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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506900Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 86693763, compound

https://huagongshe.com/reaction/1506900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantEthyl 2-amino-1-benzothiophene-3-carboxylateHCID 699464—
SolventPyridineHCID 1049—
ProductHCID 86693763HCID 8669376346.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of ethyl 2-aminobenzo(b)thiophene-3-carboxylate (0.165 g) and benzenesulphonyl chloride (0.53 g) in pyridine (7 ml) was stirred and heated at 80° C. for 5 hours. Further benzenesulphonyl chloride (0.53 g) was added and the mixture was stirred and heated at 80° C. for 24 hours. The mixture was concentrated and the residue was partitioned between ethyl acetate and water. The aqueous layer was further extracted with ethyl acetate and the combined organic layers were washed with water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and pentane (5-10%) to give ethyl 2-[bis-(benzenesulphonyl)amino]benzo[b]thiophene-3-carboxylate (0.173 g) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221787B2
Source datasetuspto-grants-2015_12
ORD IDord-075c87bff6a9458f92331a4645cf82ee
Source noteuspto-grants-2015_12