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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520972Generated: October 30, 2026

Methanesulfonyl chloride → HCID 71714815, compound

https://huagongshe.com/reaction/520972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-{2-[(3-aminobenzyl)sulfanyl]-5-chlorophenyl}-1-benzofuran-2-sulfonamideHCID 67972007—
SolventPyridineHCID 1049—
ProductHCID 71714815HCID 7171481573.1%

Reaction Steps

To a solution of N-{2-[(3-aminobenzyl)sulfanyl]-5-chlorophenyl}-1-benzofuran-2-sulfonamide (440 mg, 0.90 mmol) in pyridine (4 ml) was added methanesulfonyl chloride (70 μl, 0.90 mmol). The reaction was stirred at room temperature for 2 hours and was concentrated, diluted with 1M HCl, and extracted with EtOAc. The organic layer was dried over Na2SO4, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (4% EtOAc in hexane) to yield the title compound (344 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328067B2
Source datasetuspto-grants-2016_05
ORD IDord-e1f17127ccd849aa854ed40a8f93cd36
Source noteuspto-grants-2016_05