Issue 28, 2021

Indium-mediated annulation of 2-azidoaryl aldehydes with propargyl bromides to [1,2,3]triazolo[1,5-a]quinolines

Abstract

An efficient indium-mediated cascade annulation reaction of 2-azidoaryl aldehydes with propargyl bromides is reported. The aromatic 5/6/6-fused heterocycles, [1,2,3]triazolo[1,5-a]quinoline derivatives, could be constructed in one pot in moderate yields with a broad substrate scope. Mechanistic studies indicated that the reaction proceeded through allenol formation, azide–allene [3 + 2] cycloaddition, and dehydration. The synthetic potential of the products including the denitrogenative functionalization and the Pd-catalyzed coupling reactions has also been explored.

Graphical abstract: Indium-mediated annulation of 2-azidoaryl aldehydes with propargyl bromides to [1,2,3]triazolo[1,5-a]quinolines

Supplementary files

Article information

Article type
Paper
Submitted
19 Jun 2021
Accepted
30 Jun 2021
First published
30 Jun 2021

Org. Biomol. Chem., 2021,19, 6346-6352

Indium-mediated annulation of 2-azidoaryl aldehydes with propargyl bromides to [1,2,3]triazolo[1,5-a]quinolines

X. Zhang, J. Yang, N. Xiong, Z. Han, X. Duan and R. Zeng, Org. Biomol. Chem., 2021, 19, 6346 DOI: 10.1039/D1OB01183A

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