Electro-oxidation induced O-S cross-coupling of quinoxalinones with sodium sulfinates for synthesizing 2-sulfonyloxylated quinoxalines

The functionalization of quinoxalinones is synthetically and biologically appealing, however, C2 functionalized quinoxalinones is not reported via environmentally friendly approach. Herein, we disclosed C2-O sulfonylation of quinoxalinones via our developed electrochemical oxidative O-S coupling str...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2022-11, Vol.58 (88), p.12357-1236
Hauptverfasser: Shi, Shi-Hui, Wei, Jian, Liang, Chun-Miao, Bai, Huan, Zhu, Hai-Tao, Zhang, Yantu, Fu, Feng
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Sprache:eng
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Zusammenfassung:The functionalization of quinoxalinones is synthetically and biologically appealing, however, C2 functionalized quinoxalinones is not reported via environmentally friendly approach. Herein, we disclosed C2-O sulfonylation of quinoxalinones via our developed electrochemical oxidative O-S coupling strategy for synthesizing 2-sulfonyloxylated quinoxalines. Applying this protocol, quinoxalin-ones and sodium sulfinates as the starting materials, a wide range of 2-sulfonyloxyl quinoxaline derivatives were obtained in moderate to good yields with good functional-group tolerance under mild conditions without additional oxidants. The utility of this methodology and the sulfonyloxyl handles was demonstrated trough gram-scale preparation and the synthesis of 2-substituted quinoxaline-based bioactive molecules, respectively. The novel C2-O sulfonylation of quinoxalinones via electro-oxidation induced O-S coupling strategy under mild conditions was reported.
ISSN:1359-7345
1364-548X
DOI:10.1039/d2cc04524a