Substituted pyrazolyl urea derivatives useful in the treatment of cancer
    1.
    发明公开
    Substituted pyrazolyl urea derivatives useful in the treatment of cancer 审中-公开
    取代基吡唑基-harnstoff衍生的zur Behandlung von Krebs

    公开(公告)号:EP2295427A1

    公开(公告)日:2011-03-16

    申请号:EP10185914.8

    申请日:2005-05-02

    CPC分类号: C07D401/12 C07D405/14

    摘要: The present invention relates to compounds of formula (I), pharmaceutical compositions which contain them and methods for treating cancer using compounds of formula (I).

    wherein
    R 1 and R 2 are independently:
    (a) hydrogen;
    (b) (C 1 -C 5 )alkyl, optionally substituted with one or more of hydroxy or fluoro; or
    (c) halogen;
    A is phenyl, pyridine, or pyrimidine, optionally substituted with 1 or 2 substituents that are independently (C 1 -C 5 )alkyl, (C 1 -C 5 )alkoxy, (C 1 -C 5 )haloalkyl, (C 1 -C 5 )haloalkoxy, or halogen;
    B is phenylene or naphthylene, optionally substituted with 1 to 4 substituents that are independently (C 1 -C 5 )alkyl, (C 1 -C 5 )alkoxy, (C 1 -C 5 )haloalkyl, (C 1 -C 5 )haloalkoxy, or halogen;
    L is a bridging group which is -O-, -S-, -CH 2 -.
    M is phenyl, pyridine or pyrimidine, optionally substituted.

    摘要翻译: 本发明涉及式(I)化合物,含有它们的药物组合物和使用式(I)化合物治疗癌症的方法。 其中R 1和R 2独立地为:(a)氢; (b)(C 1 -C 5)烷基,任选被一个或多个羟基或氟取代; 或(c)卤素; A是苯基,吡啶或嘧啶,任选地被1或2个独立地为(C 1 -C 5)烷基,(C 1 -C 5)烷氧基,(C 1 -C 5)卤代烷基,(C 1 -C 5) C 5)卤代烷氧基或卤素; B是亚苯基或亚萘基,任选被1至4个独立地为(C 1 -C 5)烷基,(C 1 -C 5)烷氧基,(C 1 -C 5)卤代烷基,(C 1 -C 5) 卤代烷氧基或卤素; L是-O-,-S-,-CH 2 - 的桥接基团。 M是苯基,吡啶或嘧啶,任选被取代。

    Substituted pyrazolyl urea derivatives useful in the treatment of cancer
    6.
    发明公开
    Substituted pyrazolyl urea derivatives useful in the treatment of cancer 审中-公开
    取代基吡唑基-harnstoff衍生的zur Behandlung von Krebs

    公开(公告)号:EP2295426A1

    公开(公告)日:2011-03-16

    申请号:EP10185804.1

    申请日:2005-05-02

    CPC分类号: C07D401/12 C07D405/14

    摘要: The present invention relates to compounds of formula (I), pharmaceutical compositions which contain them and methods for treating cancer using compounds of formula (I).

    wherein
    R 1 and R 2 are independently:
    (a) hydrogen;
    (b) (C 1 -C 5 )alkyl, optionally substituted with one or more of hydroxy or fluoro; or
    (c) halogen;
    A is phenyl, pyridine, or pyrimidine, optionally substituted with 1 or 2 substituents that are independently (C 1 -C 5 )alkyl, (C 1 -C 5 )alkoxy, (C 1 -C 5 )haloalkyl, (C 1 -C 5 )haloalkoxy, or halogen;
    B is phenylene or naphthylene, optionally substituted with 1 to 4 substituents that are independently (C 1 -C 5 )alkyl, (C 1 -C 5 )alkoxy, (C 1 -C 5 )haloalkyl, (C 1 -C 5 )haloalkoxy, or halogen;
    L is a bridging group which is -O-, -S-, or -CH 2 -
    M is phenyl, pyridine or pyrimidine, optionally substituted.

    摘要翻译: 本发明涉及式(I)化合物,含有它们的药物组合物和使用式(I)化合物治疗癌症的方法。 其中R 1和R 2独立地为:(a)氢; (b)(C 1 -C 5)烷基,任选被一个或多个羟基或氟取代; 或(c)卤素; A是苯基,吡啶或嘧啶,任选地被1或2个独立地为(C 1 -C 5)烷基,(C 1 -C 5)烷氧基,(C 1 -C 5)卤代烷基,(C 1 -C 5) C 5)卤代烷氧基或卤素; B是亚苯基或亚萘基,任选被1至4个独立地为(C 1 -C 5)烷基,(C 1 -C 5)烷氧基,(C 1 -C 5)卤代烷基,(C 1 -C 5) 卤代烷氧基或卤素; L是-O-,-S-或-CH 2 - M是苯基,吡啶或嘧啶的任意取代的桥基。