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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49406Generated: October 29, 2026

Water → N-(3,4-dichloro-5-isothiazolecarbonyl)-N-(4-chlorophenyl)-4-methoxybenzenesulfonamide

https://huagongshe.com/reaction/49406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-(4-Chlorophenyl)-4-methoxybenzenesulfonamideHCID 598671—
Reactant3,4-Dichloro-5-isothiazolecarbonyl chlorideHCID 10976886—
SolventDimethylformamideHCID 6228—
ProductN-(3,4-dichloro-5-isothiazolecarbonyl)-N-(4-chlorophenyl)-4-methoxybenzenesulfonamideHCID 1140894936.7%

Reaction Steps

To a solution of N-(4-chlorophenyl)-4-methoxybenzenesulfonamide (1.98 g) in unhydrous N,N-dimethylformamide (20 ml) 60% sodium hydride (0.24 g) was added at room temperature. After stirring the reaction mixture at the same temperature for 1 hour, a solution of 3,4-dichloro-5-isothiazolecarbonyl chloride (1.1 g) in unhydrous N,N-dimethylformamide (10 ml) was added thereto dropwise. After finishing the addition, the reaction mixture was stirred at room temperature for 18 hours and poured into water. The mixture was extracted with ethyl acetate and the organic phase was washed with water and dried with unhydrous sodium sulfate. The crude product obtained by distilling off the solvent under reduced pressure was recrystallized from ethanol to obtain N-(3,4-dichloro-5-isothiazolecarbonyl)-N-(4-chlorophenyl)-4-methoxybenzenesulfonamide (0.89 g). mp 154-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706748B2
Source datasetuspto-grants-2004_03
ORD IDord-3585ca59184a4e89bbba02979f2ff0d0
Source noteuspto-grants-2004_03