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

Diaminofurazan reacted with 8-benzoyl-2-phenyl-3,4-dihydropyrrolo[1,2- a ]pyrazine-1,6,7(2 H )- 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-...

Full description

Saved in:
Bibliographic Details
Published inRussian journal of organic chemistry Vol. 54; no. 3; pp. 512 - 513
Main Authors Chervyakov, A. V., Maslivets, A. N.
Format Journal Article
LanguageEnglish
Published Moscow Pleiades Publishing 01.03.2018
Springer Nature
Springer Nature B.V
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Diaminofurazan reacted with 8-benzoyl-2-phenyl-3,4-dihydropyrrolo[1,2- a ]pyrazine-1,6,7(2 H )- 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(2 H ,9 H ,13 H )-trione by the action of N , N′ -dicyclohexylcarbodiimide.
ISSN:1070-4280
1608-3393
DOI:10.1134/S1070428018030235