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Mendeleev Communications, 2023, Volume 33, Issue 6, Pages 782–783
DOI: https://doi.org/10.1016/j.mencom.2023.10.014
(Mi mendc523)
 

Communications

Synthesis of androstane derivatives fused with polyheterocycles at the D ring

A. V. Komkov, L. G. Menchikov, A. S. Dmitrenok, I. V. Zavarzin

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
Abstract: An unusual reaction of 16α,17α-epoxypregn-5-en-20-one with 3-amino-5-mercapto-1,2,4-triazole is accompanied by the heterocyclization involving epoxy ring opening and results in a mixture of new androstane derivatives fused with polyheterocycles at the D ring. Such polyheterocycles belong to 3-thia-1,2,8,8b-tetraazaacenaphthylene and 1,2a,7,7b-tetraazacyclopenta[cd]indene-2-thione families incorporating isomeric [1,2,4]triazolopyrimidine systems
Keywords: 16α-17α-epoxypregn-5-en-20-one, fused heterocycles, androstane D ring, 3-thia-1,2,8,8b-tetraazaacenaphthylene, 1,2a,7,7b-tetraazacyclopenta[cd]indene-2-thione, [1,2,4]triazolopyrimidines, heterocyclization.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.6 Mb)


Citation: A. V. Komkov, L. G. Menchikov, A. S. Dmitrenok, I. V. Zavarzin, “Synthesis of androstane derivatives fused with polyheterocycles at the D ring”, Mendeleev Commun., 33:6 (2023), 782–783
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