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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283362Generated: November 1, 2026

2-Amino-5-methylbenzenesulfonamide → 2-[2-(4-Chloro-2-methoxy-phenyl)-ethenesulfonylamino]-5-methyl-benzenesulfonamide

https://huagongshe.com/reaction/2283362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-methylbenzenesulfonamideHCID 245584—
Reactant2-(4-Chloro-2-methoxyphenyl)-ethenesulfonyl chlorideHCID 73993005—
SolventPyridineHCID 1049—
Product2-[2-(4-Chloro-2-methoxy-phenyl)-ethenesulfonylamino]-5-methyl-benzenesulfonamideHCID 6878263454%

Reaction Steps

2-(4-Chloro-2-methoxy-phenyl)-ethenesulfonyl chloride (0.50 g, 1.87 mmol) was added slowly to a solution of 2-amino-5-methyl-benzenesulfonamide (0.38 g, 2.05 mmol) in anhydrous pyridine (10 mL) and the reaction mixture was stirred for 18 hours at room temperature. The solvent was removed in vacuo and the residue was dissolved in ethyl acetate (30 mL). The organic phase was washed with 1 M hydrochloric acid and brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by column chromatography gave 0.42 g (54% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145380B2
Source datasetuspto-grants-2015_09
ORD IDord-55df97f10b5d466da5ed2aaefe123d3a
Source noteuspto-grants-2015_09