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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430201Generated: October 29, 2026

m-Chloroperbenzoic acid → 3-Cyclopentyl-2-(4-methanesulfinyl-phenyl)-N-thiazol-2-yl-propionamide

https://huagongshe.com/reaction/430201

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Cyclopentyl-2-(4-methylsulfanyl-phenyl)-N-thiazol-2-yl-propionamideHCID 12088916—
SolventDichloromethaneHCID 6344—
Product3-Cyclopentyl-2-(4-methanesulfinyl-phenyl)-N-thiazol-2-yl-propionamideHCID 2231514732%

Reaction Steps

A solution 3-cyclopentyl-2-(4-methylsulfanyl-phenyl)-N-thiazol-2-yl-propionamide (75 mg, 0.216 mmol) in methylene chloride (1 mL) was treated with 3-chloroperoxybenzoic acid (75% grade, 50 mg, 0.216 mmol). The reaction mixture was immediately monitored by thin layer chromatography and the results indicated the immediate absence of starting material. The reaction mixture was partitioned between water and methylene chloride and then washed with a saturated aqueous sodium bicarbonate solution. The organic layer was further washed with water and then dried over magnesium sulfate, filtered, and concentrated in vacuo. Recrystallization from 1/1 hexanes/ethyl acetate afforded 3-cyclopentyl-2-(4-methanesulfinyl-phenyl)-N-thiazol-2-yl-propionamide (25 mg, 32%) as a white solid: mp 170-173° C.; EI-HRMS m/e calcd for C18H22N2O2S2 (M+) 362.1123, found 362.1121.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06320050B1
Source datasetuspto-grants-2001_11
ORD IDord-6987bb03c35e4ca2bff5429799f1401f
Source noteuspto-grants-2001_11