Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398508Generated: October 30, 2026

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

https://huagongshe.com/reaction/398508

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 numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-343b02eb0c794d979f8e1e3680bdb020
Source noteuspto-grants-2003_08