Synthesis and Antimicrobial Activity of Some New Coumarin Incorporated Pyridine-3-carbonitrile Derivatives
نویسندگان
چکیده
Drug resistance causes serious difficulties in the routine therapy for curing common microbial infections. Thus it is very essential to develop new antimicrobial agents which can offer alternative treatments. The development of potent and effective utmost importance overcome emerging multidrug strains bacteria fungi. technique involves Knoevenagel reaction between substituted salicylaldehyde ethyl acetoacetate presence piperidine as catalyst give 3-acetyl coumarin. intermediate coumarinyl chalcones was synthesized by condensing with various benzaldehyde ethanolic KOH. final pyridine-3-carbonitrile derivative prepared upon refluxing malononitrile ammonium acetate. All newly compounds were assigned on basis IR, 1H NMR mass spectral data. finalsynthesized screened their antibacterial activity tube dilution method. Most showed promising MIC method compared standard Cephalosporin.
منابع مشابه
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substituted schiff bases (hydrazones) 5a-j have been prepared from the starting material 2-chloro pyridine-3-carboxylic acid 1 by a sequence of reactions like reaction with 2-amino-6-nitro benzothiazole (ullamann condensation), thionyl chloride, hydrazine hydrate and different aromatic aldehydes. on cyclocondensation of 5a-j with thioglycolic acid in dry 1,4-dioxane furnished desired compounds ...
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ژورنال
عنوان ژورنال: Journal of pharmaceutical research international
سال: 2021
ISSN: ['2456-9119']
DOI: https://doi.org/10.9734/jpri/2021/v33i21a31364