首页> 外国专利> METHOD OF SYNTHESIS OF INDOLO1',7':1,2,3PIRROLO3',4':6,7AZEPINO4,5-BINDOL-1,3(2H,10H)-DIONE

METHOD OF SYNTHESIS OF INDOLO1',7':1,2,3PIRROLO3',4':6,7AZEPINO4,5-BINDOL-1,3(2H,10H)-DIONE

机译:吲哚并[1',7':1,2,3]吡咯并[3',4':6,7]叠氮[4,5-B]吲哚-1,3(2H,10H)-二酮的合成方法

摘要

FIELD: medicine; pharmaceuticals.;SUBSTANCE: invention refers to the new method for the preparation of indolo[1',7':1,2,3]pyrrolo[3',4':6,7]azepino[4,5-b]indole-1,3(2H,10H)-dione, which is the starting material for the preparation of the potential antitumor preparation of 6-[(4-methyl-1-1-piperazinyl)methyl]-indolo[1',7':1,2,3]pyrrolo[3',4':6,7]azepino[4,5-6]indole-1,3(2H,10H)-dione). Method includes the steps of introducing the protecting group along the indole nitrogen atom, the subsequent dehydrogenation step under the action of 2,3-dichloro-5,6-dicyanobenzoquinone, and the step of protective group removal. ; .;EFFECT: claimed method allows to increase the yield of the final product more than twice as compared with the known method.;1 cl, 6 ex
机译:领域:医学;药物:发明是指用于制备吲哚并[1',7':1,2,3]吡咯并[3',4':6,7]氮杂环庚烷[4,5-b]吲哚的新方法-1,3(2H,10H)-dione是制备6-[((4-甲基-1-1-哌嗪基)甲基]-吲哚[1',7']潜在抗肿瘤制剂的原料:1,2,3] pyrrolo [3',4':6,7] azepino [4,5-6] indole-1,3(2H,10H)-dione)。该方法包括以下步骤:沿吲哚氮原子引入保护基;在2,3-二氯-5,6-二氰基苯并醌的作用下进行随后的脱氢步骤;以及除去保护基的步骤。 ; 。;效果:声明的方法可以使最终产品的产量提高两倍以上与已知方法比较。; 1 cl,6 ex

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