Issue 13, 2024

Synthesis of trifluoroethoxy/aryloxy cinnolines, cinnolinones and indazoles from o-alkynylanilines via metal-free diazotization reagent

Abstract

A facile and user-friendly protocol for the synthesis of trifluoroethoxy/aryloxy cinnolines, cinnolinones and indazoles from o-alkynylaniline in good-to-excellent yields has been developed using a metal-free diazotization reagent (a combination of BF3·OEt2 and TBN). The methodology has been further extended to construct bis-cinnolinones and for the chemoselective synthesis of N-propargylated cinnolinones.

Graphical abstract: Synthesis of trifluoroethoxy/aryloxy cinnolines, cinnolinones and indazoles from o-alkynylanilines via metal-free diazotization reagent

Supplementary files

Article information

Article type
Paper
Submitted
11 Jan 2024
Accepted
21 Feb 2024
First published
22 Feb 2024

Org. Biomol. Chem., 2024,22, 2608-2619

Synthesis of trifluoroethoxy/aryloxy cinnolines, cinnolinones and indazoles from o-alkynylanilines via metal-free diazotization reagent

M. Kumar and A. Goswami, Org. Biomol. Chem., 2024, 22, 2608 DOI: 10.1039/D4OB00058G

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