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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283274Generated: October 30, 2026

2-Aminobenzenesulfonamide → 2-[2-(4-Chloro-2-methoxy-phenyl)-ethenesulfonylamino]-benzenesulfonamide

https://huagongshe.com/reaction/2283274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzenesulfonamideHCID 72894—
Reactant2-(4-Chloro-2-methoxyphenyl)-ethenesulfonyl chlorideHCID 73993005—
SolventPyridineHCID 1049—
Product2-[2-(4-Chloro-2-methoxy-phenyl)-ethenesulfonylamino]-benzenesulfonamideHCID 6878318741%

Reaction Steps

2-Aminobenzene sulfonamide (194 mg, 1.13 mmol) was added in one portion to a solution of 2-(4-chloro-2-methoxyphenyl)-ethenesulfonyl chloride (300 mg, 1.13 mmol) in pyridine (3 mL) at RT. After 1 h stirring, no more starting material was detected by tlc. The reaction mixture was concentrated and the residue was taken up in ethyl acetate with a small amount of methanol. The organic phase was washed with 1N HCl, saturated sodium bicarbonate, dried over MgSO4 and concentrated under reduced pressure. The crude product was purified on silica gel using DCM/methanol, 99:1 to afford material which was further purified by recrystallization from methanol to give the title compound (184 mg, 41%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-d286d92c92884b89b6e3dc6bcfcd8ac6
Source noteuspto-grants-2015_09