发明名称 3-pyridyl carboxamide-containing spleen tyrosine kinase (SYK) inhibitors
摘要 The invention provides certain 3-pyridyl carboxamide-containing compounds of the Formula (I) (I) or pharmaceutically acceptable salts thereof, wherein A and B are as defined herein. The invention also provides pharmaceutical compositions comprising such compounds, and methods of using the compounds for treating diseases or conditions mediated by Spleen Tyrosine Kinase (Syk) kinase.;
申请公布号 US8987456(B2) 申请公布日期 2015.03.24
申请号 US201214349563 申请日期 2012.10.01
申请人 Merck Sharp & Dohme Corp. 发明人 Altman Michael D.;Childers Kaleen Konrad;Donofrio Anthony;Ellis John Michael;Knowles Sandra Lee;Northrup Alan B.
分类号 C07D215/38;C07D401/12;C07D401/14;C07D405/14;A61K31/444;A61K31/4709 主分类号 C07D215/38
代理机构 代理人 Meade Eric A.;Fitch Catherine D.
主权项 1. A compound of the Formula (I) or a pharmaceutically acceptable salt thereof, wherein B is pyridyl or quinolinyl; wherein B is unsubstituted or substituted by 1 to 3 R3 moieties, wherein each R3 moiety is independently selected from the group consisting of C1-C3 alkyl, C1-C3 alkoxy, C1-C3 fluoroalkyl, C1-C3 hydroxyalkyl, halo, hydroxy, amino, (C1-C3 alkyl)amino, di(C1-C3 alkyl)amino, and E; wherein E is a 5-membered heteroaryl containing 1 to 3 N atoms, wherein E is unsubstituted or substituted by 1 to 2 moieties independently selected from the group consisting of C1-C3 alkyl; A is selected from the group consisting of: wherein Y is —CH2— or —O—;R11 and R12 are independently H or F; andn′ is 0 or 1; and wherein Ra and Rb are independently H or C1-C6 alkyl;Rc is H, C1-C6 alkyl, C1-C3 fluoroalkyl, C3-C6 cycloalkyl, or —(CH2)rOR13, wherein R13 is H or C1-C3 alkyl; andr is 1 or 2;Rd is H or C1-C6 alkyl,or Re and Rd together with the carbon atom to which they are attached form a group of the formula wherein p is 1 or 2.
地址 Rahway NJ US