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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2022 Volume 32, Issue 6, Pages 771–773 (Mi mendc794)

This article is cited in 4 papers

Communications

Synthesis of trialkyl semithioglycolurils from alkylthiourea-glyoxal cyclic adducts and dialkylureas

A. A. Galochkin, V. V. Baranov, N. G. Kolotyrkina, A. N. Kravchenko

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

Abstract: Condensation of 1-alkyl-4,5-dihydroxyimidazolidine-2-thiones (monoalkylthiourea-glyoxal cyclic adducts) with 1,3-dialkylureas affords novel 1,4,6-trialkylsemithio- glycolurils having non-substituted NH group linked to C=S function. Such compounds can be accessed in two-stage one-pot reaction sequence from alkylthioureas and glyoxal followed by treatment of the resulting adduct with 1,3-dialkylureas

Keywords: 1,4,6-trialkylsemithioglycolurils, one-pot synthesis, 4,5-dihydroxyimidazolidin-2-ones, 4,5-dihydroxyimidazolidine-2- thiones, alkylthioureas, dialkylureas.

Language: English

DOI: 10.1016/j.mencom.2022.11.021



© Steklov Math. Inst. of RAS, 2025