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Preparation of aminotriazole-thione derivatives from n-aryl-n-carboxyethyl-β-alanines

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Chemistry of Heterocyclic Compounds Aims and scope

Depending on the substituents in the aryl moiety, the fusion of N-aryl-N-ethoxycarbonyl-β-alanines with thiocarbohydrazide gives di- or monotriazole derivatives, namely, 4-amino-(2-{[2-(4-amino-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)ethyl]anilino}ethyl)-4,5-dihydro-1H-1,2,4-triazole-5-thiones, 1-[2-(4-amino- 5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)ethyl]-2,3-dihydroquinolin-4(1H)-ones, 4-amino-3-[2-(4-methylanilino))ethyl]-4,5-dihydro-1H-1,2,4-triazole-5-thione and 4-amino-3-[2-(4-ethoxyanilino)-ethyl]-4,5-dihydro-1H-1,2,4-triazole-5-thione. A ditriazolethione derivative was also obtained from the diethyl ester of N-ethoxycarbonyl-N-(4-ethoxyphenyl)- β-alanine.

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Correspondence to Z. J. Beresnevičius.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1564-1567, October, 2009.

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Tumosienė, I., Beresnevičius, Z.J. Preparation of aminotriazole-thione derivatives from n-aryl-n-carboxyethyl-β-alanines. Chem Heterocycl Comp 45, 1257–1260 (2009). https://doi.org/10.1007/s10593-010-0416-2

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  • DOI: https://doi.org/10.1007/s10593-010-0416-2

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