Shaanxi Key Laboratory of Chemical Reaction Engineering, College of Chemistry and Chemical Engineering, Yan'an University, Yan'an 716000, Shaanxi, China.
Laboratory of Chemical Genomics, School of Chemical Biology and Biotechnology, Shenzhen Graduate School of Peking University, Shenzhen 518055, China.
Chem Commun (Camb). 2022 Nov 3;58(88):12357-12360. doi: 10.1039/d2cc04524a.
The functionalization of quinoxalinones is synthetically and biologically appealing, however, C2 functionalized quinoxalinones is not reported environmentally friendly approach. Herein, we disclosed C2-O sulfonylation of quinoxalinones 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.
喹喔啉酮的功能化在合成和生物方面都很有吸引力,然而,C2 功能化的喹喔啉酮还没有报道出一种环境友好的方法。在此,我们公开了喹喔啉酮的 C2-O 磺酰化,这是我们开发的电化学氧化 O-S 偶联策略,用于合成 2-磺酰氧基喹喔啉。应用该方案,以喹喔啉酮和亚磺酸钠盐为起始原料,在温和条件下,无需额外氧化剂,通过广泛的 2-磺酰氧基喹喔啉衍生物的中等至良好产率和良好的官能团耐受性,获得了一系列 2-磺酰氧基喹喔啉衍生物。该方法和磺酰氧基的实用性分别通过克级制备和 2-取代喹喔啉基生物活性分子的合成得到了证明。