HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → HCID 67502424, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 67514192 | HCID 67514192 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Sulfite | HCID 24437 | — |
| Product | HCID 67502424 | HCID 67502424 | 111.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673950B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-3b52a0ea522c43fe92c03974cfb9bb8e |
| Source note | uspto-grants-2014_03 |