Microwave-Assisted, Solvent-Free and Parallel Synthesis of Some Novel Substituted Imidazoles of Biological Interest

被引:15
作者
Sharma, Gyanendra Kumar [1 ]
Pathak, Devender [1 ]
机构
[1] Rajiv Acad Pharm, Dept Pharmaceut Chem, Mathura 281001, Uttar Pradesh, India
关键词
aryl imidazole; anticancer activity; anthelminitic activity; VITRO ANTITUBERCULOSIS ACTIVITY; ONE-POT SYNTHESIS; TETRASUBSTITUTED IMIDAZOLES; SOLID SUPPORT; DERIVATIVES; AGENTS; CYTOTOXICITY; IRRADIATION; INHIBITORS; EFFICIENT;
D O I
10.1248/cpb.58.375
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Solvent free microwave assisted synthesis of, some novel Substituted imidazoles of biological interest is reported. First, primary aromatic or heteryl amine vas condensed with aryl or heteryl aldehydes to afford corresponding Schiff's base. The Schiff's base further on treatment with ammonium acetate (NH(4)OAC) and isatin using silica gel as the solid support, yielded the corresponding aryl imidazoles. In this paper a comparative study between the developed microwave method and conventional method is described. The synthesized compounds,were analyzed by physical and analytical data. The synthesized compounds were evaluated for their antibacterial, anthelmintic, short-term anticancer and antitubercular activity. All the synthesized substituted imidazoles have shown good antibacterial activity against grain negative bacterial strains Klebsiella pneumoniae and Escherichia coli and moderate to good anthelmintic activity. The synthesized imidazole derivative possessed significant cytotoxic activity against Ehrlich's ascites carcinoma (EAC) cell lines. None of the compounds exhibited prominent antitubercular activity.
引用
收藏
页码:375 / 380
页数:6
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