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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730204Generated: October 27, 2026

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

https://huagongshe.com/reaction/730204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
Reactant1-Benzothiophene-2-sulfonyl chlorideHCID 2776333—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductBenzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 8624001878.8%

Reaction Steps

To a solution of o-phenylenediamine (5 mmol) in DCM (25 mL) and pyridine (5 mL) at 0° C., benzo[b]thiophene-2-sulfonyl chloride (5.5 mmol) was added in small portions. The reaction mixture was then gradually warmed to RT with stirring continued until the reaction was complete as determined by TLC or LC-MS. The reaction mixture was then diluted with DCM (25 mL). The organic phase was washed with water (2×25 mL) and 25 mL of brine. 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 give 1.2 g of benzo[b]thiophene-2-sulfonic acid (2-amino-phenyl)-amide. Tr 0.94 min, MS: 305.7 (M+1)+. 1H NMR (DMSO-d6, 400 MHz): δ 6.40 (t, 1H), 6.60 (d, 1H), 6.78 (d, 1H), 6.89 (t, 1H), 7.45 (t, 1H), 7.50 (t, 1H), 7.80 (s, 1H), 7.90 (d, 1H), 8.80 (d, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582673B2
Source datasetuspto-grants-2009_09
ORD IDord-0333576690ca4bb69fc2dd94fdf11d9f
Source noteuspto-grants-2009_09