5,7-Dihydropyrrolo[3,4-d][1,2]diazepin-1(2H)-ones. Synthesis and transformations
- Authors: Kharaneko O.I.1, Bogza S.L.2
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Affiliations:
- Litvinenko Institute of Physical Organic and Coal Chemistry
- Institute of Organic Chemistry
- Issue: Vol 52, No 7 (2016)
- Pages: 1043-1049
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/214752
- DOI: https://doi.org/10.1134/S1070428016070228
- ID: 214752
Cite item
Abstract
A preparative procedure has been developed for the synthesis of substituted 5,7-dihydropyrrolo-[3,4-d][1,2]diazepines by recyclization of 6-phenylpyrano[3,4-c]pyrrol-4(2H)-one with hydrazine hydrate. The stability of the seven-membered ring in the products under acidic conditions, alkylation, and heteroring fusion to the diazepine ring have been studied.
About the authors
O. I. Kharaneko
Litvinenko Institute of Physical Organic and Coal Chemistry
Author for correspondence.
Email: o_kharaneko@mail.ru
Ukraine, ul. R. Lyuksemburg 70, Donetsk, 83114
S. L. Bogza
Institute of Organic Chemistry
Email: o_kharaneko@mail.ru
Ukraine, ul. Murmanskaya 5, Kiev, 02660
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