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使用3-溴-4-(吲哚-1-基)马来酰亚胺支架合成6H-吡咯并[3',4':2,3][1,4]二氮杂卓并[6,7,1-hi]吲哚-8,10(7H,9H)-二酮

Synthesis of 6H-pyrrolo[3',4':2,3][1,4]diazepino[6,7,1-hi]indole-8,10(7H,9H)-diones using 3-bromo-4-(indol-1-yl)maleimide scaffold.

作者信息

Lakatosh Sergey A, Luzikov Yuri N, Preobrazhenskaya Maria N

机构信息

Gause Institute of New Antibiotics, Russian Academy of Medical Sciences, B. Pirogovskaya 11, Moscow 119021, Russia.

出版信息

Org Biomol Chem. 2003 Mar 7;1(5):826-33. doi: 10.1039/b211163b.

DOI:10.1039/b211163b
PMID:12929367
Abstract

Series of 3-arylalkyl- or 3-alkylamino-4-(indol-1-yl)maleimides and bis(indol-1-yl)maleimides were synthesised. The cyclization of the 3-substituted 4-(indol-1-yl)maleimides under the action of acids resulted in the formation of diazepine[1,4] derivatives with indoline and maleimide nuclei annelated. These compounds readily produced the corresponding indolomaleimidodiazepines[1,4] after dehydrogenation.

摘要

合成了一系列3-芳基烷基-或3-烷基氨基-4-(吲哚-1-基)马来酰亚胺和双(吲哚-1-基)马来酰亚胺。3-取代的4-(吲哚-1-基)马来酰亚胺在酸的作用下环化,形成了稠合有吲哚啉和马来酰亚胺环的二氮杂卓[1,4]衍生物。这些化合物脱氢后很容易生成相应的吲哚马来酰亚胺并二氮杂卓[1,4]。

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