Abstract
The reaction of 2-chloro-N-phenacylpyridinium salts with diazonium salts in the presence of bases was studied for the first time. It was demonstrated that this reaction leads to the formation of [1,2,4]triazolo[4,3-a]pyridinium salts. It was shown that substitution of the pyridine with a thiazole moiety leads to a similar cyclization.
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