Process for the preparation of pyrazolopyridine derivatives
    4.
    发明授权
    Process for the preparation of pyrazolopyridine derivatives 失效
    吡唑并吡啶衍生物的制备方法

    公开(公告)号:US06803463B2

    公开(公告)日:2004-10-12

    申请号:US10168002

    申请日:2002-06-14

    IPC分类号: C07D48704

    摘要: A process for the preparation of a compound of formula (I) and pharmaceutically acceptable derivatives thereof in which: R0 is halogen, C1-6alkyl, C1-6alkoxy, C1-6alkoxy substituted by one or more fluorine atoms, or O(CH2)nNR4R5; R1 and R2 are independently selected from H, C1-6alkyl, C1-6alkyl substituted by one or more fluorine atoms, C1-6alkoxy, C1-6hydroxyalkyl, SC1-6alkyl, C(O)H, C(O)C1-6alkyl, C1-6alkylsulphonyl, C1-6alkoxy substituted by one or more fluorine atoms, O(CH2)nCO2C1-6alkyl, O(CH2)nSC1-6alkyl, (CH2)nNR4R5, (CH2)nSC1-6alkyl or C(O)NR4R5; with the proviso that when R0 is at the 4-position and is halogen, at least one of R1 and R2 is C1-6alkylsulphonyl, C1-6alkoxy substituted by one or more fluorine atoms, O(CH2)nCO2C1-6alkyl, O(CH2)nSC1-6alkyl, (CH2)nNR4R5 or (CH2)nSC1-6alkyl, C(O)NR4R5; R3 is C1-6alkyl or NH2; R4 and R5 are independently selected from H, or C1-6alkyl or, together with the nitrogen atom to which they are attached, form a 4-8 membered saturated ring; and n is 1-4.

    摘要翻译: 一种制备式(I)化合物及其药学上可接受的衍生物的方法,其中:R 0是卤素,C 1-6烷基,C 1-6烷氧基,被一个或多个氟原子取代的C 1-6烷氧基或O( CH 2)n NR 4 R 5; R 1和R 2独立地选自H,C 1-6烷基,被一个或多个氟原子取代的C 1-6烷基,C 1-6烷氧基,C 1-6羟烷基,SC 1 C(O)H,C(O)C 1-6烷基,C 1-6烷基磺酰基,被一个或多个氟原子取代的C 1-6烷氧基,O(CH 2)n CO 2 C 1-6烷基,O(CH 2)nSC 1-6烷基, )nNR 4 R 5,(CH 2)nSC 1-6烷基或C(O)NR 4 R 5; 条件是当R 0在4-位且是卤素时,R 1和R 2中的至少一个是C 1-6烷基磺酰基,被一个或多个氟原子取代的C 1-6烷氧基,O( O(CH 2)n C 1-6烷基,(CH 2)n NR 4 R 5或(CH 2)nSC 1-6烷基,C(O)NR 4 R 5; R 3, 是C 1-6烷基或NH 2; R 4和R 5独立地选自H或C 1-6烷基,或与它们所连接的氮原子一起形成4-8元饱和环; 而且是1-4。