Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439354Generated: October 30, 2026

Hydrochloric Acid → HCID 15453204, compound

https://huagongshe.com/reaction/439354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant4-t-Butylbenzenesulfonyl chlorideHCID 139882—
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15453204HCID 1545320421%

Reaction Steps

A solution of 5-amino-4-bromo-3-methylisoxazole (354 mg, 2.0 mmol) in dry THF (1 ml) was added to a suspension of sodium hydride (60% dispersion in mineral oil, 188 mg, 4.4 mmol)in dry THF (1 ml) at 0°-5° C. After stirring at 0°-5° C. for 10 min., the reaction was warmed to room temperature for 10 min. to complete the reaction. The reaction mixture was re-cooled to 0° C. and 4-tert-butylbenzenesulfonyl chloride (512 mg, 2.2 mmol) was added slowly. Stirring was continued for 20 min. at 0°-5° C. Excess sodium hydride was decomposed by addition of methanol (0.4 ml) followed by water (0.5 ml). The mixture was acidified with hydrochloric acid and extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate and the solvent was removed under reduced pressure to give a crude product, which was purified by recrystallization from ethyl acetate/hexanes to give a white solid in 21% yield, m.p. 170° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514691
Source datasetuspto-grants-1996_05
ORD IDord-a259a546c9d5411cbbc9024759158b7f
Source noteuspto-grants-1996_05