Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378461Generated: October 29, 2026

Benzenesulfonyl chloride → HCID 18617325, compound

https://huagongshe.com/reaction/378461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant4-Bromo-5-methyl-1,2-oxazol-3-amineHCID 2774464—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 18617325HCID 1861732572.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030991
Source datasetuspto-grants-2000_02
ORD IDord-06236f8bd3694f0a92f9cc80a2e0f453
Source noteuspto-grants-2000_02