퀴놀린계 유도체와 그의 제조방법
    121.
    发明授权
    퀴놀린계 유도체와 그의 제조방법 失效
    喹啉衍生物及其制备方法

    公开(公告)号:KR1019970005298B1

    公开(公告)日:1997-04-15

    申请号:KR1019930009768

    申请日:1993-06-01

    Abstract: Novel quinoline derivatives(I) exhibiting superior antimicrobial activity and pharmaceutically acceptable salts thereof are prepared. The carboxyl group of the quinoline compound is activated by carboxylic acid-active reagent and reacted with compound having activated methylene group and alkali or alkali earth metals to give the title compound. In formula I, R1 is C1-3 lower alkyl, halogen-substituted lower alkyl, phenyl or halogen-substituted phenyl; R2 is H, lower alkyl or amino; R3 is halogen or (substituted) heterocyclic compound; X is N or C-R4(where, R4 is H, halogen, lower alkyl, or lower alkoxy); Y and Z are H, ester, cyano, nitro, acyl, (substituted) amido, lower alkylsulfoxy, or lower alkylsulfone group.

    Abstract translation: 制备具有优异抗菌活性的新喹啉衍生物(I)及其药学上可接受的盐。 喹啉化合物的羧基被羧酸活性试剂活化,与具有活性亚甲基的化合物和碱金属或碱土金属反应,得到标题化合物。 在式I中,R 1是C 1-3低级烷基,卤素取代的低级烷基,苯基或卤素取代的苯基; R2是H,低级烷基或氨基; R3是卤素或(取代的)杂环化合物; X是N或C-R4(其中R4是H,卤素,低级烷基或低级烷氧基); Y和Z是H,酯,氰基,硝基,酰基,(取代的)酰氨基,低级烷基亚磺酰基或低级烷基砜基。

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