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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757752Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 178448444, compound

https://huagongshe.com/reaction/1757752

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 numberUS05446161
Source datasetuspto-grants-1995_08
ORD IDord-c97151f5e728467c8fa692422fb922a5
Source noteuspto-grants-1995_08