Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/12096
Title: Synthesis and antibacterial evaluation of novel heterocycles from 5-chloro-3-methyl-1-phenylpyrazole-4-carbaldehyde
Authors: Siddiqui, Zeba N
Praveen, Shagufta
Musthafa, Mohammed T N
Keywords: 3-Acetyl-4-hydroxycoumarin
Dehydroacetic acid
5-chloro-3-methyl-1-phenylpyrazole-4-carbaldehyde
Pyrazolines
<img src='/image/spc_char/alpha.gif' border=0>-bromo-<img src='/image/spc_char/beta.gif' border=0>-methoxyheteroaryl ketones
Antibacterial activity
Issue Date: Jul-2011
Publisher: NISCAIR-CSIR, India
Abstract: 5-Chloro-3-methyl-1-phenylpyrazole-4-carbaldehyde <b style="">1</b> reacts with acetylpyrone <b style="">2 </b>and acetylbenzopyrone <b style="">3</b> <i style="">via</i> Claisen-Schmidt condensation to afford heterochalcones <b style="">4a,b</b> which undergo facile cyclisation with hydrazines to give 3,5-heteroaryl-2-pyrazolines <b style="">5a-d</b> in quantitative yield. Further, heterochalcones <b style="">4a,b</b> undergo addition reaction using Br<sub>2</sub>/MeOH in the presence of Pb(NO<sub>3</sub>)<sub>2</sub> or AgNO<sub>3</sub> to afford addition products <b style="">6a,b</b>. The structures of the newly synthesized compounds have been established on the basis of their spectral studies. The newly synthesized heterochalcones and pyrazolines have been screened for their antibacterial activity against two kinds of strains using the Agar well diffusion method. Some of the compounds showed significant activity against both the strains.
Description: 910-917
URI: http://hdl.handle.net/123456789/12096
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.50B(07) [July 2011]

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