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

被引:2
|
作者
Malkova, Ksenia [1 ]
Bubyrev, Andrey [1 ]
Kalinin, Stanislav [1 ]
Dar'in, Dmitry [1 ]
机构
[1] St Petersburg State Univ, St Petersburg 199034, Russia
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2023年 / 19卷
关键词
aza-Wittig reaction; azides; cyclocondensation; quinolones; sulfonamides; ONE-POT SYNTHESIS; SUBSTITUTED QUINOLINES; EFFICIENT SYNTHESIS; DRUG; CYCLIZATION; ANNULATION; SCAFFOLD; ALKYNES;
D O I
10.3762/bjoc.19.60
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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 alpha-sulfonyl-substituted alkyl acetates providing the target quinoline derivatives in good to excellent yields.
引用
收藏
页码:800 / 807
页数:8
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