One-pot, multicomponent synthesis under microwave conditions of new imidazole and acridine benzamido acetic acid derivatives

被引:0
|
作者
Jazi, Niloofar [1 ]
Fozooni, Samieh [2 ]
Hamidian, Hooshang [1 ]
机构
[1] Payame Noor Univ, Dept Chem, Kerman, Iran
[2] Higher Educ Complex Zarand, Dept Min Engn, Zarand, Iran
关键词
4-aminohippuric acid; araldehydes; dimedone; 1,8-dioxo-decahydroacridin-9-ylbenzamido acetic acid; benzil; 4-(2,3,5-triphenylimidazole-1-yl)-benzamido acetic acid; SOLVENT-FREE SYNTHESIS; TETRASUBSTITUTED IMIDAZOLES; BIOLOGICAL EVALUATION; EFFICIENT SYNTHESIS; HIGHLY EFFICIENT; 1,8-DIOXO-DECAHYDROACRIDINES; CATALYST; GREEN; ESTER;
D O I
10.3184/174751918X15181752711035
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Starting from 4-aminohippuric acid (AHA), two novel series of heterocyclic compounds of pharmaceutical interest have been synthesised by one-pot, multicomponent reactions under microwave conditions. Reaction of AHA with various aldehydes and benzil in (1:1) EtOH/acetic acid in the presence of ammonium acetate yielded 1,2,3,5-tetra-arylated imidazole derivatives, whereas a solvent-free reaction of AHA with various aldehydes and dimedone (2 equiv.) in the presence of p-TSA yielded 4,9-diarylated 1,8-dioxo-decahydroacridine derivatives. These reactions produced good yields in short reaction times with an easy work-up, and purification of products was achieved by simple recrystallisation.
引用
收藏
页码:80 / 85
页数:6
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