SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTS
The reaction of cyanoacetylhydrazine with ω-bromoacetophenone gave the N-[2-bromo-1-phenylethylidene]-2-isocyanoacetohydrazide (3). The latter compound underwent ready cyclization when treated with potassium cyanide to give the 1-(isocyanoacetyl)-3-phenyl-1H-pyrazol-5-amine (6). Compound 6...
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Sociedad Chilena de Química
2007
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oai:scielo:S0717-970720070002000062007-09-13SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTSWARDAKHAN,WAGNAT WLOUCA,NADIA A Cyanoacetylhydrazine Pyrazole Coumarin Pyridazine The reaction of cyanoacetylhydrazine with ω-bromoacetophenone gave the N-[2-bromo-1-phenylethylidene]-2-isocyanoacetohydrazide (3). The latter compound underwent ready cyclization when treated with potassium cyanide to give the 1-(isocyanoacetyl)-3-phenyl-1H-pyrazol-5-amine (6). Compound 6 underwent a series of heterocyclization to give either coumarin, pyridazine, 1,2,4-triazine or thiophene derivatives. The antimicrobial and antifungal activities of the newly synthesized products were measured, using two Gram-negative (Escherichia coli and Pseudomonas aeruginosa), two Gram-positive bacteria (Bacillus subtilis and Bacillus cereus) and the antifungal activity using Candida albicansinfo:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.52 n.2 20072007-06-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000200006en10.4067/S0717-97072007000200006 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
English |
topic |
Cyanoacetylhydrazine Pyrazole Coumarin Pyridazine |
spellingShingle |
Cyanoacetylhydrazine Pyrazole Coumarin Pyridazine WARDAKHAN,WAGNAT W LOUCA,NADIA A SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTS |
description |
The reaction of cyanoacetylhydrazine with ω-bromoacetophenone gave the N-[2-bromo-1-phenylethylidene]-2-isocyanoacetohydrazide (3). The latter compound underwent ready cyclization when treated with potassium cyanide to give the 1-(isocyanoacetyl)-3-phenyl-1H-pyrazol-5-amine (6). Compound 6 underwent a series of heterocyclization to give either coumarin, pyridazine, 1,2,4-triazine or thiophene derivatives. The antimicrobial and antifungal activities of the newly synthesized products were measured, using two Gram-negative (Escherichia coli and Pseudomonas aeruginosa), two Gram-positive bacteria (Bacillus subtilis and Bacillus cereus) and the antifungal activity using Candida albicans |
author |
WARDAKHAN,WAGNAT W LOUCA,NADIA A |
author_facet |
WARDAKHAN,WAGNAT W LOUCA,NADIA A |
author_sort |
WARDAKHAN,WAGNAT W |
title |
SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTS |
title_short |
SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTS |
title_full |
SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTS |
title_fullStr |
SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTS |
title_full_unstemmed |
SYNTHESIS OF NOVEL PYRAZOLE, COUMARIN AND PYRIDAZINE DERIVATIVES EVALUATED AS POTENTIAL ANTIMICROBIAL AND ANTIFUNGAL AGENTS |
title_sort |
synthesis of novel pyrazole, coumarin and pyridazine derivatives evaluated as potential antimicrobial and antifungal agents |
publisher |
Sociedad Chilena de Química |
publishDate |
2007 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072007000200006 |
work_keys_str_mv |
AT wardakhanwagnatw synthesisofnovelpyrazolecoumarinandpyridazinederivativesevaluatedaspotentialantimicrobialandantifungalagents AT loucanadiaa synthesisofnovelpyrazolecoumarinandpyridazinederivativesevaluatedaspotentialantimicrobialandantifungalagents |
_version_ |
1718445371766603776 |