Issue 0, 1979

Bicyclic heterocycles with nitrogen at the ring junction 1. Synthesis and chemistry of imidazo[5,1-f]-1,2,4-triazines

Abstract

The synthesis of the potential bronchodilators 2-amino-5-methyl-7-propylimidazo[5,1-f][1,2,4]triazin-4(3H)-one (12) and fhe corresponding triazine (2) is described and some chemical reactions of this novel ring system are discussed. Although X-ray analysis of the methanesulphonate salt of (12) indicated that protonation occurred on the nitrogen atom at position 6, acylation of the primary amino-group could still be achieved using a carboxylic acid in the presence of methanesulphonyl chloride.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1979, 1120-1124

Bicyclic heterocycles with nitrogen at the ring junction 1. Synthesis and chemistry of imidazo[5,1-f]-1,2,4-triazines

R. W. Clarke, S. C. Garside, L. H. C. Lunts, D. Hartley, R. Hornby and A. W. Oxford, J. Chem. Soc., Perkin Trans. 1, 1979, 1120 DOI: 10.1039/P19790001120

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