首页> 外国专利> Use of Derivatives of M - amino phenyl imino imidazolidine for the preparation of medicaments for the treatment of incontinence of urine, Derivatives of M - amino phenyl imino imidazolidine with a New pattern of substituents on the phenyl ring, a process for their Preparation and the prepa

Use of Derivatives of M - amino phenyl imino imidazolidine for the preparation of medicaments for the treatment of incontinence of urine, Derivatives of M - amino phenyl imino imidazolidine with a New pattern of substituents on the phenyl ring, a process for their Preparation and the prepa

机译:M-氨基苯基亚氨基咪唑烷衍生物在制备用于尿失禁的药物中的用途,M-氨基苯基亚氨基咪唑烷衍生物在苯环上具有新型取代基的衍生物,其制备方法和制备方法

摘要

The use of m-amino-fenilamino-imidazolidina derivatives in general formula (1) or formula (2) was described,for the preparation of medicinal products for the treatment of urinary incontinence, in particular of stress incontinence, n where R1: F, Cl, Br, CH2F, CF2H or CF3, R2: NR6R7, with R6: Me, Et, iPr , R7: Me, Et, Pr or Pr, R3, R4, R5: are, in each case independently of each other, H, Me, F, Cl, Br, CH2F, CF2H and / or CF3 and, for the case in that R4 is Me, F, Cl, Br, CH2F, CF2H or CF3, then R1 is additionally also H or Me, and / or their pharmacologically compatible salts. The m-amino-phenylimino-imidazolidine derivatives of the general formula (1) or of the general formula (2) are also described,for the preparation of medicines, where R1: F, Cl, Br, CH2F, CF2H or CF3, R2: NR6R7, with R6: Me, Et, Pr or iPr, R7: Me, Et or Pr, R3, R4, R5 : they are, in each case independently of each other, H, Me, F, Cl, Br, CH2F, CF2H and / or CF3 and, in the case that R4 is Me, F, Cl, Br, CH2F, CF2H or CF3 , then R1 is additionally also H or Me, provided that R1 is neither chlorine nor bromine, and / or at least one of the radicals R4 or R5 is a substituent other than hydrogen,and / or its pharmacologically compatible salts. Procedures for the preparation of the above-mentioned compounds and the medicinal preparations containing them are also described. These compounds are alpha-1L agonists that selectively act on the bladder without substantially influencing the cardiocirculatory system and exhibit better properties in relation to bioavailability or metabolism.
机译:描述了在通式(1)或通式(2)中的间氨基苯甲酰氨基-咪唑啉酮衍生物在制备用于治疗尿失禁,尤其是压力性尿失禁的药物中的用途,其中n为R1:F, Cl,Br,CH2F,CF2H或CF3,R2:NR6R7,R6:Me,Et,iPr,R7:Me,Et,Pr或Pr,R3,R4,R5:在每种情况下彼此独立,Me,F,Cl,Br,CH2F,CF2H和/或CF3,并且对于R4为Me,F,Cl,Br,CH2F,CF2H或CF3的情况,则R1另外也为H或Me,和/或其药理相容的盐。还描述了通式(1)或通式(2)的间氨基氨基亚氨基咪唑烷衍生物,用于制备药物,其中R 1:F,Cl,Br,CH 2 F,CF 2 H或CF 3,R 2 :NR6R7,R6:Me,Et,Pr或iPr,R7:Me,Et或Pr,R3,R4,R5:它们分别彼此独立地为H,Me,F,Cl,Br,CH2F ,CF2H和/或CF3,并且在R4是Me,F,Cl,Br,CH2F,CF2H或CF3的情况下,则R1也是H或Me,前提是R1既不是氯也不是溴,和/或基团R 4或R 5中的至少一个是除氢和/或其药理学上相容的盐以外的取代基。还描述了制备上述化合物和含有它们的药物制剂的方法。这些化合物是α-1L激动剂,可选择性地作用于膀胱,而基本上不影响心血管系统,并且在生物利用度或代谢方面表现出更好的特性。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号