Transition metal catalyzed synthesis of 2H-indazoles
    2.
    发明授权
    Transition metal catalyzed synthesis of 2H-indazoles 有权
    过渡金属催化合成2H-吲唑

    公开(公告)号:US08283476B2

    公开(公告)日:2012-10-09

    申请号:US12644371

    申请日:2009-12-22

    IPC分类号: C07D231/56

    CPC分类号: C07D231/56

    摘要: The present invention relates to a process for the regioselective synthesis of compounds of the formula I, wherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct transition metal catalyzed process to a wide variety of multifunctional 2H-indazoles or 2H-azaindazoles of the formula (I) from 2-halo-phenylacetylenes or (2-sulfonato)phenylacetylenes and monosubstituted hydrazines.

    摘要翻译: 本发明涉及一种用于区域选择性合成式I化合物的方法,其中R 0; R1; R2; R3; R4; R5; A1; A2; A3; A4,Q和J具有权利要求中所示的含义。 本发明提供了对2-卤代苯基乙炔或(2-磺酸基)苯基乙炔和单取代肼的多种式(I)的多官能2H-吲唑或2H-氮杂吲唑的直接过渡金属催化方法。

    Regioselective palladium catalyzed synthesis of benzimidazoles and azabenzimidazoles
    3.
    发明授权
    Regioselective palladium catalyzed synthesis of benzimidazoles and azabenzimidazoles 有权
    苯并咪唑和氮杂苯并咪唑的区域选择性钯催化合成

    公开(公告)号:US08188282B2

    公开(公告)日:2012-05-29

    申请号:US12353271

    申请日:2009-01-14

    IPC分类号: C07D513/02 C07D235/00

    摘要: The present invention relates to a process for the regioselective synthesis of compounds of the formula I, wherein R0; R1; R2; R3; R4; R5; A1; A2; A3; A4, Q and J have the meanings indicated in the claims. The present invention provides a direct palladium catalyzed, regioselective process to a wide variety of unsymmetrical, multifunctional N-substituted benzimidazoles or azabenzimidazoles of formula I starting from 2-halo-nitroarenes and N-substituted amides useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.

    摘要翻译: 本发明涉及一种用于区域选择性合成式I化合物的方法,其中R 0; R1; R2; R3; R4; R5; A1; A2; A3; A4,Q和J具有权利要求中所示的含义。 本发明提供了直接钯催化的区域选择性方法,用于从2-卤代 - 硝基芳烃和用于制备药物,诊断剂的N-取代酰胺开始的各种不对称,多官能的取代的苯并咪唑或式I的氮杂苯并咪唑, 液晶,聚合物,除草剂,杀真菌剂,杀线虫剂,杀寄生虫剂,杀虫剂,杀螨剂和节肢动物杀虫剂。

    Transition metal catalyzed synthesis of N-aminoindoles
    4.
    发明授权
    Transition metal catalyzed synthesis of N-aminoindoles 有权
    过渡金属催化N-氨基吲哚的合成

    公开(公告)号:US08026375B2

    公开(公告)日:2011-09-27

    申请号:US12576339

    申请日:2009-10-09

    IPC分类号: C07D471/04 C07D209/04

    CPC分类号: C07D209/08

    摘要: The present invention relates to a process for the regioselective synthesis of compounds of the formula I, wherein R0; R1; R2; R3; R4; R5; R6; A1; A2; A3; A4, Q, T and J have the meanings indicated in the claims. The present invention provides a direct transition metal catalyzed process to a wide variety of multifunctional N-aminoindole or N-amino-azaindoles of the formula I from 2-halo-phenylacetylenes or (2-sulfonato)phenyl-acetylenes and N,N-disubstituted hydrazines, useful for the production of pharmaceuticals, diagnostic agents, liquid crystals, polymers, herbicides, fungicidals, nematicidals, parasiticides, insecticides, acaricides and arthropodicides.

    摘要翻译: 本发明涉及一种用于区域选择性合成式I化合物的方法,其中R 0; R1; R2; R3; R4; R5; R6; A1; A2; A3; A4,Q,T和J具有权利要求中所示的含义。 本发明提供了从2-卤代 - 苯基乙炔或(2-磺酸根合)苯基 - 乙炔和N,N-二取代的,由式I表示的多种多官能N-氨基吲哚或N-氨基 - 氮杂吲哚的直接过渡金属催化方法 肼,可用于生产药物,诊断剂,液晶,聚合物,除草剂,杀真菌剂,杀线虫剂,杀寄生虫剂,杀虫剂,杀螨剂和节肢动物杀虫剂。