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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899662Generated: October 25, 2026

2,3,4-Trichlorobenzenesulfonyl chloride → 2,3,4-Trichloro-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamide

https://huagongshe.com/reaction/1899662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4-Trichlorobenzenesulfonyl chlorideHCID 36904—
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
Product2,3,4-Trichloro-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamideHCID 1861734166%

Reaction Steps

2,3,4-Trichloro-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamide was prepared from 5-amino-4-bromo-3-methylisoxazole and 2,3,4-trichlorobenzenesulfonyl chloride according to the procedures described in Example 45. The crude product was purified by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 110°-113° C., yield 66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571821
Source datasetuspto-grants-1996_11
ORD IDord-ecf8d502ae2e4322860f47d5b0079ff8
Source noteuspto-grants-1996_11