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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439352Generated: October 29, 2026

Benzenesulfonyl chloride → N-Benzenesulfonyl-N-(4-bromo-3-tert-butyl-5-isoxazolyl) benzenesulfonamide

https://huagongshe.com/reaction/439352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant4-Bromo-3-(tert-butyl)isoxazol-5-amineHCID 18617312—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductN-Benzenesulfonyl-N-(4-bromo-3-tert-butyl-5-isoxazolyl) benzenesulfonamideHCID 1861730860.1%

Reaction Conditions

Temperature500 °C

Reaction Steps

5-Amino-4-bromo-3-tert-butylisoxazole (440 mg, 2.0 mmol) was dissolved in dry pyridine (2 ml). Benzenesulfonyl chloride (344 mg, 2.0 mmol) and 4-dimethylamino-pyridine (5 mg) was added and the reaction was stirred at 500° C. for 16 h. The reaction mixture was diluted with ethyl acetate (20 ml), washed with 1N HCl (2×10 ml) and the organic phase was dried over magnesium sulfate. The solvent was removed under reduced pressure to yield a crude product, which was recrystallized from ethyl acetate/hexanes to give 300 mg (60% yield) of N-benzenesulfonyl-N-(4-bromo- 3-tert-butyl-5-isoxazolyl) benzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514691
Source datasetuspto-grants-1996_05
ORD IDord-3f40b29badd04232b7d9d42d8288c2ae
Source noteuspto-grants-1996_05