신규한 퀴놀론 화합물
    23.
    发明授权
    신규한 퀴놀론 화합물 失效
    新颖的喹啉酮化合物

    公开(公告)号:KR1019930006162B1

    公开(公告)日:1993-07-08

    申请号:KR1019910003932

    申请日:1991-03-12

    Abstract: Quinolone derivs. of formula (I) and their salts are new. In (I), X=N or C-Y; Y=H,F,Cl, methoxy or methyl; Z=H, halogen or amino; R1=C1-4 alkyl, haloalkyl, hydroxyalkyl or alkenyl, C3-6 cycloalkyl, fluoro-substd. phenyl, X-O (or S) CH2CH(CH3)-N, etc.; R2=H or a cation; R3=H or lower alkyl; R4 and R5 each = H, lower alkyl, cycloalkyl or OH; m = 1 or 2. Also claimed is the prepn. of (I) which comprises a condensation reaction of the cpd. of formula (II) and the cpd. of formula (III) at 20-180 deg.C for 1-12 hr(s). The cpds. (I) have a good antibacterial activity.

    Abstract translation: 喹诺酮衍生物。 的式(I)及其盐是新的。 在(I)中,X = N或C-Y; Y = H,F,Cl,甲氧基或甲基; Z = H,卤素或氨基; R 1 = C 1-4烷基,卤代烷基,羟基烷基或烯基,C 3-6环烷基,氟取代基。 苯基,X-O(或S)CH 2 CH(CH 3)-N等; R2 = H或阳离子; R3 = H或低级烷基; R4和R5各自为H,低级烷基,环烷基或OH; m = 1或2.还要求是prepn。 的(I),其包含cpd的缩合反应。 的式(II)和cpd。 的式(III)在20-180℃下反应1-12小时(s)。 cpds。 (I)具有良好的抗菌活性。

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