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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378436Generated: October 26, 2026

p-Bromobenzenesulfonyl chloride → HCID 15453181, compound

https://huagongshe.com/reaction/378436

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
Reactant5-Amino-3-methylisoxazoleHCID 84590—
SolventPyridineHCID 1049—
ProductHCID 15453181HCID 1545318172%

Reaction Steps

4-brombenzenesulfonyl chloride (solid) was added, in five portions, to a solution of 3-methyl-5-aminoisoxazole (3.82 g, 40 mmol) in dry pyridine (30 ml). This was stirred at room temperature for 3 h and the pyridine was removed under reduced pressure. The residue was dissolved in THF (300 ml) and a 5% NaOH solution (100 ml) was added. Stirring continued for 1 h at room temperature. The THF was removed under reduced pressure and the resultant residue was neutralized to pH 2 using concentrated hydrochloric acid. This was extracted with ethyl acetate (3×200 ml) and the combined organic layer was dried over MgSO4 and concentrated. The crude product was recrystallized using hexane/ethyl acetate giving N-(3-methyl-5-isoxazolyl)-4-bromobenzenesulfonamide (9.2 g, 72% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030991
Source datasetuspto-grants-2000_02
ORD IDord-bc909251a10a467fad941be18872155e
Source noteuspto-grants-2000_02