HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → HCID 67502792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 67502424 | HCID 67502424 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Sulfite | HCID 24437 | — |
| Product | HCID 67502792 | HCID 67502792 | 114.5% |
Reaction Steps
To a stirred solution of (4S)-tert-butyl 2,2-dimethyl-4-(4-(5-(methylsulfinyl)pyrimidin-2-ylamino)phenethyl)oxazolidine-3-carboxylate (227 mg) in dichloromethane (5 ml) was added m-CPBA (155 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 (S)-tert-butyl 2,2-dimethyl-4-(4-(5-(methylsulfonyl)pyrimidin-2-ylamino)phenethyl)oxazolidine-3-carboxylate (269 mg, 70% purity, 94% yield) as a brown oil. MS (ISP): 477.4 ([M+H]+), 421.3 ([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-c9aec9c33efc48e5bacbb46b413b46dd |
| Source note | uspto-grants-2014_03 |