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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187781Generated: November 3, 2026

m-Chloroperbenzoic acid → HCID 67502424, compound

https://huagongshe.com/reaction/1187781

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 67514192HCID 67514192—
SolventDichloromethaneHCID 6344—
SolventSodium SulfiteHCID 24437—
ProductHCID 67502424HCID 67502424111.5%

Reaction Steps

To a stirred solution of (5)-tert-butyl 2,2-dimethyl-4-(4-(5-(methylthio)pyrimidin-2-ylamino)phenethyl)oxazolidine-3-carboxylate (393 mg) in dichloromethane (5 ml) was added m-CPBA (218 mg) and stirring was continued at RT for 40 min. The reaction mixture was then diluted with aq. Na2SO3 solution and extracted with dichloromethane. The organic layers were dried over MgSO4 and concentrated in vacuo to give (4S)-tert-butyl 2,2-dimethyl-4-(4-(5-(methylsulfinyl)pyrimidin-2-ylamino)phenethyl)oxazolidine-3-carboxylate (454 mg, 85% purity, 95% yield) as a yellow oil. MS (ISP): 461.4 ([M+H]+), 405.3 ([M+H—C4H8—CO2]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673950B2
Source datasetuspto-grants-2014_03
ORD IDord-3b52a0ea522c43fe92c03974cfb9bb8e
Source noteuspto-grants-2014_03