Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Linezolid impurity 3 | HCID 10944967 | — |
| Reactant | 2-Oxiranepropanamide | HCID 22246713 | — |
| Reactant | 2-Propanol, 2-methyl-, lithium salt (1:1) | HCID 23664764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | rac-Linezolid | HCID 3929 | 80% |
Reaction Steps
To a solution of (±)-glycidylacetamide (VIIIB, EXAMPLE 11, 0.1571 g, 1.365 mmol) in THF (1.63 ml) at −78° is added N carbomethoxy-3-fluoro-4-morpholinylaniline (IX, PREPARATION 2, 0.4358 g, 1.71 mmol, 1.26 eq) and lithium t-butoxide (0.1267 g, 1.583 mmol, 1.16 eq). The reaction mixture is then stirred at 0 to 11° for 17.5 hrs at which point HPLC showes an 80% yield of (±)-N-[[3-(3-fluoro-4-morpholinylphenyl)-2-oxo-5-oxazolidinyl]methyl]acetamide (retention time=0.97 min; method B; Stationary phase: 4.6×250 mm Zorbax RX C-8 column; mobile phase: 650 ml acetonitrile, 1.85 ml triethylamine, 1.30 ml acetic acid, water sufficient to make 1000 ml; flow rate: 3.0 mi/min; UV detection at 254 nm). The title compound is isolated by means known to those skilled in the art.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740754B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-d79c3ddda3d84f21aabc69d5fa29eea9 |
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| Source note | uspto-grants-2004_05 |
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