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CYANOGUANIDINE DERIVATIVES AND PHARMACEUTICAL K-CHANNEL BLOCKER COMPOSITIONS CONTAINING THEM

机译:氰基胍胺衍生物和包含它们的药物K-通道阻断剂组合物

摘要

A compound of the formula (I) or its pharmaceutically acceptable acid addition salts wherein n is 0 or 1, R1 is hydrogen or methyl; R2 is C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C5 cycloalkyl, C3-C5 cycloalkenyl, hydroxy, methyl, methoxy-C1-C5 alkyl, or R1 and R2 are combined to form a C3-C6 carbocyclic ring; R3 and R4 are each independently selected to be hydrogen, C1-C4 alkyl, F, Cl, Br, I or CF3; R5 is hydrogen, F or Cl; R6 is H, Cl, Br -NH2, -NHCH3, -NHC2H5, -NHCH(CH3)2, -N(CH3)2, -N(C2H5)2, NH(CH2)m -OC1-C3 alkyl (where m is 2 or 3), -NHC(O) C1-C3 alkyl, with the proviso that when R2 is C1-C6 alkyl, then R6 is not H, Cl or Br and n is 0 or 1, or wherein the compound of formula I is (R) N)-Cyano- (3-pyridyl)-N(- (1-phenylpropyl) guanidine or N)-Cyano-N- (3-pyridyl)-N(- [1-(3-chlorophenyl) propyl] guanidine. 4 ט" ז בטבת התשס" א - January 11, 2001
机译:式(I)化合物或其药学上可接受的酸加成盐,其中n为0或1,R 1为氢或甲基; R2是C1-C6烷基,C2-C6烯基,C2-C6炔基,C3-C5环烷基,C3-C5环烯基,羟基,甲基,甲氧基-C1-C5烷基,或R1和R2结合形成C3-C6碳环R3和R4各自独立地选自氢,C1-C4烷基,F,Cl,Br,I或CF3; R5是氢,F或Cl; R 6是H,Cl,Br -NH2,-NHCH3,-NHC2H5,-NHCH(CH3)2,-N(CH3)2,-N(C2H5)2,NH(CH2)m -OC1-C3烷基(其中m是2或3)--NHC(O)C1-C3烷基,条件是当R2是C1-C6烷基时,则R6不是H,Cl或Br并且n为0或1,或其中I为(R)N)-氰基-(3-吡啶基)-N(-(1-苯丙基)胍或N)-氰基-N-(3-吡啶基)-N(-[1-(3-氯苯基)丙基]胍。4ט"זבטבתהתשס“א-2001年1月11日

著录项

  • 公开/公告号IL106641B

    专利类型

  • 公开/公告日2001-01-11

    原文格式PDF

  • 申请/专利权人 PHARMACIA & UPJOHN COMPANY LLC;

    申请/专利号IL106641

  • 发明设计人

    申请日1993-08-10

  • 分类号C07D213/74;A61K31/44;A61P43/00;

  • 国家 IL

  • 入库时间 2022-08-22 01:25:05

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