Facile access to 3-sulfonylquinolines via Knoevenagel condensation/aza-Wittig reaction cascade involving ortho-azidobenzaldehydes and β-ketosulfonamides and sulfones

Beilstein J Org Chem. 2023 Jun 9:19:800-807. doi: 10.3762/bjoc.19.60. eCollection 2023.

Abstract

Quinoline-based sulfonyl derivatives, and especially sulfonamides, are relevant and promising structures for drug design. We have developed a new convenient protocol for the synthesis of 3-sulfonyl-substituted quinolines (sulfonamides and sulfones). The approach is based on a Knoevenagel condensation/aza-Wittig reaction cascade involving o-azidobenzaldehydes and ketosulfonamides or ketosulfones as key building blocks. The protocol is appropriate for both ketosulfonyl reagents and α-sulfonyl-substituted alkyl acetates providing the target quinoline derivatives in good to excellent yields.

Keywords: aza-Wittig reaction; azides; cyclocondensation; quinolones; sulfonamides.

Grants and funding

This research was supported by the Russian Science Foundation (project grant 21-73-00220).