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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378439Generated: October 29, 2026

Chlorosuccinimide → N-(4-chloro-3-methyl-5-isoxazolyl)-4-(4-methylphenyl)benzenesulfonamide

https://huagongshe.com/reaction/378439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 15453182HCID 15453182—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductN-(4-chloro-3-methyl-5-isoxazolyl)-4-(4-methylphenyl)benzenesulfonamideHCID 1545318358%

Reaction Steps

N-chlorosuccinimide (0.266 g, 2 mmol) was added, in one lot, to a stirred suspension of N-(3-methyl-5-isoxazolyl)-4-(4-methylphenyl)benzenesulfonamide (0.327g, 1 mmol, Example 14b) in chloroform (10 ml) and stirred at room temperature for 2 h. The reaction mixture was diluted with dichloromethane (50 ml) and washed with water (2×50 ml). The organic layer was dried over MgSO4 and concentrated. The crude product was purified by column chromatography using ethyl acetate as eluent to give N-(4-chloro-3-methyl-5-isoxazolyl)-4-(4-methylphenyl)benzenesulfonamide [210 mg, 58% yield, m.p. 260° C. (de coup)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030991
Source datasetuspto-grants-2000_02
ORD IDord-67e3b9e1eb514920a87eb0fb285241d1
Source noteuspto-grants-2000_02