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Mass spectrometry of nitrogen heterocycles. 3. Thermal intramolecular cyclization of 2-azolylaminopyridines
Authors:V. L. Rusinov  N. A. Klyuev  V. G. Baklykov  T. L. Pilicheva  A. A. Tumashov
Affiliation:(1) S. M. Kirov Ural Polytechnical Institute, Sverdlovsk
Abstract:Mass spectrometric fragmentation or decay of 2-azolylaminopyridines containing a carbonyl group in the ortho-position results in elimination of a neutral molecule (ammonia, ethanol, hydrogen sulfide). This decay process is accompanied by intramolecular cyclization to form an ion with a triazolo[1,5-a]pyrido[2,3-d]pyrimidine structure.For Communication 2, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 101–104, January, 1991.
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