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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70464Generated: October 29, 2026

Methanesulfonyl chloride → HCID 71714815, compound

https://huagongshe.com/reaction/70464

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 numberUS08822530B2
Source datasetuspto-grants-2014_09
ORD IDord-2561765ecc78480ba7b43ad56e682b0a
Source noteuspto-grants-2014_09