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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727138Generated: November 2, 2026

3-Methoxybenzenesulfonyl chloride → HCID 57566768, compound

https://huagongshe.com/reaction/1727138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxybenzenesulfonyl chlorideHCID 2737504—
ReactantHCID 68828675HCID 68828675—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 57566768HCID 5756676865.2%

Reaction Steps

A mixture of 1-(3-aminophenyl)-4-(3-cyclopentyloxy-4-methoxyphenyl)-pyrrolidin-2-one (15 mg, 0.04 mmol) and 3-methoxybenzenesulfonyl chloride (10 mg, 0.042 mol) in pyridine (30 μL) and CH2Cl2 (0.5 mL) was created in a dry round bottom flask. The mixture was stirred at r.t. for 15 h. After removal of solvent, the residue was purified by preparative LC-MS to give 14 mg of N-{3-[4-(3-cyclopentyloxy-4-methoxyphenyl)-2-oxo-pyrrolidin-1-yl]phenyl}-3-methoxybenzenesulfonamide. Yield: 65%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495016B2
Source datasetuspto-grants-2009_02
ORD IDord-b7994bf31baf404ab5f508b5f32e7411
Source noteuspto-grants-2009_02