HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54092Generated: October 29, 2026
m-Chloroperbenzoic acid → HCID 178448444, compound
https://huagongshe.com/reaction/54092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 178504641 | HCID 178504641 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178448444 | HCID 178448444 | 34.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05620987 |
|---|
| Source dataset | uspto-grants-1997_04 |
|---|
| ORD ID | ord-b03d103511ba46508cce9d5472c584ca |
|---|
| Source note | uspto-grants-1997_04 |
|---|