发明名称 |
Macrocyclic kinase inhibitors |
摘要 |
Compounds of Formula (I): wherein variables are defined herein, and pharmaceutically acceptable salts, synthesis, intermediates, formulations, and methods of disease treatment therewith, including cancers for which FAK inhibition is beneficial.; |
申请公布号 |
US9133224(B2) |
申请公布日期 |
2015.09.15 |
申请号 |
US201113990045 |
申请日期 |
2011.11.29 |
申请人 |
OSI Pharmaceuticals, LLC |
发明人 |
Crew Andrew P.;Dong Hanqing;Ferraro Caterina;Sherman Dan;Siu Kam W. |
分类号 |
A61K31/675;C07F9/6584 |
主分类号 |
A61K31/675 |
代理机构 |
Brinks Gilson & Lione |
代理人 |
Brinks Gilson & Lione |
主权项 |
1. A compound of Formula I: wherein: X is N or CH; A1 is optionally substituted phenylene or optionally substituted 5-6heteroaryl; A3 is optionally substituted 5-6heterocyclic; L2 is —O— or a bond; L3 is optionally substituted C2-6aliphatic; L4 is optionally substituted C1-2aliphatic; Q1 to Q4 are independently N,N-oxide, or optionally substituted CH; when Q1 and Q4 are independently CH or N, an optionally substituted 5-6cyclic containing one or more heteroatoms is optionally fused to Ring A2 at Q1 and Q4; R1, Ra, and Rb are each independently H or an optional substituent; and R4 is OH, C1-4aliphatic, —OC1-3aliphatic, 3-6carbocyclic, or 4-6heterocyclic; or a pharmaceutically acceptable salt thereof. |
地址 |
Northbrook IL US |