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SYNTHESIS AND BIOLOGICAL EVALUATION OF SOME NOVEL 1, 2, 3-TRIAZOL-N-ARYLIDENE ACETOHYDRAZIDE INCORPORATING BENZIMIDAZOLE RING MOIETY AS POTENTIAL ANTIMICROBIAL AGENTS

Research Authors
BAHAA GM YOUSSIF, SAMIA GALAL ABDEL-MOTY, IBRAHIM M SAYED
Research Journal
J. Curr. Chem. Pharm. Sc.ISSN 2277-2871
Research Publisher
NULL
Research Rank
1
Research Vol
4(2)
Research Website
www.sadgurupublications.com
Research Year
2014
Research_Pages
54-64
Research Abstract

Two series of new 2-[4-((1H-benzimidazol-2-ylthio)methyl)-1H-1,2,3-triazol-1-yl]N`-(arylmethylidene)
acetohydrazides (4-14) and 2-[4-((1H-benzimidazol-2-ylthio)methyl)-1H-1,2,3-triazol-1-yl]N`-(α-arylethylidene)
acetohydrazides (15-20) were prepared by the reaction of 2-[4-((1H-benzimidazol-2-ylthio)methyl)-1H-1,2,3-triazol-1-
yl]acetohydrazide (3) and the appropriate (un) substituted benzaldehyde or acetophenones. The purity of all new compounds
was checked by TLC and elucidation of their structures was confirmed by IR, 1H NMR, and mass spectrometry along with
elemental microanalyses. All the target compounds were evaluated for their possible antimicrobial activity. Most of the
tested compounds showed moderate to good antibacterial activity against most of the bacterial strains used in comparison
with ciprofloxacin as a reference drug. The most active compounds were (7), (13), (15), and (20). Results of antifungal
activity revealed that all compounds showed a good and potent antifungal activity in comparison to fluconazole as a
reference drug. Compounds (8), (9), (13) and (14) were the most active compounds