Condensation of 5-(4-methylphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione with haloacetic acids |
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Authors: | A. A. Rzhevskii N. P. Gerasimova E. M. Alov O. S. Kozlova A. S. Danilova S. A. Khapova K. Yu. Suponitskii |
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Affiliation: | 1. Yaroslavl State Technical University, 88 Moskovskii pr., 150023, Yaroslavl, Russian Federation 2. Yaroslavl State Academy of Agriculture, 58 Tutaevskoe sh., 150042, Yaroslavl, Russian Federation 3. A. N. Nesmeyanov Institute of Organoelement Compounds, 28 ul. Vavilova, 119991, Moscow, Russian Federation
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Abstract: | Reactions of triazolethiones with haloacetic acids were studied with 5-(4-methylphenyl)-2,4-dihydro-3H-1,2,4-triazole-3-thione as an example. It was proved for the first time by X-ray diffraction that the cyclocondensation of these compounds proceeds regiospecifically to give 2-(4-methylphenyl)[1,3]thiazolo[3,2-b][1,2,4]triazol-6(5H)-one rather than its isomer 3-(4-methylphenyl)[1,3]thiazolo[2,3-c][1,2,4]triazol-5(6H)-one. |
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