发明名称 ANTIVIRAL COMPOUNDS
摘要 The present invention discloses compounds of Formula I: wherein the variables in Formula I are defined as described herein. Also disclosed are pharmaceutical compositions containing such compounds and methods for using the compounds of Formula I in the prevention or treatment of HCV infection.;
申请公布号 US2016000760(A1) 申请公布日期 2016.01.07
申请号 US201414768915 申请日期 2014.03.03
申请人 HOFFMANN-LA ROCHE INC. 发明人 Bilotta Joseph Anthony;Chen Zhi;Chi Feng;Chin Elbert;Ding Qingjie;Erickson Shawn David;Gabriel Stephen Deems;Jiang Nan;Kocer Buelent;Mertz Eric;Plancher Jean-Marc;Weikert Robert J.;Zhang Jing;Zhang Qiang
分类号 A61K31/4196;A61K31/454;A61K45/06;C07D403/12;C07D249/14;C07D417/12;A61K31/428;A61K31/496;A61K31/5377;C07D495/04;C07D413/12;A61K31/538;A61K31/541;A61K31/5415;C07D405/12;C07D491/107;C07D401/12 主分类号 A61K31/4196
代理机构 代理人
主权项 1. A compound of formula I: wherein: A is phenyl, naphthyl, or bicyclic unsaturated or partially saturated heteroaryl, optionally substituted with one or more A′; each A′ is independently lower alkyl, halo, lower alkoxy, S(═O)2(CH2)mA″, C(═O)NHA″, NHC(═O)A″, —O(CH2)mA″, (CHA1)mNHS(═O)2A1; or S(═O)2NHA″; each A″ is independently lower alkyl, heterocycloalkyl or heteroaryl, optionally substituted with one or more A′″; each A′″ is independently hydroxy, lower alkyl, oxo, C(═O)OA1, halo loweralkyl, each A1 is independently H, lower alkyl, halo loweralkyl, amino, lower alkoxy, each m is independently 0, 1, 2, or 3; R1 is H, halo, lower alkyl, halo loweralkyl, SF5, and R2 is H, halo, lower alkyl, halo loweralkyl, or a pharmaceutically acceptable salt thereof.
地址 Nutley NY US