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Reaction of 4-acetyl-1,2,3-triazol-5-olate with hydrazine derivatives

I. S. Khazhieva, T. V. Glukhareva, Yu. Yu. Morzherin


1,2,3-triazole attracts attention because of the ability opening ring to form α-diazoimin and intramolecular rearrangements with the formation of various heterocyclic systems. Previously the interaction of the 1H-1,2,3-triazole-5-ol sodium salt with amine hydrochloride leading to the formation of isomeric 1,2,3-triazoles was studied. In this paper we present a research of the interaction of 4-acetyl-1,2,3-triazole-5-ol sodium salt with hydrazine derivatives. As result 5-methyl-1,2,3-triazol-4-phenylcarboxamide-phenylamide and bis-5,5’-dimethyl-[1,1’]bi[[1,2,3]triazolyl]-4,4’-dicarboxylic acid derivatives were synthesized.


1,2,3-Triazoles; rearrangement; hydrazine; bis-triazoles; organic synthesis

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Khazhieva I, Glukhareva T, Morzherin Yu. In: Problemy teoreticheskoy i eksperimental'noy khimii. XXIII Rossiyskaya molodezhnaya nauchnaya konferentsiya; 2013 Apr 23-26; Ekaterinburg, Russia. p. 506. Russian.


Copyright (c) 2015 I. S. Khazhieva, T. V. Glukhareva, Yu. Yu. Morzherin

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Chimica Techno Acta, 2014-2024
ISSN 2411-1414 (Online)
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