Issue 14, 1976

Reaction of amines with perfluoroazapropene: formation of the novel 4H-pyrido[1,2-a]-s-triazine system via unsymmetrical carbodi-imides

Abstract

Perfluoroazapropene (1) reacts with primary aromatic amines to give intermediate carbodi-imides (2) which dimerise or trimerise; intramolecular cyclisation occurs with 2-aminopyridines to give the novel hetero-cyclic system 4H-pyrido[1,2-a]-s-triazine and with aminopyrazine to give a derivative of 4H-pyrazino-[1,2-a]-s-triazine, respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1976, 567-568

Reaction of amines with perfluoroazapropene: formation of the novel 4H-pyrido[1,2-a]-s-triazine system via unsymmetrical carbodi-imides

W. T. Flowers, R. Franklin, R. N. Haszeldine and R. J. Perry, J. Chem. Soc., Chem. Commun., 1976, 567 DOI: 10.1039/C39760000567

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