Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | HCID 18684838 | HCID 18684838 | — |
| Solvent | 2-Methylpropan-2-ol--water (1/1) | HCID 71401949 | — |
| Product | HCID 10309658 | HCID 10309658 | — |
Reaction Steps
A solution of (S)-N-[[3-[4-(3,6-dihydro-1,1-dioxido-2H-thiopyran-4-yl)-3-fluorophenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (0.415 g, 1.08 mmol; prepared as described in U.S. Pat. No. 5,968,962) in 1:1 t-butanol-water (4 mL) is added to a solution of the standard reagent AD mix-β (1.51 g; available from Aldrich Co.) and methanesulfonamide (0.103 g, 1.08 mmol) in 1:1 t-butanol-water (10 mL) cooled at 0° C. The reaction mixture is stirred 5 days at 4° C. and then treated with sodium sulfite (1.5 g) and stirred 30 minutes. The solution is then extracted with four 10 mL portions of ethyl acetate and the combined organic phases dried (MgSO4), filtered and concentrated. Purification by column chromatography (0–5% MeOH-DCM) provided the title compound as a mixture of diastereomers. Yield 0.29 g (64%). 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101874B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-74ae24fce0a444e49c338316288f02c8 |
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| Source note | uspto-grants-2006_09 |
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