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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279397Erstellt: 23. Oktober 2026

Linezolid impurity 3 → rac-Linezolid

https://huagongshe.com/de/reaction/279397

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLinezolid impurity 3HCID 10944967—
Edukt2-OxiranepropanamideHCID 22246713—
Edukt2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
LösungsmittelTetrahydrofuranHCID 8028—
Produktrac-LinezolidHCID 392980%

Reaktionsschritte

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 ml/min; UV detection at 254 nm). The title compound is isolated by means known to those skilled in the art.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06362334B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-bbf218f1d6874c07b9f0b7b3b59a7e72
Quellennotizuspto-grants-2002_03