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Synthesis of Some New 1,2,4-triazole Schiff Bases and their Antibacterial Activity Studies
Journal
Letters in Organic Chemistry
ISSN
1570-1786
Date Issued
2023-09
Author(s)
Yin-Haw Hoor
Xin-Lik Boo
Chor-Chin Teh
Shih-Nee Lai
Chor-Pey Teh
DOI
http://10.2174/1570178620666230330091737
Abstract
<jats:sec>
<jats:title>Abstract:</jats:title>
<jats:p>A new 4-amino-5-mercapto-3-[(1H-indol-3-yl)propyl]-1,2,4-triazole was synthesized from
the fusion of indole-3-butyric acid with thiocarbohydrazide. The reaction of 1,2,4-triazole with a series
of benzaldehydes afforded the corresponding Schiff bases (2a-2s). All the synthesized compounds
were evaluated for their antibacterial activities using a 96-well microbroth dilution assay. The results
of the antibacterial activity revealed that Schiff base 2p with both chloro groups at meta and para positions
of the phenyl exhibited significant inhibition against Bacillus cereus and Staphylococcus aureus
at MIC 9.11 μmol/mL and against Bacillus subtilis spizizenni at 18.20 μmol/mL.</jats:p>
</jats:sec>
<jats:title>Abstract:</jats:title>
<jats:p>A new 4-amino-5-mercapto-3-[(1H-indol-3-yl)propyl]-1,2,4-triazole was synthesized from
the fusion of indole-3-butyric acid with thiocarbohydrazide. The reaction of 1,2,4-triazole with a series
of benzaldehydes afforded the corresponding Schiff bases (2a-2s). All the synthesized compounds
were evaluated for their antibacterial activities using a 96-well microbroth dilution assay. The results
of the antibacterial activity revealed that Schiff base 2p with both chloro groups at meta and para positions
of the phenyl exhibited significant inhibition against Bacillus cereus and Staphylococcus aureus
at MIC 9.11 μmol/mL and against Bacillus subtilis spizizenni at 18.20 μmol/mL.</jats:p>
</jats:sec>
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