraflutolofen) + SX, pyraclostrobin (pyraclostrobin) + SX, pyrazoxamethyl (pyraoxystrobin) + SX, pyrapropofol + SX, pyrafluumid + SX, pyrazofos (pyrazophos) + SX, pyribenzocarb (pyribencarb) + SX, pyridachlorometyl + SX, pyribenzoxim (pyrifenox) + SX, pyribenzoxim, and quindox, quizaquin (pyribenzoxim) +, quizaquin) SX, quizaquin, quindox, and quindox (e) +, quindox, and quindox, e, quindox, and quindox, e, or quindox, e, or quindox, e, or quindox, or a oa) + SX, sedaxane (sedaxane) + SX, silthiofam (silthiofam) + SX, simeconazole (simeconazole) + SX, sodium bicarbonate (sodiumhydrogencarbonate) + SX spiroxamine (spiroxamine) + SX, streptomycin (streptomycin) + SX, sulfur (sulfurfur) + SX, tebuconazole) + SX, tebuflozoline (tebuflozoline) + SX, tebufenpyrad (tebufenpyrad) + SX, tetrachlornitrobenzene) + SX, terbinafine (terbinafine) + SX, tetraconazole) + (tetraconazole) + SX, thiabendazole(s) +), thiabendazole (thiobendazole) + SX, thifluzamide (SX, sedaxamide) + (SX, S-tolfenthiuramide) + SX, S-methyl-methiocarb) +, S-S, S-S, Triadimenol (triadiminol) + SX, imidazoxazine (triazoxide) + SX, triclopyricarb (triclopyr) + SX, tricyclazole (tricyclazole) + SX, tridemorph (tridemorph) + SX, trifloxystrobin (trifloxystrobin) + SX, triflumizole) + SX, triforidine (triforine) + SX, triticonazole (tritizolium) + SX, validamycin (validamycin) + SX, validamide (valifenalate) + SX, ethephrilene (vinclozolin) + SX, wasabine (bellamur SX), yellow mustard powder (bellamustard potder) + SX, zinc thiazole) + SX, zineb (zinoamide) + SX, fenhexamide (SX), fenhexamide) + SX, fenhexamide (SX, fenhexamide) + SX, fenhexamine (SX, fenhexamine) + SX, fenhexamine (4-methyl phenyl-4-) (4) (+) SX) ]-1,2, 4-thiadiazol-5-yl } oxy) -2, 5-dimethylphenyl]-N-ethyl-N-methylmethanesulfonamide (1202781-91-6) + SX, 4- (2-bromo-4-fluorophenyl) -N- (2-chloro-6-fluorophenyl) -1, 3-dimethyl-1H-pyrazol-5-amine (1362477-26-6) + SX, 2- [ 6- (3-fluoro-4-methoxyphenyl) -5-methylpyridin-2-yl]Quinazoline (1257056-97-5) + SX, 5-fluoro-2- [ (4-methylphenyl) methoxy]-4-pyrimidineamine (1174376-25-0) + SX, 5-fluoro-4-imino-3-methyl-1-tosyl-3, 4-dihydropyrimidin-2 (1H) -one (1616664-98-2) + SX, N '- (2, 5-dimethyl-4-phenoxyphenyl) -N-ethyl-N-methylmethanimidamide (1052688-31-9) + SX, N' - { 4- [ (4, 5-dichlorothiazol-2-yl) oxy]-2, 5-dimethylphenyl } -N-Ethyl-N-methylformamidinimide (929908-57-6) + SX, ethyl (2Z) -3-amino-2-cyano-3-phenylacrylate (39491-78-6) + SX, N- [ (2-chlorothiazol-5-yl) methyl]-N-ethyl-6-methoxy-3-nitropyridin-2-amine (1446247-98-8) + SX, 5- (4-chlorobenzyl) -2-chloromethyl-2-methyl-1- (1H-1,2, 4-triazol-1-ylmethyl) cyclopent-1-ol (1394057-11-4) + SX, (1R,2S,5S) -5- (4-chlorobenzyl) -2-chloromethyl-2-methyl-1- (1H-1,2, 4-triazol-1-ylmethyl) cyclopent-1-ol (1801930-06-2) + SX, (1S,2R,5R) -5- (4-chlorobenzyl) -2-chloromethyl-2-methyl-1- (1H-1,2, 4-triazol-1-ylmethyl) cyclopent-1-ol (1801930-07-3) + SX, 2-chloromethyl-5- (4-fluorobenzyl) -2-methyl-1- (1H-1-ylmethyl) cyclopent-1-ol (1801930-07-3) + SX, 2, 4-triazol-1-ylmethyl) cyclopentanol (1394057-13-6) + SX, (1R,2S,5S) -2- (chloromethyl) -5- (4-fluorobenzyl) -2-methyl-1- (1H-1,2, 4-triazol-1-ylmethyl) cyclopent-1-ol (1801930-08-4) + SX, (1S,2R,5R) -2-chloromethyl-5- (4-fluorobenzyl) -2-methyl-1- (1H-1,2, 4-triazol-1-ylmethyl) cyclopent-1-ol (1801930-09-5) + SX, 3- [ (4-chlorophenyl) methyl ]-methyl 2-hydroxy-1-methyl-2- (1H-1, 2, 4-triazol-1-ylmethyl) cyclopentanecarboxylate (1791398-02-1) + SX, ({ 2-methyl-5- [1- (4-methoxy-2-methylphenyl) -1H-pyrazol-3-yl]Phenyl } methyl) carbamic acid methyl ester (1605879-98-8) + SX, 2- (difluoromethyl) -N- [1,1, 3-trimethyl-2, 3-dihydro-1H-inden-4-yl]Pyridine-3-carboxamide (1616239-21-4) + SX, 2- (difluoromethyl) -N- [ 3-ethyl-1, 1-dimethyl-2, 3-dihydro-1H-inden-4-yl]Pyridine-3-carboxamide (1847460-02-9) + SX, 2- (difluoromethyl) -N- [ 3-propyl-1, 1-dimethyl-2, 3-dihydro-1H-inden-4-yl]Pyridine-3-carboxamide (1847460-05-2) + SX, (2E,3Z) -5- { [1- (4-chlorophenyl) -1H-pyrazol-3-yl]Oxy } -2- (methoxyimino) -N, 3-dimethylpent-3-enamide (1445331-27-0) + SX, Agrobacterium radiobacter K1026 strain (Agrobacterium radiobacter strain K1026) + SX, Agrobacterium radiobacter K84 strain (Agrobacterium radiobacter strain K84) + SX, Bacillus amyloliquefaciens (Bacillus amyloliquefaciens strain AT332) + SX, Bacillus amyloliquefaciens B3 strain (Bacillus amyloliquefaciens strain AT332) + SXBacillus strain B3) + SX, Bacillus amyloliquefaciens strain D747(Bacillus amyloliquefaciens strain D747) + SX, Bacillus amyloliquefaciens strain DB101 (Bacillus amyloliquefaciens strain DB101) + SX, Bacillus amyloliquefaciens strain DB102 (Bacillus amyloliquefaciens strain DB102) + SX, Bacillus amyloliquefaciens strain GB03 (Bacillus amyloliquefaciens strain GB03) + SX, Bacillus amyloliquefaciens strain FZB24 (Bacillus amyloliquefaciens strain FZB 64) + SX, Bacillus amyloliquefaciens strain FZB42 (Bacillus amyloliquefaciens strain FZB42) + SX, Bacillus amyloliquefaciens strain IN 7 8693727 strain SX, Bacillus amyloliquefaciens strain SX strain No. 28, Bacillus amyloliquefaciens strain SX strain No. 7) + Bacillus amyloliquefaciens strain SX, Bacillus amyloliquefaciens strain No. SX strain No. 28, Bacillus amyloliquefaciens strain SX, Bacillus amyloliquefaciens strain SZ strain No. 36600, Bacillus amyloliquefaciens strain SX, Bacillus amyloliquefaciens strain No. 3646, Bacillus amyloliquefaciens strain SX, Bacillus amyloliquefaciens strain SX strain No. 36, Bacillus amyloliquefaciens strain SX strain SZ strain SX, Bacillus amyloliquefaciens strain No. 36, Bacillus amyloliquefaciens strain SX strain SZ strain SX strain No. 36, Bacillus amyloliquefaciens strain SX strain SZ strain No. 36, Bacillus amyloliquefaciens strain SX, Bacillus amyloliquefaciens strain No. 36, Bacillus amyloliquefaciens strain SX strain SZ strain No. 8, Bacillus amyloliquefaciens strain SX strain No. 8, Bacillus amyloliquefaciens strain SZ strain No. 8, Bacillus amyloliquefaciens strain No. 36, Bacillus amyloliquefaciens strain SX strain No. 36, Bacillus amyloliquefaciens strain SX, Bacillus amyloliquefaciens strain No. 8, Bacillus amyloliquefaciens strain SX strain No. 36, Bacillus amyloliquefaciens strain No. 8, Bacillus amyloliquefaciens strain SX strain SZ strain SX strain No. 36, Bacillus amyloliquefaciens strain SX strain SZ, Bacillus amyloliquefaciens strain SX strain SZ, Bacillus amyloliquefaciens strain No. 8, Bacillus amyloliquefaciens strain No. 36, Bacillus amyloliquefaciens strain SX strain No. 36, Bacillus amyloliquefaciens strain SX strain No. 36, Bacillus amyloliquefaciens strain No. 3, Bacillus amyloliquefaciens strain No. 36, Bacillus amyloliquefaciens strain SX strain No. 36, Bacillus amyloliquefaciens strain No. 4, Bacillus amyloliquefaciens strain SX strain No., Bacillus licheniformis HB-2 strain (Bacillus licheniformis strain HB-2) + SX, Bacillus licheniformis SB3086 strain (Bacillus licheniformis SB3086) + SX, Bacillus pumilus AQ717 strain (Bacillus pumilus strain AQ717) + SX, Bacillus pumilus BUF-33 strain (Bacillus pumilus strain BUF-33) + SX, Bacillus pumilus GB34 strain (Bacillus pumilus GB34) + SX, Bacillus pumilus QST2808 strain (Bacillus pumilus strain 280T 2808) + SX, Bacillus simplex CGF2856 strain (Bacillus pumilus CGF2856) + SX, Bacillus AQ153 strain (Bacillus subtilis strain) AQ 367, Bacillus subtilis strain (SX 1819) SX, Bacillus subtilis strain (SX 1818) + SX, Bacillus subtilis Strain (SX) SX, Bacillus subtilis strain (SX 1818) + SX, Bacillus subtilis strain (SX B747, Bacillus subtilis strain SX, Bacillus subtilis strain (SX B1818) + SX, Bacillus subtilis strain (SX B747, Bacillus subtilis strain B369B 368) and Bacillus subtilis strain, Bacillus subtilis GB03 strain (Bacillus subtilis strain GB03) + SX, Bacillus subtilis HAI0404 strain (Bacillus subtilis strain HAI0404) + SX, Bacillus subtilis IAB/BS03 strain (Bacillus subtilis strain IAB/BS03) + SX, and Bacillus subtilis MBI600 strain (Bacillus subtilis strain MBI600) Subtilis strain MBI600) + SX, Bacillus subtilis QST30002/AQ30002 strain (Bacillus subtilis strain QST30002/AQ30002) + SX, Bacillus subtilis QST30004/AQ30004 strain (Bacillus subtilis strain QST30004/AQ30004) + SX, Bacillus subtilis T713 strain (Bacillus subtilis strain QST713) + SX, Bacillus subtilis T714 strain (Bacillus subtilis strain QST714) + SX, Bacillus amyloliquefaciens variant FFJ 24 strain (Bacillus subtilis var. Amyloliquefaciens strain FZB24) + SX, Bacillus subtilis strain Y1336 (Bacillus subtilis strain Y6) SX, Candida albicans strain SXSXSXSXbI 14, Bacillus cepharacteria) + (SXSXK strain SXK 3627, Bacillus cepharacteria strain SX 366727, Bacillus cepharacterium, Bacillus cepharacteria strain SX1 strain SXK 3627, Bacillus cep strain SXK 3680, Bacillus cep strain SXhocola (SXb 3680), Bacillus cep 3680, Bacillus cep strain 3680, Candida 3680, Bacillus cep, Candida callosa strain SX 3680, Candida callosa strain (SX 3680, Candida callosa strain 3680, Pseudomonas cep, Chaetomium cupreum) + SX, Sporotrichum roseum (Clinostasys rosea) + SX, Chaetomium cupreum CGMCC8325 strain (Coniothyrium minitans CGMCC8325) + SX, Chaetomium cupreum CON/M/91-8 strain (Coniothyrium minitans CON/M/91-8) + SX, Cryptococcus albidus (Cryptococcus albidus) + SX, Erwinia carotovora CGE234M403 strain (Erwinia carotovora strain CGE234M403) + SX, Fusarium oxysporum Fo47 strain (Fusarium oxysporum strain SX 47) + SX, Polymyces streptoverticillium J1446 strain (Gliocladium vulatum strain SX 1445), Polymyces stickum SX 325, Polymyces SX 325-325 SX, Polymyces polysachrorhium SX 325, Sporotrichum Sp SX 325-325, Polymyces 0105 strain (VRase K325, Polymyces pullulan 325, Polymyces polysachromyces 325, Sp, Pseudomonas chlororaphis strain 63-28 (Pseudomonas chlororaphis strain 63-28) + SX, Pseudomonas chlororaphis strain AFS009 (Pseudomonas chlororaphis strain AFS009) + SX, Pseudomonas chlororaphis strain MA342 (Pseudomonas chlororaphis strain MA342) + SX, Pseudomonas fluorescens strain 1629RS) + SX, Pseudomonas fluorescens strain A506 (Pseudomonas fluorescens strain A506) + SX, Pseudomonas fluorescens strain CL 145A) (Pseudomonas fluorescens strains CL145A) + SX, Pseudomonas fluorescens G7090 strain (Pseudomonas fluorescens strains G7090) + SX, Pseudomonas sp.CAB-02 strain (Pseudomonas sp.strain CAB-02) + SX, Pseudomonas syringae 742RS strain (Pseudomonas syringae strain 742RS) + SX, Pseudomonas syringae MA-4 strain (Pseudomonas syringae strain MA-4) + SX, Pseudomonas floccus PF-A22UL strain (Pseudomonas oligosaccharensis PF-A22UL) + SX, Pseudomonas rosenbergii HAI-0804 strain (Pseudomonas chrysospora strain I-080 108 SX, Streptomyces chrysosporium strain W28 SX, Streptomyces strain Wfungal strain SX 28 SX, Streptomyces strain W28 SX 2 SX, Streptomyces strain Wfungal strain W103 SX 2 SX, Streptomyces strain W28 SX 2 SX, Streptomyces strain Wfungal strain W103 SX 2 SX, Streptomyces strain W103 SX, Streptomyces strain WK 4628 SX, Streptomyces strain W28 SX 2 SX, Streptomyces strain W15 SX, Streptomyces strain W103 SX, Streptomyces strain WK 4628, Streptomyces strain W15 SX, Streptomyces strain WK) + SX, Streptomyces strain W15 SX, Streptomyces strain WK, Streptomyces strain W15 SX, Streptomyces strain WK 2, Streptomyces strain W15 SX, Streptomyces strain WK, Streptomyces strain W15, Streptomyces strain WK 2, Streptomyces strain WK, Streptomyces strain W15, Streptomyces strain W15 strain WK, Streptomyces strain W28, Streptomyces strain WK 2 strain WK, Streptomyces strain WK 2 strain W28, Streptomyces strain WK 2 strain W15 strain W28 strain W15 strain WK, Streptomyces strain W15, Streptomyces strain W15 strain WK, Streptomyces strain W15 strain WK, Streptomyces strain WK 01) + SX, T.flavum V117b strain (Talaromyces flavus strain V117b) + SX, T.aculeatus ICC012 strain (Trichoderma asperellum strain ICC012) + SX, T.aculeatus SKT-1 strain (Trichoderma asperellum SKT-1) + SX, T.aculeatus T25 strain (Trichoderma asperellum strain T25) + SX, T.aculeatus T34 strain (Trichoderma asperellum strain T34) + SX, T.aculeatus TV1 strain (Trichoderma asperellum strain TV1) + SX, T.trichoderma CNCM 1-1237 strain (Trichoderma viride strain Sc 080trichoderma), trichoderma harzianum strain 21 (Trichoderma harzianum strain 21) + SX, Trichoderma harzianum DB104 strain (Trichoderma harzianum strain DB104) + SX, Trichoderma harzianum DSM14944 strain (Trichoderma harzianum strain DSM14944) + SX, Trichoderma harzianum ESALQ-1303 strain (Trichoderma harzianum strain ESALQ-1303) + SX, Trichoderma harzianum ESALQ-1306 strain (Trichoderma harzianum strain ESALQ-1306) + SX, Trichoderma IIHR-Th 2 strain (Trichoderma harzianum strain IIHR HR IIHR HR IIHR HR IIHR HR IIHR Th-2) + SX, Trichoderma harzianum ITEM908 strain (Trichoderma harzianum strain ITEM908) + SX, Trichoderma harzianum Kd strain (Trichoderma harzianum strain kd) + SX, Trichoderma harzianum MO1 strain (Trichoderma harzianum strain MO1) + SX, Trichoderma harzianum SF strain (Trichoderma harzianum strain SF) + SX, Trichoderma harzianum T22 strain (Trichoderma harzianum strain T22) + SX, Trichoderma harzianum T39 strain (Trichoderma harzianum strain T39) + SX, Trichoderma harzianum T78 strain (Trichoderma harzianum strain GL-4523) + Trichoderma harzianum strain SX, Trichoderma harzianum strain GL-4523, Trichoderma harzianum strain SX-T78) + SX, Trichoderma harzianum strain SX, Trichoderma harzianum strain SX-T4523, Trichoderma harzianum strain SX, Trichoderma harzianum strain GL-9 (Trichoderma harzianum strain GL-493T 78) + SX, Trichoderma harzianum strain SX 9 (Trichoderma harzianum strain SX 9, Trichoderma harzianum strain SX 9 (Trichoderma harzianum strain SX 9, Trichoderma harzianum strain SX 9) + Trichoderma harzianum strain SX 9, Trichoderma harzianum strain (Trichoderma harzianum strain SX 9, Trichoderma harzianum strain (Trichoderma harzianum strain SX 9, Trichoderma harzianum strain SX 9) + T5623, Trichoderma harzianum strain SX 9, Trichoderma harzianum strain (Trichoderma harzianum strain SX 9) + (Trichoderma harzianum strain SX 9, Trichoderma harzianum strain (Trichoderma harzianum strain SX 9, Trichoderma harzianum strain (Trichoderma harzianum strain, Hypersensitive protein (Harpin protein) + SX.

Combinations of the present components of the above group (c) with the compounds of the present invention:

1-methylcyclopropene (1-methylcyclopropene) + SX, 1,3-diphenylurea (1,3-diphenylurea) + SX, 2,3,5-triiodobenzoic acid (2,3,5-triiodobenzoic acid) + SX, IAA ((1H-indol-3-yl) acetic acid, (1H-indol-3-yl) acetic acid) + SX, IBA (4- (1H-indol-3-yl) butyric acid, + SX, MCPA (2- (4-chloro-2-methylphenoxy) acetic acid, 2- (4-chloro-2-methylphenoxy) acetic acid) + SX, PB (4- (4-chloro-2-methylphenoxy) butyric acid, 4- (4-chloro-2-methylphenoxy) butyric acid) + SX, 4-CPA (4-chlorophenoxyacetic acid, 4- (4-chlorophenoxyacetic acid) + SX, 5-aminolevulinic acid hydrochloride (5-aminolevulinic acid hydrochloride) + SX, 6-benzylaminopurine (6-benzylaminopurine) + SX, abscisic acid (abscisic acid) + SX, AVG (aminoethoxyvinylglycine), aminoethoxyvinylglycine) + SX, pyrimidinol (ancymidol) + SX, butraline (butralin) + SX, calcium carbonate (calceium carbonate) + SX, calcium chloride (calceium chloride) + SX, calcium formate (calceium formate) + SX, calcium peroxide) + SX, calcium polysulphide (calcium chloride) + SX, calcium chloride (SXloxycanthyl) SX, calcium chloride (SX, calcium chloride) + (SX, calcium chloride) + SX, calcium chloride (SXchloride) + SX, calcium chloride (SX, calcium chloride) + (SX, calcium chloride) + chloride (SX, calcium chloride (chloride) + chloride (SX, calcium chloride) (SX, calcium chloride (chloride) (SX, calcium chloride) (SX, SX chloride) (SX, SX chloride) (SX, SX chloride) (SX, SX chloride) (SX, SX chloride (chloride) (SX, SX chloride (chloride) (SX, SX chloride (, Decane-1-ol (decano-1-ol) + SX, 2, 4-dichlorprop (dichlorprop) + SX, furamectin (dikegulac) + SX, thionine (dimethipin) + SX, diquat) + SX, ethephon (ethephon) + SX, endothall (ethyhexazate) + SX, flumetralin (flumetralin) + SX, pyrimethanil (flumetrazol) + SX, pyrimethanil (dichlorfenoron) + SX, formononetin (formononetin) + SX, Gibberellin A (gibberlin A) + SX, Gibberellin A3(Gibberellin A3) + SX, antiepidamine (inamide), chitin lipid (SX), jasminocaprone SX, jasminozide) + SX, jasminoid SX, morpholine, Pyraflufen-ethyl) + SX, azoxystrobin (sintofen) + SX, sodium 1-naphthaleneacetate) + SX, sodium cyanate (sodium cyclamate) + SX, streptomycin (streptamycin) + SX, thidiazuron (thidiazuron) + SX, triclosan (triphenol) + SX, profenofos (tribenofos) + SX, trinexapac-ethyl) + SX, uniconazole P (uniconazole-P) + SX, 2- (naphthalen 1-yl) acetamide (2- (naphthyralen-1-yl) acetamide) + SX, [ 4-oxo-4- (2-phenylethyl) amino ] butyric acid + SX, 5- (trifluoromethyl) methyl ester [ (SX-1-yl) acetamide ], 2- (4-oxo-4- (2-phenylethyl) amino ] butyric acid + 5- (trifluoromethyl) methyl benzoate-2- [ (2-chloro-6-phenyl) thiophene-2-phenyl ] thiophene-4-phenyl-methyl benzoate) + SX, 4-chloro-tolyltriazole (SX, 3-chloro-2- (4-phenylethyl) glycine-2- (tolyloxazoline-2-yl) acetamide, 3-phenyl) benzenomycin-2-methyl benzoate) +, Inoculated Mossippinarum strain (Fusneliformis mosseae) + SX, Macrocystis margarita (Gigaspora margarita) + SX, Macrocystis rosea strain (Gigaspora rosea) + SX, Synechococcus fasciatus strain (Glomus aggregatum) + SX, Glomus desert sacculus strain (Glomus dessertoli) + SX, Glomus monospora strain (Glomus monospora) + SX, Glybioides sacculus brasiliensis strain (Paraglomus brasiliensis num) + SX, Glomus pellus strain (Rhizopus claris)) + SX, Glomus rhizogenes RTI-801 strain (Rhizogulus RTra I-801) + SX, Endocalamus daniella benthia strain (SX-SX) 197198 strain (Rhizosaccharomyces regius) strain (Rhizobolus rex) Na 2, Spirobolus benthia strain SX-SX, Spiromyces strain (SX-SX), Spirobolus benthia sp.SX, Spirobolus sp.SX Strain (SX), Spirobolus sp.sp. 5, Spirobolus sp.sp.sp.sp.sp.sp.3636 strain (SX-6), Spirobolus sp.sp.sp.sp.sp.sp., Azospirillum caulinodans + SX, Azospirillum halopraefrens + SX, Azospirillum iracillus (Azospirillum irakense) + SX, Azospirillum lipolyticum strain (Azospirillum lipoferum) + SX, Meizolobium exhizoensis strain (Meizolobium SX), Meizolobium exhizoides strain (Meizolobiobacter SX), Meizolobium sp.SX strain (Meizolobiobacter xylinum SX) 5019, Meizozobium sp.SX strain (Meizolobiobacter SX) SX strain (Meizolobiobacter SX), Meizolobiobacter SX strain (Mediazobium SX) 5019) + SX, Mediazobium sp.SX strain (Medhilobium SX), Medhilobium SX strain (Medhilobium SX) strain (Medhi SX), Medhilobium SX) strain (Medhi strain SX) strain (Medhi) + strain SX, Medhi strain SX strain (Medhi strain SX, Medhi strain SX, Medhilobium SX, Medhi strain (Medhi strain SX) strain SX, Medhi strain SX, Medhi strain (Medhi strain SX) strain SX, Medhi strain (Medhi strain SX) strain (Medhi strain SX) strain SX, Medhi strain SX strain (Medhi strain SX) strain (Medhi) + strain SX) strain SX, Medhi strain (Medhi strain SX ) strain SX, Medhi strain SX, Medhi strain SX, Medhi strain SX strain (Medhi strain S, Rhizobium japonicum bean biovar (Rhizobium leguminosa bv. phaseoli) + SX, Rhizobium japonicum clover biovar (Rhizobium leguminosa bv. trifolii) + SX, Rhizobium japonicum bean biovar (Rhizobium leguminosa bv. viciae) + SX, Rhizobium trifolium (Rhizobium trifolii) + SX, Rhizobium tropicalis (Rhizobium tropicalis) + SX, inoculated Rhizobium japonicum strain (Rhizobium japonicum) + SX, Sinorhizobium meliloti (Sinorhizobium meliloti) + SX, and mild strain of the Yellow mosaic Virus (Zucchini Yellow mosaic Virus strain) SX + SX.

Combinations of the present components of the above group (d) with the compounds of the present invention:

anthraquinone (anthraquinone) + SX, deet) + SX, ericardin (icaridin) + SX.

The ratio of the compound of the present invention to the component is not particularly limited, and examples thereof include 1000:1 to 1:1000, 500:1 to 1:500, 100:1 to 1:100, 50:1, 20:1, 10:1, 9:1, 8:1, 7:1, 6:1, 5:1, 4:1, 3:1, 2:1, 1:2, 1:3, 1:4, 1:5, 1:6, 1:7, 1:8, 1:9, 1:10, 1:20, 1:50 and the like in terms of a weight ratio (the compound of the present invention: the component).

The compound of the present invention has an effect on harmful arthropods such as harmful insects, harmful mites, and the like, harmful nematodes, and harmful molluscs. Examples of harmful arthropods, harmful nematodes, and harmful molluscs include the following.

Hemiptera pests (Hemiptera), Laodelphax striatellus (Laodelphax striatellus), Nilaparvata lugens (Nilaparvata lugens), Sogatella furcifera (Sogatella furcifera), Nilaparvata zeae (Peregrinus maidis), Orchikura (Javesella pellucida), Trapa canephora (Perkinsia sacchara), Tagosodedes orizicolus (Delphacidae), and other plant hoppers (Delphacidae); leafhopper families (Cicadellidae) such as Nephoteix cincticeps, Nephoteix striatus, Nephoteix nigra, Elaphe cinerea, Empoasca minor, Empoasca tuberosa, Empoasca zeae, Empoasca flava, Emblica albilineata, and Empoasca leucoptera (Cofana spectra); laodermaceae (Cercopideae) such as foamex (Mahanarva Posticata) and Laoderma canescens (Mahanarva fimbriolata); beet aphids (Aphis fabae), soybean aphids (Aphis dextrans), cotton aphids (Aphis gossypii), apple aphids (Aphis pomi), meadowsweet aphids (Aphis spiraecola), peach aphids (Myzus persicae), plum short tail aphids (Brachyuraea hephrix), cabbage aphids (Brevibacterium brassiccus), rose apple aphids (Dysaphena grandifolia), plant pipe aphids (Lipaphis erygium), long pipe aphids (Macrosiphumum eupatorium), net-free aphids (Aulacorthumum solani), lettuce aphids (Nasonoviia biosnigri), corn aphids (Rhopalosira), green aphids (Rhodococcus citri), green aphids (Achillea aphid), and green aphid (Achillea sinensis aphid), and green aphid (Achillea aphid), aphid (Achillea grandiflora); rhizophora vitiintended (Daktulosphaira vitifolia), Rhizoctonia pecuroides (Phylloxara devastatrix), Rhizoctonia pecuroides (Phylloxara nodabilis), Rhizoctonia southern Carya cathayensis (Phylloxara russelae), and the family of Oncorhynchaceae (Phylloxeridae); coccidioideae (Adelgidae) such as marssonia ferricens (Adelges tsugae), coccidioida fir (Adelges piceae), coccidioida fir (aphhrasiasia petiensae) and the like; oryza sativa (Scotophylla lucida), Oryza sativa (Scotophylla coarctata), Oryza sativa green (Nezara antranana), Orthosiphon aristatus (Eysarocoris aeneus), Orthosiphon aristatus (Eysarocoris lewisi), Orthosiphon aristatus (Eysarocoris ventraris), Orthosiphon aristatus (Eysarocoris armenii), Orthosiphon aristatus (Halomorphus armeniaca), Oryza sativa (Nezara virula), Orthosiphon aristatus (Euschistosus), Orthosiphon aristatus (Piezolous guilidii), Orthosiphon aristatus (Oialus pugnax), Euglena sinensis (Pilocalygus), and the like (Penaeidae); orius terrestris (Cydnidae) such as brown stinkbug (Scaptocoris castanea); apocynaceae (Alydidae) such as Neurous punctatus (Riptortus peestris), Neurous oryzophilus (Leptosporisa chinensis), and Neurous oryzae (Leptosporisa acuta); lygus lucorum (Coreidae) such as lygus lucorum (Cletus punctiger), phyllopodium angustifolia (Leptoglossus australis), etc.; long plant bugs of the family lygomorphaceae (Lygaeidae) such as sugar cane long plant bugs (Caverelius saccharovorus), calabash long plant bugs (Togo hemipterus), lygus linens (Blissus leucopterus); plant bug (Miridae) such as Lygus lucorum (Trigonotylus caelestifolium), Leptodermia gibsonii (Stenotus ruberatatus), Laptodermus dibotrys (Stenodema calgarata), Lygus pratensis (Lygus lineolaris) and the like; aleyrodidae (Aleyrodidae), such as greenhouse whitefly (Trialeurodes vaporariorum), Bemisia tabaci (bemis tabaci), citrus whitefly (Dialeurodes citri), aleuropus spiniferus (aleurocarpus spiniferus), camellia aleurocarpus (aleurocarpus camelliae), eurya emarginata (Pealius euryae), and the like; the pelagidae (Diaspididie) such as Tolyrus fascicularis (Abgrallaspis cyanhylli), Tolyrus rubescens (Aonidiella aurantii), Tolyrus piricola (Diaspiotius perniciosus), Blastus alba (Pseudoaulacaspis pentagona), Pantoea pellucida (Unnassis yanonensis), and Citrus unshiu (Unnassis citri); ericerus pela (Ceroplasmes rubens) and other Geckiaceae (Coccidae); ericerus plants (Margarodidae) such as icerus pela (Icherya purchasasi), and icerus pela (Icherya sechelarum); ericerus lycoris (Phonococcus solani), Hibiscus sordida (Phenococcus solenopsis), Helicoverpa japonica (Planococcus krauniae), Pseudococcinella longirostris (Pseudococcus comstocki), Pseudococcinella citricola (Planococcus citriodora), Pseudococcinella pseudolongata (Pseudococcineus longispinus), and Pseudococcinella rosea (Breynia rehi); psyllidae (Psyllidae) such as Diaphorina citri (Diaphorina citri), african psyllid (Trioza erytreae), european pear psyllid (cacosylla pyricularis), chinese pear psyllid (cacosylla chinensis), potato psyllid (bacicera cockelli), pear psyllid (cacosylla pyricularia), and the like; nepholididae (tingdae) such as Nepholidus deltoides (Corythucha citiata), Nepholidus deltoides (Corythucha marmorata), Nepholidus pyrifolia (Stephaniae nashi), Nepholidus crepidae (Stephaniae pyrioides), etc.; bed bugs (Cimicidae) such as Cimex lectularius, and Cimicidae; cicadae (Cicadidae) such as Giant Cicada (Giant Cicada) (quasada gigas); apolycidum plant (Reduviii dae), Apolygus genus (Triatoma spp.) such as Apolygus sinensis (Triatoma inflans), Nephocoris longiligorum (Rhodonius prolixus), etc.

Lepidoptera pests (Lepidoptera), Chilo supressalis (Chilo supplyssalis), Taiwan rice borer (Chilo polychrysus), white rice borer (Sciphaga innotata), yellow rice borer (Sciphaga incertulas), Rupela albina (Cnaphalocrocis medinalis), Ostrinia punctiferalis (Marasmia patnalis), Ostrinia punctiferalis (Marasmia exigua), Cnaphalocrocis medinalis (Notrcha elata), Asian corn borer (Ostrinia furnacalis), European corn borer (Ostrinia nubilalis), cabbage borer (Hellula undaria), grape leaf borer (Hertoperma luciduosa), blue grass borer (Diasterera), yellow rice borer (Ostrinia punctiferalis), and sugarcane borer (Cryptospira punctifera indica), and sugarcane borer (Cryptospirifera punctifera indica (Crisaria) and the like; borer families (Pyralidae) such as corn borer (Elasmopalpus lignosellus), Indian corn moth (Plodia interpunctella), cutworm (Euzophera batangensis), pink borer (Cadra cautella), and the like; spodoptera litura (Spodoptera litura), Spodoptera exigua (Spodoptera exigua), armyworm (Mythimna sepata), Spodoptera frugiperda (Mamestra brassicae), Sesamia inferens (Sesamia infensens), Spodoptera frugiperda (Spodoptera mauritia), Chrysomya frugiperda (Spodoptera frugiperda), Spodoptera frugiperda (Spodoptera exigua), Spodoptera litura (Spodoptera glauca), Spodoptera litura (Autograpevina nigra), Spodoptera frugiperda (Spodoptera nigra), Spodoptera virescens (Plumbus virescens), Spodoptera virescens (Helicosa), Helicoverpa virescens (Helicosa) and the like (Helicoverpa punctifera), Helicoverpa zea (Helicosa) and the like; pieridae (Pieridae) such as Pieris rapae; grapholitha molesta, Grapholitha dimorpha (Grapholitha), Grapholitha somnophila (Leguminosae), Choristonella torricola (Matsumura azukivora), Trichuris malalis (Adoxophyes orana fasciata), Trichuris cinerea (Adoxophyes homina), Trichuris abrotae (Homona magnania), Trichuris malpighia pomonella (Archis fusscoccus), Trichuris malpighia pomonella (Cydia pomonella), Trichuris furnature (Tetramera schericina), Trichuris arborea (Epinola obliqua), Trichuris fuliginosa (Epinota), Trichuris villosa (Cirsium villosa) and the like; the family of the fine moths (Gracilaria), such as the tea fine moth (Caloptilia theivora), the golden-banded fine moth (Phyllonorycter ringer niella) and the like; carposinidae (Carposinidae) such as Staphylocola pomifera (Carposina sasakii); polysinidae (Lyonethidae) such as coffee leaf miner (Leucoptera cofeella), peach leaf miner (Lyonetia clerkella), and leaf miner (Lyonetia prunifolia); toxidaceae (lymantriaceae) such as phacidonella (Lymantria spp.) such as gypsy moth (Lymantria dispar), phacidonella (Euproctis pseudoconspersa) such as theacrinis (Euproctis pseudospos); diamondback moth (Plutella xylostella), etc. (Plutellae); mylopideae (Gelechiaceae) such as Trypanosoma persicum (Anarsia lineolaris), Hypoglyces trichogramma (Helystomula trinnulella), Heliothis virescens (Pectinophora gossypiella), Solanum tuberosum (Phthomas operculella), and Lycopersicon esculentum (Tuta absoluta); arctidae (Arctidae) such as Hyphantria cunea (Hyphantria cunea); sphenoididae (castnidae) such as the sugarcane borer (Telchin licus); family Carpinidae (Cossidae), such as the family Carpinidae (Cossus insolaris); geometriae (Geometriade) such as Ascotis selenaria; chordariaceae (Limacodesae), such as Chordata virescens (Parasa lepida); a family of the phylocomiaceae such as the persimmon tree (Stahmopoda massinosa) (Stahmopodidae); gelididae (Sphingideae), such as Sphingideae (Achernitia lactis); serratidae (Sesidae) such as Nokona ferralis, apple paranthrene (Synanthedon hepctor), and Jatropha curcas (Synanthn tenuis); pierisceae (Hesperiaceae) such as straight grain rice Tapidula (Parnara gutta); and (3) family of rice-moth (Tieedae) such as Chlamydomonas (Tenera translucens), Glyphylla schericola (Tenera bisseliella), and the like.

Thrips (thrisanoptera) such as Frankliniella occidentalis (Frankliniella occidentalis), Cirsium palmatum (Thrips palmi), Frankliniella harderi (Thrips dorsalis), Thrips tabaci (Thrips tabaci), Thrips floribunda (Frankliniella intonas), Thrips oryzae (Stenchaminothrips biformis), Thrips americana (Echinoththrips americanus), and Thrips (Thripidae); amidothistle (Phlaothripide) such as rice thrips acutus.

Diptera (Diptera) of the family anthomyidae (Anthomyces aniformis), such as the plant fly (Delia platura), the plant fly (Delia antaqua), the plant fly (Pegomya cuniculularia), etc.; (ii) Ceramidae (Ulididae) such as beet muscardine (Tetanops myopaeformis); agromyzidae (Agromyzidae) such as rice leaf miner (Agromyza oryzae), leaf miner (Liriomyza sativa), leaf miner (Liriomyza trifolii), pea color fly (chromatia horticola); dihydroflaviviridae (Chloropidae) such as Periploca oryzae (Chlorops oryzae); bactrocera cucurbitae (Tertiaceae), Bactrocera cucurbitae (Bactrocera dorsalis), Bactrocera dorsalis (Bactrocera latifolia), Bactrocera nervosa (Bactrocera oleae), Bactrocera trembling (Bactrocera tryoni), Bactrocera murray (Ceratitis capitata), Bactrocera malabaricus (Rhagoletis pomonella), and Rhacochlaea pseudocerana japonica (Rhacochlaena japonica); amycolidaceae (Ephididae) such as Hymenophilus oryzae (Hydrellia griseola), Hymenophilus oryzae (Hydrellia philippinarum), and Hymenophilus oryzae (Hydrellia sasakii); drosophilaceae (Drosophilidae), such as Drosophila suzukii; siphonidae (Phoridae) such as Toyonia Isopsylla (Megaselia spiraculis); a family of mothicoideae (Psychodidae), such as mothflies (Clogmia albicans); eumycotina (Sciaridae) such as Bradysia difformis (Bradysia difformis) of domestic fungus; cecidomyidae (Ceridomyidae) such as the Heiteriophycidae (Mayetia destructor), Asian rice cecidomyidae (Orseolia oryzae); diopsidae (Diopsida), such as the Diopsis major eye cord (Diopsis macrophthalma); big mosquitoes (Tipulidae) of the family of the culicidae (Tipula aino), the common big mosquitoes (Tipula oleracea), the European big mosquitoes (Tipula paludosa); culex pipiens pallens (Culex pipiens), Culex tritaeniorhynchus (Culex tritaeniorhynchus), Culex pipiens (Culex pipiens f. molestus), Culex pipiens (Culex quinquefasciatus), Culex pipiens (Culex pipiens pipiens), Culex albugineus (Culex visnui), Aedes albopictus (Aedes albopictus), Aedes aegypti (Aedes aegypti), Anopheles sinensis (Anopheles sinensis), Anopheles gambiae (Anopheles gambiae), Anopheles stephensi (Anopheles stephensi), Anopheles colzzii, Anopheles albugineus (Anopheles albus), Anopheles anopheus (Anopheles Anopheles), Anopheles Anopheles (Anopheles), Anopheles nilapaceae (Anopheles), Anopheles nilapades nilapaensis, etc.); simultaneous families (Simulidae) such as Prosimulium yezoensis, Arachnocampa (Simulium ornatum); tabaniidae (Tabanidae) such as Tabanus tridentatus; muscadae (Musca domestica), Musca Stabilensis (Musca staylans), Musca stables (Stomoxys calcerns), and Musca crenata (Haematobia irritans); calliphoridae (Calliphoridae); sarcophagidae (Sarcophagidae); chironomidae (Chironomidae) such as Chironomidae (Chironomidae) including Chironomidae (Chironomidae plus), Chironomidae (Chironomidae yossui), Chironomidae (graptopteridae) and Chironomidae (graptopteridae) including Chironomidae); the family of the lavatory flies (Fannidae).

Coleoptera pests (Coleoptera) western corn rootworm (Diabrotica virgifera), southern corn rootworm (Diabrotica undaria howardi), northern corn rootworm (Diabrotica barberi), Mexican corn rootworm (Diabrotica virgifera zeae), spotted cucumber leaf Beetle (Diabrotica batata), Menuguensis (Cucurbit Beetle) (Diabrotica speciosa), Bean leaf Beetle (Ceratoma trifolium), grain leaf Beetle (Oullaria melanopsis), yellow fruit Beetle (Aulacora), yellow leaf Beetle (Phyllotreta), cabbage (Phyllotreta), Western black Beetle (Phyllotreta), southern rice Beetle (Phyllotreta), rice (Brassica juncea indica), rice (Brassica napus sativa), rice (Brassica napus), rice (Brassica napobraspa), rice (Phyllocha indica), rice (Phyllocha Septoria indica), rice (Brassica) and rice (Brassica napobraspa purpurea (Brassica) varieties, and rice (Brassica napobraspa), Phyllotaceae (Chrysomelidae) such as tobacco flea beetle (epirix hirtipenis); the brown beetles (carapidae) of the families of maize seed castanea (stemolophus lecontei), maize seed beetles (Clivina imprints), etc.; andropanaceae (aribiaceae) such as cuproid isocoryza sativa (Anomala cuprea), polychrome isocoryza sativa (Anomala rufouchae), bronchus minor (Anomala albopicosa), japanese beetle (Popillia japonica), golden bean (Heptophylla), european gold (Rhizotrogus majalis), black round gold (Tomarus gibbosus), gilles claw (Holotrichia spp.), gilles horneri (pelothrix), gilles horneri (Phyllophaga crinita), etc. (Phyllophaga spp.), and cottonthus pauciflorus (Dilobadeus spp.) such as Argentina; coffee bean (Araceae affeae), sweet potato elephant (Cylas formicarius), western sweet potato (Euscapes postfascarius), alfalfa leaf weevil (Hypera pottica), corn elephant (Sitophilus zeamais), rice elephant (Sitophilus oryzae), rice elephant (Sitophilus grandiflora), rice elephant (Echinococcus squameus), rice elephant (Lissopterus oryzae), palm weevil (Rhabdophthalus linococcus), cotton boll weevil (Anthonomonus grandis), parasitic elephant (Sphenophorus veus), southern corn beak (Sphenophorus callorhycus), soybean stem weevil (Sterculia tsusuensis), sugarcane (Sphenophorus), European corn borer (Phormidis), European corn borer (Phormis), European corn borer (Acanthopanax gracilistylus), European corn borer (Acanthopanax graciliaris, etc.); pseudostep A (Tenebrioidae) such as Tribolium castaneum (Tribolium castaneum), Tribolium convulsum (Tribolium convulsum), and Trichoides nigricans (Aliphiobius diaperinus); ladybird families (Coccinelida) such as E.solanacearum (Epilachna virginioticpuncta); family Rhynchophyllidae (Bostrochidae) such as Cydia pomonella (Lyctus brunneus) and Rhizopertha dominica (Rhizopertha dominica); arachnidae (ptidae); anoplophora malasiaca (Anoplophora malasiaica), Migdolus fryanus (Cerambycedae); click beetles (Elateridae) such as Sieve-chest combed nail (Melanotus okinawensis), fine-chest click beetles (Agriotes fusicolis), horn-chest click beetles (Melanotus legatus), Leptospira unifoliae (Anchartus spp.), Elastoidea variegata (Conoderus spp.), Flaccida (Ctenodera spp.), Customia (Limonius spp.), and Aeolus (Aeolus spp.); cryptopteridae (Staphylinidae) such as Paederus fuscipes (Paederus fuscipes); bark beetles (Dermestidae) such as small bark beetles (Anthrenus versasci), white bark beetles (Dermestis macultates), and Trogopterus griseus (Trogopterma granarium); lasioderma serricorn (Lasioderma serricorn), Stegobium panicum (Stegobium panicum) and other largehead (Anobidae); family Valley Thelaridae (Laemophiloeidae) such as Gilletia rustica (Cryptolepes ferrugineus); saurianaceae (Silveridae), such as Oryzaephilus surinaensis (Oryzaephilus surinaensis).

Orthoptera pests (Orthoptera) migratory locust (Locusta migratoria), Moroccan locusts (Docistaurus maroccanus), Australian locusts (Choristocetes terminifera), red wing locusts (Nomadacris septemfasciata), Phaseolus fulvidraco (Locustina paradalina), Tree locusts (Anagridium melando), Italian locusts (Callipramus italica), Long-negative locusts (Melanophaga diffusa), Melanopsis bivitta (Melanophagus bivittata), Melanopsis migrans (Melanopsis sanguinipes), Melanopsis sanguinipes (Melanophaga mularia), Melanophaga sanguinea (Melanophaga mulosa), Melanophycus diffusa (Catlepipes), Graphoma spicata (Acacia), Gracillus indica (Acacia), and Yellow locust (Orchikura, etc.); gryllotalpidata (Gryllotalpidata) of Gryllotalpatidae family such as Gryllotalpa (Gryllotalpa orientalis); cricket family (Gryllidar) such as cricket family (Acheta domestica), yellow-face oil gourd (Teleogryllus emma), etc.; longhorned grasshopper (Tettigniidae), such as Gryllus mojaponicae (Anabrus simplex).

Hymenoptera pest (Hymenoptera), leaf wasp (Athalia rosae), Japanese vegetable leaf wasp (Athalia japonica), and leaf wasp family (Tenthredinidae); solenopsis invicta (Solenopsis invicta), Solenopsis (Solenopsis geminata), Solenopsis spp (Solenopsis spp.), Solenopsis americana (Atta spp.), Solenopsis spp (Brown leaf-cutting ant (Atta capguera), Solenopsis americana (Atta spp.), Solenopsis spp (Acromycex spp.), Formica fusca (Paraphytoera clavata), Anthemis glabrata (Occidus glabra), Solenopsis microphylla (Monochorium pharaonis), Antenorhabditis argentea (Linepitomentoha hune), Formica fusca (Formica fusca japonica), Anthemis striatus (Prinosus punctatus), Formica fusca (Solenopsis punctata), Solenopsis invicta (Solenopsis punctifera, Solenopsis invicta, Solenopsis spp.), Solenopsis invicta (Solenopsis, Solenopsis spp.); wasp families (Vespidae) such as hornet (Vespa mandarinia japonica), vespid (Vespa similia), black-tail wasp (Vespa analis fabricius), black-chest wasp (Vespa velutina), hornet (Polistes jokahamae), etc.; apidae (Siricidae) such as Apis gigas (Urocerus gigas); family Oncomelania (Bethyidiae).

Blatta order pests (Blatta), Blatta (Blattalla germanica), and Blatta family (Blatta); blattaceae (Blattidae) such as Periplaneta fuliginosa (Periplaneta fuliginosa), Periplaneta americana (Periplaneta americana), Periplaneta fusca (Periplaneta brunnea), Blatta orientalis (Blatta orientalis), etc.; termites meretrix (Reticulitermes speratus), lactotermes formosanus (Coptotermes formosanus), Albitermes albidus (Incisiteriitermes minor), Coptotermes frustocosus (Cryptotermes domesticus), Aleurites formosanus (Odontiotermes formosanus), Neopteris aethiopica (Neotomes koshuunensis), Heteropterodon erythraeus (Glyptotermes satsumensis), Meadopteris kajimi (Glyptotermes nakajimi), Coptotermes fuscus (Glyptotermes fuscus), Proteus solenopsis (Hodotermus sjostedtii), Coptotermes guangzhous (Coptotermes guangzhounsis), Coptotermes flavus (Reticulitermes amanicanus), Micropteris amanensis (Reticulitermes amanensis), Microtermes flavipes amanicatus (Reticulitermes), Micropterocellus terreus (Reticulitermes), and Coptotermes formosanus punctatus (Simulans punctatus), Coptotermes formosanus chinensis (Simulans punctiferous termites (Simulans), Terminax punctiferous termites (Simulans, etc.).

Siphonaptera (Siphonaptera) is selected from the genera of Siphonaptera (Pulex), such as human Siphonaptans (Pulex irutans), Ctenocephalides (Ctenocephadae felis), Ctenocephalides (Ctenocephades canis), such as Ctenocephades (Ctenocephades), Ctenocephades (Ctenocephadides), Coptophlus (Xenopsylla), such as Xenopsylla (Xenopsylla), and Phlebia (Tunga) such as Periplaneta (Tunga), and the genera of Scyphylla (Echidephagana), such as Achnophtalaria (Echidnophyagana), and the genera of Achnophyta (Nosophyllus), such as Xenophylla (Nosophyllus fasciatus).

Pediculus (Pediculus) such as Pediculus humanus (Pediculus humanus capitis) belonging to Pediculus species; pubic lice (Phtirus) such as pubic pubis (Pthirus pubis); haematopinas (Haematopinaus) such as Sarcocus bovis (Haematopinaus eurystenus) and Sarcocus suis (Haematopinaus suis); philips genus (Damalinia) such as sheep blood louse (dalelliia ovis) and cattle hair louse (damelliia bovis); toxoplasma genus (Linoganthus) such as California (Linoganthus nutuli), sheep Toxoplasma (Linoganthus ovilus), etc.; tubificidae (solenopots) such as Calophyllus aquatica (solenopots); cootie (Menopon), such as cootie (Menopon); louse moulting (Trimenopon spp.); diaphorina (Trinoton spp.); rodentica (trichodictes) such as psocida canicola (trichodictes canis); catalpa (Felicola) such as Felicola substratus; bovicola (Bovicola bovis) and other Bovicola (Bovicola); pediculus gallicus (Menacanthus stramineus) and the like; werneeckiella spp; lepikentron spp; liposeelis subfamilas, Pediculus Tomentosa (Liposeelis bostrychophilus), Liposeelis simulans, Pediculus Boophilus (Liposeelis divinatorius), Pediculus insect-philic (Liposeelis entomophila), and the like, of the family Pediculidae (Liposelidae).

Thysanura (Thysanura) Laurencidae (Lepismatidae) such as Ctenoepsma villosa, silverfish (Lepisma saccharana), etc.

Tetranychidae (Tetranychus urticae), Tetranychus urticae (Tetranychus urticae), Tetranychus zeylanica (Tetranychus kanzawai), Tetranychus evansi (Tetranychus evansi), Tetranychus citrullus (Panocyhus citri), Panonychus ulmi (Panychus ulmi), Tetranychus sp.sp.Oligonchus (Tetranyhidae), etc.; cecidomycosis aurantiacae (Aculops pelekassi), cecidomycosis citrifolia (Phylloptruta citri), cecidomycosis lycopersici (Aculops lycopersici), cecidomycosis sinensis (Calacarus carinatus), cecidomycosis theacrinis (Acaphhyla theaavagrans), cecidomycosis sinensis (Eriophenops hibayensis), cecidomycosis spicata (Aculus schlecendali), kaki bud mite (Aceria diospyri), Triticum aestivum (Aceria tosichiella), Sterculiaceae (Shutcheeckenkella sp.) and the like (Eriophenopidae); tarsonchidae (Tarsonemidae) such as Tarsonemus laterosus (Polyphagarsonemus latus); leptodermidae (Tenuipipidae) such as Brevispora purpurea (Brevipus phoenicis); duke mite family (Tuckerellidae); hard tick (Ixodidae), for example, Haemaphyceae (Haemaphysalis longicornis), Haemaphysalis (Haemaphysalis flava), Haemaphysalis (Haemaphysalis californica), Dermatopteris (Dermacentor variabilis), Boophilus (Boormacentor taiwanensis), Dermacentor anharmenius (Dermacentor andersoni), Dermacentor (Ixodes ovatus), Ixophilus communis (Ixodes persulcatus), Ixophilus (Ixophysalis communis), Ixophilus (Ixophilus), Ixophilus (Ixophysalis communis), Rhipicephalus (Rhipicephalus, etc.); tyrophagus putrescentiae (Tyrophagus putrescentiae), Tyrophagus pseudophagicus (Tyrophagus similis), and other Dermatophagidae (Acaridae); dermatophagoides farinae (Dermatophagoides farinae), house dust mite (Dermatophagoides pteronyssinus) and the like (Pyroglyphidae); carnivorous family (Cheyletidae) such as common carnivorous mite (Cheyletus eruptius), malanychus (Cheyletus malaccensis), morel carnivorous mite (Cheyletus moorei), morel carnivore mite (Cheyletiella yasgugri); examples of the acarids of the genus Iridium (Argas) such as Argas persicae (Argas persicus), Dermatopyris hernialis (Ornithiomorus hermsii), Dermatopyris (Ornithiomorus turicata) such as Ornithiophaga hernialis, Dermatopyris (Ornithiomorus), Dermatophagoides ovis (Psoroptes ovis), Dermatophagoides (Psoroptes equi), Dermatophagoides (Knemophilus) such as Knemophilus (Knemophilus), Dermatophagoides (Notoepress), Dermatophagoides (Notoenophagoides), Dermatophagoides (Sarcophagoides), Dermatophagoides (Octophagoides), Dermatophagoides, Sarcophagoides, etc., Sarcophagoides, Sarcophagus, Sarcophagoides, Sarcophagus, Sarcophagoides, Sarcophagus, etc, Varroa species (Varroa), Dermatophagoides such as Varroa japonicas (Varroa), Dermatophagoides (Cheyletiella yasgugri), Dermatophagoides such as Dermatophagoides (Cheyletiella blakei), Dermatophagoides such as Dermatophagoides (Ornithocaulia spp.), Dermatophagoides (Demodex cantis), Demodex species (Demodex cati), Dermatophagoides (Myobia spp.), Dermatophagoides (Psorogates spp.), Red Trombicula akushi, Xanthium (Trombicula pallida), and Trombiculus species (Trombicula scaris).

Araneidae (Aranea), red chelidaceae (Eutichuridae) such as red chelidaceae (Cheiranthium japonicum); aranea (Latridectus hasseltii) of the family Amaranthaceae (Therididae).

Orchidaceae (Paradeoxymate) such as Orchidaceae (Polydesma), greenhouse mainland (Oxidus gracilis), and Red mainland (Nedypus tambranus).

Isopoda pest (Isopoda) such as Armadillidium vulgare (Armadillidium vulgare) and Armadillidiidae (Armadillidiidae).

Scutigeraceae (Scutigeriae), Scutigera (Thereuonema hilgendorfi), etc., Chilopoda pests (Chilopoda); scolopendra (Scolonderridae) such as Scolopendra subspinipes Vietnam (Scolonderra subspinipes); grateloupia filicina (Borthropoly rugoso) and the like (Ethopolidae).

Pest of Gastropoda (Gastropoda) of the family Limacidae (Limawarinatus), such as Limaflagena slug (Limax flagenatus), Limaflavus (Limax flavus), etc.; mucophilic slug families (philiomycedae) such as the bifilar slugs (meghimium bililinaum); pomacea canaliculata (Pomacea canaliculata) and other Bauscapidae (Ampulariidae); and (Lymnaeidae) family of Convolvulaceae such as Spirosoma microphylla (Austopeeplea olula).

Nematode (Nematoda), aphelenchoideae (Aphelenchoides besseyi), such as Aphelenchoides besseyi; pratylenchidae (Pratylenchidae) such as Pratylenchus coffeee, Pratylenchus brachyurus, Pratylenchus negatus (Pratylenchus negectius), Radopholus similis (Radopholus similis), and the like; heteroderidae (Heterodae) such as Meloidogyne javanicus (Meloidogyne javanica), Meloidogyne incognita (Meloidogyne incognita), Meloidogyne northern (Meloidogyne hapla), Heterodera glycines (Heterodera globosa), Rhixoma solani (Globodera rosestoniae), and Meloidogyne solani (Globodera pallida); lamiaceae (Hoploapidae) such as reniform nematode (Rotylenchulus reniformis); granuloridae (Anguinidae) such as strawberry bud nematode (nothylenchus acris), bulb nematode (Ditylenchus dipsaci); hemipenetraceae (Tylenchulidae), such as hemipenetrans semipenetarans (Tylenchulus semipenetarans); sword nematode (Xiphinema index) Isopeidae (Longidoridae); trichoderma family (Trichodoridae); bursaphelenchus xylophilus (Bursaphelenchus xylophilus) and the like (Parasitaphelenchadae).

The harmful arthropods such as harmful insects and harmful mites, the harmful mollusks and the harmful nematodes may be harmful arthropods such as harmful insects and harmful mites and harmful nematodes in which drug sensitivity to insecticides, acaricides, molluscicides and nematicides has been reduced or drug resistance has been developed.

The harmful arthropod control method of the present invention is carried out by applying an effective amount of the compound or the composition a of the present invention directly to harmful arthropods and/or to habitats (plants, soil, houses, animals, etc.) of harmful arthropods. Examples of the method for controlling harmful arthropods of the present invention include stem and leaf treatment, soil treatment, root treatment, spray treatment, fumigation treatment, water surface treatment, and seed treatment.

The compound or composition a of the present invention is usually mixed with an inactive carrier such as a solid carrier, a liquid carrier, or a gaseous carrier, and if necessary, a surfactant and other formulation auxiliaries to prepare an emulsion, an oil, a powder, a granule, a wettable powder, a water dispersible powder, a flowable formulation, a dry flowable formulation, a microcapsule, an aerosol, a poison bait, a resin formulation, a shampoo formulation, a paste formulation, a foam, a carbon dioxide formulation, a tablet, or the like. These preparations may be used after being processed into mosquito coils, electric mosquito coils, liquid mosquito-repellent preparations, smoking agents, fumigants, sheet preparations, spot-on agents, and oral preparations. These preparations usually contain 0.0001 to 95% by weight of the compound or the composition A of the present invention.

Examples of the solid carrier used for the preparation of the agent include clay (kaolin clay, diatomaceous earth, bentonite, acid clay, etc.), dry silica, wet silica, talc, ceramics, other inorganic minerals (sericite, quartz, sulfur, activated carbon, calcium carbonate, etc.), fine powders and granules of chemical fertilizers (ammonium sulfate, ammonium phosphate, ammonium nitrate, urea, ammonium chloride, etc.), synthetic resins (polyester resins such as polypropylene, polyacrylonitrile, polymethyl methacrylate, polyethylene terephthalate, etc., nylon resins such as nylon-6, nylon-11, nylon-66, etc., polyamide resins, polyvinyl chloride, polyvinylidene chloride, vinyl chloride-propylene copolymers, etc.).

Examples of the liquid carrier include water, alcohols (methanol, ethanol, isopropanol, butanol, hexanol, benzyl alcohol, ethylene glycol, propylene glycol, phenoxyethanol, etc.), ketones (acetone, methyl ethyl ketone, cyclohexanone, etc.), aromatic hydrocarbons (toluene, xylene, ethylbenzene, dodecylbenzene, phenylxylylethane, methylnaphthalene, etc.), aliphatic hydrocarbons (hexane, cyclohexane, kerosene, light oil, etc.), esters (ethyl acetate, butyl acetate, isopropyl myristate, oleic acid, etc.), esters (ethyl acetate, butyl acetate, isopropyl myristate, etc.), and the like Ethyl ester, diisopropyl adipate, diisobutyl adipate, propylene glycol monomethyl ether acetate, etc.), nitriles (acetonitrile, isobutyronitrile, etc.), ethers (diisopropyl ether, 1, 4-diisopropyl ether, etc.)Alkanes, 1, 2-dimethoxyethane, diethylene glycol dimethyl ether, diethylene glycol monomethyl ether, propylene glycol monomethyl ether, dipropylene glycol monomethyl ether, 3-methoxy-3-methyl-1-butanol, etc.), amides (DMF, N-dimethylacetamide, etc.), sulfoxides (DMSO, etc.), propylene carbonate, and vegetable oils (soybean oil, cottonseed oil, etc.).

As the gaseous carrier, for example, fluorocarbon (fluorocarbon), butane gas, LPG (liquefied petroleum gas), dimethyl ether, and carbon dioxide can be cited.

Examples of the surfactant include nonionic surfactants such as polyoxyethylene alkyl ethers, polyoxyethylene alkyl aryl ethers, and polyethylene glycol fatty acid esters, and anionic surfactants such as alkylsulfonates, alkylbenzenesulfonates, and alkylsulfates.

Examples of the other formulation auxiliary agents include a fixing agent, a dispersing agent, a coloring agent, and a stabilizer, and specifically include casein, gelatin, saccharides (starch, gum arabic, a cellulose derivative, alginic acid, and the like), lignin derivatives, bentonite, synthetic water-soluble polymers (polyvinyl alcohol, polyvinylpyrrolidone, polyacrylic acids, and the like), isopropyl acid phosphate, 2, 6-di-tert-butyl-4-methylphenol, and BHA (a mixture of 2-tert-butyl-4-methoxyphenol and 3-tert-butyl-4-methoxyphenol).

Examples of the base material of the resin formulation include vinyl chloride polymers and polyurethanes, and plasticizers such as phthalates (dimethyl phthalate, dioctyl phthalate, etc.), adipates, and stearic acid may be added to these base materials as necessary. The resin preparation can be obtained by kneading the compound in the base material using a usual kneading apparatus, and then molding the compound by injection molding, extrusion molding, press molding or the like, and if necessary, the resin preparation can be further processed into a plate-like, film-like, tape-like, net-like, linear or the like through steps such as molding, cutting or the like. These resin formulations are processed into collars for animals, ear tags for animals, sheet formulations, guide wires, posts for gardening, for example.

Examples of the base material of the bait agent include grain powder, vegetable oil, sugar, crystalline cellulose, and the like, and further, if necessary, antioxidants such as dibutylhydroxytoluene and nordihydroguaiaretic acid, preservatives such as dehydroacetic acid, anti-misuse agents such as capsicum powder for preventing eating by children or pets, cheese flavor, onion flavor, pest-attracting flavors such as peanut oil, and the like may be added.

In the present invention, examples of plants include whole plants, stems and leaves, flowers, scions, fruits, trunks, branches, crowns, seeds, vegetative reproductive organs, and seedlings.

The vegetative propagation organ is an organ having a growing ability when the part is cut off from the body in the root, stem, leaf, etc. of a plant and placed in the soil. Examples of the vegetative propagation organ include tuberous roots (tuber roots), creeping roots (creeping roots), bulbs (bulb), corms (corm or solid bulb), tubers (tuber), rhizomes (rhizome), creeping branches (stolon), rhizomes (rhizopus), cuttings (cane cuts), propaguses (propague), and cuttings (vine cuts). It should be noted that stolons are also called runners (runner) and propagation branches are also called bulbils (bulbils), which are classified into granulation (broad bud) and bulbil. The cuttings refer to the shoots (known as shoots) of sweet potatoes or yams and the like. Bulbs, corms, tubers, rhizomes, cuttings, root stocks, or tuberous roots are also collectively referred to as a bulbous root. Cultivation of potatoes begins by planting tubers in soil, the tubers used being generally called seed potatoes.

Examples of the method for controlling harmful arthropods by applying an effective amount of the present compound or composition a to soil include a method in which an effective amount of the present composition or composition a is applied to soil before or after transplanting a plant, a method in which an effective amount of the present composition or composition a is applied to a root ring of a crop plant to be protected from damage such as ingestion of a harmful arthropod, and a method in which an effective amount of the present composition or composition a is osmotically transferred from the root or the like into a plant body to control harmful arthropods that feed the plant. More specifically, for example, hole planting treatment (hole planting spreading, hole planting treatment soil mixing), root treatment (root spreading, root soil mixing, root irrigation, post-nursery root treatment), furrow planting treatment (furrow planting spreading, furrow planting soil mixing), furrow treatment (furrow spreading, furrow soil mixing, growth period furrow spreading), furrow treatment at the time of sowing (furrow spreading at the time of sowing, furrow soil mixing at the time of sowing), all-round treatment (all-soil spreading, all-soil mixing), side-of-ridge working treatment, surface treatment (surface application, surface application after impoundment), other soil spreading treatment (foliar spreading of growth granules, under-crown or trunk periphery spreading, soil surface mixing, hole sowing spreading, furrow surface spreading, inter-plant spreading) and other irrigation treatment (soil irrigation, soil mixing, hole spreading, furrow surface spreading, plant spreading) can be given, Seedling stage perfusion, liquid medicine injection treatment, plant basal perfusion, liquid medicine drip irrigation, chemical solution irrigation), seedling box treatment (seedling box spreading, seedling box perfusion, seedling box liquid medicine accumulation), seedling tray treatment (seedling tray spreading, seedling tray perfusion, seedling tray liquid medicine accumulation), seedbed treatment (seedbed spreading, seedbed perfusion, seedbed spreading, seedling immersion), bed soil mixing treatment (bed soil mixing, bed soil mixing before sowing, spreading before covering soil when sowing, spreading after covering soil when sowing, covering soil mixing), and other treatments (soil mixing, turning-in, surface soil mixing, rainwater droplety soil mixing, planting position treatment, granule and floral grouping spreading, pasty fertilizer mixing).

Examples of the seed treatment include treatment of seeds or vegetative reproductive organs with the compound or composition a of the present invention, and more specifically, for example, a spraying treatment in which a suspension of the compound or composition a of the present invention is sprayed onto the surface of seeds or the surface of vegetative reproductive organs, a coating treatment in which the compound or composition a of the present invention is applied to seeds or vegetative reproductive organs, an immersion treatment in which seeds are immersed for a certain period of time in a chemical solution of the compound or composition a of the present invention, and a method in which seeds or vegetative reproductive organs are coated with a carrier containing the compound or composition a of the present invention (film coating treatment, particle coating treatment, and the like). The vegetative propagation organ may be a potato seed.

When the composition a is applied to a seed or a vegetative reproductive organ, the composition a may be prepared in 1 preparation to apply the treatment to the seed or the vegetative reproductive organ, or the composition a may be prepared in a plurality of different preparations to apply the treatment to the seed or the vegetative reproductive organ in a plurality of times. Examples of the method of treating the composition A in a plurality of different preparations and divided into a plurality of times include a method of treating a preparation containing only the compound of the present invention as an active ingredient, and a method of treating a preparation containing the active ingredient after air-drying seeds or vegetative reproductive organs; and a method of treating a preparation containing the compound of the present invention and the present component as active ingredients, and treating a preparation containing the present component other than the treated present component after air-drying the seed or vegetative reproductive organ.

The seed or vegetative propagation organ holding the compound or composition a of the present invention in the present invention means a seed or vegetative propagation organ in a state where the compound or composition a of the present invention is adhered to the surface of the seed or vegetative propagation organ. The seed or vegetative propagation organ holding the compound or composition a of the present invention described above may be attached with a material other than the compound or composition a of the present invention before or after the compound or composition a of the present invention is attached to the seed or vegetative propagation organ.

In addition, when the composition A is applied as a layer on the surface of a seed or a vegetative propagation organ, the layer is composed of 1 layer or more. In the case of a plurality of layers, each layer contains 1 or more kinds of active ingredients, or contains 1 or more kinds of active ingredients and a layer containing no active ingredient.

The seed or vegetative reproductive organ holding the compound or composition a of the present invention can be obtained by applying a preparation containing the compound or composition a of the present invention to the seed or vegetative reproductive organ by the method of seed treatment described above, for example.

When the compound or the composition A of the present invention is used for controlling harmful arthropods in the agricultural field, the amount thereof to be applied is At a rate of per 10000m²The amount of the compound of the present invention is usually 1 to 10000 g. When the seed or vegetative propagation organ is treated, the amount of the compound of the present invention is usually in the range of 0.001 to 100g per 1Kg of the seed or vegetative propagation organ. When the compound or the composition A of the present invention is formulated into a preparation such as an emulsion, a wettable powder, a flowable preparation or the like, the preparation is usually diluted with water so that the concentration of the active ingredient is 0.01 to 10000ppm, and the preparation is usually applied directly as a granule, a powder or the like.

The treatment may be carried out by winding the resin preparation processed into a sheet or thread form around a crop, pulling the resin preparation around the crop, spreading the resin preparation over the soil at the root of the plant, or the like.

When the compound or the composition A of the present invention is used for controlling harmful arthropods inhabiting a house, the amount thereof to be applied is 1m per 1m when treated on a plane²The amount of the compound of the present invention in the treated area is usually 0.01 to 1000mg per 1m when the treatment is carried out in a space³The amount of the compound of the present invention in the treatment space is usually 0.01 to 500 mg. When the compound or the composition a of the present invention is formulated into a preparation such as an emulsion, a wettable powder, a flowable preparation or the like, it is usually diluted with water so that the active ingredient concentration is 0.1 to 10000ppm and applied as it is, or an oil, an aerosol, a fumigant, a bait or the like.

When the compound or the composition a of the present invention is used for controlling ectoparasites in livestock such as cattle, horses, pigs, sheep, goats, and chickens, and in small animals such as dogs, cats, rats, and mice, it can be applied to the animals by a method known in veterinary medicine. Specific methods of use include administration by tablets, mixed feeds, suppositories, and injections (intramuscular, subcutaneous, intravenous, intraperitoneal, and the like) for the purpose of systemic suppression, and use by spraying or dripping an oil or aqueous liquid preparation, washing an animal with a shampoo preparation, or wearing a resin preparation in the form of a collar or ear tag on an animal, for example, for the purpose of non-systemic suppression. The amount of the compound of the present invention administered to an animal is usually in the range of 0.1 to 1000mg per 1kg of the body weight of the animal.

The compound or the composition a of the present invention can be used as a control agent for harmful arthropods in agricultural lands such as upland fields, paddy fields, lawns, fruit tree gardens, and the like. Examples of the plant include the following.

Corn, rice, wheat, barley, rye, oat, sorghum, cotton, soybean, peanut, buckwheat, beet, rapeseed, sunflower, sugarcane, tobacco, solanaceous vegetables (eggplant, tomato, green pepper, capsicum, potato, etc.), cucurbitaceous vegetables (cucumber, pumpkin, zucchini, watermelon, melon, etc.), cruciferous vegetables (radish, turnip, horseradish, kohlrabi, cabbage, mustard, broccoli, cauliflower, etc.), compositae vegetables (burdock, garland chrysanthemum, artichoke, lettuce, etc.), liliaceae vegetables (onion, garlic, asparagus), umbelliferae vegetables (carrot, parsley, celery, parsnip, etc.), chenopodiaceae vegetables (spinach, swiss beet, etc.), labiatae vegetables (perilla, mint, basil, etc.), strawberry, sweet potato, yam, taro, pome fruits (apple, western pear, japanese pear, flower, pear, etc.), sugar beet, etc, Quince, etc.), stone fruits (peach, plum, nectarine, plum, cherry, apricot, prune, etc.), citrus fruits (satsuma mandarin, orange, lemon, lime, grapefruit, etc.), nuts (chestnut, walnut, hazelnut, almond, pistachio, cashew nut, macadamia nut, etc.), berry fruits (blueberry, cranberry, blackberry, raspberry, etc.), grape, persimmon, olive, loquat, banana, coffee, date, coconut, tea tree, mulberry, ornamental plants, forest plants, lawns, pasture grasses.

The above plants also include plants which can be produced by natural crossing, plants which can be produced by gene mutation, F1 hybrid plants and genetically recombinant crops. Examples of the genetically modified crop include paradigmsHPPD (4-hydroxyphenylpyruvate dioxygenase) inhibitors such as carfentrazone-ethyl (Isoxaflutole), ALS (acetolactate synthase) inhibitors such as Imazethapyr (Imazethapyr) and Thifensulfuron-Methyl (Thifensulfuron-Methyl), EPSP (5-enolpyruvylshikimate-3-phosphate synthase) inhibitorPlants tolerant to herbicides such as agents, glutamine synthetase inhibitors, PPO (protoporphyrinogen oxidase) inhibitors, Bromoxynil (Bromoxynil) or Dicamba (Dicamba); plants capable of synthesizing a selective toxin known to Bacillus such as Bacillus thuringiensis; a plant capable of imparting specific insecticidal activity by synthesizing a gene fragment or the like corresponding to an endogenous gene portion derived from a pest insect and inducing gene silencing (RNAi) in the target pest insect.

The plant is not particularly limited as long as it is a variety generally cultivated.

Examples

Hereinafter, the present invention will be described in more detail based on production examples, formulation examples, test examples, and the like, but the present invention is not limited to these examples.

In the present specification, Me represents a methyl group, Et represents an ethyl group, Pr represents a propyl group, i-Pr represents an isopropyl group, c-Pr represents a cyclopropyl group, c-Bu represents a cyclobutyl group, c-Pen represents a cyclopentyl group, c-Hex represents a cyclohexyl group, Ph represents a phenyl group, Py2 represents a 2-pyridyl group, Py3 represents a 3-pyridyl group, Py4 represents a 4-pyridyl group, and Bn represents a benzyl group. When c-Pr, c-Bu, c-Pen, c-Hex, Ph, Py2, Py3 and Py4 have a substituent, the substituent and the substitution position are described together before the symbol. For example, 1-CN-c-Pr represents 1-cyanocyclopropyl, 3, 4-F₂Ph represents 3, 4-difluorophenyl, 4-CF₃-Py2 represents 4- (trifluoromethyl) -2-pyridyl, 5-OCH₂CF₂CF₃-Py2 represents 5- (2, 2, 3, 3, 3-pentafluoropropoxy) -2-pyridyl.

First, production examples of the compound of the present invention are shown.

When physical property values of the compounds were measured by liquid chromatography/mass spectrometry (hereinafter, referred to as LCMS), the measured molecular ion values [ M + H ] were described]⁺Or [ M-H]^-And retention time (hereinafter, denoted as RT). The conditions for liquid chromatography (hereinafter, referred to as LC) are as follows.

[ LC Condition ]

Column: l-column2 ODS with inner diameter of 4.6mm, length of 30mm, and particle diameter of 3 μm (evaluation and research institution of chemical substance of the Pan-Seikaga Ach.)

UV measurement wavelength: 254nm

Mobile phase: solution A: 0.1% aqueous formic acid solution, solution B: 0.1% formic acid acetonitrile

Flow rate: 2.0 mL/min

A pump: LC-20AD (manufactured by Shimadzu corporation) 2 stands (high pressure gradient)

Gradient conditions: the liquid was fed at a concentration gradient described in [ Table LC1 ].

[ Table 1]

[ Table LC1]

Time (minutes)	Solution A (%)	Solution B (%)
			0.01	90	10
2.00	0	100
			4.00	0	100
4.01	90	10

[ MS conditions ]

A detector: LCMS-2020 (manufactured by Shimadzu corporation)

The ionization method comprises the following steps: DUIS

Reference production example 1

16.7mL of triethylamine was added to a mixture of 9.49g of chloroacetic acid and 15mL of water at 0 ℃ over 30 minutes. To the resulting mixture was added 16.1g of 2-amino-5- (trifluoromethyl) pyridine, and the mixture was stirred under reflux for 2 hours. The resulting mixture was filtered, and the filtrate was washed with water. The obtained solid was dried to obtain 11.0g of a crude product of intermediate 1 represented by the following formula.

Intermediate 1 LCMS:219[ M-H ]]^-RT 0.42 min

Reference production example 2

A mixture of 4.40g of the crude product of intermediate 1 obtained in reference production example 1, 22.37g of phosphorus oxybromide and 50mL of toluene was stirred under reflux for 5 hours. The resulting mixture was added dropwise to an aqueous sodium hydroxide solution, followed by extraction with toluene. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 24.7 g of an intermediate represented by the following formula.

Intermediate 2:¹H-NMR(CDCl₃)δ:8.45(1H,d),7.69(1H,s),7.67(1H,dd),7.36(1H,d).

reference production example 3

A mixture of 2.39g of intermediate 2, 6- (trifluoromethyl) -1, 2, 4-triazolo [4, 3-a ] pyridin-3 (2H) -one 1.83g, pyridine-2-carboxylic acid 885mg, copper (I) iodide 1.35g, cesium carbonate 4.39g and NMP30mL was stirred at 120 ℃ for 8 hours. To the resulting mixture was added water, followed by extraction with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to give 590mg of a crude product of intermediate 3 represented by the following formula (containing 85% of intermediate 2).

Intermediate 3 LCMS:388[ M + H ]]⁺RT 1.84 min

Reference production example 4

360mg of N-iodosuccinimide was added to a mixture of 590mg of the crude product of intermediate 3 (containing 85% of intermediate 2) produced in reference production example 3 and DMF5mL under ice-cooling, and stirred at room temperature for 3 hours. To the resulting mixture was added an aqueous sodium thiosulfate solution, and extraction was performed with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to give 4118 mg of an intermediate represented by the following formula.

Intermediate 4:¹H-NMR(CDCl₃)δ：8.59(1H，s)，8.26(1H，d)，7.78(1H，d)，7.51(1H，d)，7.30(1H，s)，7.28(1H，d).

reference production example 5

The compound produced in accordance with reference production example 1 and the physical property values thereof are shown below.

R in the Compound represented by the formula (B-1)^3bAnd R^3cIn combination of [ Table B-1]]The compound according to any one of the combinations described in (1).

[ Table 2]

[ Table B-1]

Intermediates	R3b	R3c
			5	Br	H
6	Cl	H
			7	H	CF3
49	H	Br
			50	H	Cl

Intermediate 5: LCMS: 229[ M-H]^-RT 0.34 min

Intermediate 6: LCMS: 187[ M + H ]]⁺RT 0.34 min

Intermediate 7: LCMS: 219[ M-H]^-RT 1.18 min

Intermediate 49: LCMS: 231[ M + H ]]⁺RT 0.40 min

Intermediate 50: LCMS: 187[ M + H ]]⁺RT 0.35 min

Reference production example 6

A mixture of 13.21g of the crude product of intermediate 1 produced according to reference production example 1, 18mL of phosphorus oxychloride and 150mL of toluene was stirred under reflux for 6 hours. The resulting mixture was added dropwise to an aqueous sodium hydroxide solution, followed by extraction with toluene. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 813.2 g of an intermediate represented by the following formula.

Intermediate 8:¹H-NMR(CDCl₃)δ：8.44(1H，s)，7.65(1H，d)，7.62(1H，s)，7.38(1H，d).

reference production example 7

The compound produced in accordance with reference production example 6 and the physical property values thereof are shown below.

R in the compound represented by the formula (B-2)^3bAnd R^3cIn combination of [ Table B-2]]The compound according to any one of the combinations described in (1).

[ Table 3]

[ Table B-2]

Intermediates	R3b	R3c
			9	Br	H
10	Cl	H
			11	H	CF3
12	H	Br
			13	H	Cl

Intermediate 9:¹H-NMR(CDCl₃)δ：8.21(1H，s)，7.48(1H，s)，7.44(1H，d)，7.28(1H，d).

intermediate 10:¹H-NMR(CDCl₃)δ：8.11(1H，s)，7.48-7.50(2H，m)，7.19(1H，d).

intermediate 11:¹H-NMR(CDCl₃)δ：8.17(1H，d)，7.86(1H，s)，7.64(1H，s)，7.04(1H，d).

intermediate 12:¹H-NMR(CDCl₃)δ：7.91(1H，d)，7.72(1H，s)，7.51(1H，s)，6.96(1H，d).

intermediate 13:¹H-NMR(CDCl₃)δ：7.97(1H，d)，7.54(1H，s)，7.49(1H，s)，6.85(1H，d).

reference production example 8

17.32g of N-iodosuccinimide was added to a mixture of 15.44g of intermediate 8 and DMF75mL produced according to reference production example 6 under ice-cooling, and stirred at 70 ℃ for 5 hours. To the resulting mixture was added an aqueous sodium thiosulfate solution, and the precipitated solid was filtered off. The obtained solid was washed with water and dried under reduced pressure to obtain 1418.0 g of an intermediate represented by the following formula.

Intermediate 14:¹H-NMR(CDCl₃)δ：8.41(1H，s)，7.65(1H，d)，7.44(1H，d).

reference production example 9

The compound produced in accordance with reference production example 8 and the physical property values thereof are shown below.

R in the compound represented by the formula (B-3)^3bAnd R^3cIn combination of [ Table B-3 ]]The compound according to any one of the combinations described in (1).

[ Table 4]

[ Table B-3 ]

Intermediates	R3b	R3c
			15	Br	H
16	Cl	H
			17	H	CF3
18	H	Br
			19	H	Cl

Intermediate 15:¹H-NMR(CDCl₃)δ：8.20(1H，s)，7.43(1H，d)，7.35(1H，d).

intermediate 16:¹H-NMR(CDCl₃)δ：8.46(1H，s)，7.64(1H，d)，7.47(1H，d).

intermediate 17:¹H-NMR(CDCl₃)δ：8.18(1H，d)，7.84(1H，s)，7.15(1H，d).

intermediate 18:¹H-NMR(CDCl₃)δ：7.93(1H，d)，7.72(1H，s)，7.06(1H，d).

intermediate 19:¹H-NMR(CDCl₃)δ：7.98(1H，d)，7.55(1H，s)，6.96(1H，d).

reference production example 10

18.0g of intermediate 14, 1, 4-bisA mixture of 140mL of an alkane, 2.38g of tris (dibenzylideneacetone) dipalladium (0), 3.01g of Xantphos, 27.2mL of diisopropylethylamine, and 3.75mL of ethanethiol was stirred at reflux for 3 hours. The resulting mixture was brought to room temperature and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to obtain 2013.39 g of an intermediate represented by the following formula.

Intermediate 20:¹H-NMR(CDCl₃)δ：8.74(1H，s)，7.67(1H，d)，7.48(1H，d)，2.78(2H，d)，1.24(3H，t).

reference production example 11

The compound produced in accordance with reference production example 10 and the physical property values thereof are shown below.

R in the compound represented by the formula (B-4)^3bAnd R^3cIn combination of [ Table B-4]]The compound according to any one of the combinations described in (1).

[ Table 5]

[ Table B-4]

Intermediates	R3b	R3c
			21	Br	H
22	Cl	H
			23	H	CF3
24	H	Br
			25	H	Cl

Intermediate 21:¹H-NMR(CDCl₃)δ:8.51(1H,s),7.46(1H,d),7.38(1H,d),2.73(2H,d),1.23(3H,t).

intermediate 22:¹H-NMR(CDCl₃)δ:8.42(1H,s),7.51(1H,d),7.28(1H,d),2.75(2H,d),1.23(3H,t).

intermediate 23 LCMS 281[ M + H ]]⁺RT 2.11 points

Intermediate 24:¹H-NMR(CDCl₃)δ:8.25(1H,d),7.74(1H,s),7.07(1H,d),2.73(2H,q),1.21(3H,t).

intermediate 25:¹H-NMR(CDCl₃)δ:8.31(1H,d),7.57(1H,s),6.96(1H,d),2.73(2H,q),1.21(3H,t).

reference production example 12

5.16g of mCPBA (purity 70%, containing 30% water) was added to a mixture of 2.66g of intermediate 21 and 10mL of chloroform under ice-cooling, and the mixture was stirred at room temperature for 2 hours. To the resulting mixture were added a saturated aqueous sodium bicarbonate solution and an aqueous sodium thiosulfate solution in this order, followed by extraction with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to obtain 261.79 g of an intermediate represented by the following formula.

Intermediate 26:¹H-NMR(CDCl₃)δ:9.15(1H,s),7.60(1H,d),7.57(1H,d),3.36(2H,q),1.36(3H,t).

reference production example 13

The compound produced in accordance with reference production example 12 and the physical property values thereof are shown below.

R in the Compound represented by the formula (B-5)^3bAnd R^3cIn combination of [ Table B-5]]The compound according to any one of the combinations described in (1).

[ Table 6]

[ Table B-5]

Intermediates	R3b	R3c
			27	CF3	H
28	Cl	H
			29	H	CF3
30	H	Br
			31	H	Cl

Intermediate 27:¹H-NMR(CDCl₃)δ：9.39(1H，s)，7.81(1H，d)，7.67(1H，d)，3.39(2H，q)，1.37(3H，t).

intermediate 28:¹H-NMR(CDCl₃)δ：9.07(1H，s)，7.63(1H，d)，7.49(1H，d)，3.37(2H，q)，1.36(3H，t).

intermediate 29:¹H-NMR(CDCl₃)δ：9.16(1H，d)，7.98(1H，s)，7.27(1H，d)，3.38(2H，q)，1.35(3H，t).

intermediate 30:¹H-NMR(CDCl₃)δ：8.87(1H，d)，7.86(1H，s)，7.20(1H，d)，3.34(2H，q)，1.33(3H，t).

intermediate 31:¹H-NMR(CDCl₃)δ：8.93(1H，d)，7.68(1H，s)，7.08(1H，d)，3.34(2H，q)，1.33(3H，t).

reference production example 14

A mixture of 324mg of intermediate 26, trans-N, N' -dimethylcyclohexane-1, 2-diamine (0.32 mL), sodium iodide (225 mg), copper (I) iodide (190 mg) and toluene (4 mL) was stirred at 120 ℃ for 21 hours. The resulting mixture was cooled to room temperature and then filtered. To the obtained filtrate, water was added, and extraction was performed 2 times with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography to obtain 3270mg of an intermediate represented by the following formula.

Intermediate 32:¹H-NMR(CDCl₃)δ：9.23(1H，s)，7.70(1H，d)，7.46(1H，d)，3.35(2H，q)，1.35(3H，t).

reference production example 15

936mg of intermediate 27, cesium fluoride 4.56g and DMSO10mL were stirred at 95 ℃. After the resulting mixture was allowed to reach room temperature, ethyl acetate and water were sequentially added thereto, followed by filtration. The obtained filtrate was subjected to liquid separation, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to give 330mg of a crude product of intermediate 33 represented by the following formula (containing 22% of intermediate 27).

Intermediate 33: LCMS: 297[ M + H]⁺RT 1.76 min

Reference production example 16

The compound produced in accordance with reference production example 15 and the physical property values thereof are shown below.

R in the Compound represented by the formula (B-6)^3bAnd R^3cIn combination of [ Table B-6]The compound according to any one of the combinations described in (1).

[ Table 7]

[ Table B-6]

Intermediates	R3b	R3c
			34	Br	H
35	Cl	H
			36	H	CF3
37	H	Br
			38	I	H

Intermediate 34: LCMS: 307[ M + H]⁺RT 1.64 min

Intermediate 35: LCMS: 263[ M + H]⁺RT 1.61 min

Intermediate 36: LCMS: 297[ M + H]⁺RT 1.78 min

Intermediate 37: LCMS: 307[ M + H]⁺RT 1.69 min

Intermediate 38: LCMS: 355[ M + H]⁺RT 1.72 min

Reference production example 17

A mixture of 60g of intermediate 8, 165g of sodium iodide, 307mL of 57% hydroiodic acid, and 600mL of acetonitrile was stirred under reflux for 22 hours. Acetonitrile was distilled off from the obtained mixture under reduced pressure, and the precipitated solid was collected by filtration. The obtained solid was washed with water, a 10% aqueous solution of sodium hydroxide, and water in this order. The obtained solid was dried to obtain 3940 g of an intermediate represented by the following formula.

Intermediate 39:¹H-NMR(CDCl₃)δ:8.46(1H,s),7.79(1H,s),7.68(1H,d),7.33(1H,d).

reference production example 18

The compound produced in accordance with reference production example 17 and the physical property values thereof are shown below.

Intermediate 40:¹H-NMR(CDCl₃)δ:8.23(1H,dd),7.64(1H,s),7.47(1H,d),7.24(1H,dd).

reference production example 19

To a mixture of 3.1g of 2-hydrazino-5- (trifluoromethyl) pyridine and THF20mL was added 4.2g of 1, 1' -carbonyldiimidazole at 0 ℃ and the mixture was stirred at room temperature for 3 hours. To the resulting mixture was added water, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography to obtain 412.5 g of an intermediate represented by the following formula.

Intermediate 41:¹H-NMR(CDCl₃)δ:10.55(1H,s),8.21(1H,s),7.27(1H,d),7.20(1H,dd).

reference production example 20

The compound produced in accordance with reference production example 19 and the physical property values thereof are shown below.

Intermediate 42:¹H-NMR(CDCl₃)δ:9.83(1H,s),7.89(1H,d),7.48(1H,d),6.62(1H,dd).

intermediate 43:¹H-NMR(CDCl₃)δ:11.12(1H,s),7.95(1H,s),6.96(1H,d),6.55(1H,s),6.47(1H,dd).

intermediate 44:¹H-NMR(DMSO-d₆)δ:8.99(1H,s),8.45(1H,s).

intermediate 45:¹H-NMR(CDCl₃)δ:9.27(1H,s),8.15(1H,s),7.21(1H,d),7.15(1H,d).

reference production example 21

To a mixture of 8.34g of methyl 2-chloro-5- (trifluoromethyl) pyridine-3-carboxylate and 70mL of ethanol was added dropwise 5.5mL of methylhydrazine at 0 ℃ and the mixture was stirred at room temperature for 30 minutes. After the resulting mixture was concentrated under reduced pressure, 2N hydrochloric acid was added to the resulting residue, and extraction was performed with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography to obtain 468.16 g of an intermediate represented by the following formula.

Intermediate 46:¹H-NMR(DMSO-d₆)δ:8.75(1H,s),8.56(1H,s),3.85(3H,s).

reference production example 22

A mixture of 2.18g of intermediate 39, 1.52g of intermediate 46, 345mg of pyridine-2-carboxylic acid, 533g of copper (I) iodide, 3.58g of cesium carbonate and NMP20mL was stirred at 120 ℃ for 8 hours. To the resulting mixture was added water, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to give 4770 mg of an intermediate represented by the following formula.

Intermediate 47:¹H-NMR(CDCl₃)δ:8.90(1H,s),8.57(1H,s),8.48(1H,s),8.35(1H,s),7.74(1H,d),7.43(1H,d),3.92(3H,s).

reference production example 23

The compound produced in accordance with reference production example 4 and the physical property values thereof are shown below.

Intermediate 48:¹H-NMR(CDCl₃)δ:8.89(1H,s),8.59(1H,s),8.49(1H,s),7.75(1H,d),7.53(1H,d),3.55(3H,s).

production example 1

118mg of intermediate 4, 1, 4-bisA mixture of 1mL of an alkane, 21mg of tris (dibenzylideneacetone) dipalladium (0), Xantphos27mg, 0.060mL of diisopropylethylamine, and 0.050mL of ethanethiol was stirred at reflux for 3 hours. To the resulting mixture was added water, followed by extraction with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (chloroform: methanol: 96:4) to obtain 171 mg of a compound of the present invention represented by the following formula.

Compound 1 of the present invention:¹H-NMR(DMSO-d₆)δ:9.02(1H,s),8.49(1H,d),7.97(1H,d),7.81(1H,d),7.52(2H,m),2.88(2H,q),1.06(3H,t).

production example 2

To a mixture of 71mg of compound 1 of the present invention and 3mL of chloroform was added 154mg of mCPBA (purity 70%, containing 30% water) under ice-cooling, and the mixture was stirred at room temperature for 4 hours. To the resulting mixture were added a saturated aqueous sodium bicarbonate solution and an aqueous sodium thiosulfate solution in this order, followed by extraction with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 270 mg of a compound of the present invention represented by the following formula.

Compound 2 of the present invention:¹H-NMR(DMSO-d₆)δ:9.18(1H,s),8.54(1H,d),8.15(1H,d),8.04(1H,d),7.55(2H,m),3.87(2H,q),1.32(3H,t).

production example 3

The compound produced in accordance with production example 1 and the physical property values thereof are shown below.

Compound 3 of the present invention:¹H-NMR(CDCl₃)δ:8.89-8.88(2H,m),8.48(1H,d),7.78(1H,d),7.56(1H,d),3.54(3H,s),2.95(2H,q),1.26(3H,t).

production example 4

The compound produced in accordance with production example 2 and the physical property values thereof are shown below.

Compound 4 of the present invention:¹H-NMR(DMSO-d₆)δ:9.39(1H,s),9.05(1H,s),8.58(1H,s),8.07(1H,d),7.97(1H,d),3.92(2H,t),3.59(3H,s),1.45(3H,t).

production example 5

72mg of sodium hydride (oil, 60%) was added at room temperature to a mixture of 180mg of intermediate 41, 392mg of intermediate 34 (containing 30% of intermediate 26) and DMF2mL and stirred at 70 ℃ for 2 h. To the resulting mixture was added water, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (ethyl acetate: hexane ═ 40:60) to give 5147 mg of the compound of the present invention represented by the following formula.

Compound 5 of the present invention:¹H-NMR(DMSO-d₆)δ:8.98(1H,s),8.53(1H,s),7.94-7.92(2H,m),7.54-7.53(2H,m),3.79(2H,q),1.30(3H,t).

production example 6

A mixture of 69mg of intermediate 43, 150mg of intermediate 34 (containing 30% of intermediate 26), DMF2mL and cesium carbonate 166mg was stirred at 70 ℃ for 2 hours. To the resulting mixture was added water, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (ethyl acetate: hexane ═ 40:60) to obtain 649 mg of the compound of the present invention represented by the following formula.

Compound 6 of the present invention:¹H-NMR(CDCl₃)δ:9.03(1H,s),7.93(1H,s),7.63-7.62(2H,m),6.94(1H,d),6.86(1H,s),6.51(1H,d),3.85(2H,q),1.50(3H,d).

production example 7

The compound produced in accordance with production example 6 and the physical property values thereof are shown below.

A in the compound represented by the formula (A-1)²、A⁴、A⁵、R^3bAnd R^3cIn combination of [ Table A-1 ]]The compound according to any one of the combinations described in (1).

[ Table 8]

[ Table A-1]

Compounds of the invention	A2	A4	A5	R3b	R3c
						7	N	CCF3	CH	CF3	H
8	N	CH	CCF3	H	CF3
						9	N	N	CCF3	Br	H
10	N	CH	CCF3	Cl	H
						11	N	CH	CCF3	H	Br
12	N	CH	CSCF3	Cl	H

Compound 7 of the present invention:¹H-NMR(CDCl₃)δ：9.30(1H，s)，7.94-7.89(2H，m)，7.71(1H，d)，7.49(1H，s)，6.66(1H，d)，3.83(2H，q)，1.50(3H，t).

compound 8 of the present invention:¹H-NMR(DMSO-d₆)δ：9.08(1H，d)，8.54-8.51(2H，m)，7.66(1H，d)，7.55(2H，m)，3.78(2H，q)，1.31(3H，t).

compound 9 of the present invention:¹H-NMR(CDCl₃)δ：9.05(1H，s)，8.87(1H，s)，8.14(1H，s)，7.71(1H，d)，7.68(1H，d)，3.73(2H，q)，1.51(3H，t).

compound 10 of the present invention:¹H-NMR(CDCl₃)δ：8.97(1H，s)，8.20(1H，d)，7.76(1H，d)，7.53(1H，d)，7.27(1H，s)，7.25(1H，d)，3.78(2H，q)，1.49(3H，t).

compound 11 of the present invention:¹H-NMR(DMSO-d₆)δ：8.80(1H，d)，8.52(1H，s)，8.33(1H，d)，7.57(1H，d)，7.54-7.53(2H，m)，3.73(2H，q)，1.28(3H，t).

compound 12 of the present invention:¹H-NMR(DMSO-d₆)δ：8.92(1H，s)，8.54(1H，s)，7.99(1H，d)，7.86(1H，d)，7.45-7.45(2H，m)，3.77(2H，q)，1.30(3H，t).

production example 8

A mixture of 490mg of Compound 5 of the present invention, bis (pinacol) diboron 508mg, potassium acetate 294mg, 1' -bis (diphenylphosphino) ferrocene 37mg and toluene 10mL was stirred at 110 ℃ for 3 hours. To the resulting mixture was added water, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. To the resulting mixture were added 615mg of sodium acetate, 5mL of water and 5mL of THF. To the resulting mixture, 0.22mL of 30% hydrogen peroxide water was added at 0 ℃ and the mixture was stirred at room temperature for 5 hours. To the resulting mixture was added an aqueous sodium thiosulfate solution, followed by extraction with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain 500mg of a crude product of Compound 13 of the present invention represented by the following formula.

The compound 13 of the invention is LCMS:426[ M-H]^-RT 1.54 min

Production example 9

A mixture of 500mg of the crude product of Compound 13 of the present invention obtained in production example 8, 391mg of cesium carbonate, 4mL of DMF and 0.100mL of iodoethane was stirred at room temperature for 6 hours. To the resulting mixture was added water, followed by extraction with chloroform. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (ethyl acetate: hexane ═ 40:60) to give 14209 mg of the compound of the present invention represented by the following formula.

Compound 14 of the present invention:¹H-NMR(DMSO-d₆)δ:8.51(1H,s),8.33(1H,d),7.87(1H,d),7.58(1H,d),7.53-7.52(2H,m),4.15(2H,q),3.70(2H,q),1.41(3H,t),1.27(3H,t).

production example 10

A mixture of 490mg of the compound of the present invention 5, 2-isopropenyl-4, 4,5, 5-tetramethyl-1, 3, 2-dioxaborolan 252mg, tripotassium phosphate 637mg, 1' -bis (diphenylphosphino) ferrocene 29mg, 8mL of 1, 2-dimethoxyethane, and 0.8mL of water was stirred at 80 ℃ for 4 hours. To the resulting mixture was added water, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (ethyl acetate: hexane ═ 63:37), to give 15150 mg of the compound of the present invention represented by the following formula.

Compound 15 of the present invention:¹H-NMR(CDCl₃)δ：8.91(1H，s)，8.20(1H，d)，7.74-7.73(2H，m)，7.27(1H，s)，7.25(1H，d)，5.52(1H，s)，5.30(1H，s)，3.77(2H，q)，2.22(3H，s)，1.49(3H，t).

production example 11

The compound produced in accordance with production example 10 and the physical property values thereof are shown below.

R in the compound represented by the formula (A-2)^3bAnd R^3cIn combination of [ Table A-2]]The compound according to any one of the combinations described in (1).

[ Table 9]

[ Table A-2]

Compounds of the invention	R3b	R3c
			16	c-Pr	H
17	4-F-Ph	H

Compound 16 of the present invention:¹H-NMR(DMSO-d₆)δ：8.67(1H，s)，8.52(1H，s)，7.83(1H，d)，7.53-7.52(2H，m)，7.43(1H，d)，3.71(2H，t)，2.21-2.17(1H，m)，1.28(3H，t)，

1.06-1.04(2H，m)，0.82-0.81(2H，m).

compound 17 of the present invention:¹H-NMR(CDCl₃)δ：9.03(1H，s)，8.21(1H，s)，7.86(1H，d)，7.76(1H，d)，7.58-7.55(2H，m)，7.28(1H，s)，7.25-7.20(3H，m)，3.80(2H，q)，1.51(3H，t).

production example 12

A mixture of 490mg of Compound 5 of the present invention, 0.057mL of formic acid, 0.23mL of triethylamine, 116mg of tetrakis (triphenylphosphine) palladium (0), and 10mL of N, N-dimethylacetamide was stirred at 100 ℃ for 3 hours. To the resulting mixture was added water, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (ethyl acetate: hexane ═ 71:29), to give 18390 mg of the compound of the present invention represented by the following formula.

Compound 18 of the present invention:¹H-NMR(CDCl₃)δ:8.93(1H,d),8.20(1H,s),7.81(1H,d),7.58-7.56(1H,m),7.28-7.27(1H,m),7.25-7.23(1H,m),7.17-7.15(1H,m),3.77(2H,q),1.49(3H,t).

production example 13

Compound 5 of the present invention was used instead of intermediate 26, and Compound 19 of the present invention represented by the following formula was obtained in accordance with reference production example 14.

Compound 19 of the present invention:¹H-NMR(CDCl₃)δ:9.15(1H,s),8.19(1H,s),7.75(1H,d),7.58(1H,d),7.27(1H,s),7.25(1H,s),3.78(2H,q),1.50(3H,t).

next, examples of the compound of the present invention produced according to any one of the production examples described in the examples and the production method described in the present specification are shown below. Q11 to Q30 are groups shown below.

In the compound represented by the formula (L-1) (hereinafter, referred to as the compound (L-1)), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1).

[ Table 10]

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 2).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 3).

In the compound (L-1), Q is a group represented by Q12, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound of hydrogen atom (hereinafterAnd is marked as compound group SX 4).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 5).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 6).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 7).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 8).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 9).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 10).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 11).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 12).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 13).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 14).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 15).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 16).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 17).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 18).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 19).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 20).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 21).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 22).

In the compound (L-1), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 23).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 24).

In the compound (L-1), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 25).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 26).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 27).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 28).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 29).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 30).

In the compound (L-1), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 31).

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 32).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 33).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 34).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substitution described in (1)Radical, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 35).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 36).

In the compound (L-1), Q is a group represented by Q14, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 37).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 38).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 39).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 40).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 41).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound being a hydrogen atom (hereinafter, described as chemical formula)Composition set SX 42).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 43).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 44).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 45).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 46).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 47).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 48).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 49).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoroMethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 50).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 51).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 52).

In the compound (L-1), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 53).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 54).

In the compound (L-1), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 55).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 56).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 57).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any ofA substituent, R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 58).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ] ]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 59).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 60).

In the compound (L-1), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 61).

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 62).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 63).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 64).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 65).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 66).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 67).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 68).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 69).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ] ]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 70).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 71).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 72).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 73).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 74).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 75).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 76).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 77).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 78).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 79).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 80).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 81).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 82).

In the compound (L-1), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 83).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 84).

In the compound (L-1), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 85).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 86).

In the compound (L-1), Q is a group represented by Q28, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 87).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 88).

Compound (A) to (B)In L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 89).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 90).

In the compound (L-1), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 91).

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 92).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 93).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 94).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 95).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cIs hydrogenAtomic compounds (hereinafter, referred to as compound group SX 96).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 97).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ] ]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 98).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 99).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 100).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 101).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 102).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 103).

In the compound (L-1), Q isGroup represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 104).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 105).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 106).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 107).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 108).

In the compound (L-1), Q is a group represented by Q21, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 109).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 110).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 111).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 112).

In the compound (L-1), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 113).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 114).

In the compound (L-1), Q is a group represented by Q27, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 115).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 116).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 117).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 118).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound which is a hydrogen atom (hereinafter, referred to as a compound)Set SX 119).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 120).

In the compound (L-1), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 121).

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 122).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 123).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 124).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 125).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 126).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 127).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 128).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 129).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 130).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 131).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 132).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 133).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cIs conversion of hydrogen atomsCompound (hereinafter, referred to as compound group SX 134).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 135).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 136).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 137).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 138).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 139).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 140).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 141).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cCompounds being hydrogen atoms (hereinafter referred to as compound group SX 142).

In the compound (L-1), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 143).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 144).

In the compound (L-1), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 145).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 146).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 147).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 148).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 149).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 150).

In the compound (L-1), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 151).

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 152).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 153).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 154).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 155).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 156).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 157).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 158).

In the compound (L-1), Q is a group represented by Q15, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 159).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 160).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 161).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 162).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 163).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 164).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 165).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 166).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 167).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 168).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter referred to as compound group SX 169).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 170).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA trifluoromethyl compound (hereinafter referred to as compound group SX 171).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 172).

In the compound (L-1), Q is Q25Radical, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 173).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 174).

In the compound (L-1), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R ^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 175).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 176).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 177).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 178).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 179).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cCompound having trifluoromethyl group (hereinafter, referred to as compound group SX 18)0)。

In the compound (L-1), Q is a group represented by Q11, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 181).

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 182).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 183).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 184).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 185).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 186).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 187).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 188).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 189).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 190).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 191).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 192).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 193).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 194).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 195).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 196).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 197).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 198).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 199).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 200).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 201).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 202).

In the compound (L-1), Q is a group represented by Q25, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound of chlorine atom (hereinafterAnd is marked as compound group SX 203).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 204).

In the compound (L-1), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 205).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 206).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 207).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 208).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 209).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 210).

In the compound (L-1), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substitution described in (1)Radical, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 211).

In the compound (L-1), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 212).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 213).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 214).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 215).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 216).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 217).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 218).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 219).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 220).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 221).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 222).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 223).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 224).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 225).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ watch ]2A]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 226).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 227).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 228).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 229).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 230).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 231).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 232).

In the compound (L-1), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 233).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 234).

In the compound (L-1), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 235).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R ^3cA compound having a bromine atom (hereinafter referred to as compound group SX 236).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 237).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 238).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 239).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 240).

In the compound (L-1), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 241).

Q in the compound (L-1) is Q11 A group shown, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 242).

In the compound (L-1), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 243).

In the compound (L-1), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 244).

In the compound (L-1), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 245).

In the compound (L-1), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 246).

In the compound (L-1), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 247).

In the compound (L-1), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 248).

In the compound (L-1), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cAnd compounds having an iodine atom (hereinafter referred to as compound group SX 249).

In the compound (L-1), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 250).

In the compound (L-1), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 251).

In the compound (L-1), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 252).

In the compound (L-1), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 253).

In the compound (L-1), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 254).

In the compound (L-1), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 255).

In the compound (L-1), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 256).

In the compound (L-1), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 257).

In the compound (L-1), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 258).

In the compound (L-1), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 259).

In the compound (L-1), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 260).

In the compound (L-1), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 261).

In the compound (L-1), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 262).

In the compound (L-1), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 263).

In the compound (L-1), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ] ]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 264).

In the compound (L-1), Q is Q27Radical, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 265).

In the compound (L-1), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 266).

In the compound (L-1), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 267).

In the compound (L-1), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 268).

In the compound (L-1), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 269).

In the compound (L-1), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 270).

In the compound represented by the formula (L-2) (hereinafter, referred to as the compound (L-2)), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 271).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 272).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 273).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 274).

In the compound (L-2), Q is a group represented by Q13, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 275).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 276).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 277).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 278).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 279).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 280).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 281).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 282).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 283).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 284).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 285).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cIs hydrogenAtomic compounds (hereinafter, referred to as compound group SX 286).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 287).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 288).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 289).

In the compound (L-2), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 290).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 291).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 292).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 293).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 294).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 295).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 296).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 297).

In the compound (L-2), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 298).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 299).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 300).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 301).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom,R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 302).

In the compound (L-2), Q is a group represented by Q12, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 303).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 304).

In the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 305).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 306).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 307).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 308).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound being a hydrogen atom (hereinafter, described as chemical formula)Composition set SX 309).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 310).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 311).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 312).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 313).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 314).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 315).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 316).

In the compound (L-2), Q is Q19Radical, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 317).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 318).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 319).

In the compound (L-2), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 320).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 321).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 322).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 323).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 324).

In the compound (L-2), Q is a group represented by Q27, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 325).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 326).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 327).

In the compound (L-2), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 328).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 329).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 330).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 331).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound which is a hydrogen atom (hereinafter, referred to as a compound)Set SX 332).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 333).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 334).

In the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 335).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 336).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 337).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 338).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 339).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 340).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 341).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 342).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 343).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 344).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 345).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 346).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cIs conversion of hydrogen atomsA compound (hereinafter, referred to as compound group SX 347).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 348).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 349).

In the compound (L-2), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 350).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 351).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 352).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 353).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 354).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cCompounds which are hydrogen atoms (hereinafter, referred to as compound group S)X355)。

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 356).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 357).

In the compound (L-2), Q is a group represented by Q28, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 358).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 359).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 360).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 361).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 362).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any one of the aboveSubstituent, R^3bIs a bromine atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 363).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 364).

In the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 365).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 366).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 367).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 368).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 369).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cCompounds being hydrogen atoms (hereinafter, referred to as compound group SX)370)。

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 371).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 372).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 373).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 374).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 375).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 376).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 377).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any one of the aboveSubstituent, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 378).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 379).

In the compound (L-2), Q is a group represented by Q22, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 380).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 381).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 382).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 383).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 384).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 385).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bTo hydrogen atomsSeed, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 386).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 387).

In the compound (L-2), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 388).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 389).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 390).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 391).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 392).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 393).

In the compound (L-2), Q isGroup represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 394).

In the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 395).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 396).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 397).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 398).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter, referred to as compound group SX 399).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 400).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1)、R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 401).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ] ]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 402).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 403).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 404).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 405).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 406).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 407).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 408).

In the compound (L-2), Q is QGroup represented by 21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 409).

In the compound (L-2), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 410).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 411).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 412).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 413).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 414).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 415).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 416).

In the compound (L-2), Q is Q28Group of (A), R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 417).

In the compound (L-2), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 418).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 419).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 420).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 421).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 422).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 423).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cIs a trifluoromethylA basic compound (hereinafter referred to as compound group SX 424).

In the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 425).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 426).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound (hereinafter, referred to as compound group SX427) which is a trifluoromethyl group.

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 428).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 429).

In the compound (L-2), Q is a group represented by Q15, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 430).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 431).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 432).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 433).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 434).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 435).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 436).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 437).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 438).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 439).

In the compound (L-2), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 440).

In the compound (L-2), Q is a group represented by Q23, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 441).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 442).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 443).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 444).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 445).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 446).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any one of the extracts described in (1)Substituent group, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 447).

In the compound (L-2), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter referred to as compound group SX 448).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 449).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 450).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 451).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 452).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 453).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 454).

Chemical combinationIn the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 455).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 456).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 457).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 458).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 459).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 460).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 461).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 462).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 463).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 464).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 465).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 466).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 467).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 468).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 469).

In the compound (L-2), Q is Q22Radical, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 470).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 471).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 472).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 473).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 474).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 475).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 476).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 477).

Compound (L-2) Wherein Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 478).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 479).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 480).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 481).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 482).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 483).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 484).

In the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 485).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 486).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 487).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 488).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 489).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 490).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 491).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 492).

Compound (L-2) Wherein Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 493).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 494).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 495).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R ^3cA compound having a bromine atom (hereinafter referred to as compound group SX 496).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 497).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 498).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 499).

In the compound (L-2), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 500).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 501).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 502).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 503).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 504).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 505).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 506).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 507).

In the compound (L-2), Q is a group represented by Q28, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cIs bromogenA daughter compound (hereinafter referred to as compound group SX 508).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 509).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 510).

In the compound (L-2), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 511).

In the compound (L-2), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 512).

In the compound (L-2), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 513).

In the compound (L-2), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 514).

In the compound (L-2), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 515).

In the compound (L-2), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 516).

In the compound (L-2), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 517).

In the compound (L-2), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 518).

In the compound (L-2), Q is a group represented by Q15, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 519).

In the compound (L-2), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 520).

In the compound (L-2), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 521).

In the compound (L-2), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 522).

In the compound (L-2), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cIs a iodine atomA daughter compound (hereinafter referred to as compound group SX 523).

In the compound (L-2), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R ^3cA compound having an iodine atom (hereinafter referred to as compound group SX 524).

In the compound (L-2), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 525).

In the compound (L-2), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cAnd compounds containing an iodine atom (hereinafter, referred to as compound group SX 526).

In the compound (L-2), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 527).

In the compound (L-2), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 528).

In the compound (L-2), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 529).

In the compound (L-2), Q is a group represented by Q22, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 530).

In the compound (L-2), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom,R^3cAnd compounds having an iodine atom (hereinafter referred to as compound group SX 531).

In the compound (L-2), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 532).

In the compound (L-2), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 533).

In the compound (L-2), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 534).

In the compound (L-2), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 535).

In the compound (L-2), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 536).

In the compound (L-2), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cAnd compounds having an iodine atom (hereinafter referred to as compound group SX 537).

In the compound (L-2), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 538).

In the compound (L-2), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Is described inAny substituent of (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 539).

In the compound (L-2), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 540).

In the compound represented by the formula (L-3) (hereinafter, referred to as the compound (L-3)), Q is a group represented by Q11, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 541).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 542).

In the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 543).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 544).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 545).

In the compound (L-3)Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 546).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 547).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 548).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 549).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 550).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 551).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 552).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any one of the extracts described in (1)Substituent group, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 553).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 554).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 555).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 556).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 557).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 558).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 559).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 560).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2 ]A]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 561).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 562).

In the compound (L-3), Q is a group represented by Q25, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 563).

In the compound (L-3), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 564).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 565).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 566).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 567).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 568).

In the compound (L-3), Q is QGroup represented by 29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 569).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 570).

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 571).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 572).

In the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 573).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 574).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 575).

In the compound (L-3), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 576).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 577).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 578).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 579).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 580).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 581).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 582).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 583).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 584).

In the compound (L-3), Q is a group represented by Q18, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 585).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 586).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 587).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 588).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 589).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 590).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound that is a hydrogen atom (hereinafter,as depicted for compound set SX 591).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 592).

In the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 593).

In the compound (L-3), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 594).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 595).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 596).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 597).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 598).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 599).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs trifluoromethyl, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 600).

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 601).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 602).

In the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 603).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 604).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 605).

In the compound (L-3), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 606).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 607).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 608).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 609).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 610).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 611).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 612).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 613).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1)、R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 614).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 615).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 616).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 617).

In the compound (L-3), Q is a group represented by Q20, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 618).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 619).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 620).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 621).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Chinese character' ZhongjiCarrying any substituent, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 622).

In the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 623).

In the compound (L-3), Q is a group represented by Q26, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 624).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 625).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 626).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 627).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 628).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 629).

In the compound (L-3), Q is Q30Group of (A), R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a chlorine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 630).

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 631).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 632).

In the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 633).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 634).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 635).

In the compound (L-3), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 636).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 637).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 638).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 639).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 640).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 641).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 642).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 643).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 644).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 645).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 646).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 647).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 648).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 649).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 650).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 651).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 652).

Chemical combinationIn the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 653).

In the compound (L-3), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 654).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 655).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 656).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 657).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 658).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 659).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a bromine atom, R^3cCompounds being hydrogen atoms (hereinafter, referred to as compound group)SX660)。

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 661).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 662).

In the compound (L-3), Q is a group represented by Q12, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 663).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 664).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 665).

In the compound (L-3), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 666).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 667).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ watch ]1A]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 668).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 669).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 670).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 671).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 672).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 673).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 674).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 675).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 676).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 677).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 678).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 679).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 680).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 681).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 682).

In the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound of hydrogen atom (hereinafterAnd is marked as compound group SX 683).

In the compound (L-3), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 684).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 685).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 686).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 687).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 688).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 689).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs an iodine atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 690).

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substitution described in (1)Radical, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 691).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 692).

In the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 693).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 694).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 695).

In the compound (L-3), Q is a group represented by Q13, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 696).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 697).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cCompound represented by trifluoromethyl (hereinafter, referred to as "trifluoromethyl")Compound group SX 698).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 699).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 700).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 701).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 702).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 703).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 704).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 705).

Q in the compound (L-3) is Q18A group shown, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 706).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 707).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 708).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 709).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 710).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 711).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 712).

In the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 713).

In the compound (L-3), Q is a group represented by Q26、R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 714).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 715).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 716).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 717).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 718).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 719).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 720).

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter, referred to as "chlorine atom")Compound group SX 721).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 722).

In the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 723).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 724).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 725).

In the compound (L-3), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 726).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 727).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 728).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 729).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 730).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 731).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 732).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 733).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R ^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 734).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 735).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs hydrogenAtom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 736).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 737).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 738).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 739).

In the compound (L-3), Q is a group represented by Q22, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 740).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 741).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 742).

In the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 743).

In the compound (L-3), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter, described as chemical formula)Composition set SX 744).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 745).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 746).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 747).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 748).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 749).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 750).

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 751).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 752).

In the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 753).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 754).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 755).

In the compound (L-3), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 756).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 757).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 758).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound which is a bromine atom (hereinafter, described asCompound set SX 759).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 760).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 761).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 762).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 763).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 764).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 765).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 766).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R ^3cA compound having a bromine atom (hereinafter referred to as compound group SX 767).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 768).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 769).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 770).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 771).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 772).

In the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 773).

In the compound (L-3), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 774).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Is described inAny substituent of (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 775).

In the compound (L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 776).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 777).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 778).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 779).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 780).

In the compound (L-3), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 781).

In the compound (L-3), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 782).

Chemical combinationIn the compound (L-3), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 783).

In the compound (L-3), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 784).

In the compound (L-3), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 785).

In the compound (L-3), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 786).

In the compound (L-3), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 787).

In the compound (L-3), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 788).

In the compound (L-3), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 789).

In the compound (L-3), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 790).

In the compound (L-3), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 791).

In the compound (L-3), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 792).

In the compound (L-3), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 793).

In the compound (L-3), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 794).

In the compound (L-3), Q is a group represented by Q18, R^1aIs a hydrogen atom, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 795).

In the compound (L-3), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 796).

In the compound (L-3), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 797).

In the compound (L-3), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 798).

In the compound (L-3), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 799).

In the compound (L-3), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 800).

In the compound (L-3), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 801).

In the compound (L-3), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 802).

In the compound (L-3), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 803).

In the compound (L-3), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 804).

In the compound (L-3), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 805).

Compound (A) to (B)In L-3), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R ^3cA compound having an iodine atom (hereinafter referred to as compound group SX 806).

In the compound (L-3), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 807).

In the compound (L-3), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 808).

In the compound (L-3), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 809).

In the compound (L-3), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 810).

In the compound represented by the formula (L-4) (hereinafter, referred to as the compound (L-4)), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 811).

In the compound (L-4), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 812).

In the compound (L-4), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 813).

In the compound (L-4), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 814).

In the compound (L-4), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 815).

In the compound (L-4), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 816).

In the compound (L-4), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 817).

In the compound (L-4), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 818).

In the compound (L-4), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 819).

In the compound (L-4), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 820).

In the compound (L-4), Q is Q16Radical, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 821).

In the compound (L-4), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 822).

In the compound (L-4), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 823).

In the compound (L-4), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 824).

In the compound (L-4), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 825).

In the compound (L-4), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 826).

In the compound (L-4), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 827).

In the compound (L-4), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 828).

In the compound (L-4), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter, referred to as "hydrogen atom")Compound group SX 829).

In the compound (L-4), Q is a group represented by Q22, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 830).

In the compound (L-4), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 831).

In the compound (L-4), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 832).

In the compound (L-4), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 833).

In the compound (L-4), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 834).

In the compound (L-4), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 835).

In the compound (L-4), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 836).

In the compound (L-4), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 837).

In the compound (L-4), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 838).

In the compound (L-4), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 839).

In the compound (L-4), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 840).

In the compound (L-4), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 841).

In the compound (L-4), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 842).

In the compound (L-4), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 843).

In the compound (L-4), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 844).

In the compound (L-4), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 845).

In the compound (L-4), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 846).

In the compound (L-4), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 847).

In the compound (L-4), Q is a group represented by Q14, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA trifluoromethyl compound (hereinafter referred to as compound group SX 848).

In the compound (L-4), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 849).

In the compound (L-4), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 850).

In the compound (L-4), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA trifluoromethyl group (hereinafter referred to as compound group SX 851).

In the compound (L-4), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA trifluoromethyl compound (hereinafter referred to as compound set SX 852).

In the compound (L-4), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 853).

In the compound (L-4), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 854).

In the compound (L-4), Q is a group represented by Q18,R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 855).

In the compound (L-4), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 856).

In the compound (L-4), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 857).

In the compound (L-4), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 858).

In the compound (L-4), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 859).

In the compound (L-4), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 860).

In the compound (L-4), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 861).

In the compound (L-4), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 862).

In the compound (L-4), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 863).

In the compound (L-4), Q is a group represented by Q26Group, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 864).

In the compound (L-4), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 865).

In the compound (L-4), Q is a group represented by Q27, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 866).

In the compound (L-4), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 867).

In the compound (L-4), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound which is a trifluoromethyl group (hereinafter referred to as compound group SX 868).

In the compound (L-4), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 869).

In the compound (L-4), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 870).

In the compound (L-4), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 871).

In the compound (L-4), Q is a group represented by Q11, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cIs a conversion of chlorine atomsCompound (hereinafter, referred to as compound group SX 872).

In the compound (L-4), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 873).

In the compound (L-4), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 874).

In the compound (L-4), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 875).

In the compound (L-4), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 876).

In the compound (L-4), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 877).

In the compound (L-4), Q is a group represented by Q14, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 878).

In the compound (L-4), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 879).

In the compound (L-4), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 880).

In the compound (L-4), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 881).

In the compound (L-4), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 882).

In the compound (L-4), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 883).

In the compound (L-4), Q is a group represented by Q17, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 884).

In the compound (L-4), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 885).

In the compound (L-4), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 886).

In the compound (L-4), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 887).

In the compound (L-4), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 888).

In the compound (L-4), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1),R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 889).

In the compound (L-4), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ] ]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 890).

In the compound (L-4), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 891).

In the compound (L-4), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 892).

In the compound (L-4), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 893).

In the compound (L-4), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 894).

In the compound (L-4), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 895).

In the compound (L-4), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 896).

In the compound (L-4), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 897).

In the compound (L-4), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any one of the extracts described in (1)Substituent group, R^1bIs a hydrogen atom, R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 898).

In the compound (L-4), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 899).

In the compound (L-4), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a chlorine atom (hereinafter referred to as compound group SX 900).

In the compound (L-4), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 901).

In the compound (L-4), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3cA compound having a bromine atom (hereinafter referred to as compound group SX 902).

In the compound (L-4), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 903).

In the compound (L-4), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 904).

In the compound (L-4), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 905).

In the compound (L-4), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 906).

In the compound (L-4), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 907).

In the compound (L-4), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 908).

In the compound (L-4), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 909).

In the compound (L-4), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 910).

In the compound (L-4), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 911).

In the compound (L-4), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 912).

In the compound (L-4), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 913).

In the compound (L-4), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ] ]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 914).

In the compound (L-4), Q is a group represented by Q18Group, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 915).

In the compound (L-4), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 916).

In the compound (L-4), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 917).

In the compound (L-4), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 918).

In the compound (L-4), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 919).

In the compound (L-4), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3cA compound having a bromine atom (hereinafter referred to as compound group SX 920).

In the compound (L-4), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 921).

In the compound (L-4), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 922).

In the compound (L-4), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 923).

In the compound (L-4), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 924).

In the compound (L-4), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 925).

In the compound (L-4), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 926).

In the compound (L-4), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 927).

In the compound (L-4), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 928).

In the compound (L-4), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter, referred to as compound group SX 929).

In the compound (L-4), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having a bromine atom (hereinafter referred to as compound group SX 930).

In the compound (L-4), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cAnd compounds having an iodine atom (hereinafter, referred to as compound group SX 931).

In the compound (L-4), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cCompounds being iodine atoms (hereinafter, referred to as compound group SX 932))。

In the compound (L-4), Q is a group represented by Q12, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 933).

In the compound (L-4), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 934).

In the compound (L-4), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 935).

In the compound (L-4), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 936).

In the compound (L-4), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 937).

In the compound (L-4), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 938).

In the compound (L-4), Q is a group represented by Q15, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 939).

In the compound (L-4), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 940).

In the compound (L-4), Q is QGroup represented by 16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 941).

In the compound (L-4), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 942).

In the compound (L-4), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 943).

In the compound (L-4), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 944).

In the compound (L-4), Q is a group represented by Q18, R ^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 945).

In the compound (L-4), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 946).

In the compound (L-4), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 947).

In the compound (L-4), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 948).

In the compound (L-4), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cCompounds being iodine atoms(hereinafter referred to as compound group SX 949).

In the compound (L-4), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 950).

In the compound (L-4), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3cA compound having an iodine atom (hereinafter referred to as compound group SX 951).

In the compound (L-4), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 952).

In the compound (L-4), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 953).

In the compound (L-4), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cAnd compounds having an iodine atom (hereinafter referred to as compound group SX 954).

In the compound (L-4), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 955).

In the compound (L-4), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 956).

In the compound (L-4), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 957).

In the compound (L-4), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom,R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 958).

In the compound (L-4), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 959).

In the compound (L-4), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3cA compound having an iodine atom (hereinafter referred to as compound group SX 960).

In the compound represented by the formula (L-5) (hereinafter, referred to as the compound (L-5)), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 961).

In the compound (L-5), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 962).

In the compound (L-5), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 963).

In the compound (L-5), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 964).

In the compound (L-5), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 965).

In the compound (L-5), Q is QGroup represented by 13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 966).

In the compound (L-5), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 967).

In the compound (L-5), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 968).

In the compound (L-5), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 969).

In the compound (L-5), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 970).

In the compound (L-5), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 971).

In the compound (L-5), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 972).

In the compound (L-5), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 973).

In the compound (L-5), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]The method ofAny substituent, R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 974).

In the compound (L-5), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 975).

In the compound (L-5), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 976).

In the compound (L-5), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 977).

In the compound (L-5), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 978).

In the compound (L-5), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 979).

In the compound (L-5), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 980).

In the compound (L-5), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 981).

In the compound (L-5), Q is a group represented by Q24, R^1bIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 982).

In the compound (L-5), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 983).

In the compound (L-5), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 984).

In the compound (L-5), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 985).

In the compound (L-5), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 986).

In the compound (L-5), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 987).

In the compound (L-5), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 988).

In the compound (L-5), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 989).

In the compound (L-5), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a hydrogen atom (hereinafter referred to as compound group SX 990).

In the compound (L-5), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 991).

Compound (I)In (L-5), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 992).

In the compound (L-5), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 993).

In the compound (L-5), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 994).

In the compound (L-5), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 995).

In the compound (L-5), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 996).

In the compound (L-5), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 997).

In the compound (L-5), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 998).

In the compound (L-5), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 999).

In the compound (L-5), Q is a group represented by Q15, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1000).

In the compound (L-5), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1001).

In the compound (L-5), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 1002).

In the compound (L-5), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1003).

In the compound (L-5), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1004).

In the compound (L-5), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1005).

In the compound (L-5), Q is a group represented by Q18, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1006).

In the compound (L-5), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1007).

In the compound (L-5), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1),R^3bA compound which is a trifluoromethyl group (hereinafter referred to as compound group SX 1008).

In the compound (L-5), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1009).

In the compound (L-5), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1010).

In the compound (L-5), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter referred to as compound group SX 1011).

In the compound (L-5), Q is a group represented by Q24, R ^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 1012).

In the compound (L-5), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound represented by a trifluoromethyl group (hereinafter referred to as compound group SX 1013).

In the compound (L-5), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 1014).

In the compound (L-5), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 1015).

In the compound (L-5), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1016).

In the compound (L-5), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ 2 ]TABLE 1A]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1017).

In the compound (L-5), Q is a group represented by Q28, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound represented by a trifluoromethyl group (hereinafter, referred to as compound group SX 1018).

In the compound (L-5), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1019).

In the compound (L-5), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound which is a trifluoromethyl group (hereinafter, referred to as compound group SX 1020).

In the compound (L-5), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1021).

In the compound (L-5), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1022).

In the compound (L-5), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1023).

In the compound (L-5), Q is a group represented by Q12, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1024).

In the compound (L-5), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter, described as chemical formula)Composition set SX 1025).

In the compound (L-5), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1026).

In the compound (L-5), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1027).

In the compound (L-5), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1028).

In the compound (L-5), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1029).

In the compound (L-5), Q is a group represented by Q15, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1030).

In the compound (L-5), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1031).

In the compound (L-5), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1032).

In the compound (L-5), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1033).

In the compound (L-5), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1034).

In the compound (L-5), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1035).

In the compound (L-5), Q is a group represented by Q18, R ^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1036).

In the compound (L-5), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1037).

In the compound (L-5), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1038).

In the compound (L-5), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1039).

In the compound (L-5), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1040).

In the compound (L-5), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1041).

In the compound (L-5), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1042).

In the compound (L-5), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1043).

In the compound (L-5), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1044).

In the compound (L-5), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1045).

In the compound (L-5), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1046).

In the compound (L-5), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1047).

In the compound (L-5), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1048).

In the compound (L-5), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1049).

In the compound (L-5), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a chlorine atom (hereinafter referred to as compound group SX 1050).

In the compound (L-5), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1051).

In the compound (L-5), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1052).

In the compound (L-5), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1053).

In the compound (L-5), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1054).

In the compound (L-5), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1055).

In the compound (L-5), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1056).

In the compound (L-5), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1057).

In the compound (L-5), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1058).

In the compound (L-5), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bCompounds being bromine atoms (hereinafter, referred to as compound group SX 1059))。

In the compound (L-5), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1060).

In the compound (L-5), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1061).

In the compound (L-5), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1062).

In the compound (L-5), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1063).

In the compound (L-5), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1064).

In the compound (L-5), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1065).

In the compound (L-5), Q is a group represented by Q18, R^1aIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1066).

In the compound (L-5), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1067).

In the compound (L-5), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1068).

In the compound (L-5), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1069).

In the compound (L-5), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1070).

In the compound (L-5), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1071).

In the compound (L-5), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1072).

In the compound (L-5), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1073).

In the compound (L-5), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1074).

In the compound (L-5), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1075).

In the compound (L-5), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1076).

In the compound (L-5), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1077).

In the compound (L-5), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1078).

In the compound (L-5), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1079).

In the compound (L-5), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having a bromine atom (hereinafter referred to as compound group SX 1080).

In the compound (L-5), Q is a group represented by Q11, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1081).

In the compound (L-5), Q is a group represented by Q11, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1082).

In the compound (L-5), Q is a group represented by Q12, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1083).

In the compound (L-5), Q is a group represented by Q12, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1084).

In the compound (L-5), Q is a group represented by Q13, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bIs conversion of iodine atomsCompound (hereinafter, referred to as compound group SX 1085).

In the compound (L-5), Q is a group represented by Q13, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1086).

In the compound (L-5), Q is a group represented by Q14, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1087).

In the compound (L-5), Q is a group represented by Q14, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1088).

In the compound (L-5), Q is a group represented by Q15, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1089).

In the compound (L-5), Q is a group represented by Q15, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1090).

In the compound (L-5), Q is a group represented by Q16, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1091).

In the compound (L-5), Q is a group represented by Q16, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1092).

In the compound (L-5), Q is a group represented by Q17, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1093).

In the compound (L-5), Q is a group represented by Q17, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1094).

In the compound (L-5), Q is a group represented by Q18, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1095).

In the compound (L-5), Q is a group represented by Q18, R^1aIs [ Table 1A ] ]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1096).

In the compound (L-5), Q is a group represented by Q19, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1097).

In the compound (L-5), Q is a group represented by Q20, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1098).

In the compound (L-5), Q is a group represented by Q21, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1099).

In the compound (L-5), Q is a group represented by Q22, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1100).

In the compound (L-5), Q is a group represented by Q23, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1101).

In the compound (L-5), Q is a group represented by Q24, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R ^3bCompounds containing iodine atoms (hereinafter referred to as compound group SX 1)102)。

In the compound (L-5), Q is a group represented by Q25, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1103).

In the compound (L-5), Q is a group represented by Q26, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1104).

In the compound (L-5), Q is a group represented by Q27, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1105).

In the compound (L-5), Q is a group represented by Q27, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1106).

In the compound (L-5), Q is a group represented by Q28, R^1aIs a hydrogen atom, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1107).

In the compound (L-5), Q is a group represented by Q28, R^1aIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^1bIs a hydrogen atom, R ^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1108).

In the compound (L-5), Q is a group represented by Q29, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1109).

In the compound (L-5), Q is a group represented by Q30, R^1bIs [ Table 1A ]]Or [ Table 2A ]]Any substituent described in (1), R^3bA compound having an iodine atom (hereinafter referred to as compound group SX 1110).

Q31 to Q60 are the following groups.

In the compound represented by the formula (L-6) (hereinafter, referred to as the compound (L-6)), Q is a group represented by Q31, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1111).

[ Table 11]

[ Table 12]

[ Table 13]

In the compound (L-6), Q is a group represented by Q32, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1112).

In the compound (L-6), Q is a group represented by Q33, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1113).

In the compound (L-6), Q is a group represented by Q34, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 1114).

In the compound (L-6), Q is a group represented by Q35, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1115).

In the compound (L-6), Q is a group represented by Q36, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1116).

In the compound (L-6), Q is a group represented by Q37, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1117).

In the compound (L-6), Q is a group represented by Q38, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1118).

In the compound (L-6), Q is a group represented by Q39, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1119).

In the compound (L-6), Q is a group represented by Q40, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1120).

In the compound (L-6), Q is a group represented by Q41, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 1121).

In the compound (L-6), Q is a group represented by Q42, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 1122).

In the compound (L-6), Q is a group represented by Q43, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1123).

In the compound (L-6), Q is a group represented by Q44, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1124).

In the compound (L-6), Q is a group represented by Q45, R^1bIs CF ₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1125).

In the compound (L-6), Q is a group represented by Q46, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1126).

In the compound (L-6), Q is a group represented by Q47, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1127).

In the compound (L-6), Q is a group represented by Q48, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1128).

In the compound (L-6), Q is a group represented by Q49, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1129).

In the compound (L-6), Q is a group represented by Q50, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1130).

In the compound (L-6), Q is a group represented by Q51, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1131).

In the compound (L-6), Q is a group represented by Q52, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1132).

In the compound (L-6), Q is a group represented by Q53, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1133).

In the compound (L-6), Q is a group represented by Q54, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1134).

In the compound (L-6), Q is a group represented by Q55, R^1bIs CF₃、G¹And G⁴Is CH、R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1135).

In the compound (L-6), Q is a group represented by Q56, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1136).

In the compound (L-6), Q is a group represented by Q57, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1137).

In the compound (L-6), Q is a group represented by Q58, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1138).

In the compound (L-6), Q is a group represented by Q59, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1139).

In the compound (L-6), Q is a group represented by Q60, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1140).

In the compound (L-6), Q is a group represented by Q31, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1141).

In the compound (L-6), Q is a group represented by Q32, R^1bIs C ₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1142).

In the compound (L-6), Q is a group represented by Q33, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1143).

In the compound (L-6), Q is a group represented by Q34, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1144).

In the compound (L-6), Q is a group represented by Q35, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1145).

In the compound (L-6), Q is a group represented by Q36, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1146).

In the compound (L-6), Q is a group represented by Q37, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1147).

In the compound (L-6), Q is a group represented by Q38, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1148).

In the compound (L-6), Q isGroup represented by Q39, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1149).

In the compound (L-6), Q is a group represented by Q40, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 1150).

In the compound (L-6), Q is a group represented by Q41, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1151).

In the compound (L-6), Q is a group represented by Q42, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1152).

In the compound (L-6), Q is a group represented by Q43, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1153).

In the compound (L-6), Q is a group represented by Q44, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1154).

In the compound (L-6), Q is a group represented by Q45, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound being a hydrogen atom (hereinafter, described as chemical formula)Composition set SX 1155).

In the compound (L-6), Q is a group represented by Q46, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1156).

In the compound (L-6), Q is a group represented by Q47, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1157).

In the compound (L-6), Q is a group represented by Q48, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1158).

In the compound (L-6), Q is a group represented by Q49, R^1aIs C ₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1159).

In the compound (L-6), Q is a group represented by Q50, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1160).

In the compound (L-6), Q is a group represented by Q51, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1161).

In the compound (L-6), Q is a group represented by Q52, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Is described inAny substituent of (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1162).

In the compound (L-6), Q is a group represented by Q53, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1163).

In the compound (L-6), Q is a group represented by Q54, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1164).

In the compound (L-6), Q is a group represented by Q55, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1165).

In the compound (L-6), Q is a group represented by Q56, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1166).

In the compound (L-6), Q is a group represented by Q57, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1167).

In the compound (L-6), Q is a group represented by Q58, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1168).

In the compound (L-6), Q is a group represented by Q59, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1169).

In the compound (L-6), Q is a group represented by Q60, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1170).

In the compound (L-6), Q is a group represented by Q31, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1171).

In the compound (L-6), Q is a group represented by Q32, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1172).

In the compound (L-6), Q is a group represented by Q33, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1173).

In the compound (L-6), Q is a group represented by Q34, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1174).

In the compound (L-6), Q is a group represented by Q35, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1175).

In the compound (L-6), Q is a group represented by Q36, R^1bIs CF ₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1176).

In the compound (L-6), Q is a group represented by Q37, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1177).

In the compound (L-6), Q is a group represented by Q38, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1178).

In the compound (L-6), Q is a group represented by Q39, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1179).

In the compound (L-6), Q is a group represented by Q40, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1180).

In the compound (L-6), Q is a group represented by Q41, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1181).

In the compound (L-6), Q is a group represented by Q42, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1182).

In the compound (L-6), Q is a group represented by Q43, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1183).

In the compound (L-6), Q is a group represented by Q44, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1184).

In the compound (L-6), Q is a group represented by Q45, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1185).

In the compound (L-6), Q is a group represented by Q46, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1186).

In the compound (L-6), Q is a group represented by Q47, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1187).

In the compound (L-6), Q is a group represented by Q48, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1188).

In the compound (L-6), Q is a group represented by Q49, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1189).

In the compound (L-6), Q is a group represented by Q50, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1190).

In the compound (L-6), Q is a group represented by Q51, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1191).

In the compound (L-6), Q is a group represented by Q52, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1192).

In the compound (L-6), Q is a group represented by Q53, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1193).

In the compound (L-6), Q is a group represented by Q54, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1194).

In the compound (L-6), Q is a group represented by Q55, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1195).

In the compound (L-6), Q is a group represented by Q56, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1196).

In the compound (L-6), Q is a group represented by Q57, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1197).

In the compound (L-6), Q is a group represented by Q58, R^1bIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1198).

In the compound (L-6), Q is a group represented by Q59, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1199).

In the compound (L-6), Q is a group represented by Q60, R^1aIs CF₃、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1200).

In the compound (L-6), Q is a group represented by Q31, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1201).

In the compound (L-6), Q is a group represented by Q32, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1202).

In the compound (L-6), Q is a group represented by Q33, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1203).

In the compound (L-6), Q is a group represented by Q34, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1204).

In the compound (L-6), Q is a group represented by Q35, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1205).

In the compound (L-6), Q is a group represented by Q36, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1206).

In the compound (L-6), Q is a group represented by Q37, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1207).

In the compound (L-6), Q is a group represented by Q38, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1208).

In the compound (L-6), Q is a group represented by Q39, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1209).

In the compound (L-6), Q is a group represented by Q40, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1210).

In the compound (L-6), Q is a group represented by Q41, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1211).

In the compound (L-6), Q is a group represented by Q42, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1212).

In the compound (L-6), Q is a group represented by Q43, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1213).

In the compound (L-6), Q is a group represented by Q44, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1214).

In the compound (L-6), Q is a group represented by Q45, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1215).

In the compound (L-6), Q is a group represented by Q46, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1216).

In the compound (L-6), Q is a group represented by Q47, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1217).

In the compound (L-6), Q is a group represented by Q48, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1218).

In the compound (L-6), Q is a group represented by Q49, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1219).

In the compound (L-6), Q is a group represented by Q50, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1220).

In the compound (L-6), Q is a group represented by Q51, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1221).

In the compound (L-6), Q is a group represented by Q52, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1222).

In the compound (L-6), Q is a group represented by Q53, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1223).

In the compound (L-6), Q is a group represented by Q54, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1224).

In the compound (L-6), Q is a group represented by Q55, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1225).

In the compound (L-6), Q is a group represented by Q56, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1226).

In the compound (L-6), Q is a group represented by Q57, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1227).

In the compound (L-6), Q is a group represented by Q58, R^1bIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1228).

In the compound (L-6), Q is a group represented by Q59, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1229).

In the compound (L-6), Q is a group represented by Q60, R^1aIs C₂F₅、G¹And G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1230).

Q in the compound (L-6) is Q31A group shown, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1231).

In the compound (L-6), Q is a group represented by Q32, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1232).

In the compound (L-6), Q is a group represented by Q33, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1233).

In the compound (L-6), Q is a group represented by Q34, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1234).

In the compound (L-6), Q is a group represented by Q35, R^1bIs CF₃、G¹Is a nitrogen atom, G ⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1235).

In the compound (L-6), Q is a group represented by Q36, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1236).

In the compound (L-6), Q is a group represented by Q37, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as a compound)Set SX 1237).

In the compound (L-6), Q is a group represented by Q38, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1238).

In the compound (L-6), Q is a group represented by Q39, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1239).

In the compound (L-6), Q is a group represented by Q40, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1240).

In the compound (L-6), Q is a group represented by Q41, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1241).

In the compound (L-6), Q is a group represented by Q42, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1242).

In the compound (L-6), Q is a group represented by Q43, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1243).

In the compound (L-6), Q is a group represented by Q44, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any ofA substituent, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1244).

In the compound (L-6), Q is a group represented by Q45, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1245).

In the compound (L-6), Q is a group represented by Q46, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1246).

In the compound (L-6), Q is a group represented by Q47, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1247).

In the compound (L-6), Q is a group represented by Q48, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1248).

In the compound (L-6), Q is a group represented by Q49, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1249).

In the compound (L-6), Q is a group represented by Q50, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1250).

In the compound (L-6), Q is a group represented by Q51, R^1aIs CF ₃、G¹Is nitrogenAtom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1251).

In the compound (L-6), Q is a group represented by Q52, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1252).

In the compound (L-6), Q is a group represented by Q53, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1253).

In the compound (L-6), Q is a group represented by Q54, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1254).

In the compound (L-6), Q is a group represented by Q55, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1255).

In the compound (L-6), Q is a group represented by Q56, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1256).

In the compound (L-6), Q is a group represented by Q57, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1257).

In the compound (L-6)Q is a group represented by Q58, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1258).

In the compound (L-6), Q is a group represented by Q59, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1259).

In the compound (L-6), Q is a group represented by Q60, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1260).

In the compound (L-6), Q is a group represented by Q31, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1261).

In the compound (L-6), Q is a group represented by Q32, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1262).

In the compound (L-6), Q is a group represented by Q33, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1263).

In the compound (L-6), Q is a group represented by Q34, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1264).

In the compound (L-6), Q is a group represented by Q35, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1265).

In the compound (L-6), Q is a group represented by Q36, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1266).

In the compound (L-6), Q is a group represented by Q37, R^1bIs C₂F₅、G¹Is a nitrogen atom, G ⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1267).

In the compound (L-6), Q is a group represented by Q38, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1268).

In the compound (L-6), Q is a group represented by Q39, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1269).

In the compound (L-6), Q is a group represented by Q40, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1270).

In the compound (L-6), Q is a group represented by Q41,R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1271).

In the compound (L-6), Q is a group represented by Q42, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1272).

In the compound (L-6), Q is a group represented by Q43, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1273).

In the compound (L-6), Q is a group represented by Q44, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1274).

In the compound (L-6), Q is a group represented by Q45, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1275).

In the compound (L-6), Q is a group represented by Q46, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1276).

In the compound (L-6), Q is a group represented by Q47, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substitution described in (1)Radical, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1277).

In the compound (L-6), Q is a group represented by Q48, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1278).

In the compound (L-6), Q is a group represented by Q49, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1279).

In the compound (L-6), Q is a group represented by Q50, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1280).

In the compound (L-6), Q is a group represented by Q51, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1281).

In the compound (L-6), Q is a group represented by Q52, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1282).

In the compound (L-6), Q is a group represented by Q53, R^1aIs C₂F₅、G¹Is a nitrogen atom, G ⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1283).

In the compound (L-6), Q is Q54Radical, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1284).

In the compound (L-6), Q is a group represented by Q55, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1285).

In the compound (L-6), Q is a group represented by Q56, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1286).

In the compound (L-6), Q is a group represented by Q57, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1287).

In the compound (L-6), Q is a group represented by Q58, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1288).

In the compound (L-6), Q is a group represented by Q59, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1289).

In the compound (L-6), Q is a group represented by Q60, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs [ Table 3A ]][ Table 11A)]Any ofA substituent, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1290).

In the compound (L-6), Q is a group represented by Q31, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1291).

In the compound (L-6), Q is a group represented by Q32, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1292).

In the compound (L-6), Q is a group represented by Q33, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1293).

In the compound (L-6), Q is a group represented by Q34, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1294).

In the compound (L-6), Q is a group represented by Q35, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1295).

In the compound (L-6), Q is a group represented by Q36, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1296).

In the compound (L-6), Q is a group represented by Q37, R^1bIs CF₃、G¹Is nitrogenAtom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1297).

In the compound (L-6), Q is a group represented by Q38, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1298).

In the compound (L-6), Q is a group represented by Q39, R^1bIs CF ₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1299).

In the compound (L-6), Q is a group represented by Q40, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1300).

In the compound (L-6), Q is a group represented by Q41, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1301).

In the compound (L-6), Q is a group represented by Q42, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1302).

In the compound (L-6), Q is a group represented by Q43, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1303).

In the compound (L-6)Q is a group represented by Q44, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ] ][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1304).

In the compound (L-6), Q is a group represented by Q45, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1305).

In the compound (L-6), Q is a group represented by Q46, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1306).

In the compound (L-6), Q is a group represented by Q47, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1307).

In the compound (L-6), Q is a group represented by Q48, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1308).

In the compound (L-6), Q is a group represented by Q49, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1309).

In the compound (L-6), Q is a group represented by Q50, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to asCompound set SX 1310).

In the compound (L-6), Q is a group represented by Q51, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1311).

In the compound (L-6), Q is a group represented by Q52, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1312).

In the compound (L-6), Q is a group represented by Q53, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1313).

In the compound (L-6), Q is a group represented by Q54, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1314).

In the compound (L-6), Q is a group represented by Q55, R^1bIs CF ₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1315).

In the compound (L-6), Q is a group represented by Q56, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1316).

In the compound (L-6), Q is a group represented by Q57, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1317).

In the compound (L-6), Q is a group represented by Q58, R^1bIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1318).

In the compound (L-6), Q is a group represented by Q59, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1319).

In the compound (L-6), Q is a group represented by Q60, R^1aIs CF₃、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ] ][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1320).

In the compound (L-6), Q is a group represented by Q31, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1321).

In the compound (L-6), Q is a group represented by Q32, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1322).

In the compound (L-6), Q is a group represented by Q33, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1323).

In the compound (L-6), Q is a group represented by Q34, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1324).

In the compound (L-6), Q is a group represented by Q35, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1325).

In the compound (L-6), Q is a group represented by Q36, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1326).

In the compound (L-6), Q is a group represented by Q37, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1327).

In the compound (L-6), Q is a group represented by Q38, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1328).

In the compound (L-6), Q is a group represented by Q39, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1329).

In the compound (L-6), Q is a group represented by Q40, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table of11A]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1330).

In the compound (L-6), Q is a group represented by Q41, R^1bIs C₂F₅、G¹Is a nitrogen atom, G ⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1331).

In the compound (L-6), Q is a group represented by Q42, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1332).

In the compound (L-6), Q is a group represented by Q43, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1333).

In the compound (L-6), Q is a group represented by Q44, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1334).

In the compound (L-6), Q is a group represented by Q45, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1335).

In the compound (L-6), Q is a group represented by Q46, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1336).

In the compound (L-6), Q is Q47Radical, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1337).

In the compound (L-6), Q is a group represented by Q48, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1338).

In the compound (L-6), Q is a group represented by Q49, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1339).

In the compound (L-6), Q is a group represented by Q50, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1340).

In the compound (L-6), Q is a group represented by Q51, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1341).

In the compound (L-6), Q is a group represented by Q52, R^1aIs C₂F₅、G¹Is a nitrogen atom, G ⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1342).

In the compound (L-6), Q is a group represented by Q53, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ watch ]3A][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1343).

In the compound (L-6), Q is a group represented by Q54, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1344).

In the compound (L-6), Q is a group represented by Q55, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1345).

In the compound (L-6), Q is a group represented by Q56, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1346).

In the compound (L-6), Q is a group represented by Q57, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1347).

In the compound (L-6), Q is a group represented by Q58, R^1bIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1348).

In the compound (L-6), Q is a group represented by Q59, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1349).

In the compound (L-6), Q is Q6Group represented by 0, R^1aIs C₂F₅、G¹Is a nitrogen atom, G⁴Is CH, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1350).

In the compound (L-6), Q is a group represented by Q31, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1351).

In the compound (L-6), Q is a group represented by Q32, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1352).

In the compound (L-6), Q is a group represented by Q33, R^1bIs CF ₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1353).

In the compound (L-6), Q is a group represented by Q34, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1354).

In the compound (L-6), Q is a group represented by Q35, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1355).

In the compound (L-6), Q is a group represented by Q36, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound of hydrogen atom (hereinafterAnd is marked as compound group SX 1356).

In the compound (L-6), Q is a group represented by Q37, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1357).

In the compound (L-6), Q is a group represented by Q38, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1358).

In the compound (L-6), Q is a group represented by Q39, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1359).

In the compound (L-6), Q is a group represented by Q40, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1360).

In the compound (L-6), Q is a group represented by Q41, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1361).

In the compound (L-6), Q is a group represented by Q42, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1362).

In the compound (L-6), Q is a group represented by Q43, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table of11A]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1363).

In the compound (L-6), Q is a group represented by Q44, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1364).

In the compound (L-6), Q is a group represented by Q45, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1365).

In the compound (L-6), Q is a group represented by Q46, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1366).

In the compound (L-6), Q is a group represented by Q47, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1367).

In the compound (L-6), Q is a group represented by Q48, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1368).

In the compound (L-6), Q is a group represented by Q49, R^1aIs CF ₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1369).

In the compound (L-6), Q is a group represented by Q50, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1370).

In the compound (L-6), Q is a group represented by Q51, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1371).

In the compound (L-6), Q is a group represented by Q52, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1372).

In the compound (L-6), Q is a group represented by Q53, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1373).

In the compound (L-6), Q is a group represented by Q54, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1374).

In the compound (L-6), Q is a group represented by Q55, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1375).

In the compound (L-6), Q is a group represented by Q56, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1376).

In the compound (L-6), Q is a group represented by Q57, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1377).

In the compound (L-6), Q is a group represented by Q58, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1378).

In the compound (L-6), Q is a group represented by Q59, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1379).

In the compound (L-6), Q is a group represented by Q60, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1380).

In the compound (L-6), Q is a group represented by Q31, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1381).

In the compound (L-6), Q is a group represented by Q32, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1382).

In the compound (L-6), Q is a group represented by Q33, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substitution described in (1)Radical, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1383).

In the compound (L-6), Q is a group represented by Q34, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1384).

In the compound (L-6), Q is a group represented by Q35, R^1bIs C₂F₅、G¹Is CH, G ⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1385).

In the compound (L-6), Q is a group represented by Q36, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1386).

In the compound (L-6), Q is a group represented by Q37, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1387).

In the compound (L-6), Q is a group represented by Q38, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1388).

In the compound (L-6), Q is a group represented by Q39, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1389).

In the compound (L-6), Q is Q40Radical, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1390).

In the compound (L-6), Q is a group represented by Q41, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1391).

In the compound (L-6), Q is a group represented by Q42, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1392).

In the compound (L-6), Q is a group represented by Q43, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1393).

In the compound (L-6), Q is a group represented by Q44, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1394).

In the compound (L-6), Q is a group represented by Q45, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1395).

In the compound (L-6), Q is a group represented by Q46, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any ofA substituent, R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1396).

In the compound (L-6), Q is a group represented by Q47, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1397).

In the compound (L-6), Q is a group represented by Q48, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1398).

In the compound (L-6), Q is a group represented by Q49, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1399).

In the compound (L-6), Q is a group represented by Q50, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1400).

In the compound (L-6), Q is a group represented by Q51, R^1aIs C₂F₅、G¹Is CH, G ⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1401).

In the compound (L-6), Q is a group represented by Q52, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1402).

In the compound (L-6), Q is Q5Group represented by 3, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1403).

In the compound (L-6), Q is a group represented by Q54, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1404).

In the compound (L-6), Q is a group represented by Q55, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter, referred to as compound group SX 1405).

In the compound (L-6), Q is a group represented by Q56, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R ^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1406).

In the compound (L-6), Q is a group represented by Q57, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1407).

In the compound (L-6), Q is a group represented by Q58, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1408).

In the compound (L-6), Q is a group represented by Q59, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound having a hydrogen atom (hereinafter referred to as compound group SX 1409).

In the compound (L-6), Q is a group represented by Q60, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs [ Table 3A ]][ Table 11A)]Any substituent described in (1), R^3cA compound which is a hydrogen atom (hereinafter referred to as compound group SX 1410).

In the compound (L-6), Q is a group represented by Q31, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1411).

In the compound (L-6), Q is a group represented by Q32, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1412).

In the compound (L-6), Q is a group represented by Q33, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1413).

In the compound (L-6), Q is a group represented by Q34, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1414).

In the compound (L-6), Q is a group represented by Q35, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1415).

In the compound (L-6), Q is a group represented by Q36, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1416).

In the compound (L-6), Q is a group represented by Q37, R^1bIs CF ₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1417).

In the compound (L-6), Q is a group represented by Q38, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1418).

In the compound (L-6), Q is a group represented by Q39, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1419).

In the compound (L-6), Q is a group represented by Q40, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1420).

In the compound (L-6), Q is a group represented by Q41, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1421).

In the compound (L-6), Q is a group represented by Q42, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ] ][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1422).

In the compound (L-6), Q is a group represented by Q43, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1423).

In the compound (L-6), Q is a group represented by Q44, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1424).

In the compound (L-6), Q is a group represented by Q45, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1425).

In the compound (L-6), Q is a group represented by Q46, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1426).

In the compound (L-6), Q is a group represented by Q47, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1427).

In the compound (L-6), Q is a group represented by Q48, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1428).

In the compound (L-6), Q is a group represented by Q49, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]Any substitution described in (1)A basic compound (hereinafter, referred to as compound group SX 1429).

In the compound (L-6), Q is a group represented by Q50, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1430).

In the compound (L-6), Q is a group represented by Q51, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1431).

In the compound (L-6), Q is a group represented by Q52, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1432).

In the compound (L-6), Q is a group represented by Q53, R^1aIs CF ₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1433).

In the compound (L-6), Q is a group represented by Q54, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1434).

In the compound (L-6), Q is a group represented by Q55, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1435).

In the compound (L-6), Q is a group represented by Q56, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1436).

In the compound (L-6), Q is a group represented by Q57, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1437).

In the compound (L-6), Q is a group represented by Q58, R^1bIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ] ][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1438).

In the compound (L-6), Q is a group represented by Q59, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1439).

In the compound (L-6), Q is a group represented by Q60, R^1aIs CF₃、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1440).

In the compound (L-6), Q is a group represented by Q31, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1441).

In the compound (L-6), Q is a group represented by Q32, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1442).

In the compound (L-6), Q is Q33Group of (A), R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1443).

In the compound (L-6), Q is a group represented by Q34, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1444).

In the compound (L-6), Q is a group represented by Q35, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1445).

In the compound (L-6), Q is a group represented by Q36, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1446).

In the compound (L-6), Q is a group represented by Q37, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1447).

In the compound (L-6), Q is a group represented by Q38, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1448).

In the compound (L-6), Q is a group represented by Q39, R^1bIs C₂F₅、G¹Is CH, G ⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1449).

In the compound (L-6), Q is a group represented by Q40, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1450).

In the compound (L-6), Q is a group represented by Q41, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1451).

In the compound (L-6), Q is a group represented by Q42, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1452).

In the compound (L-6), Q is a group represented by Q43, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1453).

In the compound (L-6), Q is a group represented by Q44, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A) ]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1454).

In the compound (L-6), Q is a group represented by Q45, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1455).

Q in Compound (L-6)Is a group represented by Q46, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1456).

In the compound (L-6), Q is a group represented by Q47, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1457).

In the compound (L-6), Q is a group represented by Q48, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1458).

In the compound (L-6), Q is a group represented by Q49, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1459).

In the compound (L-6), Q is a group represented by Q50, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1460).

In the compound (L-6), Q is a group represented by Q51, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1461).

In the compound (L-6), Q is a group represented by Q52, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1462).

In the compound (L-6), Q is a group represented by Q53, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1463).

In the compound (L-6), Q is a group represented by Q54, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1464).

In the compound (L-6), Q is a group represented by Q55, R^1bIs C₂F₅、G¹Is CH, G ⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1465).

In the compound (L-6), Q is a group represented by Q56, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1466).

In the compound (L-6), Q is a group represented by Q57, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1467).

In the compound (L-6), Q is a group represented by Q58, R^1bIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1468).

Chemical combinationIn the compound (L-6), Q is a group represented by Q59, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1469).

In the compound (L-6), Q is a group represented by Q60, R^1aIs C₂F₅、G¹Is CH, G⁴Is a nitrogen atom, R^3bIs a hydrogen atom, R^3cIs [ Table 3A ]][ Table 11A) ]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1470).

In the compound represented by the formula (L-7) (hereinafter, referred to as the compound (L-7)), Q is a group represented by Q31, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1471).

In the compound (L-7), Q is a group represented by Q32, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1472).

In the compound (L-7), Q is a group represented by Q33, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1473).

In the compound (L-7), Q is a group represented by Q34, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1474).

In the compound (L-7), Q is a group represented by Q35, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1475).

In the compound (L-7), Q is a group represented by Q36, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1476).

In the compound (L-7), Q is a group represented by Q37, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1477).

In the compound (L-7), Q is a group represented by Q38, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1478).

In the compound (L-7), Q is a group represented by Q39, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1479).

In the compound (L-7), Q is a group represented by Q40, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1480).

In the compound (L-7), Q is a group represented by Q41, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1481).

In the compound (L-7), Q is a group represented by Q42, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1482).

In the compound (L-7), Q is a group represented by Q43, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1483).

In the compound (L-7), Q is a group represented by Q44, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1484).

In the compound (L-7), Q is a group represented by Q45, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1485).

In the compound (L-7), Q is a group represented by Q46, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1486).

In the compound (L-7), Q is a group represented by Q47, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1487).

In the compound (L-7), Q is a group represented by Q48, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1488).

In the compound (L-7), Q is a group represented by Q49, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1489).

In the compound (L-7), Q is a group represented by Q50, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1490).

In the compound (L-7), Q is a group represented by Q51, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1491).

In the compound (L-7), Q is a group represented by Q52, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1492).

In the compound (L-7), Q is a group represented by Q53, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1493).

In the compound (L-7), Q is a group represented by Q54, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1494).

In the compound (L-7), Q is a group represented by Q55, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1495).

In the compound (L-7), Q is a group represented by Q56, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1496).

In the compound (L-7), Q is a group represented by Q57, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1497).

In the compound (L-7), Q is a group represented by Q58, R^1bIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1498).

In the compound (L-7), Q is a group represented by Q59, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound set SX 1499).

In the compound (L-7), Q is a group represented by Q60, R^1aIs CF₃、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1500).

In the compound (L-7), Q is a group represented by Q31, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1501).

In the compound (L-7), Q is a group represented by Q32, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1502).

In the compound (L-7), Q is a group represented by Q33, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1503).

In the compound (L-7), Q is a group represented by Q34, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1504).

In the compound (L-7), Q is a group represented by Q35, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1505).

In the compound (L-7), Q is a group represented by Q36, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1506).

In the compound (L-7), Q is a group represented by Q37, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1507).

In the compound (L-7), Q is a group represented by Q38, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1508).

In the compound (L-7), Q is a group represented by Q39, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1509).

In the compound (L-7), Q is a group represented by Q40, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1510).

In the compound (L-7), Q is a group represented by Q41, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1511).

In the compound (L-7), Q is a group represented by Q42, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1512).

In the compound (L-7), Q is a group represented by Q43, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1513).

In the compound (L-7), Q is a group represented by Q44, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1514).

In the compound (L-7), Q is a group represented by Q45, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1515).

In the compound (L-7), Q is a group represented by Q46, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1516).

In the compound (L-7), Q is a group represented by Q47, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1517).

In the compound (L-7), Q is a group represented by Q48, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1518).

In the compound (L-7), Q is a group represented by Q49, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1519).

In the compound (L-7), Q is a group represented by Q50, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1520).

In the compound (L-7), Q is a group represented by Q51, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1521).

In the compound (L-7), Q is a group represented by Q52, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1522).

In the compound (L-7), Q is a group represented by Q53, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1523).

In the compound (L-7), Q is a group represented by Q54, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1524).

In the compound (L-7), Q is a group represented by Q55, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1525).

In the compound (L-7), Q is a group represented by Q56, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1526).

In the compound (L-7), Q is a group represented by Q57, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1527).

In the compound (L-7), Q is a group represented by Q58, R^1bIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1528).

In the compound (L-7), Q is Q59A group shown, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1529).

In the compound (L-7), Q is a group represented by Q60, R^1aIs C₂F₅、R^3cIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1530).

In the compound represented by the formula (L-8) (hereinafter, referred to as the compound (L-8)), Q is a group represented by Q31, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1531).

In the compound (L-8), Q is a group represented by Q32, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1532).

In the compound (L-8), Q is a group represented by Q33, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1533).

In the compound (L-8), Q is a group represented by Q34, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1534).

In the compound (L-8), Q is a group represented by Q35, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1535).

In the compound (L-8), Q is a group represented by Q36, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1536).

Compound (A) to (B)L-8) wherein Q is a group represented by Q37, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1537).

In the compound (L-8), Q is a group represented by Q38, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1538).

In the compound (L-8), Q is a group represented by Q39, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1539).

In the compound (L-8), Q is a group represented by Q40, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1540).

In the compound (L-8), Q is a group represented by Q41, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1541).

In the compound (L-8), Q is a group represented by Q42, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1542).

In the compound (L-8), Q is a group represented by Q43, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1543).

In the compound (L-8), Q is a group represented by Q44, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1544).

In the compound (L-8), Q is a group represented by Q45, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1545).

In the compound (L-8), Q is Q46, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1546).

In the compound (L-8), Q is a group represented by Q47, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1547).

In the compound (L-8), Q is a group represented by Q48, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1548).

In the compound (L-8), Q is a group represented by Q49, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1549).

In the compound (L-8), Q is a group represented by Q50, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any of the substituents described in (1) (hereinafter, referred to as compound group SX 1550).

In the compound (L-8), Q is a group represented by Q51, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1551).

In the compound (L-8), Q is a group represented by Q52, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1552).

In the compound (L-8), Q is a group represented by Q53, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1553).

In the compound (L-8), Q is a group represented by Q54, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1554).

In the compound (L-8), Q is a group represented by Q55Group, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1555).

In the compound (L-8), Q is a group represented by Q56, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1556).

In the compound (L-8), Q is a group represented by Q57, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1557).

In the compound (L-8), Q is a group represented by Q58, R^1bIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1558).

In the compound (L-8), Q is a group represented by Q59, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1559).

In the compound (L-8), Q is a group represented by Q60, R^1aIs CF₃、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1560).

In the compound (L-8), Q is a group represented by Q31, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1561).

In the compound (L-8), Q is a group represented by Q32, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1562).

In the compound (L-8), Q is a group represented by Q33, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1563).

Compound (L-8)Wherein Q is a group represented by Q34, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1564).

In the compound (L-8), Q is a group represented by Q35, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1565).

In the compound (L-8), Q is a group represented by Q36, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1566).

In the compound (L-8), Q is a group represented by Q37, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1567).

In the compound (L-8), Q is a group represented by Q38, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1568).

In the compound (L-8), Q is a group represented by Q39, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1569).

In the compound (L-8), Q is a group represented by Q40, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1570).

In the compound (L-8), Q is a group represented by Q41, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1571).

In the compound (L-8), Q is a group represented by Q42, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]A compound of any substituent described in (1)Substance (hereinafter, referred to as compound group SX 1572).

In the compound (L-8), Q is a group represented by Q43, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1573).

In the compound (L-8), Q is a group represented by Q44, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1574).

In the compound (L-8), Q is a group represented by Q45, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1575).

In the compound (L-8), Q is a group represented by Q46, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1576).

In the compound (L-8), Q is a group represented by Q47, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1577).

In the compound (L-8), Q is a group represented by Q48, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1578).

In the compound (L-8), Q is a group represented by Q49, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1579).

In the compound (L-8), Q is a group represented by Q50, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1580).

In the compound (L-8), Q is a group represented by Q51, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1581).

In the compound (L-8), Q is a group represented by Q52, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1582).

In the compound (L-8), Q is a group represented by Q53, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1583).

In the compound (L-8), Q is a group represented by Q54, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1584).

In the compound (L-8), Q is a group represented by Q55, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1585).

In the compound (L-8), Q is a group represented by Q56, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1586).

In the compound (L-8), Q is a group represented by Q57, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1587).

In the compound (L-8), Q is a group represented by Q58, R^1bIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1588).

In the compound (L-8), Q is a group represented by Q59, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1589).

In the compound (L-8), Q is a group represented by Q60, R^1aIs C₂F₅、R^3bIs [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1590).

In the compound represented by the formula (L-9) (hereinafter, referred to as the compound (L-9)), n is 1 and R²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]The compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1591).

In the compound (L-9), n is 0 and R²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1592).

In the compound (L-9), n is 2 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1593).

In the compound (L-9), n is 1 and R ²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1594).

In the compound (L-9), n is 0 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1595).

In the compound (L-9), n is 1 and R²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1596).

In the compound (L-9), n is 0 and R²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1597).

In the compound (L-9), n is 2 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1598).

In the compound (L-9), n is 1 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1599).

In the compound (L-9), n is 0 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]Compounds having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1600).

In the compound represented by the formula (L-10) (hereinafter, referred to as the compound (L-10)), n is 1 and R is²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1601).

In the compound (L-10), n is 0 and R²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1602).

In the compound (L-10), n is 2 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF ₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1603).

In the compound (L-10), n is 1 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1604).

In the compound (L-10), n is 0 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1605).

In the compound (L-10), n is 1 and R²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1606).

In the compound (L-10), n is 0 and R²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1607).

In the compound (L-10), n is 2 and R ²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]In the substituent(s) described in (1)A compound having any one of the substituents (hereinafter, referred to as compound group SX 1608).

In the compound (L-10), n is 1 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1609).

In the compound (L-10), n is 0 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]Compounds having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1610).

In the compound represented by the formula (L-11) (hereinafter, referred to as the compound (L-11)), n is 1 and R is²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1611).

In the compound (L-11), n is 0 and R²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ] ][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1612).

In the compound (L-11), n is 2 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1613).

In the compound (L-11), n is 1 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And, and[ Table 3A)][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1614).

In the compound (L-11), n is 0 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1615).

In the compound (L-11), n is 1 and R²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1616).

In the compound (L-11), n is 0 and R ²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1617).

In the compound (L-11), n is 2 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1618).

In the compound (L-11), n is 1 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 16119).

In the compound (L-11), n is 0 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1620).

In the compound represented by the formula (L-12) (hereinafter, referred to as the compound (L-12)), n is 1 and R²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ] ][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1621).

In the compound (L-12), n is 0 and R²Is ethyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1622).

In the compound (L-12), n is 2 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1623).

In the compound (L-12), n is 1 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1624).

In the compound (L-12), n is 0 and R²Is methyl, R^3cIs a hydrogen atom, R^3bIs hydrogen atom, chlorine atom, bromine atom, iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1625).

In the compound (L-12), n is 1 and R²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1626).

In the compound (L-12), n is 0 and R²Is ethyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1627).

In the compound (L-12), n is 2 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1628).

In the compound (L-12), n is 1 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1629).

In the compound (L-12), n is 0 and R²Is methyl, R^3bIs a hydrogen atom, R^3cIs a chlorine atom, a bromine atom, an iodine atom, CF₃And [ Table 3A ]][ Table 11A)]A compound having any one of the substituents described in (1) (hereinafter, referred to as compound group SX 1630).

Next, formulation examples of the compound of the present invention are shown. Parts are parts by weight. The compound S of the present invention is a compound described in compound groups SX1 to SX 1630.

Formulation example 1

Any 1 kind of 10 parts of the compound S of the present invention is mixed with a mixture of 35 parts of xylene and 35 parts of DMF, and 14 parts of polyoxyethylene styryl phenyl ether and 6 parts of calcium dodecylbenzenesulfonate are added thereto and mixed to obtain a preparation.

Preparation example 2

Sodium lauryl sulfate 4 parts, calcium lignosulfonate 2 parts, wet silica 20 parts, and diatomaceous earth 54 parts were mixed, and then any 1 of the compounds S of the present invention was added in 20 parts, and mixed to obtain a preparation.

Preparation example 3

To 1 or 2 parts of any of the compounds S of the present invention, wet silica 1 part, calcium lignosulfonate 2 parts, bentonite 30 parts and kaolin clay 65 parts were added and mixed. Next, an appropriate amount of water was added to the mixture, and the mixture was further stirred, granulated by a granulator, and air-dried to obtain a preparation.

Preparation example 4

1 part of any 1 of the compounds S of the present invention was mixed with an appropriate amount of acetone, 5 parts of wet silica, 0.3 part of isopropyl acid phosphate and 93.7 parts of kaolin clay were added thereto, mixed with stirring thoroughly, and acetone was evaporated off to give a preparation.

Preparation example 5

35 parts of a mixture (weight ratio 1:1) of polyoxyethylene alkyl ether ammonium sulfate salt and wet silica, 20 parts of any 1 of the compounds S of the present invention, and 45 parts of water were thoroughly mixed to obtain a preparation.

Preparation example 6

10 parts of any one of 1 type of the compounds S of the present invention was mixed with a mixture of 18 parts of benzyl alcohol and 9 parts of DMSO, and 6.3 parts of GERONOL (registered trademark) TE250, Ethylan (trademark) NS-500LQ 2.7 parts and 54 parts of solvent naphtha were added thereto and mixed to obtain a preparation.

Preparation example 7

0.1 part of any 1 of the compounds S of the present invention was mixed with a mixture of 5 parts of xylene and 5 parts of trichloroethane, and then mixed with 89.9 parts of kerosene to obtain a preparation.

Preparation example 8

10mg of any 1 of the compounds S of the present invention was mixed with 0.5mL of acetone, and the solution was added dropwise to 5g of an animal solid feed powder (a solid feed powder for breeding CE-2, commercially available from CLEA, Japan) and mixed uniformly. Then, acetone is evaporated and dried to obtain the poison bait.

Preparation example 9

An oil aerosol was obtained by charging 0.1 part of any 1 of the compounds S of the present invention and 49.9 parts of NEOTHIOZOL (available from CENTRAL CHEMICAL CO., LTD.) into an aerosol can, mounting an aerosol valve, filling 25 parts of dimethyl ether and 25 parts of LPG, applying vibration, and mounting an actuator.

Preparation example 10

0.6 part of any 1 of the compounds S of the present invention, 0.01 part of 2, 6-di-t-butyl-4-methylphenol, 5 parts of xylene, 3.39 parts of kerosene and 1 part of RHEODOL (registered trademark) MO-60 were mixed, and the resulting mixture and 50 parts of distilled water were charged into an aerosol container, and after a valve was attached, 40 parts of LPG were charged through the valve to obtain an aqueous aerosol.

Preparation example 11

0.1g of any 1 of the compounds S of the present invention was mixed with 2mL of propylene glycol, and the mixture was impregnated into a ceramic plate of 4.0 cm. times.4.0 cm and 1.2cm in thickness to obtain a heated fumigant.

Preparation example 12

5 parts of any 1 of the compounds S of the present invention and 95 parts of an ethylene-methyl methacrylate copolymer (the ratio of methyl methacrylate to the total weight of the copolymer: 10% by weight) were melt-kneaded, and the resulting kneaded product was extruded from an extrusion molding machine to obtain a rod-shaped molded article having a length of 15cm and a diameter of 3 mm.

Preparation example 13

5 parts of any 1 of the compounds S of the present invention and 95 parts of a soft vinyl chloride resin were melt-kneaded, and the resulting kneaded product was extruded from an extrusion molding machine to obtain a rod-shaped molded article having a length of 15cm and a diameter of 3 mm.

Preparation example 14

100mg of any 1 of the compounds S of the present invention, 68.75mg of lactose, 237.5mg of corn starch, 43.75mg of microcrystalline cellulose, 18.75mg of polyvinylpyrrolidone, 28.75mg of sodium carboxymethyl starch, and 2.5mg of magnesium stearate were mixed, and the resulting mixture was compressed into an appropriate size to obtain tablets.

Preparation example 15

25mg of any 1 of the compounds S of the present invention, 60mg of lactose, 25mg of corn starch, 6mg of carboxymethylcellulose calcium and an appropriate amount of 5% hydroxypropylmethylcellulose were mixed, and the resulting mixture was filled in a hard shell gelatin capsule or a hydroxypropylmethylcellulose capsule to obtain a capsule.

Preparation example 16

To 100mg of any 1 of the compounds S of the present invention, 500mg of fumaric acid, 2000mg of sodium chloride, 150mg of methyl paraben, 50mg of propyl paraben, 25000mg of granulated sugar, 13000mg of sorbitol (70% solution), Veegum (registered trademark) K100mg, 35mg of flavor and 500mg of coloring material was added distilled water so that the final volume became 100ml, followed by mixing to obtain a suspension for oral administration.

Preparation example 17

A liquid preparation for oral administration is obtained by mixing 5 parts of any 1 type of compound S of the present invention with 5 parts of an emulsifier, 3 parts of benzyl alcohol and 30 parts of propylene glycol, adding a phosphate buffer so that the pH of the solution becomes 6.0 to 6.5, and then adding water as the remainder.

Preparation example 18

To fractionated coconut oil 57 parts and polysorbate 85 3 parts, aluminum distearate 5 parts was added and dispersed by heating. It was cooled to room temperature and 25 parts of saccharin were dispersed in the oily vehicle. 10 parts of any 1 of the compounds S of the present invention were mixed therein to obtain a paste preparation for oral administration.

Preparation example 19

Granules for oral administration are obtained by mixing 5 parts of any 1 of the compounds S of the present invention with 95 parts of limestone powder and using a wet particle formation method.

Preparation example 20

Any 1 kind of 5 parts of the compound S of the present invention was mixed with 80 parts of diethylene glycol monoethyl ether, and 15 parts of propylene carbonate was mixed therein to obtain an ejection liquid.

Preparation example 21

10 parts of any 1 of the compounds S of the present invention were mixed with 70 parts of diethylene glycol monoethyl ether and 20 parts of 2-octyldodecanol were mixed therewith to obtain a drench solution.

Preparation example 22

0.1 part of any 1 of the compounds S of the present invention, 40 parts of sodium polyoxyethylene lauryl ether sulfate (25% aqueous solution), 5 parts of lauramidopropyl betaine, 5 parts of coconut fatty acid ethanolamide, 0.5 part of carboxyvinyl polymer and 49.4 parts of purified water were added thereto and mixed well to obtain a shampoo preparation.

Preparation example 23

0.15 part of any 1 of the compounds S of the present invention, 95 parts of animal feed, and 4.85 parts of a mixture composed of calcium hydrogen phosphate, diatomaceous earth, Aerosil (registered trademark), and carbonate (or chalk) were thoroughly mixed with stirring to obtain a feed premix for animals.

Preparation example 24

7.2g of any 1 of the compounds S of the present invention and 92.8g of VOSCO (registered trademark) S-55 were mixed at 100 ℃ and injected into a suppository mold, followed by cooling and solidification to obtain a suppository.

Next, the efficacy of the compound of the present invention against harmful arthropods is shown by test examples. In the following test examples, the test was carried out at 25 ℃.

Test method 1

A test compound was formulated as described in formulation example 6, and water containing 0.03 vol% of sinpain (registered trademark) was added thereto to prepare a diluted solution containing the test compound at a predetermined concentration.

Cucumber (Cucumis sativus) seedlings (2 nd true leaf development stage) planted in a container were inoculated with about 30 cotton aphids (whole stage). After 1 day, the dilution was applied to the seedlings at a rate of 10 mL/seedling. The number of surviving insects was further examined 5 days later, and the control value was obtained from the following equation.

Control limit value (%) { 1- (Cb × Tai)/(Cai × Tb) } × 100

The characters in the formula represent the following meanings.

Cb test number of insects in untreated area

Cai-number of surviving insects under investigation in non-treated area

Tb test insect number in treatment area

Tai-number of surviving insects in investigation of treatment area

Here, the non-treatment zone refers to a zone where the same operation as the treatment zone is performed except that the test compound is not used.

Test examples 1-1

The test was carried out according to test method 1 using the following compound of the present invention as a test compound with the predetermined concentration set at 200ppm, and as a result, the following compound of the present invention showed a control value of 90% or more.

Compound 2 of the present invention

Test examples 1 to 2

The test was carried out according to test method 1 using the following compounds of the present invention as test compounds with the predetermined concentration set at 50ppm, and all of the following compounds of the present invention showed a control value of 90% or more.

Compounds of the invention 2, 4, 5, 7, 8, 9, 10, 11, 14, 15, 16, 17, 18, 19

Test method 2

The test compound was formulated as described in formulation example 5, and water was added to the formulation to prepare a diluted solution containing the test compound at a predetermined concentration.

The dilution was poured into the container-planted cucumber seedlings (2 nd main leaf development stage) at a rate of 5 mL/seedling from the roots of the plants. After 7 days, the leaves of the seedlings were inoculated with about 30 cotton aphids (full stage). The number of surviving insects was further examined after 6 days, and the control value was obtained according to the following formula.

Control limit value (%) { 1- (Cb × Tai)/(Cai × Tb) } × 100

The characters in the formula represent the following meanings.

Cb test number of insects in untreated area

Cai-number of surviving insects under investigation in non-treated area

Tb test insect number in treatment area

Tai-number of surviving insects in investigation of treatment area

Here, the non-treatment zone refers to a zone where the same operation as the treatment zone is performed except that the test compound is not used.

Test example 2

The test was carried out according to test method 2 using the following compounds of the present invention as test compounds with the predetermined concentration set to 250ppm, and all of the following compounds of the present invention showed a control value of 90% or more.

Compounds of the invention 2, 4, 5, 8, 19

Test method 3

The test compound was formulated as described in formulation example 6, and water containing 0.03 vol% of sinpain (registered trademark) was added to the formulation to prepare a diluted solution containing the test compound at a predetermined concentration.

The dilution was applied to cabbage (Brassicae oleracea) seedlings (2. sup. nd to 3. sup. rd true leaf development stage) planted in a container at a ratio of 20 mL/seedling. Then, the stem and leaf parts of the seedlings are cut and put into a container paved with filter paper. 5 prodenia litura 3-instar larvae are thrown into the soil. After 5 days, the number of surviving worms was counted, and the dead worm rate was determined according to the following equation.

The dead insect ratio (%) (1-number of surviving insects/5). times.100

Test example 3-1

When the test was carried out according to test method 3 using the following compound of the present invention as a test compound with the predetermined concentration set at 200ppm, the following compound of the present invention showed a ratio of dead insects of 80% or more.

Compound 2 of the present invention

Test examples 3 and 2

When the test was carried out according to test method 3 using the following compounds of the present invention as test compounds with the predetermined concentration set at 50ppm, the following compounds of the present invention all showed a ratio of dead insects of 80% or more.

Compounds of the invention 2, 4, 5, 6, 8, 10, 11, 17, 19

Test method 4

The test compound was formulated as described in formulation example 6, and water containing 0.03 vol% of sinpain (registered trademark) was added to the formulation to prepare a diluted solution containing the test compound at a predetermined concentration.

The diluted solution was applied to cabbage seedlings (2 nd to 3 rd leaf development period) planted in a container at a ratio of 20 mL/seedling. Then, the stem and leaf parts of the seedlings are cut and put into a container paved with filter paper. 5 plutella xylostella 3-instar larvae are thrown into the larvae. After 5 days, the number of surviving worms was counted, and the dead worm rate was determined according to the following equation.

The dead insect ratio (%) (1-number of surviving insects/5). times.100

Test example 4-1

When the test was carried out according to test method 4 using the following compound of the present invention as a test compound with the predetermined concentration set at 200ppm, the following compound of the present invention showed a ratio of dead insects of 80% or more.

Compound 2 of the present invention

Test example 4-2

When the test was carried out according to test method 4 using the following compounds of the present invention as test compounds with the predetermined concentration set at 50ppm, the following compounds of the present invention all showed a ratio of dead insects of 80% or more.

Compounds of the invention 2, 4, 5, 6, 7, 8, 9, 10, 11, 16, 17, 18, 19

Test method 5

The test compound was dissolved in 50. mu.L of a mixed solution of polyoxyethylene sorbitan monolaurate and acetone at a volume ratio of 5:95 (1 mg). To this, water containing 0.03 vol% of sinpain (registered trademark) was added to prepare a diluted solution containing a test compound at a predetermined concentration.

Seedlings of maize (Zea mays) were immersed in this dilution for 30 seconds. The 2 seedlings were then placed in a shallow tray (90 mm diameter) and 10 western corn rootworm 2-instar larvae were applied. After 5 days, the number of dead insects was counted, and the dead insect ratio was determined according to the following equation.

Dead insect ratio (%) (dead insect number/10) × 100

Test example 5

When the test was carried out according to test method 5 using the following compounds of the present invention as test compounds with the predetermined concentration set at 50ppm, the following compounds of the present invention all showed a dead insect ratio of 80% or more.

Compounds of the invention 2, 4, 5, 6, 8

Test method 6

A diluted solution a containing a compound of the present invention at a predetermined concentration was prepared by dissolving 1mg of the compound of the present invention in 10 μ L of a mixed solution of xylene, DMF, and a surfactant (volume ratio), and diluting with water containing 0.02 volume% of a spreader.

A mixed solution of this component (1 mg) in xylene, DMF and a surfactant (4: 4:1 by volume) was diluted with water containing 0.02 vol% of a spreader in 10 μ L to prepare a diluted solution B containing this component at a predetermined concentration.

And mixing the diluent A and the diluent B to obtain a diluent C.

Leaves (length 1.5cm) of cucumber cotyledons are accommodated in each hole of a 24-hole micropore plate, 2 cotton aphid wingless adults and 8 larvae are thrown in each 1 hole, and 20 mu L of diluent C is scattered in each 1 hole. It is used as a treatment area.

In addition, 20. mu.L of water containing 0.02 vol% of a spreader was sprayed instead of the holes of the diluent C to form untreated areas.

After the dilution C was dried, the upper part of the microplate was covered with a membrane. After 5 days, the number of surviving worms in each well was investigated.

The control value was calculated from the following equation.

Control value (%) { 1- (Tai)/(Cai) } × 100

The symbols in the formulae represent the following meanings.

Cai-number of surviving insects under investigation in non-treated area

Tai-number of surviving insects in investigation of treatment area

Specific diluent C whose effect can be confirmed by test method 6 is shown in the following 1) to 5).

1) A diluent C having a concentration of the compound of the present invention of 200ppm and a concentration of the present component of 2000ppm in the combinations shown in Table A. In the list a, Comp X represents 1 compound selected from the compounds 1 to 19 of the present invention.

List a:

compx + clothianidin; compx + thiamethoxam; CompX + Imidacloprid; CompX + thiacloprid; compx + fluropyranone; compx + flonicamid; compx + trifluorobenzene pyrimidine; CompX + Dikemeishi; compx + beta-cyfluthrin; compx + tefluthrin; compx + fipronil; CompX + chlorantraniliprole; CompRX + cyantraniliprole; CompX + Fluorocyantraniliprole; CompX + thiodicarb; compx + carbofuran; compx + fluorine Azoleamide; compx + Aforana; compx + flurarana; compx + bromobenezene bisamide; CompX + avermectin; compx + fluopyram; compx + fluthiaA sulfone; compx + trifluropyrimidine amide; CompX + tioxazafen; compx + flupyrimin; CompX + mycorrhizal fungi; compx + bradyrhizobium japonicum strain TA-11; CompX + Bacillus firmus; CompX + Bacillus firmus strain I-1582; CompX + Bacillus amyloliquefaciens; CompX + Bacillus amyloliquefaciens FZB42 strain; compx + Pasteurella; CompX + Pasteurella Pn1 strain; CompX + invaded Pasteurella multocida; compx + tebuconazole; CompX + prothioconazole; CompX + metconazole; comp x + ipconazole; comp x + triticonazole; CompX + difenoconazole; CompX + imazalil; compx + triadimenol; CompX + tetraconazole; compx + flutriafol; compx + Mandesbin; compx + azoxystrobin; compx + pyraclostrobin; compx + trifloxystrobin; compx + fluoxastrobin; compx + picoxystrobin; compx + fenamidone; compx + metalaxyl; compx + metalaxyl-M; compx + fludioxonil; compx + sedaxane; compx + penflufen; CompX + fluxapyroxad; CompX + propiconazole; compx + boscalid; comp x + carboxin; compx + penthiopyrad; compx + flutolanil; CompX + captan; compx + thiram; CompX + tolclofos-methyl; CompX + thiabendazole; compx + ethaboxam; CompX + mancozeb; compx + tetrazolyl pyritinome; compx + fluorothiazolepyrithylone; compx + silthiopham; CompX + inpyrfluxam.

2) A diluent C having a concentration of the compound of the present invention of 200ppm and a concentration of the present component of 200ppm in the combinations shown in Table A.

3) A dilution C having a concentration of the compound of the present invention of 500ppm and a concentration of the present component of 50ppm in the combinations shown in Table A.

4) A diluent C having a concentration of the compound of the present invention of 500ppm and a concentration of the present component of 5ppm in the combinations shown in Table A.

5) A dilution C having a concentration of the compound of the present invention of 500ppm and a concentration of the present component of 0.5ppm in the combinations shown in Table A.

Industrial applicability

The compound of the present invention exhibits an excellent control effect on harmful arthropods.