Selective synthesis of a novel glycoluril-based hybrid compound with high application potential

Highly selective synthesis of a new antipyrine-substituted tetracycle was implemented on the basis of a modified Mannich reaction as a result of the condensation of glycoluril with 4-aminoantipyrine in formalin without the use of catalysts.

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Bibliographic Details
Published in:Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2021-06, Vol.57 (6), p.700-703
Main Authors: Mamaeva, Elena А., Leppa, Anastasiya V., Bakibayev, Abdigali А.
Format: Article
Language:English
Subjects:
Chemistry
Chemistry and Materials Science
Formaldehyde
Organic Chemistry
Pharmacy
Synthesis
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Description
Summary:Highly selective synthesis of a new antipyrine-substituted tetracycle was implemented on the basis of a modified Mannich reaction as a result of the condensation of glycoluril with 4-aminoantipyrine in formalin without the use of catalysts.
ISSN:0009-3122
1573-8353
DOI:10.1007/s10593-021-02970-y