HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439359Generated: October 29, 2026
Benzenesulfonyl chloride → HCID 18617325, compound
https://huagongshe.com/reaction/439359
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 4-Bromo-5-methyl-1,2-oxazol-3-amine | HCID 2774464 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18617325 | HCID 18617325 | 72.9% |
Reaction Steps
3-Amino-4-bromo-5-methylisoxazole (5.31 g, 30 mmol) was dissolved in dry pyridine (30 ml). Benzenesulfonyl chloride (5.24 ml, 42 mmol) was added dropwise with stirring at ambient temperature. N,N-(Dimethyl)aminopyridine (100 mg) was added and stirring was continued at 50° C. for 25 h. The reaction mixture was diluted with dichloromethane (200 ml), washed with 1N HCl (6×100 ml) and the organic phase was dried over magnesium sulfate. The solvent was removed under reduced pressure to yield a crude product which was purified by column chromatography using 9: 1, hexanes/ethyl acetate as eluent to give N-(benzenesulfonyl)-N-(4-bromo-5-methyl-3-isoxazolyl)benzenesulfonamide (7 g, 51% yield, Rf =0.27 using 3:1, hexanes/ethyl acetate as eluent) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05514691 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-67ff44c862de4040ab48a65e60fe88c0 |
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| Source note | uspto-grants-1996_05 |
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