Synthesis of biheteroaryls via 2-methyl quinoline C(sp3)-H functionalization under metal-free conditions

被引:6
作者
Wang, Dahan [1 ,2 ]
Yang, Yuhan [1 ]
Xiao, Fuhong [1 ]
Liu, Jinbing [2 ]
Mao, Guojiang [3 ]
Deng, Guo-Jun [1 ]
机构
[1] Xiangtan Univ, Hunan Prov Key Lab Green Organ Synth & Applicat, Key Lab Environm Friendly Chem & Applicat, Minist Educ,Coll Chem, Xiangtan 411105, Peoples R China
[2] Shaoyang Univ, Dept Food & Chem Engn, Shaoyang 422100, Peoples R China
[3] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Peoples R China
来源
GREEN SYNTHESIS AND CATALYSIS | 2024年 / 5卷 / 01期
基金
中国国家自然科学基金;
关键词
C(sp3)-H functionalization; Multicomponent reactions; Biheteroaryls; Elemental sulfur; Metal-free; ATOM ECONOMICAL APPROACH; ELEMENTAL SULFUR; ACCESS; STRAIGHTFORWARD; CONDENSATION; HETEROARENES;
D O I
10.1016/j.gresc.2022.10.006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An acetic acid-promoted C(sp3)-H functionalization of 2-methyl quinoline, enaminoesters and elemental sulfur for the synthesis of 3,4,5-trisubstituted isothiazoles under metal-free conditions has been developed. This approach provides viable access to various 5-(quinolin-2-yl)isothiazoles in moderate to good yields with good functional group tolerance. Moreover, the success of the gram-scale reaction gives this reaction a great potential application.
引用
收藏
页码:73 / 76
页数:4
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