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Synthesis and Antibacterial Screening of 4-Arylidene-5-oxo-imidazoles having Carboxamide Linkage with 5-(benzofuran-2-yl)-1-phenylpyrazole Moiety

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1TitleTitle of DocumentSynthesis and Antibacterial Screening of 4-Arylidene-5-oxo-imidazoles having Carboxamide Linkage with 5-(benzofuran-2-yl)-1-phenylpyrazole Moiety
2CreatorAuthor's name, affiliation, country MOHAMMAD IDREES* R. D. NASARE and N. J. SIDDIQUI
Department of Chemistry, Government Institute of Science, Nagpur-440001, Maharashtra, India
Department of Chemistry, Government Science College, Gadchiroli- 442605, Maharashtra, India
3SubjectDicipline(s) Chemical Science
3SubjectKeywords 5-Oxo imidazole, 4-Arylidene oxazolones, Carbohydrazides
4DescriptionAbstract Synthesis of 5-(H/Br benzofuran-2-yl)-1-phenyl 1H-pyrazole-3-carbohydrazides (1a-b) and condensation with different 4-(arylidene)-2 phenyloxazol-5(4H)-one (2a-g) in acetic acid medium, a series of 5-(H/Br benzofuran -2-yl)-N-(4-arylidene-5-oxo-2-phenyl-4,5-dihydro-imidazol-1-yl)-1-phenyl-1H-pyrazole-3-carboxamide derivatives (3a-g) have been carried out. Different 4-(arylidene)-2-phenyloxazol-5(4H)-one (2a-g) were synthesized from substituted benzaldehyde with hippuric acid. The structures of the novel compounds were elucidated on the basis of elemental analysis and spectral studies such as FT-IR, 1H NMR, further supported by Mass spectra. The synthesized 5-(benzofuran-2-yl)-N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydroimidazol-1-yl)-1-phenyl-1H-pyrazole-3-carboxamide (3a) was assayed in vitro for their antimicrobial activity at different concentration against four different bacterial strains namely B. thurengienesis, S. aureus, E. Coli and E. Areogenes. The investigation of antibacterial screening reveals that 3a exhibited excellent activity against Gram +ve and poor activity against Gram ?ve bacteria when compared to chloramphenicol as standard drug
5PublishersOrganizing agency, location WWW Publications, India
6Contributor Sponsor(s) -
7DateDate (YYYY-MM-DD) -
8TypeStatus & genre Peer-reviewed Article
8TypeType
9FormateFile Formate PDF
10IdentifierUniform Resource Identifier Click Here
10IdentifierDigital Object Identifier
11SourceJournal/conference title; vol., no. (Year)Chemical Science Transactions, Volume  5 , Number  (4), (2016)
12LanuguageEnglish=en en
13RelationSupp.files
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15CopyrightCopyright and permissions
Chemical Science Transactions | Chem Sci Trans | CST | Online Chemistry Journal | Open Access
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