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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730206Generated: October 26, 2026

Benzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amide → Benzo[b]thiophene-2-sulfonic acid

https://huagongshe.com/reaction/730206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
Reactant2-Methoxy-5-(propane-2-sulfonyl)benzenesulfonyl chlorideHCID 86240025—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductBenzo[b]thiophene-2-sulfonic acidHCID 18176377214.7%

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-(propane-2-sulfonyl)benzenesulfonyl 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 460 mg of benzo[b]thiophene-2-sulfonic acid {2-[2-methoxy-5-(propane-2 sulfonyl) benzenesulfonylamino]phenyl-amide. Tr 1.09 min; MS: 581.4 (M+1)+. 1H NMR (DMSO-d6, 400 MHz): δ 0.97 (d, 6H), 3.58 (m, 1H), 4.02 (s, 3H), 6.84 (dd, 1H), 7.96 (td, 1H), 7.10 (td, 1H), 7.23 (dd, 1H), 7.44-7.54 (m, 3H), 7.86 (d, 1H), 7.90 (s, 1H), 7.96 (d, 1H), 8.03 (dd, 2H), 9.22 (bs, 1H), 9.79 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582673B2
Source datasetuspto-grants-2009_09
ORD IDord-2c6e626166434788b43f5928cd7ee125
Source noteuspto-grants-2009_09