On Triazoles. XIII. The reaction of 5‐benzalimino‐1,2,4‐triazoles with substituted acetyl chlorides

József Reiter, László Pongó, P. Sohár, Péter Dvortsák

Research output: Contribution to journalArticle

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Abstract

The reaction of Schiff bases prepared from 1‐ and 2‐substituted‐5‐amino‐1,2,4‐triazoles with phenoxyacetyl chlorides in the presence of triethylamine and a mixture of phosphorus oxychloride and dichloroacetic acid in dimethylformamide to yield β‐lactam 4, a dihydro‐1,2,4‐triazolo[4,3‐a]pyrimidine‐5(1H)‐one 5, a 1,2,4‐triazolo[1,5‐a]pyrimidin‐5(3H)‐one 9 and the corresponding 1,2,4‐triazolo[4,3‐a]pyrimidine‐5(1H)‐one 10 derivatives was studied.

Original languageEnglish
Pages (from-to)173-176
Number of pages4
JournalJournal of Heterocyclic Chemistry
Volume25
Issue number1
DOIs
Publication statusPublished - 1988

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Dichloroacetic Acid
Lactams
Dimethylformamide
Triazoles
Schiff Bases
Chlorides
Derivatives
triethylamine
acetyl chloride
phosphoryl chloride

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

On Triazoles. XIII. The reaction of 5‐benzalimino‐1,2,4‐triazoles with substituted acetyl chlorides. / Reiter, József; Pongó, László; Sohár, P.; Dvortsák, Péter.

In: Journal of Heterocyclic Chemistry, Vol. 25, No. 1, 1988, p. 173-176.

Research output: Contribution to journalArticle

Reiter, József ; Pongó, László ; Sohár, P. ; Dvortsák, Péter. / On Triazoles. XIII. The reaction of 5‐benzalimino‐1,2,4‐triazoles with substituted acetyl chlorides. In: Journal of Heterocyclic Chemistry. 1988 ; Vol. 25, No. 1. pp. 173-176.
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