首页> 外国专利> Process for Preparation of Therapeutically Active 4- 4- / 4- / 4- / 2- (2,4-difluorophenyl) -2- (1H-azolylmethyl) -1,3-dioxolan-4-yl / methoxy / phenyl -1-piperazinyl / phenylsubstituted triazolones and imidazolones

Process for Preparation of Therapeutically Active 4- 4- / 4- / 4- / 2- (2,4-difluorophenyl) -2- (1H-azolylmethyl) -1,3-dioxolan-4-yl / methoxy / phenyl -1-piperazinyl / phenylsubstituted triazolones and imidazolones

机译:具有治疗活性的4- [4- / 4- / 4- / 2-(2,4-二氟苯基)-2-(1H-偶氮甲基)-1,3-二氧戊环-4-基/甲氧基/苯基的制备方法-1-哌嗪基/苯基取代的三唑酮和咪唑酮

摘要

4-[4-[4-[4-[[2-(2,4-difluorophenyl)-2-(1H-azolylmethyl)-1,3-dioxolan-4 -yl]methoxy]pheny l ]-1-piperazinyl]phenyl]triazolones and imidazolones of formula CHEM wherein Q is CH or N; Y is a radical of formula CHEM R1 is C5-7cycloalkyl or mono-, di-, tri-, tetra- or pentahaloC1-4alkyl; and R2 is C1-6alkyl, C5-7cycloalkyl or mono-, di-, tri-, tetra- or pentahaloC1-4alkyl, the acid addition salts and stereoisomeric forms thereof; said compounds having antifungal properties. Pharmaceutical compositions containing such compounds as an active ingredient; methods of preparing said compounds and pharmaceutical compositions.
机译:4- [4- [4- [4-[[2-(2,4-二氟苯基)-2-(1H-偶氮基甲基)-1,3-二氧戊环-4-基]甲氧基]苯基l] -1-哌嗪基式的]苯基]三唑酮和咪唑酮,其中Q为CH或N; Y为式的基团。R 1为C5-7环烷​​基或单,二,三,四或五卤代C1-4烷基; R 2为C 1-6烷基,C 5-7环烷​​基或单,二,三,四或五卤代C 1-4烷基,其酸加成盐及其立体异构体形式;所述化合物具有抗真菌特性。含有这类化合物作为有效成分的药物组合物;所述化合物和药物组合物的制备方法。

著录项

  • 公开/公告号FI96031B

    专利类型

  • 公开/公告日1996-01-15

    原文格式PDF

  • 申请/专利权人 JANSSEN PHARMACEUTICA N.V.;

    申请/专利号FI19900002882

  • 发明设计人 HEERES JAN;BACKX LEO JACOBUS JOZEF;

    申请日1990-06-08

  • 分类号C07D405/14;

  • 国家 FI

  • 入库时间 2022-08-22 03:54:21

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