Synthesis and antibacterial evaluation of some new 4-substituted-3-aryl-1-(2,6-dimethylpyrimidin-4-yl)pyrazoles
β 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
- DOI
- 10.1002/jhet.701
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β¦ 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.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
The preparation and the cytotoxic properties of new derivatives of the planar pyrido [3',2':5,6]thiopyrano-[4,3-c]pyrazole system, carrying an arylic side group in the 1 or 2 positions, are described. The novel substituted derivatives were obtained by reaction of suitable arylhydrazines with the app
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