Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641739Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 57736442, compound

https://huagongshe.com/reaction/1641739

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 57736468HCID 57736468—
SolventDichloromethaneHCID 6344—
ProductHCID 57736442HCID 5773644248%

Reaction Steps

To a solution of 5-[(2,5-difluorophenyl)[(4-fluorophenyl)thio]methyl]-N-(2-hydroxyethyl)-4-methylpyridine-2-carboxamide (478 mg, 1.11 mmol) in methylene chloride (15 ml), 3-chloroperbenzoic acid (293 mg, 1.11 mmol) was added at 0° C. After stirring for 3 hours at the same temperature, the reaction mixture was washed with 1 N aqueous sodium hydroxide, the organic layer was dried over anhydrous sodium sulfate and filtered, and then the filtrate was concentrated under reduced pressure. The resulting residue was subjected to flash silica gel chromatography, and the fraction obtained from an elution with hexane:ethyl acetate=1:2 was concentrated under reduced pressure. The resulting residue was washed with hexane, and then the residue was dried under reduced pressure, to obtain the title compound (238 mg, 0.53 mmol, 48%) as a colorless foamy substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-c50140f104f74fb3b3d6828c38f2ee6f
Source noteuspto-grants-2012_02