Pyridine 3-carboxillic acid 1 on treatment with phosphorous pentachloride and anhydrous carbon tetrachloride followed by reaction with hydrazine hydrate gave nicotinohydrazide 2. And compound 2 on further reaction with acetyl acetone, ethyl acetoacetate, ethylcyanoacetate and different substituted aromatic acids yielded the corresponding (3,5-dimethyl-1H-pyrazol-1-yl)(pyridine-3-yl)methanone 3, 3-methyl-1-nicotinoyl-1H-pyrazol-5(4H)-one 4, 3-amino-1-nicotinoyl-1H-pyrazol-5(4H)-one 5 and 3-(5-substituted-1,3,4 oxadiazole) pyridine 6a-d, respectively. All the synthesized compounds have been screened for their antimycobacterial activity.
CITATION STYLE
. R. V. S., . A. E. D., . K. M., & . G. A. (2011). Synthesis, antimicrobial and antimycobacterial activity of nicotinic acid hydrazide derivatives. Journal of Current Pharma Research, 1(2), 135–139. https://doi.org/10.33786/jcpr.2011.v01i02.008
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