9-aminoacridine derivatives and process for the preparation thereof
    2.
    发明申请
    9-aminoacridine derivatives and process for the preparation thereof 失效
    9-氨基吖啶衍生物及其制备方法

    公开(公告)号:US20020111491A1

    公开(公告)日:2002-08-15

    申请号:US09855530

    申请日:2001-05-16

    CPC classification number: C07D219/10 Y02P20/55

    Abstract: The present invention relates to new 9-aminoacridine derivatives of general formula (I), wherein A is hydrogen or (II) (wherein X is oxygen or sulfur, R1, R2, R3, R4 and R5 are independently hydrogen, halogen, nitro, amino, hydroxy, C1-C4 lower alkylhydroxy, C1-C4 lower alkylamino, C1-C8 alkyl, C1-C4 lower alkoxy or C1-C4 lower alkyloxycarbonyl and m and n are independently an integer of 0, 1 or 2), R6, R7, R8 and R9 are independently C1-C8 alkyl or C1-C4 lower alkoxy, and Y is hydrogen, amino, -NnullCHRnull(wherein Rnull is hydrogen, benzyl, C1-C8 alkyl or C1-C6 lower alkylamino), (III) (wherein Rnull is hydrogen, benzyl, C1-C8 alkyl or C1-C6 lower alkylamino, and Rnullnull is hydrogen, benzyl, C1-C8 alkyl or amino protecting group) or (IV) (wherein, X is as defined above, R1null, R2null, R3null, R4null and R5null are independently hydrogen, halogen, nitro, amino, hydroxy, C1-C4 lower alkylhydroxy, C1-C4 lower alkylamino, C1-C8 alkyl, C1-C4 lower alkoxy or C1-C4 lower alkylcarboxy, and q and r are independently an integer of 0, 1 or 2) or its pharmaceutically acceptable salt, and process for the preparation thereof.

    Abstract translation: 本发明涉及通式(I)的新的9-氨基吖啶衍生物,其中A是氢或(II)(其中X是氧或硫,R1,R2,R3,R4和R5独立地是氢,卤素,硝基, 氨基,羟基,C1-C4低级烷基羟基,C1-C4低级烷基氨基,C1-C8烷基,C1-C4低级烷氧基或C1-C4低级烷氧基羰基,m和n分别为0,1或2的整数),R6, R7,R8和R9独立地为C1-C8烷基或C1-C4低级烷氧基,Y为氢,氨基,-N = CHR'(其中R'为氢,苄基,C1-C8烷基或C1-C6低级烷基氨基) ,(III)(其中R“为氢,苄基,C 1 -C 8烷基或C 1 -C 6低级烷基氨基,R”'为氢,苄基,C 1 -C 8烷基或氨基保护基)或(Ⅳ)(其中 ,X'如上定义,R 1',R 2',R 3',R 4'和R 5'独立地是氢,卤素,硝基,氨基,羟基,C 1 -C 4低级烷基羟基,C 1 -C 4低级烷基氨基, C1-C4低级烷氧基或C1-C4低级烷基羧基,q和r独立地为a 0,1或2的整数)或其药学上可接受的盐,以及其制备方法。

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