s-Triazolo-N-oxides from sulphimides and nitrile oxides. Valence tautomerism of 5,7-dimethyl-2-p-tolyl-s-triazolo[1,5-α]pyrimidine 1-oxide
Abstract
The pyrido-, pyrimidino-, and amidino-sulphimides (1)–(3) react with nitrile oxides at room temperature to give the s-triazolo-N-oxides (4)–(6); the N-oxide (5c) undergoes a reversible, degenerate valence tautomerism at 90–110°.