A series of 18 3-tetrazolyl-tetrazolo[1,5- a ]quinolines were synthesized in 21–90% yields via a novel one-pot Ugi-azide/S N Ar/ring–chain azido-tautomerization process. We report also the synthesis of 10 3-imidazo[1,2- a ]pyridin-tetrazolo[1,5- a ]quinolines in 28–94% yields via a novel one-pot Groebke–Blackburn–Bienaymé/S N Ar/ring–chain azido-tautomerization process. Both synthetic strategies involve the use of microwaves or ultrasound, and catalyst-free conditions. Finally, we show the synthesis of the tetrazolo[1,5- a ]quinoline-3-carbaldehyde and tetrazolo[1,5- a ]quinoline-3-dimethyl acetal at room temperature in methanol as solvent.
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Unnamatla et al. (2016) studied this question.
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