Sustainable Synthetic Approaches for 3-Aminoimidazo-fused Heterocycles via Groebke-Blackburn-Bienayme Process

被引:11
|
作者
Mathavan, Sivagami [1 ]
B. R. D. Yamajala, Rajesh [1 ]
机构
[1] SASTRA, Dept Chem, Sch Chem & Biotechnol, Thanjavur 613401, India
来源
CHEMISTRYSELECT | 2020年 / 5卷 / 34期
关键词
Groebke-Blackburn-Bienayme reaction; 3-Aminoimidazo fused heterocycle; Multicomponent reaction; Surfactant; Thiamine hydrochloride; ONE-POT SYNTHESIS; SOLVENT-FREE SYNTHESIS; THIAMINE HYDROCHLORIDE; MULTICOMPONENT SYNTHESIS; 3-COMPONENT REACTION; COMBINATORIAL SYNTHESIS; ANNULATED PYRIDINES; RAPID SYNTHESIS; EFFICIENT; DERIVATIVES;
D O I
10.1002/slct.202002894
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two different sustainable and efficient synthetic methods have been developed for the synthesis of a variety of 3-aminoimidazo fused heterocycles by one-pot three component reaction of 2-aminoazines, aldehydes and isocyanides. The methods adopted were (a) aqueous micellar mediated condition (method A) (b) VB(1)catalyzed reaction under solvent-free condition (method B). Excellent yields were obtained for a broad range of biologically significant imidazopyridine core molecules under green conditions at room temperature. Synthesis in aqueous micellar medium, mild reaction conditions, organocatalyst, easy work-up and isolation, and gram scale synthesis, are some of the advantages of these protocols.
引用
收藏
页码:10637 / 10642
页数:6
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