发明名称
摘要 The present invention concerns the compounds of formula (I), the N-oxide forms, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein m represents 1, n represents 1, Z represents N or C, in particular N; —X1— represents C1-4alkyl, in particular methyl; —X2— represents —C1-4alkyl- or —C1-4alkyl-NR7—, in particular propyl, -ethyl-NR7— or -propyl-NR7—; —Y— represents-NR2—C1-6alkyl-CO—NR4—, -Het1-C1-6alkyl-CO—NR5— or -Het2-CO—NR6— and wherein the —C1-6alkyl-linker of —NR2—C1-6alkyl-CO—NR4— or -Het1-C1-6alkyl-CO—NR5— is optionally substituted with one or where possible two or more substituents selected from hydroxy, halo and phenyl; R1 represents hydrogen, chloro, fluoro or bromo; R2 represents —C1-4alkyl-, in particular ethyl or methyl; R7 represents hydrogen; R8 represents hydrogen; R4, R5 and R6 represent hydrogen; Het1 is selected from piperazinyl or piperidinyl, in particular -piperazinyl; Het2 selected from pyrrolidinyl or piperidinyl, in particular pyrrolidinyl wherein said pyrrolidinyl is optionally substituted with hydroxy.
申请公布号 JP2009500307(A) 申请公布日期 2009.01.08
申请号 JP20080518811 申请日期 2006.06.26
申请人 发明人
分类号 C07D471/22;A61K31/53;A61K31/5395;A61P3/10;A61P9/10;A61P11/06;A61P13/08;A61P17/06;A61P19/02;A61P25/04;A61P25/24;A61P25/28;A61P35/00;A61P37/08;A61P43/00;C07D251/42;C07D401/04;C07D401/12;C07D471/18;C07D487/08;C07D487/18;C07D498/18;C07D498/22 主分类号 C07D471/22
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