Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance

A new series of 3-chloro-1-{[2-(6-nitro-1H-indazol-1-yl)ethyl]amino}-4-(substituted phenyl)-2-azetidinones (4a-j) was synthesized in four steps from 6-nitro-1H-indazole and characterized by IR, ¹H NMR, 13C NMR, FAB-mass spectrometry and chemical methods. Compounds 4(a-j) were screened in vitro for their antibacterial, antifungal and antitubercular activities against some selected microorganism and for their antiinflammatory activity (in vivo) against albino rats (either sex). All above activities of compounds 4(a-j) showed acceptable results.

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Main Authors: Samadhiya,Pushkal, Sharma,Ritu, Srivastava,Santosh K., Srivastava,S. D.
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2012
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000500010
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spelling oai:scielo:S0100-404220120005000102012-07-02Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importanceSamadhiya,PushkalSharma,RituSrivastava,Santosh K.Srivastava,S. D. synthesis azetidinone biosignificance A new series of 3-chloro-1-{[2-(6-nitro-1H-indazol-1-yl)ethyl]amino}-4-(substituted phenyl)-2-azetidinones (4a-j) was synthesized in four steps from 6-nitro-1H-indazole and characterized by IR, ¹H NMR, 13C NMR, FAB-mass spectrometry and chemical methods. Compounds 4(a-j) were screened in vitro for their antibacterial, antifungal and antitubercular activities against some selected microorganism and for their antiinflammatory activity (in vivo) against albino rats (either sex). All above activities of compounds 4(a-j) showed acceptable results.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaQuímica Nova v.35 n.5 20122012-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000500010en10.1590/S0100-40422012000500010
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Samadhiya,Pushkal
Sharma,Ritu
Srivastava,Santosh K.
Srivastava,S. D.
spellingShingle Samadhiya,Pushkal
Sharma,Ritu
Srivastava,Santosh K.
Srivastava,S. D.
Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance
author_facet Samadhiya,Pushkal
Sharma,Ritu
Srivastava,Santosh K.
Srivastava,S. D.
author_sort Samadhiya,Pushkal
title Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance
title_short Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance
title_full Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance
title_fullStr Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance
title_full_unstemmed Synthesis of 2-azetidinone derivatives of 6-nitro-1H-indazole and their biological importance
title_sort synthesis of 2-azetidinone derivatives of 6-nitro-1h-indazole and their biological importance
description A new series of 3-chloro-1-{[2-(6-nitro-1H-indazol-1-yl)ethyl]amino}-4-(substituted phenyl)-2-azetidinones (4a-j) was synthesized in four steps from 6-nitro-1H-indazole and characterized by IR, ¹H NMR, 13C NMR, FAB-mass spectrometry and chemical methods. Compounds 4(a-j) were screened in vitro for their antibacterial, antifungal and antitubercular activities against some selected microorganism and for their antiinflammatory activity (in vivo) against albino rats (either sex). All above activities of compounds 4(a-j) showed acceptable results.
publisher Sociedade Brasileira de Química
publishDate 2012
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000500010
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AT srivastavasantoshk synthesisof2azetidinonederivativesof6nitro1hindazoleandtheirbiologicalimportance
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