TY - JOUR
T1 - Synthesis and antimicrobial activities of some ethyl 2-arylthio-6- arylimidazo[2,1-b]thiazole-3-carboxylates and their sulfones
AU - Shetty, Nitinkumar S.
AU - Koti, Rajesh S.
AU - Lamani, Ravi S.
AU - Badiger, Naveenkumar P.
AU - Khazi, I. A M
PY - 2008/10
Y1 - 2008/10
N2 - A series of new 2-arylthio-3-ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles (4a-4h) and 2-arenesulfonyl-3-ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles (5a-5h) have been prepared and characterized by analytical and spectral methods. The title compounds 4a-4h and 5a-5h were obtained by the reaction of 2-amino-4-ethoxycarbonyl-5-arylthiothiazoles (2a and 2b)/2-amino-4- ethoxycarbonyl-5-arenesulphonyl-thiazoles (3a and 3b) with various phenacyl bromides in anhydrous ethanol. These newly synthesized compounds (4a-4h and 5a-5h) were screened for their antibacterial activity against Gram-negative bacterium Escherichia coli, Gram-positive bacterium Staphylococcus aureus, and antifungal properties against Aspergillus niger and Candida albicans.
AB - A series of new 2-arylthio-3-ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles (4a-4h) and 2-arenesulfonyl-3-ethoxycarbonyl-6-arylimidazo[2,1-b]thiazoles (5a-5h) have been prepared and characterized by analytical and spectral methods. The title compounds 4a-4h and 5a-5h were obtained by the reaction of 2-amino-4-ethoxycarbonyl-5-arylthiothiazoles (2a and 2b)/2-amino-4- ethoxycarbonyl-5-arenesulphonyl-thiazoles (3a and 3b) with various phenacyl bromides in anhydrous ethanol. These newly synthesized compounds (4a-4h and 5a-5h) were screened for their antibacterial activity against Gram-negative bacterium Escherichia coli, Gram-positive bacterium Staphylococcus aureus, and antifungal properties against Aspergillus niger and Candida albicans.
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U2 - 10.1080/17415990802105747
DO - 10.1080/17415990802105747
M3 - Article
AN - SCOPUS:54049126118
SN - 1741-5993
VL - 29
SP - 539
EP - 547
JO - Journal of Sulfur Chemistry
JF - Journal of Sulfur Chemistry
IS - 5
ER -