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Synthesis and antibacterial evaluation of some new 4-substituted-3-aryl-1-(2,6-dimethylpyrimidin-4-yl)pyrazoles

✍ Scribed by Ravi Kumar; Reshmi R. Nair; Saurabh Sudha Dhiman; Jitender Sharma; Om Prakash


Publisher
Journal of Heterocyclic Chemistry
Year
2011
Tongue
English
Weight
168 KB
Volume
48
Category
Article
ISSN
0022-152X

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✦ Synopsis


Synthesis of a series of new 4-substituted-3-aryl-1-(2,6-dimethylpyrimidin-4-yl)pyrazoles (2a-g, 3ag, and 4a-g) is described. All the synthesized compounds were evaluated in vitro for their antibacterial activity against two gram-positive and two gram-negative bacteria, namely, Bacillus subtilis (MTCC 8509), Bacillus stearothermophilus (MTCC 8508), Escherichia coli (MTCC 51), and Pseudomonas putida (MTCC 121), and their activity was compared with two commercial antibiotics, streptomycin and chloramphenicol. Two compounds, namely, 3-(4-anisyl)-1-(2,6-dimethylpyrimidin-4-yl)pyrazole-4carboxaldehyde (2b) and 3-(2-thienyl)-1-(2,6-dimethyl pyrimidin-4-yl)pyrazole-4-carboxaldehyde (2g) were found to be equipotent to streptomycin and chloramphenicol against gram-negative bacteria, E. coli having minimum inhibitory concentration (MIC) value ΒΌ 4 lg/mL. Compounds 4b and 4d also displayed good activity against E. coli with MIC ΒΌ 8 lg/mL.


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