Synthesis of some Mannich base derivatives and their antimicrobial activity study
A series of 2-(phenyl)-2-(morpholin-4-yl)-N-phenylacetamide I–VII were synthesized by Mannich base method. Synthesized compounds I–VII were confirmed by IR, 1H NMR, 13C NMR, mass and elemental analyses. Synthesized compounds I–VII were screened for antibacterial activity against various bacterial st...
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doaj-c3a4ab1f8aca4077a64952c2857970542020-11-24T21:28:14ZengElsevierArabian Journal of Chemistry1878-53522014-12-017699499910.1016/j.arabjc.2010.12.025Synthesis of some Mannich base derivatives and their antimicrobial activity studyA. Idhayadhulla0R. Surendra Kumar1A. Jamal Abdul Nasser2J. Selvin3Aseer Manilal4P.G. & Research Department of Chemistry, Jamal Mohamed College, Tiruchirappalli 620 020, Tamil Nadu, IndiaP.G. & Research Department of Chemistry, Jamal Mohamed College, Tiruchirappalli 620 020, Tamil Nadu, IndiaP.G. & Research Department of Chemistry, Jamal Mohamed College, Tiruchirappalli 620 020, Tamil Nadu, IndiaDepartment of Microbiology, Bharathidasan University, Tiruchirappalli 620 024, Tamil Nadu, IndiaDepartment of Microbiology, Bharathidasan University, Tiruchirappalli 620 024, Tamil Nadu, IndiaA series of 2-(phenyl)-2-(morpholin-4-yl)-N-phenylacetamide I–VII were synthesized by Mannich base method. Synthesized compounds I–VII were confirmed by IR, 1H NMR, 13C NMR, mass and elemental analyses. Synthesized compounds I–VII were screened for antibacterial activity against various bacterial strains and compared with standard Ciprofloxacin at concentration 100 μg/mL and for antifungal activity against various fungal strains and compared with Clotrimazole at concentration 100 μg/mL; particularly 3-(4-chlorophenyl)-3-(morp holin-4-yl)-N-phenylpropanamide lll that has high antibacterial activity against Streptococcus epidermidis was compared with standard Ciprofloxacin.http://www.sciencedirect.com/science/article/pii/S1878535210002893Mannich condensationAntibacterial activityAntifungal activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
A. Idhayadhulla R. Surendra Kumar A. Jamal Abdul Nasser J. Selvin Aseer Manilal |
spellingShingle |
A. Idhayadhulla R. Surendra Kumar A. Jamal Abdul Nasser J. Selvin Aseer Manilal Synthesis of some Mannich base derivatives and their antimicrobial activity study Arabian Journal of Chemistry Mannich condensation Antibacterial activity Antifungal activity |
author_facet |
A. Idhayadhulla R. Surendra Kumar A. Jamal Abdul Nasser J. Selvin Aseer Manilal |
author_sort |
A. Idhayadhulla |
title |
Synthesis of some Mannich base derivatives and their antimicrobial activity study |
title_short |
Synthesis of some Mannich base derivatives and their antimicrobial activity study |
title_full |
Synthesis of some Mannich base derivatives and their antimicrobial activity study |
title_fullStr |
Synthesis of some Mannich base derivatives and their antimicrobial activity study |
title_full_unstemmed |
Synthesis of some Mannich base derivatives and their antimicrobial activity study |
title_sort |
synthesis of some mannich base derivatives and their antimicrobial activity study |
publisher |
Elsevier |
series |
Arabian Journal of Chemistry |
issn |
1878-5352 |
publishDate |
2014-12-01 |
description |
A series of 2-(phenyl)-2-(morpholin-4-yl)-N-phenylacetamide I–VII were synthesized by Mannich base method. Synthesized compounds I–VII were confirmed by IR, 1H NMR, 13C NMR, mass and elemental analyses. Synthesized compounds I–VII were screened for antibacterial activity against various bacterial strains and compared with standard Ciprofloxacin at concentration 100 μg/mL and for antifungal activity against various fungal strains and compared with Clotrimazole at concentration 100 μg/mL; particularly 3-(4-chlorophenyl)-3-(morp holin-4-yl)-N-phenylpropanamide lll that has high antibacterial activity against Streptococcus epidermidis was compared with standard Ciprofloxacin. |
topic |
Mannich condensation Antibacterial activity Antifungal activity |
url |
http://www.sciencedirect.com/science/article/pii/S1878535210002893 |
work_keys_str_mv |
AT aidhayadhulla synthesisofsomemannichbasederivativesandtheirantimicrobialactivitystudy AT rsurendrakumar synthesisofsomemannichbasederivativesandtheirantimicrobialactivitystudy AT ajamalabdulnasser synthesisofsomemannichbasederivativesandtheirantimicrobialactivitystudy AT jselvin synthesisofsomemannichbasederivativesandtheirantimicrobialactivitystudy AT aseermanilal synthesisofsomemannichbasederivativesandtheirantimicrobialactivitystudy |
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1725971552841760768 |