페닐아세트아미드 유도체 및 그의 제조방법
    24.
    发明授权
    페닐아세트아미드 유도체 및 그의 제조방법 失效
    苯乙酸衍生物及其制备方法

    公开(公告)号:KR1019920009574B1

    公开(公告)日:1992-10-19

    申请号:KR1019900001274

    申请日:1990-02-02

    Abstract: Phenylacetamide derivs. of formula (I) and their acid addn. salts are new. In (I), R=C1-8 alkyl or cyclid alkyl; X= halogen, nitro, R1, OR1, SR1, or NR1R2; R1 and R2 each =H, C1-8 alkyl, cyclic alkyl or substd. phenyl; l = 0-5; m = 0-5; n = 1-6. Also claimed is the prepn. of (I) which comprises condensing a cpd. of formula (II) with phenylacetic acid of formula (III). The cpds. (I) may be used as an anti-inflammatory analgesic.

    Abstract translation: 苯乙酰胺衍生物。 的式(I)和它们的酸加成。 盐是新的。 在(I)中,R = C 1-8烷基或环烷基; X =卤素,硝基,R 1,OR 1,SR 1或NR 1 R 2; R1和R2各自为H,C1-8烷基,环烷基或取代基。 苯基; l = 0-5; m = 0-5; n = 1-6。 还声称是prepn。 (I),其包括冷凝cpd。 式(II)与式(III)的苯乙酸反应。 cpds。 (I)可以用作消炎止痛剂。

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