Interaction of 1,5,6,8-tetrahydropyrazolo[3,4-е][1,4]diazepine-4,7-diones with some electrophilic reagents


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Abstract

1,5,6,8-Tetrahydropyrazolo[3,4-e][1,4]diazepine-4,7-diones undergo acylation with acetic anhydride and carbamoylation with p-toluensulfonyl isocyanate at the atom N5. Interaction with Vilsmeier- Haack reagent occurs at the atom N8, it is followed with the opening of the diazepine cycle and leads to the formation of 2-(1Н-pyrazol-4-yl)-1,3-oxazol-5(4Н)-one derivatives.

About the authors

S. V. Kemskii

Institute of Organic Chemistry

Email: mvovk@i.com.ua
Ukraine, Murmanskaya ul. 5, Kiev, 02660

A. V. Bol’but

Institute of Organic Chemistry; R&D Enterprise “Enamin,”

Email: mvovk@i.com.ua
Ukraine, Murmanskaya ul. 5, Kiev, 02660; Kiev

S. V. Shishkina

Institute of Single Crystals; Kharkiv State University

Email: mvovk@i.com.ua
Ukraine, Kharkiv; Kharkiv

D. A. Mel’nik

Ivano-Frankivsk National Medical University

Email: mvovk@i.com.ua
Ukraine, Ivano-Frankivsk

M. V. Vovk

Institute of Organic Chemistry

Author for correspondence.
Email: mvovk@i.com.ua
Ukraine, Murmanskaya ul. 5, Kiev, 02660

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