A Green, Scalable, and Catalyst-Free One-Minute Synthesis of Quinoxalines

被引:10
|
作者
Elumalai, Vijayaragavan [1 ]
Hansen, Jorn H. [1 ]
机构
[1] UiT Arctic Univ Norway, Dept Chem, Chem Synth & Anal Div, Hansine Hansens Veg 54, N-9037 Tromso, Norway
来源
SYNOPEN | 2021年 / 05卷 / 01期
关键词
quinoxaline; diamine; condensation; diketone; green; EFFICIENT SYNTHESIS; O-PHENYLENEDIAMINES; OXIDATION PROCESSES; MOLECULAR-IODINE; DERIVATIVES; PROTOCOL; ACID; DNA; BENZIMIDAZOLES; CYCLIZATION;
D O I
10.1055/s-0040-1706021
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly efficient and catalyst-free protocol is reported for the synthesis of quinoxalines via the classical cyclocondensation reaction between aryldiamines and dicarbonyl compounds. Remarkably simple and green reaction conditions employing methanol as solvent afforded medium to excellent yield of quinoxalines after only one-minute reaction time at ambient temperature. The conditions allow at least 10 gram scale synthesis of quinoxalines and should be a preferred starting point for optimization and method of choice for applications in the synthetic community.
引用
收藏
页码:43 / 48
页数:6
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