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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730218Generated: October 30, 2026

4-Methoxy-2-nitrobenzenesulphonyl chloride → Benzo[b]thiophene-2-sulfonic acid [2-(4-methoxy-2-nitro-benzenesulfonylamino)phenyl]-amide

https://huagongshe.com/reaction/730218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-2-nitrobenzenesulphonyl chlorideHCID 87452—
ReactantBenzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductBenzo[b]thiophene-2-sulfonic acid [2-(4-methoxy-2-nitro-benzenesulfonylamino)phenyl]-amideHCID 1161329467%

Reaction Steps

To a solution of benzo[b]thiophene-2-sulfonic acid (2-aminophenyl) amide (1 mmol, prepared as in Example 1) in DCM (2 mL) and pyridine (2 mL), 4-methoxy-2-nitrobenzenesulfonyl chloride (1.1 mmol) was added at RT and the reaction mixture was then allowed to stir at RT overnight. The reaction mixture was then diluted with DCM (10 mL). The organic phase was washed with 10% aqueous HCl (10 mL), water (10 mL) and brine (10 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue obtained was purified by flash column chromatography eluting with DCM/EtOAc to obtain 348 mg of benzo[b]thiophene-2-sulfonic acid [2-(4-methoxy-2-nitro-benzenesulfonylamino)phenyl]-amide. LC: Tr 1.09 min; MS: 520.7 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582673B2
Source datasetuspto-grants-2009_09
ORD IDord-527c11158a444d93bf584513855c198a
Source noteuspto-grants-2009_09