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