Abstract
In this study, a new series of N-alkyl/arakyl derivatives of N-(4-(N-(5-chloro-2-methoxyphenyl)sulfamoyl)phenyl)acetamide (5a-k) was synthesized and screened for enzyme inhibition activity. Target compounds, N-alkyl/arakyl sulfamoylacetamides (5a-k) were synthesized by stirring N-(4-(N-(5-chloro-2-methoxyphenyl)sulfamoyl)phenyl)acetamide (3) with different electrophiles (4a-k) in the presence of sodium hydride (NaH) and N, N-dimethylformamide (DMF). The structures of all the synthesized compounds have been deduced from their spectral (1H-NMR, IR, EI-MS) data. All the new compounds displayed antiurease activity to varying degree.
| Original language | English |
|---|---|
| Pages (from-to) | 1516-1521 |
| Number of pages | 6 |
| Journal | Journal of the Chemical Society of Pakistan |
| Volume | 35 |
| Issue number | 6 |
| State | Published - Dec 2013 |
| Externally published | Yes |
Keywords
- 1H-NMR
- 2-amino-4-chloroanisol
- 4-acetamidobenzenesulfonyl chloride
- EI-MS
- IR
- Urease
ASJC Scopus subject areas
- General Chemistry
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