Abstract
1,3,4-Oxadiazole bearing compounds are one of the most attractive class for researchers due to their biological activities. In the undertaken research, a number of N-substituted derivatives of 2-(5-(1-(phenylsulfonyl)piperidin-4-yl)-1,3,4-oxadiazol-2-ylthio)acetamide (6a–n) were synthesized through a series of steps. The reaction of benzenesulfonyl chloride with ethyl isonipecotate yielded ethyl 1-(phenylsulfonyl)piperidin-4-carboxylate (1), which was further converted into 1-(phenylsulfonyl)piperidin-4-carbohydrazide (2) and 5-(1-(phenylsulfonyl)piperidin-4-yl)-1,3,4-oxadiazol-2-thiol (3) respectively. The target compounds 6a–n were synthesized by the reaction of compound 3 with different N-aralkyl/aryl substituted 2-bromoacetamides (5a–n) in the presence of a weak base and polar aprotic solvent. The structures of the synthesized compounds were elucidated through 1H-NMR, IR and mass spectral data. The synthesized compounds were screened against Gram-negative and Gram-positive bacteria and exhibited moderate to talented activity.
| Original language | English |
|---|---|
| Pages (from-to) | S615-S623 |
| Journal | Journal of Saudi Chemical Society |
| Volume | 20 |
| DOIs | |
| State | Published - 1 Sep 2016 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2013
Keywords
- 1,3,4-Oxadiazole
- Acetamides
- EIMS
- Ethyl isonipecotate
- H-NMR
- IR
ASJC Scopus subject areas
- General Chemistry