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The synthesis of 4-acylamino-1,2,4-triazole derivatives in the reaction of α-hydroxyacid hydrazidesand orthoesters

✍ Scribed by W. Zieliński; A. Kudelkoand; W. Czardybon


Book ID
102344927
Publisher
Journal of Heterocyclic Chemistry
Year
2005
Tongue
English
Weight
121 KB
Volume
42
Category
Article
ISSN
0022-152X

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✦ Synopsis


The reaction of α-hydroxyacid hydrazides and orthoesters in ethanol-acetic acid solution has been studied and a series of 4-acylamino-1,2,4-triazoles has been obtained as the final products. Some acyclic intermediates: 1-acyl-2-ethoxymethylenehydrazines and N,N'-bis(methanecarbonylamino)formamidine derivative have been also separated during the process. The structures of products was confirmed by typical spectroscopic methods and X-ray analysis.


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Heterocyclization reactions of azinoisoc
✍ Kee-Jung Lee; Jin Lyang Kim; Mun Ki Hong; Jung Yong Lee 📂 Article 📅 1999 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 347 KB

## Abstract The reaction of 1‐aminoethylidenehydrazones 9 with di‐__tert__‐butyl dicarbonate and 4‐dimethylaminopyridine led to the corresponding azinoisocyanates 10, which underwent thermal rearrangement under the reaction conditions to give 4‐(__tert__‐butoxycarbonyl)‐5‐methyl‐2__H__‐1,2,4‐triazo