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A convenient synthesis of 3,5-disubstituted-1,2,4-triazoles

✍ Scribed by J.E. Francis; L.A. Gorczyca; G.C. Mazzenga; H. Meckler


Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
220 KB
Volume
28
Category
Article
ISSN
0040-4039

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A number of symmetrically 3,5-disubstituted 4-amino-1,2,4-triazoles have been prepared by the reaction of aromatic nitriles with hydrazine dihydrochloride or sulfate with an excess of hydrazine hydrate in ethylene or diethylene glycol under a nitrogen atmosphere. The structures of the new triazoles