HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466912Generated: October 30, 2026
Benzenesulfonamide → HCID 53965777, compound
https://huagongshe.com/reaction/466912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | HCID 19747149 | HCID 19747149 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53965777 | HCID 53965777 | — |
Reaction Steps
Triethylamine (2.84 g, 0.028 mol) was added to 2.00 g (0.0102 mol) of the product of (b) in dry acetonitrile (100 ml) and then, at 50° C., 3.00 g, 0.0118 mol, of 2-chloro-N-methyl pyridinium iodide was also added. The mixture was stirred at 50° C. for 30 minutes and then 3.32 g (0.0212 mol) of benzene sulphonamide and 1.42 g (0.014 mol) of triethylamine were added and the stirring continued at 50° C. for a further 30 minutes. The mixture was allowed to cool to ambient temperature (~20° C.) and left overnight, stirring being maintained for the entire period. The acetonitrile was then removed by evaporation, 50 ml of water added, the mixture acidified to a pH of 2, 50 ml of diethyl ether added and the solution vigorously stirred for 1 hour. The desired product, a beige solid, formed and was filtered off and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158599 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-21c1dfabb00d4d2f96d7ece961f6dde4 |
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| Source note | uspto-grants-1992_10 |
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