ISSN : 0975-9492
CODEN : IJPSQQ





INTERNATIONAL JOURNAL OF PHARMA SCIENCES AND RESEARCH


Open Access

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ABSTRACT

Title : Synthesis and Antibacterial Activity of 3-Chloro 4-(Substitutedphenyl) Azetidinonyl/Thiazolidinonyl-4-(3-Acetanilido) Oxa/Thiazoles
Authors : Indu Singh, Hemlata Kaur, Sunil Kumar, Suman Lata, Arun Kumar, Ashok Kumar
Keywords : Azetidinonyloxazole, Thiazolidinonyloxazole, Azetidinonylthiazole, Thiazolidinonylthiazole.
Issue Date : March 2010
Abstract :
Cyclocandensation of 2-[(substitutedbenzylidene)amino]-4-(3-acetanilido)oxazoles (3a-3j) and 2- [(substitutedbenzylidene)amino]-4-(3-acetanilido)thiazoles (7a-7j) with chloroacetyl chloride give and N-2- [3-chloro-4-(substitutedphenyl)-2-oxoazetidin-1-yl]-4-(3-acetanilido)oxazoles (4a-4j) and N-2-[3-chloro-4-(substitutedphenyl)-2-oxoazetidin-1-yl]-4-(3-acetanilido)thiazoles (8a-8j) respectively. N-2-[2- (substitutedphenyl)-4-oxo-1-thiazolidinyl]-4-(3-acetanilido)oxazoles (5a-5j) and N-2-[2-(substitutedphenyl)-4-oxo-1-thiazolidinyl]-4-(3-acetanilido)oxazoles (5a-5j) have been synthesized by reaction of compounds (3a-3j) and (7a-7j) with thioglycolic acid in presence of anhydrous zinc chloride. All the synthesized compounds were screened for their antibacterial activity and compared with reference drugs ampicillin and ciprofloxacin. The compound was the most potent compound of this series. Structure of all the synthesized compounds have been characterized by elemental (C, H, N) and spectral (IR and 1H NMR) analysis.
Page(s) : 148-168
ISSN : 0975-9492
Source : Vol. 1, No.2