首页> 外国专利> method for preparing a medicine with adrenolytische properties that a 8 beta - aminomethyl - 6 - methyl 10 alpha ergolinederivaat contains, and the resulting product formed.and method for the preparation of appropriate 8 beta - aminomethyl - 6 - methyl 10 alpha ergolinederivaten.

method for preparing a medicine with adrenolytische properties that a 8 beta - aminomethyl - 6 - methyl 10 alpha ergolinederivaat contains, and the resulting product formed.and method for the preparation of appropriate 8 beta - aminomethyl - 6 - methyl 10 alpha ergolinederivaten.

机译:制备含有8β-氨基甲基-6-甲基10α麦角灵碱的具有肾上腺皮质激素性质的药物的方法,以及形成的产物。以及制备适当的8β-氨基甲基-6-甲基10α麦角灵碱的方法。

摘要

Title derivs. of formula (I) (where R is H or CH3 R1 and R2 are H, 1-3C alkyl or phenyl, and R3 is H, halogen, CH3, C2H5, OCH3, OC2H5 phenyl, NO2, (acyl)amino CN or carboxamido) which are long-acting adrenolytics with low toxicity, are prepd. by reacting dihydrolysergamine or 1-methyl-dihydrolysergamine with a cpd. which is capable of converting the amino gp. into a guanidino gp. reacting the resulting 6-methyl-or 1,6-dimethyl-8 beta-guanidinomethyl-10 alpha-ergoline with a beta-dicarbonyl cpd. of the formula R1-CO-CHR3-CO-R2 at 10-150 degrees C for 1 hr. to 6 days; and isolating and pyrifying the resulting (I).
机译:头衔衍生。式(I)的化合物(其中R是H或CH 3 R 1和R 2是H,1-3C烷基或苯基,并且R 3是H,卤素,CH 3,C 2 H 5,OCH 3,OC 2 H 5苯基,NO 2,(酰基)氨基CN或羧酰胺基制备低毒的长效肾上腺素。使二氢麦角胺或1-甲基-二氢麦角胺与cpd反应能够转换氨基gp。变成胍基GP。使所得的6-甲基-或1,6-二甲基-8β-胍基甲基-10α-麦角灵与β-二羰基cpd反应。式R1-CO-CHR3-CO-R2在10-150℃下反应1小时。至6天;分离并热解所得的(I)。

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