Synthesis of Angular [1,2,5]Oxadiazolo[3,4-b]pyrazino-[1′,2′ : 1,2]pyrrolo[2,3-e][1,4]diazepine by Stepwise Reaction of Pyrrolo[1,2-a]pyrazinetrione with 3,4-Diaminofurazan


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

Diaminofurazan reacted with 8-benzoyl-2-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazine-1,6,7(2H)- trione to give addition product of the amino group to the double bond of the pyrrole ring, which underwent cyclization to 2,8-diphenyl-3,4-dihydro[1,2,5]oxadiazolo[3,4-b]pyrazino[1′,2′: 1,2]pyrrolo[2,3-e][1,4]diazepine-1,6,7(2H,9H,13H)-trione by the action of N,N′-dicyclohexylcarbodiimide.

About the authors

A. V. Chervyakov

Perm National State Research University

Email: koh2@psu.ru
Russian Federation, ul. Bukireva 15, Perm, 614990

A. N. Maslivets

Perm National State Research University

Author for correspondence.
Email: koh2@psu.ru
Russian Federation, ul. Bukireva 15, Perm, 614990

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2018 Pleiades Publishing, Ltd.