发明公开
EP2094699A2 NOUVEAUX DERIVES IMIDAZOLONES, LEUR PREPARATION A TITRE DE MEDICAMENTS, COMPOSITIONS PHARMACEUTIQUES, UTILISATION COMME INHIBITEURS DE PROTEINES KINASES NOTAMMENT CDC7 有权
新的咪唑啉衍生物积极的准备,其药物组合物及其作为蛋白激酶抑制剂,特别是CDC7

  • 专利标题: NOUVEAUX DERIVES IMIDAZOLONES, LEUR PREPARATION A TITRE DE MEDICAMENTS, COMPOSITIONS PHARMACEUTIQUES, UTILISATION COMME INHIBITEURS DE PROTEINES KINASES NOTAMMENT CDC7
  • 专利标题(英): New imidazolone derivatives, preparation thereof as drugs, pharmaceutical compositions, and use thereof as protein kinase inhibitors, in particular cdc7
  • 专利标题(中): 新的咪唑啉衍生物积极的准备,其药物组合物及其作为蛋白激酶抑制剂,特别是CDC7
  • 申请号: EP07858418.2
    申请日: 2007-10-10
  • 公开(公告)号: EP2094699A2
    公开(公告)日: 2009-09-02
  • 发明人: LEROY, VincentBACQUE, EricCONSEILLER, EmmanuelSTEINMETZ, AnkeRONAN, BaptisteLETALLEC, Jean-Philippe
  • 申请人: Sanofi-Aventis
  • 申请人地址: 174 Avenue de France 75013 Paris FR
  • 专利权人: Sanofi-Aventis
  • 当前专利权人: Sanofi-Aventis
  • 当前专利权人地址: 174 Avenue de France 75013 Paris FR
  • 代理机构: Kugel, Dominique
  • 优先权: FR0608924 20061012
  • 国际公布: WO2008046982 20080424
  • 主分类号: C07D471/04
  • IPC分类号: C07D471/04 A61K31/437 A61P35/00
NOUVEAUX DERIVES IMIDAZOLONES, LEUR PREPARATION A TITRE DE MEDICAMENTS, COMPOSITIONS PHARMACEUTIQUES, UTILISATION COMME INHIBITEURS DE PROTEINES KINASES NOTAMMENT CDC7
摘要:
The invention relates to products of the formula (I) in which : X-Y is NH-C(S), N=C-NR7R8, N=C-SR, N=C-R or N=C-OR; R and R1 are H or optionally substituted cycloalkyl, alkyl, heterocycloalkyl, aryl or heteroaryl,; R2 is H, Hal or alkyl; R3 is H, Hal, OH, alkyl or alkoxy; R4 is H, Hal, CN or alkyl; R5 is essentially H, Hal, OH, NR7R8, cycloalkyl, alkyl, alkoxy, heterocycloalkyl, aryl or heteroaryl, optionally substituted; R6 is H, Hal, OH, NH2, NHalk, N(alk)2, alkyl or alkoxy; with R7 et R8 being such that one is H or optionally substituted alk, while the other is H or optionally substituted cycloalkyl, alkyl, heterocycloalkyl, heteroaryl or aryl; or with R7 and R8 forming together with N an optionally substituted cyclic radical optionally containing O, S or N. The invention also relates to isomers and salts thereof used as drugs and essentially as protein kinase inhibitors, in particular CDC7.
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