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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730207Generated: October 26, 2026

Methyl 3-(chlorosulfonyl)-4-methoxybenzoate → 3-[2-(Benzo[b]thiophene-2-sulfonylamino)phenylsulfamoyl]-4-methoxybenzoic acid methyl ester

https://huagongshe.com/reaction/730207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-(chlorosulfonyl)-4-methoxybenzoateHCID 2794613—
ReactantBenzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product3-[2-(Benzo[b]thiophene-2-sulfonylamino)phenylsulfamoyl]-4-methoxybenzoic acid methyl esterHCID 1168519065.7%

Reaction Steps

To a solution of benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)-amide (1 mmol) in DCM (2 mL) and pyridine (2 mL), methyl 3-(chlorosulfonyl)-4-methoxybenzoate (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 350 mg of 3-[2-(benzo[b]thiophene-2-sulfonylamino)phenylsulfamoyl]-4-methoxybenzoic acid methyl ester. Tr 1.10 min, MS: 533.7 (M+1)+. 1H NMR (CDCl3, 400 MHz): δ 3.84 (s, 3H), 4.18 (s, 3H), 7.0-7.2 (m, 5H), 7.4-7.6 (m, 3H), 7.66 (s, 1H), 7.80 (d, 1H), 7.83 (d, 1H), 8.22 (dd, 1H), 8.34 (d, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582673B2
Source datasetuspto-grants-2009_09
ORD IDord-489cef9e3c8142ecbab82c1b31076875
Source noteuspto-grants-2009_09