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

9 Citations (Scopus)

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

    Fingerprint

ASJC Scopus subject areas

  • Organic Chemistry

Cite this