发明名称 Amidobenzamide derivatives which are useful as cytokine inhibitors
摘要 The invention concerns amide derivatives of the Formula (I)wherein R<3 >is (1-6C)alkyl or halogeno; Q is aryl or heteroaryl which optionally bears 1, 2, 3 or 4 substituents such as hydroxy, halogeno, trifluoromethyl, cyano, (1-6C)alkyl, (1-6C)alkoxy, halogeno(1-6C)alkyl, hydroxy-(1-6C)alkyl, di-[(1-6C)alklyl]amino-(1-6C)alkyl, hydroxy-(2-6C)alkoxy, (1-6)alkoxy-(2-6C)alkoxy, di-[(1-6C)alkyl]amino-(2-6C)alkoxy, amino-2(2-6C)alkylamino, N-(1-6C)alkyl-(1-6C)alkylamino-(2-6C)alkylamino, aryl, aryl-(1-6C)alkoxy, heteroaryl, heteroaryl-(1-6C)alkoxy, heterocyclyl, heterocyclyl-(1-6C)alkyl, heterocyclyloxy and heterocyclyl-(1-6C)alkoxy; p is 0-2 and R<2 >is a substituent such as hydroxy and halogeno; q is 0-4; and R<4 >includes optionally substituted aryl, cycloalkyl, heteroaryl and heterocyclyl; or pharmaceutically-acceptable salts or in-vivo-cleavable esters thereof; processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases or medical conditions mediated by cytokines.
申请公布号 US6821965(B1) 申请公布日期 2004.11.23
申请号 US20010762106 申请日期 2001.02.02
申请人 ASTERZENECA AB 发明人 BROWN DEARG S;BROWN GEORGE R
分类号 C07D295/12;A61K31/165;A61K31/167;A61K31/395;A61K31/402;A61K31/4025;A61K31/42;A61K31/435;A61K31/44;A61K31/4465;A61K31/451;A61K31/47;A61K31/496;A61K31/5375;A61K31/5377;A61K31/551;A61P1/04;A61P9/04;A61P11/06;A61P17/08;A61P19/02;A61P29/00;A61P31/18;A61P37/00;A61P43/00;C07C231/02;C07C231/10;C07C235/56;C07C237/42;C07C255/57;C07D207/08;C07D207/12;C07D211/22;C07D211/34;C07D211/46;C07D213/82;C07D215/48;C07D223/08;C07D243/08;C07D261/08;C07D261/18;C07D277/24;C07D295/13;C07D295/135;C07D295/14;C07D295/155;C07D317/68;C07D401/04;C07D413/12;(IPC1-7):C07C233/73;A61K31/166 主分类号 C07D295/12
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