N,N ‐Dimethylazidochloromethyleniminium chloride (azidophosgeniminium chloride) ( 1 ) reacts by diazo group transfer with 1,3‐dimethyl‐4‐aryl‐(and alkyl)aminouracils 4 to give, under mild “one pot” reaction conditions, a very good yield of 3‐aryl‐(and 3‐alkyl)‐4,6‐dimethyl‐5,7‐dioxo‐1,2,3‐triazolo[4,5‐ d ]pyrimidines (8‐azatheophyllines) 8 . That reaction proceeds, very likely, through formation of non‐isolated 4‐imino‐5‐diazouracils 6 .
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Kokel et al. (1987) studied this question.
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