Interaction of 1,5,6,8-tetrahydropyrazolo[3,4-е][1,4]diazepine-4,7-diones with some electrophilic reagents
- Authors: Kemskii S.V.1, Bol’but A.V.1,2, Shishkina S.V.3,4, Mel’nik D.A.5, Vovk M.V.1
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Affiliations:
- Institute of Organic Chemistry
- R&D Enterprise “Enamin,”
- Institute of Single Crystals
- Kharkiv State University
- Ivano-Frankivsk National Medical University
- Issue: Vol 52, No 8 (2016)
- Pages: 1162-1167
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/214828
- DOI: https://doi.org/10.1134/S107042801608011X
- ID: 214828
Cite item
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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