发明名称 INDOLE CARBOXAMIDE DERIVATIVES AS P2X7 RECEPTOR ANTAGONIST
摘要 The invention relates to indole carboxamide derivatives of formula (I),;;wherein R1, R2, R3, R4, R5 and R6 are as defined in the description, their preparation and their use as pharmaceutically active compounds.
申请公布号 US2015322008(A1) 申请公布日期 2015.11.12
申请号 US201314651922 申请日期 2013.12.11
申请人 ACTELION PHARMACEUTICALS LTD 发明人 HILPERT KURT;HUBLER FRANCIS;KIMMERLIN THIERRY;RENNEBERG DORTE;STAMM SIMON
分类号 C07D209/08;C07D401/14;C07D491/08;C07D403/14;C07D405/14;C07D413/12;C07D403/12;C07D401/12 主分类号 C07D209/08
代理机构 代理人
主权项 1. A compound of the formula (I),wherein R1 represents a heteroaryl or an aryl group which groups are independently unsubstituted, mono-, di-, or tri-substituted, wherein the substituents are independently selected from the group consisting of (C1-C4)alkyl, (C3-C6)cycloalkyl, (C1-C4)alkoxy, (C1-C3)fluoroalkyl, (C1-C3)fluoroalkoxy, hydroxy, halogen and phenoxy; R2 represents heterocyclyl which is unsubstituted, mono- or di-substituted, wherein the substituents are independently selected from (C1-C4)alkyl, (C1-C4)alkylcarbonyl, (C1-C4)alkoxycarbonyl, (C1-C4)alkylsulfonyl, and halogen;heterocyclyloxy;(C3-C6)cycloalkyl which is unsubstituted or mono- or di-substituted with halogen;(C3-C6)cycloalkyloxy;N—(C3-C6)cycloalkyl-amino;N—(C3-C6)cycloalkylmethyl-amino;(C3-C6)alkyl;(C2-C6)alkoxy;N—(C1-C4)alkylamino;N,N-di-[(C1-C4)alkyl]-amino; orN-arylmethyl-N—(C1-C4)alkyl-amino; R3 represents hydrogen or halogen; R4 represents hydrogen, fluoro, chloro, (C1-C4)alkyl, (C1-C4)alkoxy, (C1-C4)alkyl-carbonyl, hydroxy-(C1-C4)alkyl, hydroxy-(C2-C4)alkoxy, (C1-C2)alkoxy-(C1-C4)alkyl or (C1-C4)alkoxy-(C2-C4)alkoxy; R5 represents hydrogen or (C1-C4)alkyl; and R6 represents fluoro, chloro, methyl, ethyl or (C1-C2)fluoroalkyl;or a salt of such a compound.
地址 Allschwil CH