Condensation of acetophenone with thiourea in presence of Iodine gives 2-amino-4-phenylthiazole (I). 4-(2-Amino-4-phenyl-thiazol-5-yl-azo)-benzoic acid ethyl ester (III) was prepared by coupling of 4-ethoxycarbonylphenyldiazonium chloride with 2-amino-4-phenylthiazole. A series of amide (V) can be synthesized by treatment of appropriate substituted acid chlorides with compound (III) using pyridine as solvent. All the synthesized compounds are characterized by the combination of elemental analysis and standard spectroscopic method. They are screened for anti-bacterial activity against Escherichia coli and Staphylococcus aureus as well as screened for antifungal activity against aspergillus niger and apergillus oryzae by cup plate method at 1µg/mL concentration in DMF. All the synthesized compounds showed moderate or good microbial activity.
Cite this article:
AK Prajapati, Vishal P Modi. Synthesis and Biological Evaluation of Amides of Aminothiazole Derivatives. Asian J. Research Chem. 3(1): Jan.-Mar. 2010; Page 121-125.
AK Prajapati, Vishal P Modi. Synthesis and Biological Evaluation of Amides of Aminothiazole Derivatives. Asian J. Research Chem. 3(1): Jan.-Mar. 2010; Page 121-125. Available on: https://www.ajrconline.org/AbstractView.aspx?PID=2010-3-1-31