A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying Indole

The title compounds (7a-h) were prepared by esterification of indole-5-carboxylic acid (1) and subsequent treatment with hydrazine hydrate in methanol via the hydrazide (3). Finally hydrazide (3) condensed with different substituted aldol (6) in acetic acid / PTSA catalytic media produced (3,5-subsi...

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Main Authors: K. Narasimha Sarma, M. C. S. Subha, K. Chowdoji Rao
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2010/979401
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author K. Narasimha Sarma
M. C. S. Subha
K. Chowdoji Rao
author_facet K. Narasimha Sarma
M. C. S. Subha
K. Chowdoji Rao
author_sort K. Narasimha Sarma
collection DOAJ
description The title compounds (7a-h) were prepared by esterification of indole-5-carboxylic acid (1) and subsequent treatment with hydrazine hydrate in methanol via the hydrazide (3). Finally hydrazide (3) condensed with different substituted aldol (6) in acetic acid / PTSA catalytic media produced (3,5-subsituted-4,5-dihydropyrazol-1-yl)(1H-indol-5-yl)methanone (7a-h) in good yields. All the newly synthesized compounds are by elemental analysis and spectral studies and evaluated for antimicrobial activities.
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series E-Journal of Chemistry
spelling doaj-art-7851932c96cc44d882347e4b4f2439ea2025-08-20T03:35:11ZengWileyE-Journal of Chemistry0973-49452090-98102010-01-017374575010.1155/2010/979401A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying IndoleK. Narasimha Sarma0M. C. S. Subha1K. Chowdoji Rao2Department of Chemistry, Sri Krishnadevaraya University, Anantapur-515003, A.P., IndiaDepartment of Chemistry, Sri Krishnadevaraya University, Anantapur-515003, A.P., IndiaDepartment of Chemistry, Sri Krishnadevaraya University, Anantapur-515003, A.P., IndiaThe title compounds (7a-h) were prepared by esterification of indole-5-carboxylic acid (1) and subsequent treatment with hydrazine hydrate in methanol via the hydrazide (3). Finally hydrazide (3) condensed with different substituted aldol (6) in acetic acid / PTSA catalytic media produced (3,5-subsituted-4,5-dihydropyrazol-1-yl)(1H-indol-5-yl)methanone (7a-h) in good yields. All the newly synthesized compounds are by elemental analysis and spectral studies and evaluated for antimicrobial activities.http://dx.doi.org/10.1155/2010/979401
spellingShingle K. Narasimha Sarma
M. C. S. Subha
K. Chowdoji Rao
A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying Indole
E-Journal of Chemistry
title A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying Indole
title_full A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying Indole
title_fullStr A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying Indole
title_full_unstemmed A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying Indole
title_short A Facial Synthesis and Antimicrobial Activity of Some Pyrazole Derivatives Carrying Indole
title_sort facial synthesis and antimicrobial activity of some pyrazole derivatives carrying indole
url http://dx.doi.org/10.1155/2010/979401
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