Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity

Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole derivatives have been synthesized with different aromatic aldehyde. 1,3,4-thiadiazole derivatives were prepared by the reaction of thiosemicarbazide, sodium acetate and aromatic aldehyde. The structures of the titled Schiff bases were elucidated by IR...

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Main Authors: Alok Pandey, R. Rajavel, Sandeep Chandraker, Deepak Dash
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2012/145028
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author Alok Pandey
R. Rajavel
Sandeep Chandraker
Deepak Dash
author_facet Alok Pandey
R. Rajavel
Sandeep Chandraker
Deepak Dash
author_sort Alok Pandey
collection DOAJ
description Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole derivatives have been synthesized with different aromatic aldehyde. 1,3,4-thiadiazole derivatives were prepared by the reaction of thiosemicarbazide, sodium acetate and aromatic aldehyde. The structures of the titled Schiff bases were elucidated by IR and 1H NMR spectral measurements. All the compounds were evaluated for their analgesic activity against swiss albino mice, anti-inflammatory activity against Wister albino rats. The compounds showed significant antibacterial activity against Staphylococcus aureus (gram-positive) bacteria and E. coli (gram-negative) bacteria.
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institution Kabale University
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publisher Wiley
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series E-Journal of Chemistry
spelling doaj-art-314077b99e074cd58ef439b8f79d112e2025-02-03T05:46:22ZengWileyE-Journal of Chemistry0973-49452090-98102012-01-01942524253110.1155/2012/145028Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial ActivityAlok Pandey0R. Rajavel1Sandeep Chandraker2Deepak Dash3Department of Pharmaceutical Chemistry, Nandha College of Pharmacy and Research Institute, Erode-52 Tamilnandu, IndiaDepartment of Pharmaceutical Chemistry, Nandha College of Pharmacy and Research Institute, Erode-52 Tamilnandu, IndiaRoyal College of Pharmacy Science Raipur, (C.G.) 492101, IndiaRoyal College of Pharmacy Science Raipur, (C.G.) 492101, IndiaSchiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole derivatives have been synthesized with different aromatic aldehyde. 1,3,4-thiadiazole derivatives were prepared by the reaction of thiosemicarbazide, sodium acetate and aromatic aldehyde. The structures of the titled Schiff bases were elucidated by IR and 1H NMR spectral measurements. All the compounds were evaluated for their analgesic activity against swiss albino mice, anti-inflammatory activity against Wister albino rats. The compounds showed significant antibacterial activity against Staphylococcus aureus (gram-positive) bacteria and E. coli (gram-negative) bacteria.http://dx.doi.org/10.1155/2012/145028
spellingShingle Alok Pandey
R. Rajavel
Sandeep Chandraker
Deepak Dash
Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity
E-Journal of Chemistry
title Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity
title_full Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity
title_fullStr Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity
title_full_unstemmed Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity
title_short Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity
title_sort synthesis of schiff bases of 2 amino 5 aryl 1 3 4 thiadiazole and its analgesic anti inflammatory and anti bacterial activity
url http://dx.doi.org/10.1155/2012/145028
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AT sandeepchandraker synthesisofschiffbasesof2amino5aryl134thiadiazoleanditsanalgesicantiinflammatoryandantibacterialactivity
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