피롤로[3,2-c]피리딘 유도체 및 그의 제조 방법
    2.
    发明公开
    피롤로[3,2-c]피리딘 유도체 및 그의 제조 방법 有权
    吡咯并[3,2-C]吡啶衍生物及其制备方法

    公开(公告)号:KR1020120040980A

    公开(公告)日:2012-04-30

    申请号:KR1020100102522

    申请日:2010-10-20

    Abstract: PURPOSE: A pyrrolo[3,2-c]pyridine derivative and a pharmaceutical composition containing the same are provided to ensure anti-proliferatioin activity of melanoma and to prevent or treat melanoma. CONSTITUTION: A pyrrolo[3,2-c]pyridine derivative is denoted by chemical formula I. A method for preparing the pyrrolo[3,2-c]pyridine derivative of chemical formula I' or pharmaceutically acceptable salt thereof comprises: a step of reacting 4-chloro-1-pyrrolo[2,3-b]pyridine of chemical formula II with nitroaniline to prepare a compound of chemical formula III; a step of reacting a compound of chemical formula III with benzoyl chloride to prepare a compound of chemical formula IV; a step of reducing the compound of chemical formula IV to prepare a compound of chemical formula V; and a step of reacting the compound of chemical formula V with a compound of chemical formula VI or formula VII.

    Abstract translation: 目的:提供吡咯并[3,2-c]吡啶衍生物和含有它们的药物组合物,以确保黑色素瘤的抗增殖活性并预防或治疗黑素瘤。 构成:化学式I表示吡咯并[3,2-c]吡啶衍生物。制备化学式I'吡咯并[3,2-c]吡啶衍生物或其药学上可接受的盐的方法包括: 使化学式II的4-氯-1-吡咯并[2,3-b]吡啶与硝基苯胺反应制备化学式Ⅲ化合物; 使化学式III的化合物与苯甲酰氯反应以制备化学式IV的化合物的步骤; 降低化学式IV化合物以制备化学式V的化合物的步骤; 以及使化学式V的化合物与化学式VI或式VII的化合物反应的步骤。

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