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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2022 Volume 32, Issue 5, Pages 678–679 (Mi mendc765)

This article is cited in 5 papers

Communications

Synthesis of 7-oxindolylidene-3a,9a-diphenylimidazothiazolo[2,3-c][1,2,4]triazines by skeletal rearrangement of their [3,2-b]-fused isomers

A. N. Izmest’ev, A. N. Kravchenko, G. A. Gazieva

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Previously unavailable 7-oxindolylidene-1,3-dimethyl-3a,9adiphenylimidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazines were obtained in 63–90% yields by skeletal amidine rearrangement of the thiazolo-triazine system in the corresponding imidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazines on treatment with sodium methoxide.

Keywords: oxindolylidene derivatives, imidazothiazolotriazines, thiazolidinones, skeletal amidine rearrangement, isatin.

Language: English

DOI: 10.1016/j.mencom.2022.09.037



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