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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984723Generated: November 1, 2026

m-Chloroperbenzoic acid → 2-(2-Acetylaminopyridin-4-ylmethylsulfinyl)-N-(3,5-dimethylphenyl)pyridine-3-carboxamide

https://huagongshe.com/reaction/1984723

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(2-Acetylaminopyridin-4-ylmethylthio)-N-(3,5-dimethylphenyl)pyridine-3-carboxamideHCID 11188964—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-(2-Acetylaminopyridin-4-ylmethylsulfinyl)-N-(3,5-dimethylphenyl)pyridine-3-carboxamideHCID 2315087848%

Reaction Steps

m-Chloroperbenzoic acid(75%, 60 mg, 0.26 mmol) was added to a solution of 2-(2-acetylaminopyridin-4-ylmethylthio)-N-(3,5-dimethylphenyl)pyridine-3-carboxamide (Compound No. 4-1, 60 mg, 0.15 mmol) in methylene chloride (3 mL) under ice-cooling, and the mixture was stirred for 1 hour. The reaction mixture was diluted with ethyl acetate (30 mL), the whole was washed with saturated aqueous sodium hydrogen carbonate solution (10 mL) twice and brine (10 mL), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the precipitated solid was filtered off with ethyl acetate to give 30 mg of the target compound as a colorless solid. (Yield 48%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544703B2
Source datasetuspto-grants-2009_06
ORD IDord-8bdfe4c71b694f21b3f8c41700195319
Source noteuspto-grants-2009_06