Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267139Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 178448444, compound

https://huagongshe.com/reaction/267139

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 178504641HCID 178504641—
SolventMethanolHCID 887—
ProductHCID 178448444HCID 17844844434.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 154 mg of N2 -[3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphinyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide (two diastereomers) in 5 ml of methanol was treated with 84 mg of 3-chloroperbenzoic acid and the solution was stirred at 20° C. for 16 hours. The solvent was removed by evaporation and the residue was partitioned between dichloromethane and 2M sodium hydroxide solution. The organic phase was evaporated and the residue was crystallized from ethyl acetate/n-hexane to give 28 mg of N2 -[3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphonyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide monohydrate; MS: m/e 633 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652369
Source datasetuspto-grants-1997_07
ORD IDord-a5297d32393e4779bc38e91eb4438ab7
Source noteuspto-grants-1997_07