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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395259Erstellt: 26. Oktober 2026

Methyl morpholine oxide → Pnu-288034

https://huagongshe.com/reaction/395259

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl morpholine oxideHCID 82029—
EduktN-({(5S)-3-[3,5-difluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamideHCID 10109766—
EduktPropan-2-one--water (1/1)HCID 18366337—
KatalysatorOsmium TetroxideHCID 30318—
ProduktPnu-288034HCID 993100383%

Reaktionsschritte

N-({(5S)-3-[3,5-difluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide (13.36 g, 35.97 mmol) is dissolved in a solution of 25% water/acetone and then treated sequentially with 4-Methylmorpholine N-oxide (3 eq, 12.64 g, 107.91 mmol) and a catalytic amount of osmium tetroxide (2.8 mL). The reaction is stirred overnight at room temperature under nitrogen. In the morning, another 2 mL of osmium tetroxide is added. Another 2 eq of 4-Methylmorpholine N-oxide and 2.5 mL of osmium tetroxide are added a few hours later. The reaction is stirred overnight again under nitrogen. The following morning, the reaction is complete. The reaction mixture is quenched with a solution of sodium hydrosulfite and then extracted with methylene chloride three times. The organic layer is washed with sodium hydrosulfite and brine, dried with sodium sulfate, filtered, and concentrated. The crude product is then chomatographed on silica gel, eluting with methylene chloride and then 2% and 5% methanol/methylene chloride solutions. Appropriate fractions are combined and concentrated to yield 11.99 g (83%) of the title compound as a white solid, mp: 187-189.5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605609B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-eb7c889ddbf840c1bf7be46c3dbc5558
Quellennotizuspto-grants-2003_08