Abstract
4-Bromomethylidene-2-imino(phenylimino, acetylimino)-1,3-thiazolidine hydrobromides and 4-bromomethylidene-2-acetylimino-1,3-thiazolidine are synthesized by the reaction of thiourea, N-phenylthiourea, N,N′-diphenylthiourea and N-acetylthiourea with 1,3-dibromopropyne in glacial acetic acid, absolute methanol, acetonitrile at 20°C or upon heating (60°C).
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Original Russian Text © V.N. Elokhina, T.I. Yaroshenko, A.S. Nakhmanovich, S.V. Amosova, 2008, published in Zhurnal Obshchei Khimii, 2008, vol. 78, No. 10, pp. 1713–1715.
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Elokhina, V.N., Yaroshenko, T.I., Nakhmanovich, A.S. et al. Reaction of thiourea and substituted thioureas with 1,3-dibromopropyne. Russ J Gen Chem 78, 1949–1951 (2008). https://doi.org/10.1134/S1070363208100228
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DOI: https://doi.org/10.1134/S1070363208100228