Published September 1985 | Version v1
Journal article

Aminonitrile rearrangement of s-triazolo[1,5-c]pyrimidines upon reaction with aryl (alkyl) halides

  • 1. S.M. Kirov Ural Polytechnic Institute, Sverdlovsk, USSR

Description

Aminonitrile cleavage of the cyclic system was observed in the reaction of s-triazolo[1,5-c]pyrimidine derivatives with aryl (alkyl) halides in an alkaline medium or in dimethylformamide. It is shown that this transformation proceeds through the formation of intermediate quaternary salts. The effect of electron-acceptor and electron-donor substituents on their stability was ascertained. The structures of the substances were established by means of IR, UV, PMR, and mass spectroscopy

Additional details

Publishing Information

Journal Title
Chem. Heterocycl. Compd. (Engl. Transl.)
Journal Volume
21
Journal Issue
3
Series
Chem. Heterocycl. Compd. (Engl. Transl.).
Journal Page Range
355-358
ISSN
0069-3154
CODEN
CHCCA

Optional Information

Notes
Translated from Khim. Geterotsikl. Soedin.; 21: No.3, 421-425(Mar 1985).