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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730220Generated: October 25, 2026

6-Methoxy-m-toluenesulfonyl chloride → Benzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide

https://huagongshe.com/reaction/730220

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-m-toluenesulfonyl chlorideHCID 145149—
ReactantBenzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductBenzo[b]thiophene-2sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amideHCID 1151877679.8%

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), 2-methoxy-5-methylbenzenesulfonyl 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 390 mg of benzo[b]thiophene-2-sulfonic acid [2-(2-methoxy-5-methylbenzenesulfonylamino)phenyl]-amide. LC: Tr 1.25 min; MS: 489.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582673B2
Source datasetuspto-grants-2009_09
ORD IDord-a1631ad6ce614e76885649047060fa4d
Source noteuspto-grants-2009_09