阅读说明：本技术 芳杂环化合物、其药物组合物及其应用 (Heteroaromatic compounds, its pharmaceutical composition and its application ) 是由 张健存 邹晴安 陈延维 康宁 张礼军 胡洋 张菊福 于 2019-05-22 设计创作，主要内容包括：本发明提供了作为ATX(Autotaxin)抑制剂的一类新的芳杂环化合物,包含所述化合物的药物组合物,以及使用所述化合物和组合物治疗哺乳动物具有ATX(Autotaxin)表达增加的病理学特征的疾病,其中所述化合物具有式(I)所示结构,或其药学上可接受的盐、水合物、溶剂化物、立体异构体、互变异构体、氮氧化物、代谢物、前药、或混合物；<Image he="251" wi="700" file="DDA0002068588950000011.GIF" imgContent="drawing" imgFormat="GIF" orientation="portrait" inline="no"></Image>其中,R<Sup>1</Sup>、Ar<Sup>1</Sup>、Ar<Sup>2</Sup>、Ar<Sup>3</Sup>、W、Y、Z和Cy均具有本发明所述定义。(The present invention provides a new class of heteroaromatic compounds as ATX (Autotaxin) inhibitor, pharmaceutical composition comprising the compound, and there is the disease of the increased pathological characteristics of ATX (Autotaxin) expression using the compound and composition treatment mammal, wherein the compound has structure or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolin, prodrug or mixture shown in formula (I)； Wherein, R 1 、Ar 1 、Ar 2 、Ar 3 , W, Y, Z and Cy all have definition of the present invention.)

1. compound, be the pharmaceutically acceptable salt of compound shown in compound shown in formula (I) or formula (I), hydrate, Solvate, stereoisomer, tautomer, nitrogen oxides, metabolin, prodrug or mixture:

Wherein,

W is-N (R^1a)-,-O- ,-S- ,-S (=O)_1-2,-C (=O)-,-(C (R^2a)(R^2b))_1-4-、-N(R^1a)(C(R^2a) (R^2b))_1-4-、-N(R^1a) C (=O)-or-O (C (R^2a)(R^2b))_1-4-；

Ar¹And Ar²Five molecular heteroaryls of original are each independently, wherein Ar¹And Ar²Individually optionally by 1,2 or 3 R² Replace；

Ar³For aryl or heteroaryl, wherein the Ar³Individually optionally by 1,2,3 or 4 R³Replace；

Cy is naphthenic base, heterocycle, spiral shell bicyclic group, the miscellaneous bicyclic group of spiral shell, condensed-bicyclic base, to condense miscellaneous bicyclic group, bridged ring base, bridge miscellaneous Ring group, aryl or heteroaryl, wherein the Cy is optionally by 1,2,3 or 4 R⁴Replace；

Y is-(L¹-W¹)_m-L²-；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br, I ,-OH ,- NH₂、-NO₂,-CN and C_1-6The group of alkoxy replaces；

L²It is not present or L²For-O- ,-C (=O)-,-OC (=O)-,-C (=O) O- ,-C (=O)-C (=O)-,-C (=O)-C (=O) N (R^a)-、-N(R^b)-,-C (=O) N (R^c)-、-N(R^c) C (=O)-,-C (=O) N (R^c)-R¹⁵- C (=O) O- ,-C (= O)N(R^c)-R¹⁵- C (=O) N (R^a)-、-N(R^d) C (=O) N (R^c)-、-N(R^g) C (=O) O- ,-S (=O)_0-2,-S (=O)_{1- 2}N(R^e)-、-N(R^f) S (=O)_1-2Or-N (R^f) S (=O)_1-2-R¹⁵-N(R^a)-；

Z is H ,-CN, alkyl, alkenyl, alkynyl, halogenated alkyl, naphthenic base, heterocycle, heterocyclylalkyl group, cycloalkyl-alkyl, spiral shell are double Ring group, spiral shell miscellaneous bicyclic group, condense miscellaneous bicyclic group, bridged ring base, bridge heterocycle, aryl or heteroaryl at condensed-bicyclic base, wherein institute State alkyl, alkenyl, alkynyl, halogenated alkyl, naphthenic base, heterocycle, spiral shell bicyclic group, the miscellaneous bicyclic group of spiral shell, condensed-bicyclic base, condense it is miscellaneous Bicyclic group, bridge ring alkyl, bridge Heterocyclylalkyl, aryl and heteroaryl are optionally by one or more R⁵Replace；

R¹For alkyl, alkenyl, alkynyl, aryl, heteroaryl, naphthenic base or heterocycle, wherein the R¹Individually optionally by 1,2,3 Or 4 R⁶Replace；

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, cyano Substituted alkyl, hydroxyalkyl, alkoxy, alkoxyalkyl, sweet-smelling alkoxy alkyl, aryloxy alkyl, halogenated alkoxy ,-S (= O)_0-2R⁷,-C (=O) R⁸,-C (=O) OR^8a,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、- R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2aAnd R^2bIt is each independently H ,-CN ,-OH ,-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, cyano takes Alkyl, hydroxyalkyl, alkoxy, halogenated alkoxy, aryl, aralkyl, heteroaryl or the heteroaryl alkyl in generation；

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, cyanogen Alkyl, the hydroxyalkyl, alkoxy, halogenated alkoxy ,-S (=O) of base substitution_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a、-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_{1- 2}R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴-OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_{1- 2}R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁴It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogen Alkyl, the hydroxyalkyl, alkoxy, halogenated alkoxy ,-S (=O) that substituted alkyl, cyano replace_0-2R⁷,-C (=O) R⁸,-OS (= O)_1-2R^7a,-C (=O) OR^8a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、- NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、- R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴- NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁵It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, alkane Alkyl, the hydroxyalkyl, alkoxy, halogenated alkoxy, aryl, aralkyl ,-S (=O) that amino, halogenated alkyl, cyano replace_{0- 2}R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、- R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁶It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, cyano Substituted alkyl, hydroxyalkyl, alkoxy, halogenated alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (= O)R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N (R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr- R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, halogenated C_1-6Alkyl, cyanogen The C that base replaces_1-6Alkyl, aryl, aralkyl, heteroaryl, heteroaryl alkyl, naphthenic base, cycloalkyl-alkyl, heterocycle or heterocycle Base alkyl；Each R^9a、R¹⁰And R^10aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6Alkyl, Or halogenated C_1-6Alkyl；

Each R¹¹And R^11aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, halogenated C_1-6The C that alkyl, cyano replace_1-6 Alkyl or aralkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6Alkyl, Or halogenated C_1-6Alkyl；

R^1aIt is separately H, the alkyl that alkyl, alkenyl, alkynyl, halogenated alkyl, cyano replace, hydroxyalkyl, naphthenic base, cycloalkanes Base alkyl, aryl or aralkyl；

Each R^a、R^b、R^c、R^d、R^e、R^f、R^g、R^hAnd RⁱIt is separately H, the alkyl that alkyl, alkenyl, alkynyl, cyano replace, hydroxyl Alkyl, halogenated alkyl, R¹⁶- C (=O)-or cycloalkyl-alkyl；

Each R¹⁴And R¹⁵It is separately alkylidene, the alkylidene or halogeno alkylen that alkenylene, alkynylene, cyano replace；

R¹⁶It is H, C_1-6Alkyl or halogenated C_1-6Alkyl；With

M is 0,1 or 2.

2. compound according to claim 1, wherein Ar³For C_6-10Aryl or C_1-9Heteroaryl, wherein the Ar³It is independent Optionally by 1,2,3 or 4 R³Replace.

3. compound according to claim 1, wherein Ar³Are as follows:

Wherein, X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；With

Y¹、Y^1aAnd Y²It is each independently-N- ,-CH- or-C (R³)-。

4. compound according to claim 1, wherein Ar³For

Wherein, the Ar³Individually optionally by 0,1 or 2 R³Replace.

5. compound according to claim 1, wherein the compound has structure shown in formula (Ia):

Wherein,

X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；

Y¹And Y²It is each independently-N- or-C (R³)-；

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolism Object, prodrug or mixture.

6. compound according to claim 1-5, wherein by Ar¹And Ar²Composition Ring is

Wherein,

X²For-O- ,-S- ,-C (R²)(R^2c)-or-N (R^2d)-；

Y³、Y⁴、Y⁵、Y⁶、Y⁷And Y⁸It is each independently-N- or-C (R²)-；

R^2cFor H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, cyano Substituted C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、- R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2dFor H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, halogenated C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸、-OS (=O)_1-2R^7a,-OC (=O) R^8aOr-OC (=O) NR¹⁰R^10a、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (= O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N (R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene is halogenated C_1-4Alkylidene.

7. compound according to claim 1-5, wherein by Ar¹And Ar²Composition Ring is

Wherein,

X²For-O- ,-S- ,-C (R²)(R^2c)-or-N (R^2d)-；

Y³For-N- or-C (R²)-；

Y⁶For-N- or-C (R²)-；

R^2cFor H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, cyano Substituted C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、- R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2dFor H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, halogenated C_1-4Alkyl, C_1-4Hydroxyalkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-OC (=O) NR¹⁰R^10a、-R¹⁴- S (=O)_0-2R⁷、- R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene is halogenated C_1-4Alkylidene.

8. compound according to claim 1-5, wherein by Ar¹And Ar²Composition Ring is

Wherein, 0,1 or 2 n.

9. compound according to claim 1-5, wherein R¹For C_6-10Aryl, C_1-9Heteroaryl, C_3-8Naphthenic base, Or C_2-7Heterocycle, wherein the R¹Individually optionally by 1,2,3 or 4 R⁶Replace.

10. compound according to claim 1-5, wherein R¹For phenyl or pyridyl group, wherein the phenyl is only It stands optionally by 1,2,3 or 4 R⁶Replace.

11. compound according to claim 1, wherein the compound has structure shown in formula (Ib):

Wherein,

X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；

X²For-O- ,-S- ,-C (R²)(R^2c)-or-N (R^2d)-；

Y¹And Y²It is each independently-N- or-C (R³)-；

Y³、Y⁴、Y⁵And Y⁶It is each independently-N- or-C (R²)-；

T is 0,1,2,3 or 4；

R^2cFor H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, cyano Substituted C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、- R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2dFor H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-OC (=O) NR¹⁰R^10a、-R¹⁴- S (=O)_0-2R⁷、- R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene is halogenated C_1-4Alkylidene；Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxidation Object, metabolin, prodrug or mixture.

12. -5 and 11 described in any item compounds according to claim 1, wherein

W is-N (R^1a)-or-C (R^2a)(R^2b)-；

R^1aFor H, C_1-4Alkyl or halogenated C_1-4Alkyl；With

R^2aAnd R^2bIt is each independently H ,-CN ,-OH ,-NH₂、F、Cl、Br、I、C_1-4Alkyl, halogenated C_1-4Alkyl, cyano replace C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_6-10Aryl, C_6-10Aryl C_1-4Alkyl, C_1-9Heteroaryl or C_1-9Heteroaryl C_1-4 Alkyl.

13. -5 and 11 described in any item compounds according to claim 1, wherein

W is-N (R^1a)-；With

R^1aFor H, methyl, ethyl, propyl ,-CF₃Or-CH₂CF₃。

14. the compound according to claim 5 or 11, wherein

X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；

Y¹And Y²It is each independently-N- or-C (R³)-；

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, halogenated C_1-4Alkyl, cyano replace C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、- N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、- R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, cyanogen The C that base replaces_1-4Alkyl, aryl, aralkyl, heteroaryl, heteroaryl alkyl, naphthenic base, cycloalkyl-alkyl, heterocycle or heterocycle Base alkyl；Each R^9a、R¹⁰And R^10aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, Or halogenated C_1-4Alkyl；

Each R¹¹And R^11aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4 Alkyl or C_6-10Aryl C_1-6Alkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, Or halogenated C_1-4Alkyl；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene is halogenated C_1-4Alkylidene.

15. compound according to claim 1, wherein the compound has structure shown in formula (Ic):

Wherein,

R^1aFor H, C_1-4Alkyl or halogenated C_1-4Alkyl；

T is 0,1,2,3 or 4；

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolism Object, prodrug or mixture.

16. the described in any item compounds in -5,11 and 15 according to claim 1, wherein Cy C_3-8Naphthenic base, C_2-7Heterocycle, C_5-12Spiral shell bicyclic group, C_5-12The miscellaneous bicyclic group of spiral shell, C_5-12Condensed-bicyclic base, C_5-12Condense miscellaneous bicyclic group, C_5-12Bridged ring base, C_5-12Bridge is miscellaneous Ring group, C_6-10Aryl or C_1-9Heteroaryl, wherein the Cy is optionally by 1,2,3 or 4 R⁴Replace.

17. the described in any item compounds in -5,11 and 15 according to claim 1, wherein Cy is

Wherein,

X³、X⁴And X⁵It is each independently-O- ,-S- ,-NH- ,-(CH₂)_m1-NH-(CH₂)_m2-、-(CH₂)_m1-O-(CH₂)_m2-、- (CH₂)_m1-S-(CH₂)_m2Or-(CH₂)_m3-；

Each m1 is separately 1,2,3 or 4；

Each m2 is separately 0,1,2,3 or 4；

Each m3 is separately 1,2,3 or 4；With

N1 is 0,1,2,3 or 4.

18. the described in any item compounds in -5,11 and 15 according to claim 1, wherein Cy is

Wherein, the Cy is optionally by 1,2,3 or 4 R⁴Replace.

19. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Y is-(L¹-W¹)_m-L²-；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br ,-OH ,- NH₂、-NO₂,-CN and C_1-4The group of alkoxy replaces；

L²It is not present or L²For-O- ,-C (=O)-,-OC (=O)-,-C (=O) O- ,-C (=O)-C (=O)-,-C (=O)-C (=O) N (R^a)-、-N(R^b)-,-C (=O) N (R^c)-、-N(R^c) C (=O)-,-N (R^d) C (=O) N (R^c)-,-C (=O) N (R^c)-R¹⁵- C (=O) O- ,-C (=O) N (R^c)-R¹⁵- C (=O) N (R^a)-、-N(R^g) C (=O) O- ,-S (=O)_0-2,-S (= O)_1-2N(R^e)-、-N(R^f) S (=O)_1-2Or-N (R^f) S (=O)_1-2-R¹⁵-N(R^a)-；

Each R^a、R^b、R^c、R^d、R^e、R^f、R^g、R^hAnd RⁱIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, cyano replace C_1-4Alkyl, C_1-4Hydroxyalkyl, halogenated C_1-4Alkyl, R¹⁶- C (=O)-, C_3-6Naphthenic base C_1-4Alkyl；

R¹⁵For C_1-6Alkylidene；

R¹⁶It is H, C_1-4Alkyl or halogenated C_1-4Alkyl；With

M is 0,1 or 2.

20. the described in any item compounds in -5,11 and 15 according to claim 1, wherein Z H,-CN, C_1-4Alkyl, C_2-4Alkene Base, C_2-4Alkynyl, halogenated C_1-4Alkyl, C_3-8Naphthenic base, C_2-7Heterocycle, C_2-7Heterocycle C_1-4Alkyl, C_3-8Naphthenic base C_1-4Alkyl, C_5-12Spiral shell bicyclic group, C_5-12The miscellaneous bicyclic group of spiral shell, C_5-12Condensed-bicyclic base, C_5-12Condense miscellaneous bicyclic group, C_5-12Bridged ring base, C_5-12Bridge is miscellaneous Ring group, C_6-10Aryl or C_1-9Heteroaryl, wherein the C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, C_3-8Cycloalkanes Base, C_2-7Heterocycle, C_5-12Spiral shell bicyclic group, C_5-12The miscellaneous bicyclic group of spiral shell, C_5-12Condensed-bicyclic base, C_5-12Condense miscellaneous bicyclic group, C_5-12Bridge Ring group, C_5-12Bridge heterocycle, C_6-10Aryl and C_1-9Heteroaryl is optionally by one or more R⁵Replace.

21. the described in any item compounds in -5,11 and 15 according to claim 1, wherein Z H,-CN, C_1-4Alkyl, C_2-4Alkene Base, C_2-4Alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl ,-C_1-4Alkyl-NR¹¹R^11aOr C_3-6Cycloalkanes Base or Z are as follows:

Wherein, X⁶For N or CH₂；

X⁷For-O- ,-S- ,-NH- ,-(CH₂)_m4-NH-(CH₂)_m5-、-(CH₂)_m4-O-(CH₂)_m5-、-(CH₂)_m4-S-(CH₂)_m5-、 Or-(CH₂)_m6-；

Each m4 is separately 1,2,3 or 4；

Each m5 is separately 0,1,2,3 or 4；

Each m6 is separately 1,2,3 or 4；With

N2 is 0,1,2,3 or 4.

22. the described in any item compounds in -5,11 and 15 according to claim 1, wherein Z H,-CN, methyl, ethyl, propyl, Tert-butyl ,-CF₃、-CH₂CF₃、-CH₂CH₂CN、-CH₂CH₂OH or Z are

23. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4It is alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, C_6-10Aryl C_1-4Alkane Oxygroup C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、- N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、- R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

24. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, methyl, ethyl, propyl, methoxy, first Oxygroup ethyl, methoxy-propyl, ethoxyl methyl, ethoxyethyl group, benzyloxymethyl, Benzyloxyethyl, phenoxymethyl, benzene Oxygroup ethyl ,-CH₂CH₂CN、-CH₂CH₂OH、-CH₂OH、-CF₃、-CH₂CF₃Or-CH₂CH₂C (=O) NH₂。

25. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4It is alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_{1- 2}R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N (R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr- R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

26. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R⁴It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、- R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

27. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R⁵It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, C_1-4Alkylamino, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_6-10Aryl, C_6-10Aryl C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N (R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、- R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

28. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R⁶It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4It is alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_{1- 2}R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N (R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr- R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

29. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R⁶Separately for H ,-CN, F, Cl, Br, I, methyl, ethyl, propyl, tert-butyl, methoxyl group, ethyoxyl ,- OCH₂CF₃、-CF₃、-CH₂CF₃、-CH₂CH₂CN、-CH₂CH₂OH ,-C (=O) CH₃,-C (=O) CF₃,-C (=O) OCH₃,-C (= O)NH₂Or-NHC (=O) CH₃。

30. the described in any item compounds in -5,11 and 15 according to claim 1, wherein

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-4Alkyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, C_6-10Aryl, C_6-10Aryl C_1-4Alkyl, C_1-9Heteroaryl, C_1-9Heteroaryl C_1-4Alkyl, C_3-8Naphthenic base, C_3-8Naphthenic base C_1-4Alkyl, C_2-7Heterocycle or C_2-7Heterocycle C_1-4Alkyl；

Each R^9a、R¹⁰And R^10aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl or halogen For C_1-4Alkyl；

Each R¹¹And R^10aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4 Alkyl or C_6-10Aryl C_1-4Alkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, Or halogenated C_1-4Alkyl；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene is halogenated C_1-4Alkylidene.

31. compound according to claim 1, wherein the compound has any shown structure of formula (Id)-(Ig):

Wherein,

R^1aFor H, methyl, ethyl, propyl ,-CF₃Or-CH₂CF₃；

R²And R³It is each independently H ,-CN, F, Cl, Br, methyl, ethyl, propyl, methoxy, methoxy ethyl, methoxy Base propyl, ethoxyl methyl, ethoxyethyl group ,-CF₃、-CH₂CF₃、-CH₂CH₂CN、-CH₂CH₂OH or-CH₂CH₂C (=O) NH₂；

R⁴For H, oxo (=O) ,-CN, F, Cl, Br, I, methyl, ethyl, propyl, tert-butyl, methoxyl group, ethyoxyl ,- OCH₂CF₃、-CF₃、-CH₂CF₃、-CH₂CH₂CN、-CH₂CH₂OH、-CH₂OH ,-C (=O) CH₃,-C (=O) CF₃,-C (=O) OCH₃,-C (=O) NH₂,-C (=O) NHCH₃,-C (=O) NHCH₂CH₃Or-NHC (=O) CH₃；

R⁶For H ,-CN, F, Cl, Br, I, methyl, ethyl, propyl, tert-butyl, methoxyl group, ethyoxyl ,-OCH₂CF₃、-CF₃、- CH₂CF₃、-CH₂CH₂CN、-CH₂CH₂OH ,-C (=O) CH₃,-C (=O) CF₃,-C (=O) OCH₃,-C (=O) NH₂Or-NHC (=O) CH₃；

X³For N or CH；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br ,-OH ,- NH₂、-NO₂,-CN and C_1-4The group of alkoxy replaces；

R^hAnd RⁱIt is each independently H, methyl, ethyl, propyl, tert-butyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkane Base, C_1-4Hydroxyalkyl, halogenated C_1-4Alkyl, Cvclopropvlmethvl, HC (=O)-, CH₃C (=O)-or cyclopropylethyl；

M1 is 1,2,3 or 4；With

N1 is 0,1,2,3 or 4；

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolism Object, prodrug or mixture.

32. it is the compound one of having following structure compound according to claim 1:

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolism Object, prodrug or mixture.

33. pharmaceutical composition, described pharmaceutical composition includes compound and pharmacy described in any one of claim 1-32 Upper acceptable auxiliary material, diluent or carrier.

34. pharmaceutical composition according to claim 33, further includes additional therapeutic agent.

35. the described in any item compounds of claim 1-32 or the described in any item pharmaceutical compositions of claim 33-34 exist It prepares for preventing or treating the purposes in drug of the mammal with the ATX disease for expressing increased pathological characteristics.

36. purposes according to claim 35, wherein the disease packet for expressing increased pathological characteristics with ATX It includes: cancer, fibrotic disease, metabolic disease, myelodysplastic syndrome, cardiovascular disease, autoimmune disease, inflammation Disease, the nervous system disease or pain.

37. purposes according to claim 35, wherein described to express the diseases of increased pathological characteristics with ATX and be Idiopathic pulmonary fibrosis or liver fibrosis.

Invention field

The present invention relates to field of medicinal chemistry, more particularly to a new class of virtue as ATX (Autotaxin) inhibitor is miscellaneous Cycle compound, the pharmaceutical composition comprising the compound, and there is ATX in treatment using the compound or composition (Autotaxin) application in the disease of increased pathological characteristics is expressed.

Background of invention

Autotaxin (ATX) was separated from A2058 melanoma cells for the first time in 1992, was referred to as " autocrine Dynamic factor " is a secreting type glycoprotein.ATX has the activity of phosphodiesterase (PDE), is extracellular pyrophosphatase/phosphoric acid A member of diesterase (ENPP) family.ATX also has Lysophospholipase D (lysoPLD) activity, can be with lysophosphatidyl choline (lysophosphatidylcholine, LPC) be substrate catalysis generate lysophosphatidic acid (lysophosphatidic acid, LPA).The LPA precursor that still phosphatide does not synthesize, and extensive biological effect can be caused by various signal transduction paths. LPA is once generate, receptor protein (LPA1-6) that can be special by six cell surfaces, i.e. g protein coupled receptor (GPCR) Mediation plays a role.According to endothelial cell differentiation gene (Edg) and ventricle area unnamed gene, LPA1-6 is respectively LPA1/Edg- 2/VZG-1, LPA2/Edg-4, LPA3/Edg-7, LPA4/p2y9/GPR23, LPA5/GPR92 and LPA6/p2Y5, each receptor It is mediated by gα protein (Gs, Gi, Gq and G12/13), and then causes a series of cell signalling cascade effect.Wherein, main The access wanted includes the hydrolysis of phosphatidylinositol diphosphate ester (PIP2), and then causes intracellular calcium ion release and albumen and swash Enzyme C (PKC) activation；Inhibit adenyl cyclase (cAMP) signal path；Ras-MAPK is activated, MERK, ERK access, regulation is carefully Born of the same parents' proliferation activity；Activating phosphatase inositol PI3K-AKT access, modulating apoptosis in platelets and apoptosis activity；Finally, activation Rho access tune Control cytoskeleton remodeling, shape change and cell migration activity.Under many pathological conditions, especially in tumour cell, ATX In high expression status, lead to LPA excessive concentration.In tumour cell, LPA concentration can be increased to 10 μm of ol/L, be much higher than The normal level of 100nmol/L.Excessive LPA increases the generation of vascular endothelial growth factor (VEGF), promotes angiogenesis； The expression for reducing cancer suppressorfactor p53, increases the survival and transfer of tumour cell.ATX-LPA signal path is related to many physiology And pathologic process, to have important relation with many serious diseases, mainly include cardiovascular disease, autoimmune disease, Cancer, fibrotic disease, inflammation, the nervous system disease, pain etc..LPA has multi-functional in tumour generation, promotes tumour Drug resistance is shifted and occurred to the growth of cell, at angiogenesis.So reducing the concentration level of LPA, be conducive to the treatment of tumour With control.It is corresponding, inhibit the activity of AXT, block the constructive ways of LPA, is the research hotspot for treating a variety of serious diseases.

As the research to ATX deepens continuously, promote much using it as the appearance of the new inhibitor of target spot, wherein grind Studying carefully most concentrate is cancer and fibrotic disease.Fibrotic disease is mainly idiopathic pulmonary fibrosis (IPF) and liver fibrosis. IPF is that one kind shows as Diffuse alveolar inflammation and alveolar structure disorder, and interstitial lung fibrosis is caused to carry out the one of sexual development Kind fatal disease, prognosis is poor, and the mean survival time is 2 to 5 years.IPF may be most close with ATX-LPA pathways Disease, because in lung tissue, the expression highest of ATX concentrates on bronchial epithelial cell and pulmonary alveolar macrophage, and these Cell can be with juxtaposition fibroblast stove.

Currently, GLPG-1690 comes into the phase II clinical trials stage as Autotaxin inhibitor, for special hair The treatment of property pulmonary fibrosis；ATX concentration is closely related with liver fibrosis and liver hardness number in serum, is that predictive hepatocirrhosis is best One of index.In addition, ATX is highly expressed in many tumor tissues, including melanoma, non-small cell lung cancer, liver cancer, kidney Cancer, breast cancer, thyroid cancer, oophoroma and Hodgkin lymphoma.LPA/ATX can promote thin during growth of tumour cell Born of the same parents' invasion and transfer.So ATX inhibitor, disabling signal conduction path, provide for clinical anticancer and fibrotic disease One new way.

Compared with traditional kinase inhibitor, ATX inhibitor inhibits to influence a plurality of and cell Proliferation, life while ATX activity The relevant signal paths such as long and apoptosis generate preferable inhibitory effect to some drug-resistant type tumours, and with multiple organs Fibrosis is closely related, and is the important target of research and development tencel disease medicament.

The present invention provides a new class of heteroaromatic class compounds, have good inhibitory activity to ATX.Of the present inventionization Closing object has excellent drug effect, medicine for property and/or toxicology property, has preferable potential applicability in clinical practice.

Abstract of invention

Only summarize some aspects of the invention below, however, it is not limited to this.These aspects and other parts will be There is more complete explanation below.In this specification all bibliography pass through reference its be integrally incorporated herein.Work as this specification When disclosure and citation are variant, it is subject to this disclosure content.

The active compound of ATX can effectively be inhibited the present invention provides a new class of, can be used for preparing treatment has ATX table Up to the disease of increased pathological characteristics, for example, cancer, fibrotic disease (such as idiopathic pulmonary fibrosis or liver fibrosis), generation Thank disease, myelodysplastic syndrome, cardiovascular disease, autoimmune disease, inflammation, the nervous system disease or pain Drug.Present invention provides the methods for preparing compound of the present invention, treat mammal using these compounds, especially It is the method for the above-mentioned disease of the mankind and the pharmaceutical composition comprising these compounds.

On the one hand, the present invention provides a kind of new heteroaromatic compounds, as shown in formula (I) or chemical combination shown in formula (I) It is the pharmaceutically acceptable salt of object, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolin, preceding Medicine or mixture:

Wherein,

W is-N (R^1a)-,-O- ,-S- ,-S (=O)_1-2,-C (=O)-,-(C (R^2a)(R^2b))_1-4-、-N(R^1a)(C(R^2a) (R^2b))_1-4-、-N(R^1a) C (=O)-or-O (C (R^2a)(R^2b))_1-4-；

Ar¹And Ar²Five molecular heteroaryls of original are each independently, wherein Ar¹And Ar²Individually optionally by 1,2 or 3 R²Replace；

Ar³For aryl or heteroaryl, wherein the Ar³Individually optionally by 1,2,3 or 4 R³Replace；

Cy be naphthenic base, heterocycle, spiral shell bicyclic group, the miscellaneous bicyclic group of spiral shell, condensed-bicyclic base, condense miscellaneous bicyclic group, bridged ring base, Bridge heterocycle, aryl or heteroaryl, wherein the Cy is optionally by 1,2,3 or 4 R⁴Replace；

Y is-(L¹-W¹)_m-L²-；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br, I ,- OH、-NH₂、 -NO₂,-CN and C_1-6The group of alkoxy replaces；

L²It is not present or L²For-O- ,-C (=O)-,-OC (=O)-,-C (=O) O- ,-C (=O)-C (=O)-,-C (= O)-C (=O) N (R^a)-、-N(R^b)-,-C (=O) N (R^c)-、-N(R^c) C (=O)-,-C (=O) N (R^c)-R¹⁵- C (=O) O- ,-C (=O) N (R^c)-R¹⁵- C (=O) N (R^a)-、-N(R^d) C (=O) N (R^c)-、 -N(R^g) C (=O) O- ,-S (=O)_0-2-、-S (=O)_1-2N(R^e)-、-N(R^f) S (=O)_1-2Or-N (R^f) S (=O)_1-2-R¹⁵-N(R^a)-；

Z be H ,-CN, alkyl, alkenyl, alkynyl, halogenated alkyl, naphthenic base, heterocycle, heterocyclylalkyl group, cycloalkyl-alkyl, Spiral shell bicyclic group, spiral shell miscellaneous bicyclic group, condense miscellaneous bicyclic group, bridged ring base, bridge heterocycle, aryl or heteroaryl at condensed-bicyclic base, Described in alkyl, alkenyl, alkynyl, halogenated alkyl, naphthenic base, heterocycle, spiral shell bicyclic group, the miscellaneous bicyclic group of spiral shell, condensed-bicyclic base, thick Miscellaneous bicyclic group, bridge ring alkyl, bridge Heterocyclylalkyl, aryl and heteroaryl are closed optionally by one or more R⁵Replace；

R¹For alkyl, alkenyl, alkynyl, aryl, heteroaryl, naphthenic base or heterocycle, wherein the R¹Individually optional ground quilt 1,2,3 or 4 R⁶Replace；

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, Alkyl, the hydroxyalkyl, alkoxy, alkoxyalkyl, sweet-smelling alkoxy alkyl, aryloxy alkyl ,-S (=O) of cyano substitution_0-2R⁷、- C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、- NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、- R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴- NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2aAnd R^2bIt is each independently H ,-CN ,-OH ,-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, cyanogen Alkyl, hydroxyalkyl, alkoxy, aryl, aralkyl, heteroaryl or the heteroaryl alkyl that base replaces；

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, alkyl halide Alkyl, the hydroxyalkyl, alkoxy ,-S (=O) that base, cyano replace_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、 -N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N (R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12a、 Or-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁴It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynes Alkyl, the hydroxyalkyl, alkoxy ,-S (=O) that base, halogenated alkyl, cyano replace_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a、- C (=O) OR^8a,-OC (=O) R^8a、 -N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N (R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、 -R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (= O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、 -R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N (R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁵It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynes Alkyl, the hydroxyalkyl, alkoxy, aryl, aralkyl ,-S (=O) that base, alkylamino, halogenated alkyl, cyano replace_0-2R⁷,-C (= O)R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、- NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、- R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴- NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁶It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, Alkyl, the hydroxyalkyl, alkoxy ,-S (=O) of cyano substitution_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-C (=O) OR^8a、 -N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³)C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、- R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴- N(R¹³) C (=O) NR^13aR^13b；

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, halogenated C_1-6Alkane The C that base, cyano replace_1-6Alkyl, aryl, aralkyl, heteroaryl, heteroaryl alkyl, naphthenic base, cycloalkyl-alkyl, heterocycle, Or heterocyclylalkyl group；

Each R^9a、R¹⁰And R^10aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6Alkyl, Or halogenated C_1-6Alkyl；

Each R¹¹And R^11aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, halogenated C_1-6Alkyl, cyano replace C_1-6Alkyl or aralkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6 Alkyl or halogenated C_1-6Alkyl；

R^1aSeparately for H, alkyl, alkenyl, alkynyl, halogenated alkyl, cyano replace alkyl, hydroxyalkyl, naphthenic base, Cycloalkyl-alkyl, aryl or aralkyl；

Each R^a、R^b、R^c、R^d、R^e、R^f、R^g、R^hAnd RⁱIt is separately H, the alkane that alkyl, alkenyl, alkynyl, cyano replace Base, halogenated alkyl, R¹⁶- C (=O)-or cycloalkyl-alkyl；

Each R¹⁴And R¹⁵It is separately alkylidene, the alkylidene or halogenated alkylene that alkenylene, alkynylene, cyano replace Base；

R¹⁶It is H, C_1-6Alkyl or halogenated C_1-6Alkyl；With

M is 0,1 or 2.

On the other hand, the present invention provides a kind of pharmaceutical composition, described pharmaceutical composition includes of the present inventionization Close object or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolism Object, prodrug, and pharmaceutically acceptable auxiliary material, diluent or carrier.

In some embodiments, pharmaceutical composition of the present invention further includes additional therapeutic agent.

On the other hand, compound of the present invention or pharmaceutical composition of the present invention are used the present invention provides a kind of Object is preparing the use in the drug for preventing or treating the disease that mammal expresses increased pathological characteristics with ATX On the way.

In some embodiments, wherein described, there is ATX to express the disease of increased pathological characteristics includes: cancer, fibre Dimensionization disease, metabolic disease, myelodysplastic syndrome, cardiovascular disease, autoimmune disease, inflammation, nervous system Disease or pain.

In some embodiments, wherein the disease for expressing increased pathological characteristics with ATX is that idiopathic lung is fine Dimensionization or liver fibrosis.

Detailed description of the invention

Definition and general terms

Unless otherwise stated, all scientific and technical terminologies used in the present invention have with those skilled in the art of the invention's It is generally understood identical meaning.All patents of the present invention and public publication are integrally incorporated this hair by reference It is bright.

Unless otherwise stated, following definition should be obtained using used herein.For purposes of the present invention, chemical element with The periodic table of elements CAS editions, and " Handbook of Chemistry and Physics ", the 75th edition, 1994 is consistent.In addition, organic chemistry General Principle can join It examines " Organic Chemistry ", Thomas Sorrell, University Science Books, Sausalito:1999, With " March's Advanced Organic Chemistry " by Michael B. Smith and Jerry March, Description in John Wiley&Sons, New York:2007, entire contents are incorporated herein by reference.

There is apparent conflict unless otherwise indicated or in context, the article " one " used herein, " one (kind) " " described " is intended to include "at least one" or " one or more ".Therefore, these articles used herein refer to one or The article of more than one (i.e. at least one) object.For example, " component " refers to one or more components, it is possible to have more than one Component be taken into account in the embodiment of the embodiment and use or use.

Term " mammal " used in the present invention refers to, such as primate (such as mankind, sex), Ox, sheep, goat, horse, pig, dog, cat, rabbit, rat, mouse, fish, bird etc..In certain embodiments, the mammal is Primate.In other embodiments, the mammal is people.

Term " patient " used in the present invention refers to people (including adult and children) or other animals.In some implementations Scheme, " patient " refer to people.

Term "comprising" is open language, that is, includes content specified by the present invention, but be not precluded otherwise Content.

" stereoisomer " refers to identical chemical constitution, but the spatially different change of arrangement mode of atom or group Close object.Stereoisomer includes enantiomter, diastereoisomer, conformer (rotational isomer), geometric isomer (cis/trans) isomers, atropisomer, etc..

" chirality " be with its mirror image cannot be overlapped property molecule；And " achirality " refer to can be overlapped with its mirror image Molecule.

" enantiomter " refers to two isomers that cannot be overlapped but be mutually mirror of a compound.

" diastereoisomer " refer to there are two or multiple chiral centres and its molecule not alloisomerism of mirror image each other Body.Diastereoisomer has different physical properties, such as fusing point, boiling point, spectral property and reactivity.Diastereoisomer is mixed Such as electrophoresis and chromatography, such as HPLC can be operated by high resolution analysis to separate by closing object.

Stereochemical definitions used in the present invention and rule generally follow S.P.Parker, Ed., McGraw-Hill Dictionary of Chemical Terms (1984) McGraw-Hill Book Company, New York；and Eliel, E.and Wilen, S., " Stereochemistry of Organic Compounds ", John Wiley&Sons, Inc., New York, 1994.

Many organic compounds exist with optical active forms, i.e., they, which have, rotates the plane of linearly polarized light Ability.When describing optically active compound, indicate molecule about one or more hand using prefix D and L or R and S The absolute configuration at property center.Prefix d and l or (+) and (-) are the symbols for the rotation of linearly polarized light caused by appointed compound, Wherein (-) or l indicate that compound is left-handed.Prefix is (+) or the compound of d is dextrorotation.A kind of specific alloisomerism Body is enantiomter, and the mixture of this isomers is referred to as enantiomeric mixture.The 50:50 mixture of enantiomter Referred to as racemic mixture or racemic modification, when chemical reaction or in the process without stereoselectivity or stereospecificity when, It may occur in which such case.

Any asymmetric atom (for example, carbon etc.) of disclosed compound of present invention can be enriched with racemic or enantiomer Form exist, such as (R)-, (S)-or (R, S)-configuration exist.In certain embodiments, each asymmetric atom exists (R)-or (S)-configuration in terms of have at least 50% enantiomeric excess, at least 60% enantiomeric excess, at least 70% enantiomer mistake Amount, at least 80% enantiomeric excess, at least 90% enantiomeric excess, at least 95% enantiomeric excess, or at least 99% enantiomer It is excessive.

According to the selection of starting material and method, the compounds of this invention can with one in possible isomers or they Mixture, such as the form of racemic modification and non-corresponding isomer mixture (this depends on the quantity of asymmetric carbon atom) deposits In.Chiral synthon or chiral reagent preparation can be used in optically active (R)-or (S)-isomers, or is torn open using routine techniques Point.If compound contains a double bond, substituent group may be E or Z configuration；If containing disubstituted cycloalkanes in compound The substituent group of base, naphthenic base may have cis or trans configuration.

The mixture of resulting any stereoisomer can be separated into according to the difference in component physicochemical properties Pure or substantially pure geometric isomer, enantiomter, diastereoisomer, for example, passing through chromatography and/or fractional crystallization Method.

The racemic modification of any gained final product or intermediate can be passed through into those skilled in the art by known method Known method splits into optical antipode, e.g., is separated by its diastereoisomeric salt to acquisition.Racemic production Object can also be separated by chiral chromatogram, e.g., use the high performance liquid chromatography (HPLC) of chiral sorbent.Particularly, mapping Isomers can be prepared by asymmetric syntheses, for example, can refer to Jacques, et al., Enantiomers, Racemates and Resolutions(Wiley Interscience,New York,1981)；Principles of Asymmetric Synthesis(2^ndEd.Robert E.Gawley,Jeffrey Aubé,Elsevier,Oxford,UK,2012)；Eliel, E.L.Stereochemistry of Carbon Compounds(McGraw-Hill,NY,1962)；Wilen,S.H.Tables of Resolving Agents and Optical Resolutions p.268(E.L.Eliel,Ed.,Univ.of Notre Dame Press,Notre Dame,IN 1972)；Chiral Separation Techniques:A Practical Approach(Subramanian,G.Ed.,Wiley-VCH Verlag GmbH&Co.KGaA, Weinheim,Germany, 2007)。

Term " tautomer " or " tautomeric form " refer to that with different energy can be by low energy barrier (low Energy barrier) mutually inversion of phases constitutional isomer.If tautomerism is possible (as in the solution), can achieve The chemical balance of tautomer.For example, (also referred to as proton translocation mutually makes a variation proton tautomer (protontautomer) Structure body (prototropic tautomer)) include the mutual inversion of phases carried out by proton transfer, such as keto-enol isomerization and Imine-enamine isomerizations.Valence tautomerism body (valence tautomer) include by the recombination of some bonding electrons come The mutual inversion of phases carried out.The specific example of ketoenol tautomerization is that pentane -2,4- diketone and the amyl- 3- alkene -2- ketone of 4- hydroxyl are mutual The interconversion of tautomeric.Another tautomeric example is phenol-keto tautomerism.One of phenol-keto tautomerism is specific real Example is the interconversion of pure and mild pyridine -4 (1H) the -one tautomer of pyridine -4-.Unless otherwise noted, the compounds of this invention is all Tautomeric forms are within the scope of the present invention." pharmaceutically acceptable " refers to compounds some in this way, raw material, group Close object and/or dosage form, they within the scope of reasonable medical judgment, be suitable for contact with patient tissue and without excessive toxicity, pierce Swash property, allergy or other problems relative to a reasonable benefit/risk ratio and complication, and effective for set use On the way.

As described in the invention, the compound of the present invention can be optionally replaced one or more substituent groups, such as General formula compound above, or as example special inside embodiment/embodiment, subclass, and the present invention included one Class compound.

In general, term it is " substituted " indicate taken to one or more hydrogen atoms in structure by specific substituent group Generation.Unless otherwise indicated, the group of a substitution can have a substituent group to carry out at various substitutable position of that group Replace.When in given structural formula more than one position can by selected from specific group one or more substituent groups replaced, So substituent group can replace at various locations identical or differently.

Term " unsubstituted " indicates specified group without substituent group.

Term " optionally by ... replaces " can be used interchangeably, i.e. institute with term " unsubstituted or by ... replaced .. " Stating structure is unsubstituted or is replaced by one or more substituent groups of the present invention, substituent group packet of the present invention It includes, but is not limited to D, F, Cl, Br, I, N₃、 CN、NO₂、OH、SH、NH₂, alkyl, halogenated alkyl, alkenyl, alkynyl, alkoxy, alkane Base amino, hydroxyalkyl, the alkyl of cyano substitution, naphthenic base, heterocycle, aryl, heteroaryl ,-S (=O)_0-2R⁷,-C (=O) R⁸、- OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、 -N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、 -R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、 -R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12a、-R¹⁴-N(R¹³) C (=O) NR^13aR^13bEtc., wherein R⁷、 R^7a、R⁸、R^8a、R⁹、R^9a、R¹⁰、R^10a、R¹¹、R^11a、R¹²、R^12a、R¹³、R^13a、R^13bAnd R¹⁴With definition of the present invention.

In addition, it is necessary to explanation, unless otherwise explicitly point out, in the present invention used by describing mode " each ... independently be " and " ... be each independently " and " ... independently be " can be interchanged, and shall be understood in a broad sense, both may be used To refer among the different groups, does not influence mutually, can also indicate in phase between expressed specific option between the same symbol In same group, do not influenced mutually between expressed specific option between the same symbol.

It is disclosed in the substituent group of each section of this specification, disclosed compound of present invention according to radical species or range.It is special It does not point out, the present invention includes each independent sub-combinations thereof of each member of these radical species and range.For example, term “C_1-6Alkyl " refers in particular to the methyl being individually disclosed, ethyl, C₃Alkyl, C₄Alkyl, C₅Alkyl and C₆Alkyl.

In each section of the invention, connect substituent is described.When the structure clearly needs linking group, for Markush variable cited by the group is interpreted as linking group.For example, if the structure need linking group and " alkyl " or " aryl " is listed for the Markush group definition of the variable, then it should be understood that " alkyl " or " aryl " Respectively represent the alkylidene group or arylene group of connection.

Terminology used in the present invention " alkyl " or " alkyl group ", indicate contain 1 to 20 carbon atom, the straight chain of saturation or Branch univalent hydrocarbyl group, wherein the substituent group institute that the alkyl group can be described optionally by one or more present invention Replace.Unless otherwise detailed instructions, alkyl group contains 1-20 carbon atom.In one embodiment, alkyl group contains 1- 12 carbon atoms；In another embodiment, alkyl group contains 1-6 carbon atom；In yet another embodiment, alkyl base 1-4 carbon atom is contained in group；Also in one embodiment, alkyl group contains 1-3 carbon atom.The alkyl group can appoint Replaced the substituent group that selection of land is described by one or more present invention.

The example of alkyl group includes, but is not limited to, methyl (Me ,-CH₃), ethyl (Et ,-CH₂CH₃), n-propyl (n- Pr、-CH₂CH₂CH₃), isopropyl (i-Pr ,-CH (CH₃)₂), normal-butyl (n-Bu ,-CH₂CH₂CH₂CH₃), isobutyl group (i-Bu ,- CH₂CH(CH₃)₂), sec-butyl (s-Bu ,-CH (CH₃)CH₂CH₃), tert-butyl (t-Bu ,-C (CH₃)₃), n-pentyl (- CH₂CH₂CH₂CH₂CH₃), 2- amyl (- CH (CH₃)CH₂CH₂CH₃), 3- amyl (- CH (CH₂CH₃)₂), 2- methyl -2- butyl (- C (CH₃)₂CH₂CH₃), 3- methyl -2- butyl (- CH (CH₃)CH(CH₃)₂), 3- methyl-1-butyl (- CH₂CH₂CH(CH₃)₂), 2- Methyl-1-butyl (- CH₂CH(CH₃)CH₂CH₃), n-hexyl (- CH₂CH₂CH₂CH₂CH₂CH₃), 2- hexyl (- CH (CH₃) CH₂CH₂CH₂CH₃), 3- hexyl (- CH (CH₂CH₃)(CH₂CH₂CH₃)), 2- methyl -2- amyl (- C (CH₃)₂CH₂CH₂CH₃), 3- Methyl -2- amyl (- CH (CH₃)CH(CH₃)CH₂CH₃), 4- methyl -2- amyl (- CH (CH₃)CH₂CH(CH₃)₂), 3- methyl -3- Amyl (- C (CH₃)(CH₂CH₃)₂), 2- methyl -3- amyl (- CH (CH₂CH₃)CH(CH₃)₂), 2,3- dimethyl -2- butyl (- C (CH₃)₂CH(CH₃)₂), 3,3- dimethyl -2- butyl (- CH (CH₃)C(CH₃)₃), n-heptyl, n-octyl, etc..

Two obtained saturations of hydrogen atom are removed in term " alkylidene " expression from the linear chain or branched chain alkyl of saturation Bivalent hydrocarbon radical group.Unless otherwise detailed instructions, alkylidene group contains 1-12 carbon atom.In one embodiment, alkylene Base group contains 1-6 carbon atom；In another embodiment, alkylidene group contains 1-4 carbon atom；In another embodiment party In case, alkylidene group contains 1-3 carbon atom；Also in one embodiment, alkylidene group contains 1-2 carbon atom.This The example of sample includes methylene (- CH₂), ethylidene (- CH₂CH₂), isopropylidene (- CH (CH₃)CH₂) etc..The alkylene Replaced the substituent group that base group can be described optionally by one or more present invention.

Term " alkenyl " indicates the linear chain or branched chain monovalent hydrocarbon containing 2-12 carbon atom, wherein at least one insatiable hunger And site, that is, there is a carbon-to-carbon sp²Double bond comprising the positioning of " suitable " and negation, or the positioning of " E " and " Z ".It is real one It applies in scheme, alkenyl group includes 2-8 carbon atom；In another embodiment, alkenyl group includes 2-6 carbon atom；In In another embodiment, alkenyl group includes 2-4 carbon atom.The example of alkenyl group includes, but is not limited to, vinyl (- CH=CH₂), allyl (- CH₂CH=CH₂) etc..The alkenyl group can be optionally by one or more present invention descriptions Substituent group replaced.

Term " alkenylene " indicates the linear chain or branched chain bivalent hydrocarbon radical containing 2-12 carbon atom, and wherein at least one is not It is saturated site, that is, has a carbon-to-carbon sp²Double bond comprising the positioning of " suitable " and negation, or the positioning of " E " and " Z ".Unless In addition it is described in detail, alkenylene group contains 2-12 carbon atom.In one embodiment, alkenylene group contains 2-6 carbon Atom；In another embodiment, alkenylene group contains 2-4 carbon atom；In yet another embodiment, alkenylene group contains There is 2-3 carbon atom；Also in one embodiment, alkenylene group contains 2 carbon atoms.Such example includes sub- ethylene Base (- CH=CH-), acrol (- CH₂CH=CH-) etc..The alkylidene group can be optionally by one or more sheets Replaced the substituent group for inventing description.

Term " alkynyl " indicates the linear chain or branched chain monovalent hydrocarbon containing 2-12 carbon atom, wherein at least one insatiable hunger And site, that is, there is tri- key of carbon-to-carbon sp.In one embodiment, alkynyl group includes 2-8 carbon atom；In another implementation In scheme, alkynyl group includes 2-6 carbon atom；In yet another embodiment, alkynyl group includes 2-4 carbon atom.Alkynyl The example of group includes, but is not limited to, acetenyl (- C ≡ CH), propargyl (- CH₂C ≡ CH), 1- propinyl (- C ≡ C-CH₃) Etc..Replaced the substituent group that the alkynyl group can be described optionally by one or more present invention.

Term " alkynylene " indicates the linear chain or branched chain bivalent hydrocarbon radical containing 2-12 carbon atom, and wherein at least one is not It is saturated site, that is, has tri- key of carbon-to-carbon sp.In one embodiment, alkynylene group includes 2-8 carbon atom；Another In embodiment, alkynylene group includes 2-6 carbon atom；In yet another embodiment, alkynylene group includes 2-4 carbon Atom.The example of alkynylene group includes, but is not limited to, ethynylene (- C ≡ C-), sub- propargyl (- CH₂C ≡ C-) etc. Deng.Replaced the substituent group that the alkynylene group can be described optionally by one or more present invention.

Term " alkoxy " indicates that alkyl group is connected by oxygen atom with molecule rest part, and wherein alkyl group has Definition as described in the present invention.Unless otherwise detailed instructions, the alkoxy base contains 1-12 carbon atom.In an embodiment party In case, alkoxy base contains 1-6 carbon atom；In another embodiment, alkoxy base contains 1-4 carbon atom；In In another embodiment, alkoxy base contains 1-3 carbon atom.The alkoxy base can be optionally one or more Replaced the substituent group that the present invention describes.

The example of alkoxy base includes, but is not limited to, methoxyl group (MeO ,-OCH₃), ethyoxyl (EtO ,- OCH₂CH₃), 1- propoxyl group (n-PrO, n- propoxyl group ,-OCH₂CH₂CH₃), 2- propoxyl group (i-PrO, i- propoxyl group ,-OCH (CH₃)₂), 1- butoxy (n-BuO, n- butoxy ,-OCH₂CH₂CH₂CH₃), 2- methyl-l- propoxyl group (i-BuO, i- fourth oxygen Base ,-OCH₂CH(CH₃)₂), 2- butoxy (s-BuO, s- butoxy ,-OCH (CH₃)CH₂CH₃), 2- methyl -2- propoxyl group (t- BuO, t- butoxy ,-OC (CH₃)₃), 1- amoxy (n- amoxy ,-OCH₂CH₂CH₂CH₂CH₃), 2- amoxy (- OCH (CH₃) CH₂CH₂CH₃), 3- amoxy (- OCH (CH₂CH₃)₂), 2- methyl -2- butoxy (- OC (CH₃)₂CH₂CH₃), 3- methyl -2- fourth Oxygroup (- OCH (CH₃)CH(CH₃)₂), 3- methyl-l- butoxy (- OCH₂CH₂CH(CH₃)₂), 2- methyl-l- butoxy (- OCH₂CH(CH₃)CH₂CH₃), etc..

Term " halogenated alkyl ", " halogenated alkenyl " or " halogenated alkoxy " indicate alkyl, and alkenyl or alkoxy base are by one Replaced a or multiple halogen atoms, such example includes, but is not limited to, trifluoromethyl, trifluoroethyl, 2, and 2,3,3- tetra- Fluoropropyl, trifluoromethoxy etc..

Terminology used in the present invention " hydroxyalkyl " indicate alkyl group replaced one or more hydroxyl groups, wherein alkane Base group has to be defined as described in the present invention, and such example includes, but is not limited to ethoxy, 2- hydroxypropyl, hydroxyl first Base etc..

One or more hetero atoms can be inserted in term " miscellaneous alkyl " expression alkyl chain, wherein alkyl group and hetero atom With definition as described in the present invention.Unless otherwise detailed instructions, miscellaneous alkyl group contains 1-10 carbon atom, and other is real The scheme of applying is that miscellaneous alkyl group contains 1-8 carbon atom, and other embodiment is that it is former that miscellaneous alkyl group contains 1-6 carbon Son, other embodiment are that miscellaneous alkyl group contains 1-4 carbon atom, and other embodiment is miscellaneous alkyl group Contain 1-3 carbon atom.Such example includes, but is not limited to, CH₃OCH₂, CH₃CH₂OCH₂, CH₃SCH₂, (CH₃)₂NCH₂, (CH₃)₂CH₂OCH₂, CH₃OCH₂CH₂, CH₃CH₂OCH₂CH₂Etc..

Terminology used in the present invention " naphthenic base " refers to that monovalence saturation or part are unsaturated (but non-aromatic unless otherwise indicated Fragrant race) monocycle or polycyclic hydrocarbon.In some embodiments, the group of naphthene base can be bridge joint or unbridged, loop coil Or non-loop coil, and/or condensed or non-condensed bicyclic radicals.In some embodiments, the group of naphthene base includes 3-10 carbon atom, i.e. C₃To C₁₀Naphthenic base.In some embodiments, the naphthenic base has 3-15 (C_3-15)、3-10 (C_3-10) or 3-7 (C_3-7) a carbon atom.In some embodiments, the group of naphthene base is monocycle or bicyclic.In some realities Scheme is applied, the group of naphthene base is monocycle.In some embodiments, the group of naphthene base is bicyclic.In some embodiment party Case, the group of naphthene base are tricyclics.In some embodiments, the group of naphthene base is fully saturated.In some implementations Scheme, the group of naphthene base are fractional saturations.In some embodiments, the group of naphthene base be cyclopropyl, cyclobutyl, Cyclopenta, cyclohexyl, suberyl, bicyclic [2.1.1] hexyl, bicyclic [2.2.1] heptyl, decahydro naphthalene or adamantyl.Work as ring , can be on any ring when alkyl is substituted, i.e., it, can be independently on any aromatic rings or non-aromatic ring for including by naphthenic base Replaced one or more substituent groups described in the invention.

Term " heterocycle " and " heterocycle " are used interchangeably here, unless otherwise indicated, refer to non-comprising at least one The monovalent monocyclic non-aromatic ring system and/or polycyclic system of aromatic rings；Wherein one or more in the non-aromatic monocyclic atom It is a to be independently selected from O, S (O) (in certain embodiments, 1,2,3 or 4)_0-2It is former with the hetero atom of N and remaining described ring Son is carbon atom；Wherein one or more of annular atom of the polycyclic system (in certain embodiments, 1,2,3 or 4 It is a) it is independently selected from O, S (O)_0-2It is carbon atom with the hetero atom of N and remaining described annular atom.In some embodiments, The heterocycle includes 1 or 2 hetero atom, and the hetero atom is nitrogen-atoms.In some embodiments, the heterocycle is polycyclic And include a hetero atom in non-aromatic ring, perhaps comprising a hetero atom or in aromatic rings in aromatic rings Comprising two hetero atoms, or comprising two hetero atoms one of them in aromatic rings, and another is in non-aromatic ring.One A little embodiments, the heterocyclyl groups have 3-20,3-15,3-10,3-8,4-7 or 5-6 annular atoms.In some implementations Scheme, the heterocycle are monocycle, bicyclic, tricyclic or tetracyclic ring system.In some embodiments, the heterocyclyl groups can be with Be bridge joint or unbridged, loop coil or non-loop coil, and/or condensed or non-condensed bicyclic radicals.It is one or more Nitrogen-atoms and sulphur atom are optionally oxidized, and one or more nitrogen-atoms are optionally quaternized, and one or more carbon are former Son optionally byReplacement.Some rings can be partially or completely being saturated or aromatic, and condition is heterocycle It is non-fully armaticity.The monocyclic heterocycles and polycyclic heterocycle can be in any hetero atoms or carbon atom for leading to stable compound It is upper to be connect with the main structure.The multiring heterocyclic can by its any ring, including any aromatic rings or non-aromatic ring, without It manages whether the ring contains hetero atom, is connected in the main structure.In some embodiments, heterocycle is " Heterocyclylalkyl ", It is 1) unsaturated (but non-aromatic) monovalence list of the saturation containing at least one ring hetero atom or part as described in the present invention Unsaturated (but non-aromatic) the monovalence bicyclic radicals of cyclic group or 2) saturation or part or three cyclic groups, wherein at least one ring Contain at least one hetero atom as described in the present invention.It, can be on any ring, i.e., when heterocycle and Heterocyclylalkyl are substituted It is substituted on any aromatic rings or non-aromatic ring for being included by heterocycle and Heterocyclylalkyl.It is such in some embodiments Heterocycle includes, but are not limited to Oxyranyle, azelidinyl, oxetanylmethoxy, thietanyl, pyrrolidinyl, 2- pyrrole Cough up quinoline base, 3- pyrrolinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, tetrahydrofuran base, dihydrofuryl, Tetrahydro-thienyl, dihydrothiophene, 1,3- dioxy cyclopenta, two sulphur cyclopenta, THP trtrahydropyranyl, dihydro pyranyl, 2H- pyrrole It mutters base, 4H- pyranose, tetrahydro thiapyran base, piperidyl, morpholinyl, thio-morpholinyl, piperazinyl, dioxanes base, dithianyl, Thiophene oxane base, high piperazine base, homopiperidinyl, oxepane alkyl, thia cycloheptyl alkyl, oxygen azepineBase, diazaBase, sulphur AzepineBase, benzdioxan base, benzodioxole base, benzofuran ketone group, chromene ketone group, chromene Base, dihydro benzo furyl, benzo tetrahydro-thienyl, benzothiopyran derivative base, benzoxazinyl-, B-carboline base, benzodihydropyran Base, chromone base, cinnoline base, cumarin base, decahydroquinolyl, Decahydroisoquinolinpreparation base, dihydrobenzo isothiazine base, dihydrobenzo are different Oxazines base, dihydrofuryl, dihydro-iso indolyl, dihydro pyranyl, pyrazoline base, dihydro pyrazine base, dihydropyridine base, two Hydrogen pyrimidine radicals, pyrrolin base, dioxolanyl ,-two thiapyran base of Isosorbide-5-Nitrae, furanonyl, imidazolidinyl, 2,4- dioxies-imidazolidine Base, imidazolinyl, indoline base, 2- oxygen-indoline base, different benzo tetrahydrofuran base, different benzo tetrahydro-thienyl, different benzo two Hydrogen pyranose, isocoumarin base, iso-dihydro-indole-group (isoindoline base), 1- oxygen-iso-dihydro-indole-group, 1,3- dioxy-different two Hydrogen indoles base, isothiazole alkyl, isoxazolidinyl, 3- oxygen-isoxazolidinyl, morpholinyl, 3,5- dioxies-morpholinyl, octahydro Yin Diindyl base, octahydro isoindolyl, 1- oxygen-octahydro isoindolyl, 1,3- dioxy-hexahydro isoindolyl, oxazolidine ketone group, oxazolidine Base, Oxyranyle, piperazinyl, 2,6- dioxies-piperazinyl, piperidyl, 2,6- dioxies-piperidyl, 4- piperidone base, 2- oxygen pyrrole Cough up alkyl, 2,5- dioxypyrrole alkyl, quininuclidinyl, tetrahydro isoquinolyl, 3,5- dioxido-thiomorpholine bases, thiazolidinyl, 2, 4- dioxy-thiazolidinyl, tetrahydric quinoline group, phenothiazinyl, phenoxazine base, oxa- anthryl and 1,3,5- trithian bases. - CH in heterocycle₂Group includes, but are not limited to 2- oxo-pyrrolidine base, oxo -1,3- by-C (=the O)-example substituted Thiazolidinyl, 2- piperidone base, 3,5- dioxy piperazine piperidinyl and hybar X base.The example packet that sulphur atom is oxidized in heterocycle It includes, but is not limited to, sulfolane base, 1,1- dioxothiomorpholinyl.The heterocyclyl groups can optionally by one or Replaced multiple substituent groups described in the invention.

In one embodiment, heterocycle is 3-8 former molecular heterocycle, refers to satisfying comprising 3-8 annular atom And/or the unsaturated monocycle in part, wherein at least one annular atom are selected from nitrogen, sulphur and oxygen atom.Unless otherwise stated, 3-8 original Molecular heterocycle can be carbon-based or nitrogen base, and-CH₂Group can be substituted optionally by-C (=O)-.The sulphur atom of ring S- oxide can be optionally oxidized to.The nitrogen-atoms of ring can optionally be oxidized to N- oxygen compound.3-8 atom group At the example of heterocycle include, but are not limited to: azelidinyl, oxetanylmethoxy, thietanyl, pyrrolidinyl, 2- pyrrole Cough up quinoline base, 3- pyrrolinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, tetrahydrofuran base, dihydrofuryl, Tetrahydro-thienyl, dihydrothiophene, 1,3- dioxy cyclopenta, two sulphur cyclopenta, THP trtrahydropyranyl, dihydro pyranyl, 2H- pyrans Base, 4H- pyranose, tetrahydro thiapyran base, piperidyl, morpholinyl, thio-morpholinyl, piperazinyl, dioxanes base, dithianyl, thiophene Oxane base, high piperazine base, homopiperidinyl, oxepane alkyl, thia cycloheptyl alkyl, oxygen azepineBase, diazaBase, sulphur nitrogen It is miscellaneousBase.- CH in heterocycle₂Group includes, but are not limited to 2- oxo-pyrrolidine base, oxo-by-C (=the O)-example substituted 1,3- thiazolidinyl, 2- piperidone base, 3,5- dioxy piperazine piperidinyl and hybar X base.Sulphur atom is oxidized in heterocycle Example includes, but are not limited to sulfolane base, 1,1- dioxothiomorpholinyl.The former molecular heterocycle of described 3-8 Group can be optionally replaced one or more substituent groups described in the invention.

In one embodiment, heterocycle is 3-6 former molecular heterocycle, refers to satisfying comprising 3-6 annular atom And/or the unsaturated monocycle in part, wherein at least one annular atom are selected from nitrogen, sulphur and oxygen atom.Unless otherwise stated, 3-6 original Molecular heterocycle can be carbon-based or nitrogen base, and-CH₂Group can be substituted optionally by-C (=O)-.The sulphur atom of ring S- oxide can be optionally oxidized to.The nitrogen-atoms of ring can optionally be oxidized to N- oxygen compound.Described 3-6 Former molecular heterocyclyl groups can be optionally replaced one or more substituent groups described in the invention.

In another embodiment, heterocycle is the 5-6 molecular heterocycle of original, is referred to comprising 5-6 annular atom Saturation or the unsaturated monocycle in part, wherein at least one annular atom are selected from nitrogen, sulphur and oxygen atom.Unless otherwise stated, 5-6 Former molecular heterocycle can be carbon-based or nitrogen base, and-CH₂Group can be substituted optionally by-C (=O)-.The sulphur of ring is former Son can optionally be oxidized to S- oxide.The nitrogen-atoms of ring can optionally be oxidized to N- oxygen compound.5-6 atom The example of the heterocycle of composition includes, but are not limited to: pyrrolidinyl, 2- pyrrolinyl, 3- pyrrolinyl, pyrazolinyl, pyrazoles Alkyl, imidazolinyl, imidazolidinyl, tetrahydrofuran base, dihydrofuryl, tetrahydro-thienyl, dihydrothiophene, 1,3- dioxy ring Amyl, two sulphur cyclopenta, 2- oxo-pyrrolidine base, oxo -1,3-thiazoles alkyl, sulfolane base, THP trtrahydropyranyl, dihydropyran Base, 2H- pyranose, 4H- pyranose, tetrahydro thiapyran base, piperidyl, morpholinyl, thio-morpholinyl, piperazinyl, dioxanes base, two Thiophene alkyl, thiophene oxane base, 2- piperidone base, 3,5- dioxy piperazine piperidinyl and hybar X base, 1,1- dioxothiomorpholinyl. The former molecular heterocyclyl groups of described 5-6 can be optionally by one or more substituent group institutes described in the invention Replace.

Term " cycloalkyl-alkyl " indicates that alkyl group can be replaced one or more groups of naphthene base, wherein naphthenic base Have with alkyl and define as described herein, such example includes, but is not limited to, Cvclopropvlmethvl, cyclopropylethyl, ring Propyl propyl, cyclobutylmethyl, cyclobutylethyl, cyclopentyl-methyl, cyclopentyl ethyl, cyclopentylpropyi, cyclohexyl-ethyl etc..

Term " heterocyclylalkyl group " includes the alkyl that heterocycle replaces；Term " heterocyclylalkoxy " includes that heterocycle replaces Alkoxy, wherein oxygen atom is connected with the rest part of molecule；Term " heterocycle alkylamino " includes the alkane that heterocycle replaces Amino, wherein nitrogen-atoms is connected with the rest part of molecule.Wherein heterocycle, alkyl, alkoxy and alkylamino all have such as this The definition is invented, such example includes, but is not limited to, azetidine -1- ylmethyl, azetidine -1- base second Base, azetidine -1- base propyl, pyrroles's -1- ylmethyl, pyrroles's -1- base ethyl, pyrroles's -1- base propyl, morpholine -4- base second Base, morpholine -4- base oxethyl, piperazine -4- base oxethyl, piperidin-4-yl ethylamino etc..

Term " condensed-bicyclic ", " condensed ring ", " condensed-bicyclic base ", " condensed ring radical " indicate saturated or unsaturated fused ring system System is related to the bicyclic system of non-aromatic, and as shown in formula (a1), i.e. ring B and ring B ' share a key.Such system can be with Comprising independent or conjugation undersaturated condition, but its nuclear structure does not include aromatic rings or heteroaromatic (but aromatic series can be with As substituent group thereon).Each of condensed-bicyclic ring is either carbocyclic ring or is heteroalicyclic, such example packet It includes, but is not limited to, hexahydro-furans simultaneously [3,2-b] furans, 2,3,3a, 4,7,7a- hexahydro -1H- indenes, 7- azabicyclo [2.3.0] heptane, condensed-bicyclic [3.3.0] octane, condensed-bicyclic [3.1.0] hexane, these are included within condensed-bicyclic. And the condensed-bicyclic base can be substituted or unsubstituted, and wherein substituent group can be, but be not limited to, D, F, Cl, Br, I、N₃、CN、NO₂、OH、SH、NH₂, oxo, alkyl, halogenated alkyl, alkenyl, alkynyl, alkoxy, alkyl amino, hydroxyalkyl, cyano Substituted alkyl, naphthenic base, heterocycle, aryl, heteroaryl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a、-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、 -N (R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (= O)_1-2R^7a、 -R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N (R¹²) S (=O)_1-2R^12a、 -R¹⁴-N(R¹³) C (=O) NR^13aR^13bEtc., wherein R⁷、R^7a、R⁸、R^8a、R⁹、R^9a、R¹⁰、R^10a、 R¹¹、R^11a、R¹²、R^12a、R¹³、 R^13a、R^13bAnd R¹⁴With definition of the present invention.

Term " condensing miscellaneous bicyclic group " indicates saturated or unsaturated fused ring system or bridged-ring system, is related to non-aromatic Bicyclic system or bridged-ring system.Such system may include independent or conjugation undersaturated condition, but its nuclear structure is not Include aromatic rings or heteroaromatic (but aromatic series can be used as substituent group thereon).And at least one ring system include one or Multiple hetero atoms, wherein each ring system includes 3-7 member ring, i.e., comprising 1-6 carbon atom and selected from N, O, P, the 1-3 of S is a Hetero atom optionally obtains such as SO, SO in this S or P replaced one or more oxygen atoms₂, PO, PO₂Group, in this way Example include, but is not limited to hexahydro-furans simultaneously [3,2-b] furans, 7- azabicyclo [2.3.0] heptane, 2- azabicyclo [2.2.1] heptane, octahydro pyrroles [3,2-b] pyrroles, octahydro pyrroles [3,4-c] pyrroles, octahydro -1H- pyrroles [3,2-b] pyridine Deng.And described to condense miscellaneous bicyclic group and can be substituted or unsubstituted, wherein substituent group can be, but be not limited to, D, F, Cl、Br、I、N₃、CN、NO₂、OH、SH、NH₂, oxo, alkyl, halogenated alkyl, alkenyl, alkynyl, alkoxy, alkyl amino, hydroxyl alkane Base, the alkyl of cyano substitution, naphthenic base, heterocycle, aryl, heteroaryl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_{1- 2}R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、- NR¹¹R^11a、 -N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、- R¹⁴- OS (=O)_1-2R^7a、 -R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴- NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12a、 -R¹⁴-N(R¹³) C (=O) NR^13aR^13bEtc., wherein R⁷、R^7a、R⁸、R^8a、R⁹、 R^9a、R¹⁰、R^10a、R¹¹、R^11a、R¹²、R^12a、R¹³、 R^13a、R^13bAnd R¹⁴With definition of the present invention.

Term " loop coil base ", " loop coil ", " spiral shell bicyclic group ", " spiral shell is bicyclic " indicate a ring originating from special on another ring Cyclic annular carbon.For example, sharing a carbon atom in the ring system that ring A and ring B is saturated at two, then it is referred to as " loop coil ".Loop coil Each ring of the inside is either carbocyclic ring or is heteroalicyclic.Such example includes, but is not limited to 2,7- diaza spiro [4.4] nonane -2- base, 7- oxygen -2- azaspiro [4.5] decane -2- base, 4- azaspiro [2.4] heptane -5- base, 4- oxaspiro [2.4] heptane -5- base, 5- azaspiro [2.4] heptane -5- base, spiral shell [2.4] heptane base, spiral shell [4.4] nonyl, 7- hydroxyl -5- Azaspiro [2.4] heptane -5- base etc..And the spiral shell bicyclic group can be substituted or unsubstituted, and wherein substituent group can be, But it is not limited to, D, F, Cl, Br, I, N₃、CN、NO₂、OH、SH、NH₂, oxo, alkyl, halogenated alkyl, alkenyl, alkynyl, alcoxyl Base, alkyl amino, hydroxyalkyl, the alkyl of cyano substitution, naphthenic base, heterocycle, aryl, heteroaryl ,-S (=O)_0-2R⁷、-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹、 -OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、- R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12a、-R¹⁴-N(R¹³) C (=O) NR^13aR^13bEtc., wherein R⁷、 R^7a、R⁸、R^8a、R⁹、R^9a、R¹⁰、R^10a、 R¹¹、R^11a、R¹²、R^12a、R¹³、R^13a、R^13bAnd R¹⁴With definition of the present invention.

Term " sub- spiral shell bicyclic group " indicates that spiral shell bicyclic group system tool is connected there are two tie point with molecule rest part, wherein Spiral shell bicyclic group has definition as described in the present invention.

Term " the miscellaneous bicyclic group of spiral shell " indicates a ring originating from particularly ring-shaped carbon on another ring.For example, such as institute above Description, a carbon atom is shared in the ring system that ring A and ring B are saturated at two, then is referred to as " loop coil ".And at least one Ring system includes one or more hetero atoms, and wherein each ring system includes 3-7 member ring, that is, includes 1-6 carbon atom and choosing From N, O, P, the 1-3 hetero atom of S optionally obtains such as SO, SO in this S or P replaced one or more oxygen atoms₂, PO, PO₂Group, such example includes, but is not limited to 4- azaspiro [2.4] heptane -5- base, 4- oxaspiro [2.4] heptan Alkane -5- base, 5- azaspiro [2.4] heptane -5- base, 7- hydroxyl -5- azaspiro [2.4] heptane -5- base, 2,6- diaza spiros [3.3] heptane, 2,6- diaza spiros [3.4] octane, 1,6- diaza spiro [3.4] octane, 2,7- diaza spiros [3.5] nonane, 1,7- diaza spiro [3.5] nonane, 3,9- diaza spiros [5.5] hendecane etc..And the miscellaneous bicyclic group of spiral shell can be substitution Or it is unsubstituted, wherein substituent group can be, but be not limited to, D, F, Cl, Br, I, N₃、CN、NO₂、OH、SH、NH₂, oxo, alkane Base, halogenated alkyl, alkenyl, alkynyl, alkoxy, alkyl amino, hydroxyalkyl, the alkyl of cyano substitution, naphthenic base, heterocycle, virtue Base, heteroaryl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a)C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12a、-R¹⁴-N(R¹³)C (=O) NR^13aR^13bEtc., wherein R⁷、R^7a、R⁸、R^8a、R⁹、R^9a、R¹⁰、R^10a、 R¹¹、R^11a、R¹²、R^12a、R¹³、R^13a、R^13bAnd R¹⁴ With definition of the present invention.

Terminology used in the present invention " bridged ring base " indicates saturated or unsaturated bridged-ring system, is related to the bridged ring of non-aromatic System, as shown in formula (a2), i.e. ring A1 and ring A2 share an alkane chain or a miscellaneous alkane chain, and wherein j is 1,2,3 or 4.In this way System may include independent or conjugation undersaturated condition, but its nuclear structure does not include aromatic rings or heteroaromatic (still Aromatic series can be used as substituent group thereon).Each of bridge joint ring ring is either carbocyclic ring or is heteroalicyclic, such Example includes, but is not limited to, bicyclic [2.2.1] heptane, 2- azabicyclo [2.2.1] heptane, and 1,2,3,4,4a, 5,8,8a- Octahydro naphthalene, these are included within the system of condensed-bicyclic or bridged ring.And the bridged ring base can be substituted or unsubstituted , wherein substituent group can be, but be not limited to, D, F, Cl, Br, I, N₃、 CN、NO₂、OH、SH、NH₂, it is oxo, alkyl, halogenated Alkyl, alkenyl, alkynyl, alkoxy, alkyl amino, hydroxyalkyl, the alkyl of cyano substitution, naphthenic base, heterocycle, aryl, heteroaryl Base ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、 -N(R^9a) C (=O) R⁹、- C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、 - R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、 -R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12a、-R¹⁴-N(R¹³) C (=O) NR^13aR^13bDeng Deng wherein X³、 R⁷、R^7a、R⁸、R^8a、R⁹、R^9a、R¹⁰、R^10a、R¹¹、R^11a、R¹²、R^12a、R¹³、R^13a、R^13bAnd R¹⁴With institute of the present invention State definition.

Term " bridge heterocycle " indicates saturated or unsaturated bridged-ring system, is related to the bridged-ring system of non-aromatic.In this way System may include independent or conjugation undersaturated condition, but its nuclear structure does not include aromatic rings or heteroaromatic (still Aromatic series can be used as substituent group thereon).And at least one ring system includes one or more hetero atoms, wherein each ring System includes 3-7 member ring, i.e., comprising 1-6 carbon atom and selected from N, O, P, the 1-3 hetero atom of S, this S or P optionally by Such as SO, SO are obtained replaced one or more oxygen atoms₂, PO, PO₂Group, such example includes, but is not limited to 2- Azabicyclo [2.2.1] heptane, (1R, 5S) -3,6- diazabicyclo [3.1.1] heptane, 2,5- diazabicyclos [2.2.1] heptan Alkane, (1R, 5S) -8- azabicyclo [3.2.1] octane etc..And the bridge heterocycle can be it is substituted or unsubstituted, wherein Substituent group can be, but be not limited to, D, F, Cl, Br, I, N₃、CN、NO₂、OH、 SH、NH₂, oxo, alkyl, halogenated alkyl, alkene Base, alkynyl, alkoxy, alkyl amino, hydroxyalkyl, cyano replace alkyl, naphthenic base, heterocycle, aryl, heteroaryl ,-S (= O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (= O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴-OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12a、-R¹⁴-N(R¹³) C (=O) NR^13aR^13bEtc., Middle R⁷、R^7a、R⁸、R^8a、R⁹、R^9a、R¹⁰、R^10a、 R¹¹、R^11a、R¹²、R^12a、R¹³、R^13a、R^13bAnd R¹⁴With definition of the present invention.

As described in the present invention, be connected with molecule rest part in ring system there are two tie point, such as formula (a3) or (a4) shown in, indicate either the end E be also possible to E ' end be connected with molecule rest part, i.e., the connection type at both ends can be mutual It changes.

E-N(R^g) C (=O) O-E ' (a4)

Term " n former molecular ", wherein n is integer, the number of ring member nitrogen atoms in molecule is typically described, described The number of ring member nitrogen atoms is n in molecule.For example, piperidyl is 6 molecular Heterocyclylalkyls of original, and 1,2,3,4- naphthane is 10 molecular groups of naphthene base of original.In " unsaturated " the expression group of term as used in the present invention containing one or Multiple degrees of unsaturation.

Term " hetero atom " refers to O, S, N, P and Si, the form including any oxidation state of N, S and P；Primary, secondary, tertiary amine and season The form of ammonium salt；Or the substituted form of hydrogen in heterocycle on nitrogen-atoms, for example, N is (as in 3,4- dihydro-2 h-pyrrole base N), NH (as the NH in pyrrolidinyl) or NR (NR in pyrrolidinyl replaced as N-).

Term " halogen " refers to fluorine (F), chlorine (Cl), bromine (Br) or iodine (I).

Terminology used in the present invention " aryl " refers to the monovalence C comprising at least one aromatic ring unless otherwise indicated₆-C₁₄Carbon Ring system, wherein the aromatic ring system is monocycle, two rings or tricyclic.The aryl can pass through its any ring, that is, any aromatic rings Or non-aromatic ring is connected in main structure.In some embodiments, aryl is phenyl, naphthalene, two rings [4.2.0] octyl- 1,3,5- Trialkenyl, indanyl, fluorenyl or tetralyl.When aryl is substituted, can appoint include by aryl on any ring What it is substituted on aromatic rings or non-aromatic ring.In some or any embodiment, aryl is phenyl, naphthalene, tetralyl, fluorenes Base or indanyl；The phenyl, naphthalene, tetralyl, fluorenyl and indanyl respectively optionally can be with by the aryl group Individually optionally replaced one or more substituent groups described in the invention, in some embodiments, including by independently Selected from D, F, Cl, Br, I, N₃、CN、NO₂、OH、SH、NH₂, alkyl, halogenated alkyl, alkenyl, alkynyl, alkoxy, alkyl amino, hydroxyl Alkyl, the alkyl of cyano substitution, naphthenic base, heterocycle, aryl, heteroaryl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_{1- 2}R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、- NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、- R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴- NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12a、 -R¹⁴-N(R¹³) C (=O) NR^13aR^13bDeng group replace, wherein R⁷、R^7a、 R⁸、R^8a、R⁹、R^9a、R¹⁰、R^10a、R¹¹、R^11a、R¹²、 R^12a、R¹³、R^13a、R^13bAnd R¹⁴With definition of the present invention.

Terminology used in the present invention " aralkyl " refers to by one or two as defined herein unless otherwise indicated The alkyl group that a aryl group replaces, wherein the alkyl group is the point connecting with molecule rest part.In some implementations Scheme, aralkyl are benzyl, benzene second -1- base, benzene second -2- base, diphenyl methyl, 2,2- diphenyl-ethyl, 3,3- diphenyl Propyl or 3- phenyl propyl；The benzyl, benzene second -1- base, benzene second -2- base, diphenyl methyl, 2,2- diphenyl-ethyl, 3, 3- diphenyl propyl and 3- phenyl propyl are respectively taken optionally on ring by one or more substituent groups described in the invention Generation.

Terminology used in the present invention " heteroaryl " refers to monovalent monocyclic or polycyclic aromatic groups unless otherwise indicated, wherein At least one described (in certain embodiments, 1,2,3 or 4) annular atom is independently selected from O, S (O) in the ring_0-2With The hetero atom of N.The heteroaryl groups are by any atom in ring system, in the case of chemical valence rule allows, connection To molecule rest part.1 or 2 O atom, 1 or 2 S original can be contained in each ring of some embodiments, heteroaryl groups Sub, and/or 1 to 4 N atom, or combinations thereof, condition is that heteroatomic sum is that 4 or less and each ring contain in each ring There is at least one carbon atom.In some embodiments, the heteroaryl has 5-20,5-15 or 5-10 annular atoms.Work as heteroaryl When base is substituted, it can be replaced on any ring.In certain embodiments, single ring heteroaryl group includes but is not limited to, Furyl, imidazole radicals, isothiazolyl, isoxazolyl, oxadiazoles base, oxazolyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridyl group, Pyrimidine radicals, pyrrole radicals, thiadiazolyl group, thiazolyl, thienyl, tetrazole radical, triazine radical and triazolyl.It is double in certain embodiments Heteroaryl group includes, but are not limited to benzofuranyl, benzimidazolyl, benzo isoxazolyl, benzopyranyl, benzo Thiadiazolyl group, benzothiazolyl, benzothienyl, benzotriazole base, benzoxazolyl, furopyridyl, imidazopyridine Base, Imidazothiazole base, indolizine base, indyl, indazolyl, isobenzofuran-base, isobenzo-thienyl, isoindolyl, isoquinoline Quinoline base, isothiazolyl, naphthyridines base, oxazole and pyridyl group, phthalazinyl, pteridyl, purine radicals, pyridopyridine base, pyrrolo- pyrrole Piperidinyl, quinolyl, quinoxalinyl, quinazolyl, thiadiazoles and pyrimidine radicals and thienopyridine base.In certain embodiments, three Heteroaryl group includes, but are not limited to acridinyl, benzindole base, carbazyl, dibenzofuran group, Huo piperidinyl, phenanthroline Base, phenanthridinyl and phenazinyl.In some or any embodiment, heteroaryl is indyl, furyl, pyridyl group, pyrimidine radicals, miaow Oxazolyl or pyrazolyl；Its respectively optionally by 1,2,3 or 4 this specification in the whole text defined in group replace, in some realities Scheme is applied, including is independently selected from D, F, Cl, Br, I, N₃、CN、NO₂、OH、SH、 NH₂, alkyl, halogenated alkyl, alkenyl, alkynes Base, alkoxy, alkyl amino, hydroxyalkyl, the alkyl of cyano substitution, naphthenic base, heterocycle, aryl, heteroaryl ,-S (=O)_{0- 2}R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (= O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴-OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12a、-R¹⁴-N(R¹³) C (=O) NR^13aR^13bDeng group Replace, wherein R⁷、R^7a、R⁸、R^8a、R⁹、R^9a、R¹⁰、 R^10a、R¹¹、R^11a、R¹²、R^12a、R¹³、R^13a、R^13bAnd R¹⁴With institute of the present invention State definition.

Terminology used in the present invention " heteroaryl alkyl " refers to by one as defined herein unless otherwise indicated Or the alkyl group that two heteroaryl groups replace, wherein the alkyl group is the point connecting with molecule rest part.It is described The example of heteroaryl alkyl includes, but is not limited to imidazoles -2- methyl, thiazole -2- methyl, furans -2- ethyl, indoles -3- first Base etc.；It is respectively optionally on any ring replaced one or more substituent groups described in the invention.

Term " alkyl amino " includes " N- alkyl amino " and " N, N- dialkyl amido ", and wherein amino group is independently Ground is replaced one or two alkyl group.Some of embodiments are that alkyl amino is one or two C_1-6Alkyl connection The alkylamino group of lower level on to nitrogen-atoms.Other embodiment is that alkyl amino is C_1-3Lower level alkyl Amino group.Suitable alkylamino group can be alkyl monosubstituted amino or dialkyl amido, and such example includes, but not It is limited to, N- methylamino, N- ethylamino, N, N- dimethylamino, N, N- lignocaine etc..

Term " aminoalkyl " includes the C replaced one or more amino_1-10Linear or branched alkyl group group.Wherein Some embodiments are that aminoalkyl is the C replaced one or more amino groups_1-6" aminoalkyl of lower level ", it is another A little embodiments are that aminoalkyl is the C replaced one or more amino groups_1-4" aminoalkyl of lower level ", it is such Example includes, but is not limited to, aminomethyl, aminoethyl, aminopropyl, ammonia butyl and ammonia hexyl.

Term " cyano substitution alkyl " includes the C replaced one or more cyano_1-10Linear or branched alkyl group group. Some of embodiments are that the alkyl that cyano replaces is the C replaced one or more cyano groups_1-6" the cyano of lower level Alkyl ", other embodiments are that the alkyl that cyano replaces is the C replaced one or more cyano groups_1-4" lower level Cyanoalkyl ", such example include, but is not limited to, CNCH₂-、CNCH₂CH₂-、CNCH₂CH₂CH₂-、CNCH₂CHCNCH₂- Deng.

As described in the invention, substituent group draws one and is keyed to the ring system (as follows) formed on the ring at center Representing substituent group can replace any substitutive position on any ring.For example, formula b is represented and any on A ring or B ring may be taken The position in generation can be substituted, as shown in formula c, d, e, f, g, h, i, j, k, l, m, n, o, p, q etc..

Term " prodrug " used in the present invention represents a compound and is converted into formula (I) compound represented in vivo. Such conversion is hydrolyzed in blood by pro-drug or is that precursor structure is influenced through enzymatic conversion in blood or tissue.This hair Bright pro-drug compounds can be ester, and ester can be used as the phenyl ester class that has of pro-drug, aliphatic in existing invention (C₁-C₂₄) esters, pivaloyloxymethyl esters, carbonic ester, carbamates and amino acid esters.Such as one in the present invention Compound includes hydroxyl, it can is acylated to obtain the compound of prodrug form.Other prodrug forms include Phosphate, if these phosphate compounds are obtaining through the di on parent.It is completely begged for about pro-drug By following documents can be referred to: T.Higuchi and V.Stella, Pro-drugs as Novel Delivery Systems,Vol.14of the A.C.S.Symposium Series,Edward B.Roche,ed.,Bioreversible Carriers in Drug Design,American Pharmaceutical Association and Pergamon Press,1987,J.Rautio et al.,Prodrugs:Design and Clinical Applications,Nature Review Drug Discovery,2008,7,255-270,and S.J.Hecker et al.,Prodrugs of Phosphates and Phosphonates,Journal of Medicinal Chemistry,2008,51,2328-2345。

" metabolin " refers to specific compound or its salt product obtained by metabolic action in the body.One chemical combination The metabolite of object can be identified that activity can be by as described in the present invention by technology well-known in the art As adopt and experimentally characterized.Such product can be by, by aoxidizing, restoring, water to drug compound Solution, amidated, deamidation, esterification, degreasing, the methods of enzymatic lysis etc. obtain.Correspondingly, the present invention includes compound Metabolite, including the compound of the present invention and mammal are come into full contact with into metabolite caused by a period of time.

" pharmaceutically acceptable salt " used in the present invention refers to the organic salt and inorganic salts of the compound of the present invention.Medicine Acceptable salt is known to us in fields on, such as document: S.M.Berge et al., describe pharmaceutically acceptable salts in detail in J. Pharmaceutical Sciences, 1977,66:1-19. documented.The salt that pharmaceutically acceptable nontoxic acid is formed includes, but is not limited to, with amino base The inorganic acid salt such as hydrochloride that group's reaction is formed, hydrobromate, phosphate, sulfate, perchlorate and acylate such as acetic acid Salt, oxalates, maleate, tartrate, citrate, succinate, malonate, or by recorded in books, literature Other methods such as ion-exchanges obtain these salt.Other pharmaceutically acceptable salts include adipate, and alginates resist Bad hematic acid salt, aspartate, benzene sulfonate, benzoate, bisulphate, borate, butyrate, camphor hydrochlorate, camphor sulphur Hydrochlorate, cyclopentyl propionate, digluconate, lauryl sulfate, esilate, formates, fumarate, Portugal Heptose hydrochlorate, glycerophosphate, gluconate, Hemisulphate, enanthate, caproate, hydriodate, 2- hydroxy-ethanesulfonic acid Salt, lactobionate, lactate, laruate, lauryl sulfate, malate, malonate, mesylate, 2- naphthalene sulphur Hydrochlorate, nicotinate, nitrate, oleate, palmitate, pamoate, pectate, persulfate, 3- phenylpropionic acid salt, bitter taste Hydrochlorate, pivalate, propionate, stearate, rhodanate, tosilate, undecylate, valerate, etc..Pass through The salt reacted with alkali appropriate includes alkali metal, alkaline-earth metal, ammonium and N⁺(C₁-C₄Alkyl)₄Salt.The present invention is also intended to structure The compound for having thought the group of any included N is formed by quaternary ammonium salt.Water-soluble or oil-soluble or dispersion product can pass through Quaternization obtains.Alkali or alkaline earth metal salt includes sodium, lithium, potassium, calcium, magnesium, etc..Pharmaceutically acceptable salt is into one Step includes appropriate, nontoxic ammonium, the amine cation that quaternary ammonium salt and gegenions are formed, such as halide, hydroxide, carboxylation Object, hydrosulphate, phosphoric acid compound, nitric acid compound, C_1-8Sulphonic acid compound and aromatic sulphonic acid compound.

" solvate " of the invention refers to that one or more solvent molecules and the compound of the present invention are formed by association Object.The solvent for forming solvate includes, but is not limited to, water, isopropanol, ethyl alcohol, methanol, dimethyl sulfoxide, ethyl acetate, second Acid and ethylaminoethanol.Term " hydrate " refers to that solvent molecule is that water is formed by associated matter.

When the solvent is water, term " hydrate " can be used.In some embodiments, a compounds of this invention Molecule can be combined with a hydrone, such as monohydrate；In other embodiments, a compounds of this invention point Son can be combined with more than one hydrone, such as dihydrate, in further embodiments, a compounds of this invention Molecule can be combined with the hydrone less than one, such as semihydrate.It should be noted that hydrate of the present invention remains with The biological effectiveness of the compound of nonhydrated form.

Any disease of term " treatment " or illness as used in the present invention, refer to improvement disease in some of these embodiments Disease or illness (development for slowing down or prevent or mitigate disease or its at least one clinical symptoms).In other embodiments In, " treatment " refers to mitigation or improves at least one body parameter, including the body parameter that may not be discovered by patient.Another In a little embodiments, " treatment " refers to from body (such as stablizing perceptible symptom) or physiologically (such as stable body Parameter) or above-mentioned two aspect adjust disease or illness.In other embodiments, " treatment ", which refers to, prevents or delays disease or disease Breaking-out, generation or the deterioration of disease.

Summary of the invention

Heteroaromatic compounds provided by the invention can effectively inhibit ATX active, and can be used for preparing treatment has ATX expression The disease of increased pathological characteristics, for example, cancer, fibrotic disease (such as idiopathic pulmonary fibrosis or liver fibrosis), metabolism Disease, myelodysplastic syndrome, cardiovascular disease, autoimmune disease, inflammation, the nervous system disease or pain medicine Object.

On the one hand, the present invention provides the pharmaceutically acceptable of compound shown in compound shown in formula (I) or formula (I) Salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolin, prodrug or mixture:

Wherein,

W is-N (R^1a)-,-O- ,-S- ,-S (=O)_1-2,-C (=O)-,-(C (R^2a)(R^2b))_1-4-、-N(R^1a)(C(R^2a) (R^2b))_1-4-、-N(R^1a) C (=O)-or-O (C (R^2a)(R^2b))_1-4-；

Ar¹And Ar²Five molecular heteroaryls of original are each independently, wherein Ar¹And Ar²Individually optionally by 1,2 or 3 R²Replace；

Ar³For aryl or heteroaryl, wherein the Ar³Individually optionally by 1,2,3 or 4 R³Replace；

Cy be naphthenic base, heterocycle, spiral shell bicyclic group, the miscellaneous bicyclic group of spiral shell, condensed-bicyclic base, condense miscellaneous bicyclic group, bridged ring base, Bridge heterocycle, aryl or heteroaryl, wherein the Cy is optionally by 1,2,3 or 4 R⁴Replace；

Y is-(L¹-W¹)_m-L²-；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br, I ,- OH、-NH₂、 -NO₂,-CN and C_1-6The group of alkoxy replaces；

L²It is not present or L²For-O- ,-C (=O)-,-OC (=O)-,-C (=O) O- ,-C (=O)-C (=O)-,-C (= O)-C (=O) N (R^a)-、-N(R^b)-,-C (=O) N (R^c)-、-N(R^c) C (=O)-,-C (=O) N (R^c)-R¹⁵- C (=O) O- ,-C (=O) N (R^c)-R¹⁵- C (=O) N (R^a)-、-N(R^d) C (=O) N (R^c)-、 -N(R^g) C (=O) O- ,-S (=O)_0-2-、-S (=O)_1-2N(R^e)-、-N(R^f) S (=O)_1-2Or-N (R^f) S (=O)_1-2-R¹⁵-N(R^a)-；

Z be H ,-CN, alkyl, alkenyl, alkynyl, halogenated alkyl, naphthenic base, heterocycle, heterocyclylalkyl group, cycloalkyl-alkyl, Spiral shell bicyclic group, spiral shell miscellaneous bicyclic group, condense miscellaneous bicyclic group, bridged ring base, bridge heterocycle, aryl or heteroaryl at condensed-bicyclic base, Described in alkyl, alkenyl, alkynyl, halogenated alkyl, naphthenic base, heterocycle, spiral shell bicyclic group, the miscellaneous bicyclic group of spiral shell, condensed-bicyclic base, thick Miscellaneous bicyclic group, bridge ring alkyl, bridge Heterocyclylalkyl, aryl and heteroaryl are closed optionally by one or more R⁵Replace；

R¹For alkyl, alkenyl, alkynyl, aryl, heteroaryl, naphthenic base or heterocycle, wherein the R¹Individually optional ground quilt 1,2,3 or 4 R⁶Replace；

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, Alkyl, the hydroxyalkyl, alkoxy, alkoxyalkyl, sweet-smelling alkoxy alkyl, aryloxy alkyl, halogenated alkoxy ,-S of cyano substitution (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (= O)NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2aAnd R^2bIt is each independently H ,-CN ,-OH ,-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, cyanogen Alkyl, hydroxyalkyl, alkoxy, halogenated alkoxy, aryl, aralkyl, heteroaryl or the heteroaryl alkyl that base replaces；

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, alkyl halide Alkyl, the hydroxyalkyl, alkoxy, halogenated alkoxy ,-S (=O) that base, cyano replace_0-2R⁷,-C (=O) R⁸,-OS (=O)_{1- 2}R^7a,-OC (=O) R^8a,-C (=O) OR^8a、 -N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (= O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、- R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (= O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁴It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynes Alkyl, the hydroxyalkyl, alkoxy, halogenated alkoxy ,-S (=O) that base, halogenated alkyl, cyano replace_0-2R⁷,-C (=O) R⁸、-OS (=O)_1-2R^7a,-C (=O) OR^8a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁵It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynes Base, alkylamino, halogenated alkyl, cyano replace alkyl, hydroxyalkyl, alkoxy, halogenated alkoxy, aryl, aralkyl ,-S (= O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴-C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁶It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, alkyl, alkenyl, alkynyl, halogenated alkyl, Alkyl, the hydroxyalkyl, alkoxy, halogenated alkoxy ,-S (=O) of cyano substitution_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a、- OC (=O) R^8a,-C (=O) OR^8a、 -N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_{1- 2}R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴-OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_{1- 2}R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, halogenated C_1-6Alkane The C that base, cyano replace_1-6Alkyl, aryl, aralkyl, heteroaryl, heteroaryl alkyl, naphthenic base, cycloalkyl-alkyl, heterocycle, Or heterocyclylalkyl group；

Each R^9a、R¹⁰And R^10aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6Alkyl, Or halogenated C_1-6Alkyl；

Each R¹¹And R^11aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, halogenated C_1-6Alkyl, cyano replace C_1-6Alkyl or aralkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6 Alkyl or halogenated C_1-6Alkyl；

R^1aSeparately for H, alkyl, alkenyl, alkynyl, halogenated alkyl, cyano replace alkyl, hydroxyalkyl, naphthenic base, Cycloalkyl-alkyl, aryl or aralkyl；

Each R^a、R^b、R^c、R^d、R^e、R^f、R^g、R^hAnd RⁱIt is separately H, the alkane that alkyl, alkenyl, alkynyl, cyano replace Base, halogenated alkyl, R¹⁶- C (=O)-or cycloalkyl-alkyl；

Each R¹⁴And R¹⁵It is separately alkylidene, the alkyl or halogenated alkylene that alkenylene, alkynylene, cyano replace Base；

R¹⁶It is H, C_1-6Alkyl or halogenated C_1-6Alkyl；With

M is 0,1 or 2.

In some embodiments, wherein Ar³For C_6-10Aryl or C_1-9Heteroaryl, wherein the Ar³Individually optionally by 1, 2,3 or 4 R³Replace.

In other embodiments, wherein Ar³Are as follows:

Wherein, X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；With

Y¹、Y^1aAnd Y²It is each independently-N- ,-CH- or-C (R³)-。

In other embodiments, wherein Ar³For

Wherein, the Ar³Individually optionally by 0,1 or 2 R³Replace.

In some embodiments, wherein the compounds of this invention has structure shown in formula (Ia):

Wherein,

X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；

Y¹And Y²It is each independently-N- or-C (R³)-；

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, Metabolin, prodrug or mixture.

In some embodiments, in which: by Ar¹And Ar²CompositionRing is

Wherein,

X²For-O- ,-S- ,-C (R²)(R^2c)-or-N (R^2d)-；

Y³、Y⁴、Y⁵、Y⁶、Y⁷And Y⁸It is each independently-N- or-C (R²)-；

R^2cFor H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkane The C that base, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、 -N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (= O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴-OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2dFor H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, halogenated C_1-4Alkyl, C_1-4Hydroxyl alkane Base, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸、- OS (=O)_1-2R^7a,-OC (=O) R^8aOr-OC (=O) NR¹⁰R^10a、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴-OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、 -R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、- R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene or Halogenated C_1-4Alkylidene.

In other embodiments, wherein by Ar¹And Ar²CompositionRing is

Wherein,

X²For-O- ,-S- ,-C (R²)(R^2c)-or-N (R^2d)-；

Y³For-N- or-C (R²)-；

Y⁶For-N- or-C (R²)-；

R^2cFor H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkane The C that base, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、 -N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (= O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、 -R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴-OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2dFor H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, halogenated C_1-4Alkyl, C_1-4Hydroxyl alkane Base ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-OC (=O) NR¹⁰R^10a、-R¹⁴- S (= O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、 -R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴-OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene or Halogenated C_1-4Alkylidene.

In other embodiments, wherein by Ar¹And Ar²CompositionRing is

Wherein, 0,1 or 2 n.

In some embodiments, wherein R¹For C_6-10Aryl, C_1-9Heteroaryl, C_3-8Naphthenic base or C_2-9Heterocycle, wherein The R¹Individually optionally by 1,2,3 or 4 R⁶Replace.

In some embodiments, wherein R¹For C_6-10Aryl, C_1-9Heteroaryl, C_3-6Naphthenic base or C_2-7Heterocycle, wherein The R¹Individually optionally by 1,2,3 or 4 R⁶Replace.

In other embodiments, wherein R¹For phenyl or pyridyl group, wherein the phenyl is individually optionally by 1,2,3 Or 4 R⁶Replace.

In some embodiments, wherein the compounds of this invention has structure shown in formula (Ib):

Wherein,

X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；

X²For-O- ,-S- ,-C (R²)(R^2c)-or-N (R^2d)-；

Y¹And Y²It is each independently-N- or-C (R³)-；

Y³、Y⁴、Y⁵And Y⁶It is each independently-N- or-C (R²)-；

T is 0,1,2,3 or 4；

R^2cFor H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkane The C that base, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, aralkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、 -N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (= O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、 -R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴-OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；

R^2dFor H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyl alkane Base ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-OC (=O) NR¹⁰R^10a、-R¹⁴- S (= O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、 -R¹⁴- OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴-OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene or Halogenated C_1-4Alkylidene；Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxygen Compound, metabolin, prodrug or mixture.

In some embodiments, wherein W is-N (R^1a)-or-C (R^2a)(R^2b)-；R^1aFor H, C_1-4Alkyl or halogenated C_1-4 Alkyl；R^2aAnd R^2bIt is each independently H ,-CN ,-OH ,-NH₂、F、Cl、Br、I、C_1-4Alkyl, halogenated C_1-4Alkyl, cyano replace C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_6-10Aryl, C_6-10Aryl C_1-4Alkyl, C_1-9Heteroaryl or C_1-9Heteroaryl C_1-4Alkyl.

In some embodiments, wherein W is-N (R^1a)-；R^1aFor H, methyl, ethyl, propyl ,-CF₃Or-CH₂CF₃。

In some embodiments, wherein

X¹For-O- ,-S- ,-N (R³)-,-N=C (R³)-、-C(R³)=N- or-C (R³)=C (R³)-；

Y¹And Y²It is each independently-N- or-C (R³)-；

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, halogenated C_1-4Alkyl, cyano Substituted C_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (= O)R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N (R¹³) C (=O) NR^13aR^13b；

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkane The C that base, cyano replace_1-4Alkyl, aryl, aralkyl, heteroaryl, heteroaryl alkyl, naphthenic base, cycloalkyl-alkyl, heterocycle, Or heterocyclylalkyl group；

Each R^9a、R¹⁰And R^10aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, Or halogenated C_1-4Alkyl；

Each R¹¹And R^11aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, cyano replace C_1-4Alkyl or C_6-10Aryl C_1-6Alkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4 Alkyl or halogenated C_1-4Alkyl；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene or Halogenated C_1-4Alkylidene.

In some embodiments, wherein the compounds of this invention has structure shown in formula (Ic):

Wherein,

R^1aFor H, C_1-4Alkyl or halogenated C_1-4Alkyl；

T is 0,1,2,3 or 4；

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, Metabolin, prodrug or mixture.

In some embodiments, wherein Cy is C_3-8Naphthenic base, C_2-7Heterocycle, C_5-12Spiral shell bicyclic group, C_5-12Spiral shell is miscellaneous bicyclic Base, C_5-12Condensed-bicyclic base, C_5-12Condense miscellaneous bicyclic group, C_5-12Bridged ring base, C_5-12Bridge heterocycle, C_6-10Aryl or C_1-9Heteroaryl Base, wherein the Cy is optionally by 1,2,3 or 4 R⁴Replace.

In some embodiments, wherein Cy is

Wherein,

X³、X⁴And X⁵It is each independently-O- ,-S- ,-NH- ,-(CH₂)_m1-NH-(CH₂)_m2-、-(CH₂)_m1-O- (CH₂)_m2-、-(CH₂)_m1-S-(CH₂)_m2Or-(CH₂)_m3-；

Each m1 is separately 1,2,3 or 4；

Each m2 is separately 0,1,2,3 or 4；

Each m3 is separately 1,2,3 or 4；With

N1 is 0,1,2,3 or 4.

In some embodiments, wherein Cy is

Wherein, the Cy is optionally by 1,2,3 or 4 R⁴Replace.

In some embodiments, wherein

Y is-(L¹-W¹)_m-L²-；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-6Alkylidene, the C_1-6Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br ,- OH、-NH₂、-NO₂,-CN and C_1-4The group of alkoxy replaces；

L²It is not present or L²For-O- ,-C (=O)-,-OC (=O)-,-C (=O) O- ,-C (=O)-C (=O)-,-C (= O)-C (=O) N (R^a)-、-N(R^b)-,-C (=O) N (R^c)-、-N(R^c) C (=O)-,-N (R^d) C (=O) N (R^c- C)-, (=O) N(R^c)-R¹⁵- C (=O) O- ,-C (=O) N (R^c)-R¹⁵- C (=O) N (R^a)-、 -N(R^g) C (=O) O- ,-S (=O)_0-2-、-S (=O)_1-2N(R^e)-、-N(R^f) S (=O)_1-2Or-N (R^f) S (=O)_1-2-R¹⁵-N(R^a)-；

Each R^a、R^b、R^c、R^d、R^e、R^f、R^g、R^hAnd RⁱIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, cyano Substituted C_1-6Alkyl, C_1-6Hydroxyalkyl, halogenated C_1-6Alkyl, R¹⁶- C (=O)-or C_3-6Naphthenic base C_1-4Alkyl；

R¹⁵For C_1-6Alkylidene；

R¹⁶It is H, C_1-6Alkyl or halogenated C_1-6Alkyl；With

M is 0,1 or 2.

In some embodiments, wherein

Y is-(L¹-W¹)_m-L²-；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br ,- OH、-NH₂、-NO₂,-CN and C_1-4The group of alkoxy replaces；

L²It is not present or L²For-O- ,-C (=O)-,-OC (=O)-,-C (=O) O- ,-C (=O)-C (=O)-,-C (= O)-C (=O) N (R^a)-、-N(R^b)-,-C (=O) N (R^c)-、-N(R^c) C (=O)-,-N (R^d) C (=O) N (R^c)-, C (=O) N (R^c)-R¹⁵- C (=O) O- ,-C (=O) N (R^c)-R¹⁵- C (=O) N (R^a)-、 -N(R^g) C (=O) O- ,-S (=O)_0-2,-S (= O)_1-2N(R^e)-、-N(R^f) S (=O)_1-2Or-N (R^f) S (=O)_1-2-R¹⁵-N(R^a)-；

Each R^a、R^b、R^c、R^d、R^e、R^f、R^g、R^hAnd RⁱIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, cyano Substituted C_1-4Alkyl, C_1-4Hydroxyalkyl, halogenated C_1-4Alkyl, R¹⁶- C (=O)-or C_3-6Naphthenic base C_1-4Alkyl；

R¹⁵For C_1-6Alkylidene；

R¹⁶It is H, C_1-4Alkyl or halogenated C_1-4Alkyl；With

M is 0,1 or 2.

In some embodiments, wherein

Y is-(L¹-W¹)_m-L²-；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br ,- OH、-NH₂、-NO₂,-CN and C_1-4The group of alkoxy replaces；

L²It is not present or L²For-O- ,-C (=O)-,-OC (=O)-,-C (=O) O- ,-C (=O)-C (=O)-,-C (= O)-C (=O) N (R^a)-、-N(R^b)-,-C (=O) N (R^c)-、-N(R^c) C (=O)-,-N (R^d) C (=O) N (R^c- C)-, (=O) N(R^c)-R¹⁵- C (=O) O- ,-C (=O) N (R^c)-R¹⁵- C (=O) N (R^a)-、 -N(R^g) C (=O) O- ,-S (=O)_0-2-、-S (=O)_1-2N(R^e)-、-N(R^f) S (=O)_1-2Or-N (R^f) S (=O)_1-2-R¹⁵-N(R^a)-；

Each R^a、R^b、R^c、R^d、R^e、R^f、R^g、R^hAnd RⁱIt is separately H, methyl, ethyl, propyl, CNCH₂-、 CNCH₂CH₂-、 HOCH₂CH₂-、-CF₃、-CH₂CF₃, halogenated C_1-4Alkyl, Cvclopropvlmethvl, R¹⁶- C (=O)-or cyclopropyl second Base；

R¹⁵For methylene, ethylidene, propylidene or butylidene；

R¹⁶It is H, methyl, ethyl, propyl, butyl ,-CF₃Or CH₂CF₃With

M is 0,1 or 2.

In some embodiments, wherein Z H ,-CN, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, C_3-8 Naphthenic base, C_2-7Heterocycle, C_2-7Heterocycle C_1-4Alkyl, C_3-8Naphthenic base C_1-4Alkyl, C_5-12Spiral shell bicyclic group, C_5-12Spiral shell is miscellaneous bicyclic Base, C_5-12Condensed-bicyclic base, C_5-12Condense miscellaneous bicyclic group, C_5-12Bridged ring base, C_5-12Bridge heterocycle, C_6-10Aryl or C_1-9Heteroaryl Base, wherein the C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, C_3-8Naphthenic base, C_2-7Heterocycle, C_5-12Spiral shell is bicyclic Base, C_5-12The miscellaneous bicyclic group of spiral shell, C_5-12Condensed-bicyclic base, C_5-12Condense miscellaneous bicyclic group, C_5-12Bridged ring base, C_5-12Bridge heterocycle, C_6-10 Aryl and C_1-9Heteroaryl is optionally by one or more R⁵Replace.

In other embodiments, wherein Z H ,-CN, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, cyanogen The C that base replaces_1-4Alkyl, C_1-4Hydroxyalkyl ,-C_1-4Alkyl-NR¹¹R^11aOr C_3-6Naphthenic base or Z are as follows:

Wherein, X⁶For N or CH₂；

X⁷For-O- ,-S- ,-NH- ,-(CH₂)_m4-NH-(CH₂)_m5-、-(CH₂)_m4-O-(CH₂)_m5-、-(CH₂)_m4-S- (CH₂)_m5Or-(CH₂)_m6-；

Each m4 is separately 1,2,3 or 4；

Each m5 is separately 0,1,2,3 or 4；

Each m6 is separately 1,2,3 or 4；With

N2 is 0,1,2,3 or 4.

In other embodiments, wherein Z H ,-CN, methyl, ethyl, propyl, tert-butyl ,-CF₃、-CH₂CF₃、- CH₂CH₂CN、 -CH₂CH₂OH or Z are

In some embodiments, wherein

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, Halogenated C_1-6The C that alkyl, cyano replace_1-6Alkyl, C_1-6Hydroxyalkyl, C_1-6Alkoxy, C_1-6Alkoxy C_1-6Alkyl, C_6-10Aryl C_1-6Alkoxy C_1-6Alkyl, C_6-10Aryloxy group C_1-6Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N (R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, Halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_1-4Alkoxy C_1-4Alkyl, C_6-10Aryl C_1-4Alkoxy C_1-4Alkyl, C_6-10Aryloxy group C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N (R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R²It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, methyl, ethyl, propyl, methoxy methyl Base, methoxy ethyl, methoxy-propyl, ethoxyl methyl, ethoxyethyl group, benzyloxymethyl, Benzyloxyethyl, phenoxy group first Base, Phenoxyethyl ,-CH₂CH₂CN、-CH₂CH₂OH、-CH₂OH、-CF₃、-CH₂CF₃Or-CH₂CH₂C (=O) NH₂。

In some embodiments, wherein

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, Halogenated C_1-6The C that alkyl, cyano replace_1-6Alkyl, C_1-6Hydroxyalkyl, C_1-6Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸、-OS (=O)_1-2R^7a,-OC (=O) R^8a、 -N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_{1- 2}R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴-OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_{1- 2}R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, Halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸、-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_{1- 2}R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴-OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_{1- 2}R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R³It is separately H ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, methyl, ethyl, propyl, butyl, tertiary fourth Base, trifluoromethyl, trifluoroethyl ,-CH₂CH₂CN、-CH₂CH₂OH、-CH₂CH₂C (=O) NH₂, methoxyl group, ethyoxyl ,-S (= O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、- NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、- R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴- NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

In some embodiments, wherein

Each R⁴It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-6Alkyl, C_2-6Alkene Base, C_2-6Alkynyl, halogenated C_1-6The C that alkyl, cyano replace_1-6Alkyl, C_1-6Hydroxyalkyl, C_1-6Alkoxy ,-S (=O)_0-2R⁷、-C (=O) R⁸,-OS (=O)_1-2R^7a,-C (=O) OR^8a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹、-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、- R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R⁴It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkene Base, C_2-4Alkynyl, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷、-C (=O) R⁸,-OS (=O)_1-2R^7a,-C (=O) OR^8a,-OC (=O) R^8a、-N(R^9a) C (=O) R⁹,-C (=O) NR^9aR⁹、-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、 -N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、- R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、 -R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、-R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R⁴It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, methyl, ethyl, third Base, butyl, tert-butyl, trifluoromethyl, trifluoroethyl ,-CH₂CH₂CN、-CH₂CH₂OH、-CH₂OH、-CH₂CH₂C (=O) NH₂, first Oxygroup, ethyoxyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-C (=O) OR^8a,-OC (=O) R^8a、-N(R^9a)C (=O) R⁹,-C (=O) NR^9aR⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N (R¹³) C (=O) NR^13aR^13b。

In some embodiments, wherein

Each R⁵It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-6Alkyl, C_2-6Alkene Base, C_2-6Alkynyl, C_1-6Alkylamino, halogenated C_1-6The C that alkyl, cyano replace_1-6Alkyl, C_1-6Hydroxyalkyl, C_1-6Alkoxy, C_6-10 Aryl, C_6-10Aryl C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N (R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R⁵It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkene Base, C_2-4Alkynyl, C_1-4Alkylamino, halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy, C_6-10 Aryl, C_6-10Aryl C_1-4Alkyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N (R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R⁵It is separately H, oxo (C=O) ,-CN ,-NO₂、-OH、-NH₂, F, Cl, Br, I, methyl, ethyl, third Base, butyl, tert-butyl, trifluoromethyl, trifluoroethyl ,-CH₂CH₂CN、-CH₂CH₂OH、-CH₂CH₂C (=O) NH₂, methoxyl group, second Oxygroup, phenyl, benzyl, phenethyl ,-S (=O)_0-2R⁷,-C (=O) R⁸,-OS (=O)_1-2R^7a,-OC (=O) R^8a,-C (=O) OR^8a、-N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_1-2R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、 -R¹⁴- OS (=O)_1-2R^7a、-R¹⁴- OC (=O) R^8a、-R¹⁴-N (R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_1-2R^12aOr-R¹⁴-N (R¹³) C (=O) NR^13aR^13b。

In some embodiments, wherein

Each R⁶It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, Halogenated C_1-6The C that alkyl, cyano replace_1-6Alkyl, C_1-6Hydroxyalkyl, C_1-6Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸、-OS (=O)_1-2R^7a,-OC (=O) R^8a、 -N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_{1- 2}R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、 -R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴-OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_{1- 2}R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R⁶It is separately H ,-CN ,-NO₂、-OH、-NH₂、F、Cl、Br、I、C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, Halogenated C_1-4The C that alkyl, cyano replace_1-4Alkyl, C_1-4Hydroxyalkyl, C_1-4Alkoxy ,-S (=O)_0-2R⁷,-C (=O) R⁸、-OS (=O)_1-2R^7a,-OC (=O) R^8a、 -N(R^9a) C (=O) R⁹,-OC (=O) NR¹⁰R^10a、-NR¹¹R^11a、-N(R¹²) S (=O)_{1- 2}R^12a、-N(R¹³) C (=O) NR^13aR^13b、-R¹⁴- S (=O)_0-2R⁷、-R¹⁴- C (=O) R⁸、-R¹⁴- OS (=O)_1-2R^7a、-R¹⁴-OC (=O) R^8a、-R¹⁴-N(R^9a) C (=O) R⁹、-R¹⁴- OC (=O) NR¹⁰R^10a、-R¹⁴-NR¹¹R^11a、 -R¹⁴-N(R¹²) S (=O)_{1- 2}R^12aOr-R¹⁴-N(R¹³) C (=O) NR^13aR^13b。

In other embodiments, wherein

Each R⁶Separately for H ,-CN, F, Cl, Br, I, methyl, ethyl, propyl, tert-butyl, methoxyl group, ethyoxyl ,- OCH₂CF₃、 -CF₃、-CH₂CF₃、-CH₂CH₂CN、-CH₂CH₂OH ,-C (=O) CH₃,-C (=O) CF₃,-C (=O) OCH₃,-C (= O)NH₂Or-NHC (=O) CH₃。

In some embodiments, wherein

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-6Alkyl, halogenated C_1-6The C that alkyl, cyano replace_1-6 Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, C_6-10Aryl, C_6-10Aryl C_1-6Alkyl, C_1-9Heteroaryl, C_1-9Heteroaryl C_1-6Alkyl, C_3-8Ring Alkyl, C_3-8Naphthenic base C_1-6Alkyl, C_2-9Heterocycle or C_2-9Heterocycle C_1-6Alkyl；

Each R^9a、R¹⁰And R^10aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6Alkyl, Or halogenated C_1-6Alkyl；

Each R¹¹And R^10aIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6Alkynyl, halogenated C_1-6Alkyl, cyano replace C_1-6Alkyl or C_6-10Aryl C_1-6Alkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-6Alkyl, C_2-6Alkenyl, C_2-6The C that alkynyl, cyano replace_1-6 Alkyl or halogenated C_1-6Alkyl；With

Each R¹⁴It is separately C_1-6Alkylidene, C_2-6Alkenylene, C_2-6The C that alkynylene, cyano replace_1-6Alkylidene or Halogenated C_1-6Alkylidene.

In other embodiments, wherein

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, C_1-4Alkyl, halogenated C_1-4The C that alkyl, cyano replace_1-4 Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, C_6-10Aryl, C_6-10Aryl C_1-4Alkyl, C_1-9Heteroaryl, C_1-9Heteroaryl C_1-4Alkyl, C_3-8Ring Alkyl, C_3-8Naphthenic base C_1-4Alkyl, C_2-7Heterocycle or C_2-7Heterocycle C_1-4Alkyl；

Each R^9a、R¹⁰And R^10aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4Alkyl, Or halogenated C_1-4Alkyl；

Each R¹¹And R^10aIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4Alkynyl, halogenated C_1-4Alkyl, cyano replace C_1-4Alkyl or C_6-10Aryl C_1-4Alkyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, C_1-4Alkyl, C_2-4Alkenyl, C_2-4The C that alkynyl, cyano replace_1-4 Alkyl or halogenated C_1-4Alkyl；With

Each R¹⁴It is separately C_1-4Alkylidene, C_2-4Alkenylene, C_2-4The C that alkynylene, cyano replace_1-4Alkylidene or Halogenated C_1-4Alkylidene.

In other embodiments, wherein

Each R⁷、R^7a、R⁸、R^8a、R⁹And R^12aIt is separately H, methyl, ethyl, propyl, tert-butyl ,-CF₃、- CH₂CF₃、-CH₂CH₂CN、 -CH₂CH₂OH, vinyl, acrylic, acetenyl, phenyl, benzyl, phenethyl, C_1-9Heteroaryl, C_1-9Heteroaryl C_1-4Alkyl, C_3-8Naphthenic base, C_3-8Naphthenic base C_1-4Alkyl, C_2-7Heterocycle or C_2-7Heterocycle C_1-4Alkyl；

Each R^9a、R¹⁰And R^10aIt is separately H, methyl, ethyl, propyl, tert-butyl ,-CF₃、-CH₂CF₃、- CH₂CH₂CN, vinyl, acrylic or acetenyl；

Each R¹¹And R^10aIt is separately H, methyl, ethyl, propyl, tert-butyl ,-CF₃、-CH₂CF₃、-CH₂CH₂CN, second Alkenyl, acrylic, acetenyl, benzyl or phenethyl；

Each R¹²、R¹³、R^13aAnd R^13bIt is separately H, methyl, ethyl, propyl, tert-butyl ,-CF₃、-CH₂CF₃、- CH₂CH₂CN, vinyl, acrylic or acetenyl；With

Each R¹⁴It is separately methylene, ethylidene, propylidene, butylidene, ethenylidene, allylidene, sub- acetylene Base ,-CH₂CH (CN)-or-CH₂CH(F)-。

In some embodiments, wherein the compound has any shown structure of formula (Id)-(Ig):

Wherein,

R^1aFor H, methyl, ethyl, propyl ,-CF₃Or-CH₂CF₃；

R²And R³Be each independently H ,-CN, F, Cl, Br, methyl, ethyl, propyl, methoxy, methoxy ethyl, Methoxy-propyl, ethoxyl methyl, ethoxyethyl group, benzyloxymethyl, Benzyloxyethyl ,-CF₃、-CH₂CF₃、-CH₂CH₂CN、- CH₂CH₂OH or-CH₂CH₂C (=O) NH₂；

R⁴For H, oxo (=O) ,-CN, F, Cl, Br, I, methyl, ethyl, propyl, tert-butyl, methoxyl group, ethyoxyl ,- OCH₂CF₃、 -CF₃、-CH₂CF₃、-CH₂CH₂CN、-CH₂CH₂OH、-CH₂OH ,-C (=O) CH₃,-C (=O) CF₃,-C (=O) OCH₃,-C (=O) NH₂,-C (=O) NHCH₃,-C (=O) NHCH₂CH₃Or-NHC (=O) CH₃；

R⁶For H ,-CN, F, Cl, Br, I, methyl, ethyl, propyl, tert-butyl, methoxyl group, ethyoxyl ,-OCH₂CF₃、- CF₃、-CH₂CF₃、 -CH₂CH₂CN、-CH₂CH₂OH ,-C (=O) CH₃,-C (=O) CF₃,-C (=O) OCH₃,-C (=O) NH₂Or- NHC (=O) CH₃；

X³For N or CH；

L¹It is not present or L¹For-O- ,-C (=O)-,-N (Rⁱ)-、-N(R^h) C (=O)-or-S (=O)_0-2-；

W¹For C_1-4Alkylidene, the C_1-4Alkylidene optionally by 1,2,3 or 4 independently selected from H, F, Cl, Br ,- OH、-NH₂、-NO₂,-CN and C_1-4The group of alkoxy replaces；

R^hAnd RⁱIt is each independently H, methyl, ethyl, propyl, tert-butyl, C_2-4Alkenyl, C_2-4Alkynyl, cyano replace C_1-4Alkyl, C_1-4Hydroxyalkyl, halogenated C_1-4Alkyl, Cvclopropvlmethvl, HC (=O)-, CH₃C (=O)-or cyclopropylethyl；

M1 is 1,2,3 or 4；

N1 is 0,1,2,3 or 4；With

Z has definition of the present invention；

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, Metabolin, prodrug or mixture.

In some embodiments, the compounds of this invention is the compound one of having following structure:

Or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, Metabolin, prodrug or mixture.

On the other hand, the present invention provides a kind of pharmaceutical composition, described pharmaceutical composition includes of the present inventionization Close object or its pharmaceutically acceptable salt, hydrate, solvate, stereoisomer, tautomer, nitrogen oxides, metabolism Object, prodrug, and pharmaceutically acceptable auxiliary material, diluent or carrier.

In some embodiments, pharmaceutical composition of the present invention further includes additional therapeutic agent.

In some embodiments, composition of the present invention, wherein the additional therapeutic agent be with fibrotic conditions, Proliferative diseases, inflammatory disease, autoimmune disease, respiratory disorder, cardiovascular disease, neurodegenerative disease, dermatology barrier Hinder and/or abnormal vascular generates treating correlative diseases agent.

In some embodiments, pharmaceutical composition of the present invention, wherein the additional therapeutic agent includes but is not limited to, Immunomodulator, analgestic, non-steroidal anti-inflammatory drugs, steroids, synthesis DMARDS, the drug for treating proliferative diseases, sugared cortex Hormone, cytostatic agent, alkylating agent, antimetabolite, cytotoxic antibiotic, antibody class etc..

On the other hand, compound of the present invention or pharmaceutical composition of the present invention are used the present invention provides a kind of Object is preparing the use in the drug for preventing or treating the disease that mammal expresses increased pathological characteristics with ATX On the way.

In some embodiments, wherein described, there is ATX to express the disease of increased pathological characteristics includes: cancer, fibre Dimensionization disease, metabolic disease, myelodysplastic syndrome, cardiovascular disease, autoimmune disease, inflammation, nervous system Disease or pain.

In some embodiments, wherein the disease for expressing increased pathological characteristics with ATX is that idiopathic lung is fine Dimensionization or liver fibrosis.In some embodiments, the compounds of this invention or its pharmaceutical composition can be combined with other therapeutic agent Application.

In some embodiments, purposes of the present invention includes being enough to realize the treatment or prevention to mammal application Amount compound of the present invention or pharmaceutical composition.

Pharmaceutical composition, preparation and purposes

When being used as drug, the compounds of this invention is usually applied with pharmaceutical compositions.The composition can be with system Well known mode prepares and includes at least one according to Formulas I, the present invention of Ia, Ib, Ic, Id, Ie, If or Ig in medicine technology The compound.In general, the compounds of this invention is applied with medicine effective quantity.The amount for the compounds of this invention actually applied usually will Determined by doctor according to relevant situation, the situation include illness to be treated, selected administration method, applied it is of the invention Practical compound, the age of few patients, weight and response, the severity of patient symptom etc..

Pharmaceutical composition of the invention can be applied through a variety of ways, including oral, rectum, percutaneous, subcutaneous, joint It is interior, intravenous, intramuscular and intranasal.Depending on expected route of delivery, the compounds of this invention is preferably formulated as injectable or oral Composition or as ointment, as lotion or as patch (being used to transdermal administration).

In certain embodiments, composition provided by the invention is pharmaceutical composition or single unit dosage forms.The present invention mentions The pharmaceutical composition of confession and single unit dosage forms include the one or more prophylactics or therapeutic agent (example of prevention or therapeutically effective amount Such as, compound provided by the invention or other prophylactics or therapeutic agent) and it is typical one or more pharmaceutically acceptable Carrier or auxiliary material.In specific embodiment and the present invention, term " pharmaceutically acceptable " refers to by federal or state government Regulatory agency's approval, or what is listed in United States Pharmacopeia or other generally acknowledged pharmacopeia are used for animal, particularly for the mankind's Drug.Term " carrier " includes the diluent applied together with therapeutic agent, adjuvant (for example, Freund's adjuvant is (completely and endless Entirely)), auxiliary material or medium.Such pharmaceutical carrier can be sterile liquid, such as water and oils, including petroleum, animal oil, plant Those of oil or synthesis source, such as peanut oil, soybean oil, mineral oil, sesame oil.When intravenously application pharmaceutical composition, Water can be used as carrier.Saline solution and glucose solution and glycerite also are used as liquid-carrier, especially for infusing Penetrate solution.The case history of suitable pharmaceutical carrier is in Remington:The Science and Practice of Pharmacy；Pharmaceutical Press (Pharmaceutical Press)；In 22 editions (on Septembers 15th, 2012).

Typical pharmaceutical composition and dosage form includes one or more auxiliary materials.Technology people of the suitable auxiliary material to pharmaceutical field Member for be it is well known, in certain embodiments, suitable auxiliary material include starch, glucose, lactose, sucrose, gelatin, malt, Rice, flour, chalk, silica gel, odium stearate, glyceryl monostearate, talcum powder, sodium chloride, skimmed milk power, glycerol, propylene, Ethylene glycol, water, ethyl alcohol etc..Specific auxiliary material if appropriate for incorporation pharmaceutical composition or dosage form, depend on it is well known in the art that Various factors, including but not limited to by the dosage form be applied to the given activity in the mode and the dosage form of subject at Point.If desired, the composition or single unit dosage forms can also contain a small amount of wetting agent or emulsifier or pH buffer.

The composition of oral administration can take the form of bulk liquids solution or suspension or powder in bulk.However, more logical Chang Di, composition exist accurately to be administered with unit dosage forms.Term " unit dosage forms ", which refers to, is suitable for individual human and other The physically discontinuous unit of the unit dose of mammal, each unit, which contains, to be computed to generate the pre- of required therapeutic effect Quantitative active material, with suitable excipient substance, medium or carrier etc..Typical unit dosage forms include the pre- of liquid composition Filling, the ampoule or syringe or pill, tablet, capsule under the situation of solid composite etc. measured in advance.At described group Close object in, Formulas I, Ia, Ib, Ic, Id, Ie, If or Ig the compounds of this invention be usually accessory constituent (about 0.1 to about 50 weight Measure %, or preferably from about 1 to about 40 weight %), remaining a variety of medium for contributing to form required form of medication or carrier and Handle auxiliary agent.

On the other hand, it the present invention provides the compounds of this invention or comprising the pharmaceutical composition of the compounds of this invention, uses In medicine.In a particular embodiment, the present invention provides the compounds of this invention or include the pharmaceutical composition of the compounds of this invention Object, be used to prevent and/or treat fibrotic conditions, proliferative diseases, inflammatory disease, autoimmune disease, respiratory disorder, Cardiovascular disease, neurodegenerative disease, dermatological disorders and/or abnormal vascular generate related disease.

In some embodiments, the present invention provides the compounds of this invention or include the pharmaceutical composition of the compounds of this invention Object, be used to prepare for prevent and/or treat fibrotic conditions, proliferative diseases, inflammatory disease, autoimmune disease, Respiratory disorder, cardiovascular disease, neurodegenerative disease, dermatological disorders and/or abnormal vascular generate the drug of related disease.

In some embodiments, the present invention provides the pharmaceutical compositions comprising the compounds of this invention and other therapeutic agents. In a particular embodiment, other therapeutic agents be with fibrotic conditions, proliferative diseases, inflammatory disease, autoimmune disease, Respiratory disorder, cardiovascular disease, neurodegenerative disease, dermatological disorders and/or abnormal vascular generate treating correlative diseases agent.

In the other method in terms for the treatment of, the present invention provides preventions and/or treatment with fibrotic conditions, increases Growing property disease, inflammatory disease, autoimmune disease, respiratory disorder, cardiovascular disease, neurodegenerative disease, dermatological disorders And/or the method that abnormal vascular generates the mammal of related disease, it is a effective amount of of the present invention the method includes applying Compound or one or more of pharmaceutical composition for treating or preventing the illness.

In other embodiments, the present invention provides the compounds of this invention or include the pharmaceutical composition of the compounds of this invention Object, the purposes being used to prepare in the drug of prevention and/or treatment fibrotic conditions.In specific embodiments, fiber becomes Property disease be selected from idiopathic pulmonary fibrosis (IPF), cystic fibrosis, different pathogeny other diffusivity substance lung diseases Sick (fibre modification including the drug-induced fibre modification of medicine origin, occupation and/or environmental induction), Granulomatous Disease (tubercle Disease, hylactic pneumonia), collagen vascular disease, alveolar protein deposition, Langerhans cell granuloma, lymphatic smooth muscle hyperplasia, Genetic disease (the general moral clarke syndrome of Theo Hermans base one, tuberous sclerosis, neurofibroma, metabolic storage obstacle, familial Ask matter tuberculosis), radiation-induced fibre modification, chronic obstructive pulmonary disease (COPD), chorionitis, bleomycin induction lung Fibre modification, chronic asthma, silicosis, the pnemnofibrosis of asbestos induction, acute respiratory distress syndrome (ARDS), kidney fiber Denaturation, renal tubule ask matter fibre modification, glomerulonephritis, partial section glomerulosclerosis, IgA nephropathy, hypertension, Ao Er Pott's disease (Alport), intestines fibre modification, hepatic fibrosis, hardening, alcohol-induced hepatic fibrosis, toxin/drug-induced Hepatic fibrosis, hemochromatosis, non-alcohol steatohepatitis (NASH), bile duct injury, primary biliary cirrhosis, infection The hepatic fibrosis of induction, the hepatic fibrosis of virus induction and the insane trace of autoimmune hepatitis, cornea, hypertrophica insane trace, teepee Special bright disease, insane trace pimple, dermatofibrosis, skin chorionitis, Systemic sclerosis, spinal cord injury/fibre modification, marrow are fine Tie up denaturation, reangiostenosis, atherosclerosis, artery sclerosis, wegener granulomatosis, peyronie's disease or chronic lymphocytic Property.More particularly, fibrotic conditions are idiopathic pulmonary fibrosis (IPF).

The special projects of the method for the present invention include applied to the individual with fibrotic conditions a effective amount of Formulas I, Ia, The compounds of this invention of Ib, Ic, Id, Ie, If or Ig continue one period, and the period is enough to reduce fiber in individual and becomes Property it is horizontal, and preferably terminate and cause the fibrotic process.The specific embodiment of the method includes to hair The individual patient of exhibition idiopathic pulmonary fibrosis applies a effective amount of Formulas I, the present inventionization of Ia, Ib, Ic, Id, Ie, If or Ig It closes object to continue for some time, the period is enough to reduce or prevent the idiopathic pulmonary fibrosis of the patient, and preferably Terminate the process for causing the idiopathic pulmonary fibrosis.

Injection dosage horizontal extent is about 0.1mg/kg/h at least 10mg/kg/h, all small for about 1 to about 120 When, especially continue 24 to 96 hours.The preloading that about 0.1mg/kg can also be applied to about 10mg/kg or more inject agent with Obtain appropriate steady-state level.Undesirable 40 are more than about 1g/ days to the maximum accumulated dose of 80kg human patient.

Prevention and/or treatment for long-term illness (such as degenerative disorders), therapeutic scheme usually extend many months Perhaps for many years, therefore oral administration is preferred for patient convenience and tolerance.In oral administration, daily One to four (1-4) secondary routine dose, especially daily one to three (1-3) secondary routine dose, usual daily one to two (1-2) are secondary often Dosage is advised, and most commonly the daily secondary routine dose in one (1) is representative scheme.Optionally, for the drug that effect is lasting, It is representative scheme once, once a week and once a day every other week in oral administration.Specifically, agent Amount scheme can be every 1-14 days, more particularly 1-10 days, even more particularly 1-7 days, and most particularly 1-3 It.

Using these described mode of administration, each dosage provides about 1 to about 1000mg the compounds of this invention, wherein each Specific dosage provides about 10 to about 500mg, preferably about 30 to about 250mg.

When for preventing illness breaking-out, the compounds of this invention will be usually in the case where doctor suggests and supervises described herein above dose Amount level is applied in the patient developed among disease risk.It is generally included in the patient developed among specific disease risk The patient of family history with the illness or oneself identified by heredity test or screening to be especially susceptible to develop the illness Patient.

The compounds of this invention can be used as unique activating agent application or its and can be administered in combination with other therapeutic agents, other Therapeutic agent includes showing same or like therapeutic activity and being measured as safe and efficient of the invention to the combined administration Other compounds.In special embodiment, the co-administration of two kinds of (or a variety of) activating agents allows to significantly reduce used The dosage of every kind of activating agent, to reduce visible side effect.

It is applied in some embodiments, the compounds of this invention or pharmaceutical composition comprising the compounds of this invention as drug With.In a particular embodiment, the pharmaceutical composition also includes other active components.

In some embodiments, the compounds of this invention is co-administered with other therapeutic agent for treating and/or preventing It is related to the disease of inflammation, concrete activity agent includes but is not limited to immunomodulator, such as imuran (azathioprine), skin Matter steroids (such as prednisolone (prednisolone) or dexamethasone (dexamethasone)), cyclophosphamide, ring spore bacterium Plain A (cyclosporin A), tacrolimus (tacrol imus), mycophenolate mofetil (mycophenolate, Mofetil), muromonab-CD3 (muromonab-CD3, OKT3, such as [email protected]), ATG, aspirin, vinegar ammonia Phenol, brufen (ibuprofen), naproxen (naproxen) and piroxicam (piroxicam).

In some embodiments, the compounds of this invention is co-administered with other therapeutic agent for treating and/or preventing Arthritis (such as rheumatoid arthritis), concrete activity agent include but is not limited to, analgestic, non-steroidal anti-inflammatory drugs (NSAID), Steroids, synthesis DMARDS (such as, but not limited to, Methylaminopterin (methotrexate), leflunomide (l eflunomide), Salicylazosulfapyridine (sulfasalazine), Anranofin (auranofin), sodium aurothiomalate (sodium Aurothiomalate), penicillamine (penici llamine), chloroquine (chloroquine), hydroxychloroquine, imuran (azathioprine), tropsch imatinib (tofaci tinib), Barry for Buddhist nun (barici tinib), good fortune he replace Buddhist nun (fostamatinib) and cyclosporin) and biology DMARDS (such as, but not limited to, infliximab (infliximab), Etanercept (etanercept), adalimumab (adal imumab), Rituximab (ri Tuximab) and Orencia (abatacept)).

In some embodiments, the compounds of this invention is co-administered with other therapeutic agent for treating and/or preventing Proliferative disorder, specific activating agent include but is not limited to methotrexate (MTX), folinic acid (leukovorin), adriamycin (adriamycin), prednisone (prednisone), bleomycin (bleomycin), cyclophosphamide, 5 FU 5 fluorouracil, Japanese yew Alcohol (paclitaxel), docetaxel (docetaxel), vincristine (vincristine), vincaleukoblastinum (vinblastine), vinorelbine (vinorelbine), Doxorubicin (doxorubicin), tamoxifen (tamoxifen), Toremifene (toremifene), megestrol acetate (megestrol acetate), Anastrozole (anastrozole), Goserelin (goserelin), anti-HER2 monoclonal antibody (such as Herceptin^TM), capecitabine (capecitabine), RALOXIFENE HCL (raloxifene hydrochloride), EGFR inhibitor (such as Iressa, Erlotinib, Erbitux), VEGF inhibitor (such as Arastin), proteasome inhibitor (such as Bortezomib), Gleevec and Hsp90 inhibitor (such as 17-AAG).In addition, Formulas I, Ia, Ib, Ic, Id or Ie the compounds of this invention can with include but unlimited It is administered in combination in radiotherapy or the other therapies of operation.In a particular embodiment, proliferative disorder is selected from cancer, marrow increases Growing property disease or leukaemia.

In some embodiments, the compounds of this invention is co-administered with other therapeutic agent for treating and/or preventing Autoimmune disease, specific activating agent include but is not limited to, and (such as purine is similar for glucocorticoid, cytostatic agent Object), alkylating agent (such as mustargen (cyclophosphamide), nitroso ureas, platinum compounds of the invention and other), antimetabolite (such as Methotrexate (MTX), imuran and to purinethol), cytotoxic antibiotic (such as actinomycin D (dactinomycin), anthracene nucleus Mycin (anthracycline), mitomycin C (mi tomycin C), bleomycin and mithramycin (mithramycin)), Antibody (such as anti-CD20, anti-CD25 or AntiCD3 McAb (OTK3) monoclonal antibody,With), ring spore bacterium Element, tacrolimus (tacro1imus), rapamycin (rapamycin) (sirolimus (sirolimus)), interferon (such as IFN-β), TNF binding protein (such as infliximab, Etanercept or adalimumab), mycophenolate, fingomode (fingo1imod) and myriocin (myriocin).

As will be apparent to those skilled in the art, be co-administered includes delivering two or more therapeutic agents to patient's work For any mode of a part of same therapeutic scheme.Although two or more activating agents (can be made in single formulation simultaneously For single drug composition) in application, but this is not necessary.The activating agent can also in different preparations, in different time Application.

Specific embodiment

For the description present invention, it is listed below embodiment.But it is to be understood that the present invention is not limited to these Examples, only Method of the invention is practiced in offer.

Generally, the compound of the present invention described method can be prepared through the invention, unless there are further Explanation, wherein the definition of substituent group is as shown in Formulas I, Ia, Ib, Ic, Id, Ie, If or Ig.Following reaction scheme and implementation Example is for being further illustrated the contents of the present invention.

The professional of fields will be appreciated that chemical reaction described in the invention can be used to suitably prepare perhaps Other compounds mostly of the invention, and other methods for the preparation of the compounds of the present invention are considered as in model of the invention Within enclosing.For example, the synthesis of the compound of those non-illustrations can be successfully by those skilled in the art according to the present invention It is completed by method of modifying, such as protection interference group appropriate, by utilizing other known reagent in addition to described in the invention , or reaction condition is made into some conventional modifications.In addition, reaction disclosed in this invention or known reaction condition are also generally acknowledged Ground is suitable for the preparation of other compounds of the invention.

The embodiments described below, unless other aspects show that all temperature are set to degree Celsius.Reagent purchase is in quotient Product supplier such as Aldrich Chemical Company, Arco Chemical Company and Alfa Chemical Company, all without by not being further purified when use, unless other aspects show.General reagent is from the western Gansu Province chemical industry in Shantou Factory, Guangdong Guanghua Chemical Reagent Factory, Guangzhou Chemical Reagent Factory, tianjin haoyuyu chemicals co., ltd., Tianjin good fortune morning chemistry Chemical reagent work, Wuhan Xin Huayuan development in science and technology Co., Ltd, Qingdao Tenglong Chemical Reagent Co., Ltd. and Haiyang Chemical Plant, Qingdao's purchase It can buy.

Anhydrous tetrahydro furan, dioxane, toluene, ether are dried to obtain by sodium metal reflux.Anhydrous methylene chloride It with chloroform is dried to obtain by calcium hydride reflux.Ethyl acetate, petroleum ether, n-hexane, n,N-dimethylacetamide and N, N- Dimethylformamide is used through anhydrous sodium sulfate is dry in advance.

Reaction is usually to cover a drying tube under positive pressure of nitrogen or argon or on anhydrous solvents (unless other aspects below Show), reaction flask all squeezed by syringe beyond the Great Wall by suitable rubber stopper, substrate.Glassware is all dried.

Chromatographic column is using silicagel column.Silica gel (300-400 mesh) is purchased from Haiyang Chemical Plant, Qingdao.

¹H H NMR spectroscopy is recorded using Bruker 400MHz or 600MHz nuclear magnetic resonance spectrometer.¹H H NMR spectroscopy is with CDC1₃、 DMSO-d₆、CD₃OD or acetone-d₆For solvent (as unit of ppm), use TMS (0ppm) or chloroform (7.26ppm) as reference Standard.When there is multiplet, following abbreviation: s (singlet, unimodal), d (doublet, bimodal), t will be used (triplet, triplet), m (multiplet, multiplet), br (broadened, broad peak), dd (doublet of Doublets, double doublet), dt (doublet of triplets, double triplets).Coupling constant is indicated with hertz (Hz).

The determination condition of low resolution mass spectrometry (MS) data is: 6120 level four bars HPLC-M of Agilent (column model: Zorbax SB-C18,2.1x 30mm, 3.5 microns, 6min, flow velocity 0.6mL/min.Mobile phase: 5%-95% ((contains The CH of 0.1% formic acid₃CN) in (H containing 0.1% formic acid₂O the ratio in)), using electrospray ionisation (ESI), in 210nm/ Under 254nm, detected with UV.

Pure compound uses Agilent 1260pre-HPLC or Calesep pump 250pre-HPLC (pillar type Number: NOVASEP 50/80mm DAC), detected in 210nm/254nm with UV.

The use of logogram word below is through the present invention:

CD₃OD deuterated methanol

CDC1₃Deuterated chloroform

DMF N,N-dimethylformamide

DMSO-d₆Deuterated dimethyl sulfoxide

G grams

H hours

ML, ml milliliters

RT, rt, r.t. room temperature

Boc tertbutyloxycarbonyl

Cbz benzyloxycarbonyl group

PMB is to methoxy-benzyl

Pd₂(dba)₃Tris(dibenzylideneacetone) dipalladium

JohnPhos 2- (di-t-butyl phosphine) biphenyl

The typical synthesis step of disclosed compound of present invention is prepared as shown in following synthetic schemes 1,2 and 3.

Synthetic schemes 1:

Wherein, E¹、E²Selected from Cl, Br or I；E³Selected from Cl, Br, I, OMs, OTs or OTf；Pr¹Selected from Boc, Cbz or PMB； Z、Y、 Cy、Ar¹、Ar²、W、Ar³And R¹All have definition of the present invention.

By intermediate 1-1 and intermediate 1-2 in alkali (such as triethylamine, N, N- diisopropylethylamine, potassium carbonate, cesium carbonate, uncle Butanol potassium or sodium tert-butoxide) in the presence of and heating (50 DEG C to 150 DEG C) under the conditions of, intermediate is obtained by nucleophilic substitution 1-3；Then after intermediate 1-3 is first reacted with highly basic (such as sodium hydrogen, potassium tert-butoxide or sodium tert-butoxide), then pass through with intermediate 1-4 Nucleophilic substitution obtains intermediate 1-5；Gained intermediate 1-5 can be under acid condition (such as trifluoroacetic acid, hydrogen chloride) or palladium Catalytic hydrogenation, or reacted with Iodotrimethylsilane and slough protecting group Pr¹To obtain intermediate 1-6；By intermediate 1-6 in Mesosome 1-7 in the presence of alkali (such as triethylamine, N, N- diisopropylethylamine, potassium carbonate, cesium carbonate) and heating (25 DEG C to 120 DEG C) under the conditions of, Formulas I compound represented is obtained by nucleophilic substitution.

Synthetic schemes 2:

Wherein, E¹And E²It is each independently selected from Cl, Br or I；E³Selected from Cl, Br, I, OMs, OTs or OTf；Pr²Selected from uncle Butyl or the amyl- 2- base of 2,4,4- trimethyl；Pr¹、Z、Y、Cy、X¹、X²、Y¹、Y²、Y³、Y⁴、R^1a、R²、R⁶And t all has the present invention The definition.

By intermediate 2-1 and Pr²NC and aldehyde R²CHO is anti-by three components under lewis acid (such as magnesium chloride) catalytic action Intermediate 2-2 should be generated；Reaction obtains intermediate 2-3 under conditions of intermediate 2-2 is heated in formic acid；Gained intermediate 2- 3 and intermediate 1-2 is in alkaline (such as triethylamine, N, N- diisopropylethylamine, potassium carbonate, cesium carbonate, potassium tert-butoxide or the tert-butyl alcohol Sodium) and heating (50 DEG C to 150 DEG C) under the conditions of, intermediate 2-4 is obtained by nucleophilic substitution；Intermediate 2-4 is first and strong Alkali (such as sodium hydrogen, potassium tert-butoxide or sodium tert-butoxide) reaction after, then with intermediate 2-5 carry out nucleophilic substitution, then again with take The alkyl R in generation^1aE⁴Reaction obtains intermediate 2-6；Intermediate 2-6 can be under acid condition (such as trifluoroacetic acid, hydrogen chloride) or palladium Catalytic hydrogenation reacts with Iodotrimethylsilane and sloughs protecting group Pr¹To obtain intermediate 2-7；Intermediate 2-7 and intermediate 1-7 is in alkaline (such as triethylamine, N, N- diisopropylethylamine, potassium carbonate, cesium carbonate) and heating (25 DEG C to 120 DEG C) condition Under, Formulas I f compound represented is obtained by nucleophilic substitution.

Synthetic schemes 3:

Wherein, Pr²Selected from tert-butyl or the amyl- 2- base of 2,4,4- trimethyl；Pr¹、Cy、X²、Y³And R²All have institute of the present invention State definition.

Intermediate 3-1 and Pr²NC and aldehyde R²CHO passes through three component reactions under lewis acid (such as magnesium chloride) catalytic action Generate intermediate 3-2；Reaction obtains intermediate 2-4 under conditions of gained intermediate 3-2 is heated in formic acid.