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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816435Generated: November 2, 2026

4-Methylmorpholine → HCID 10193784, compound

https://huagongshe.com/reaction/1816435

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 67550133HCID 67550133—
SolventDichloromethaneHCID 6344—
ProductHCID 10193784HCID 10193784—

Reaction Steps

Trifluoroacetic anhydride (2.98 mL, 21.1 mmol) is added dropwise at room temperature to a solution of N-[[(5S)-3-[4-(tetrahydro-1-oxido-2H-thiopyran-4-yl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (2.46 g, 7.02 mmol; prepared as described in International Publication WO 97/09328) and N-methylmorpholine (3.86 mL, 35.1 mmol) in dichloromethane (60 mL). The reaction mixture is stirred overnight at room temperature and then evaporated to dryness. The resulting crude N-[[(5S)-3-[4-(3,4-dihydro-2H-thiopyran-4-yl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (2.77 g) is dissolved in tetrahydrofuran (100 mL) and peracetic acid (7.01 mL of a 32% solution in acetic acid) added dropwise at 0° C. The reaction mixture is allowed to warm to room temperature, stirred overnight, and then evaporated to dryness. The residue is purified by flash column chromatography (ethyl acetate) to give the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884813B2
Source datasetuspto-grants-2005_04
ORD IDord-b0e671cdabdd4246b2ddcabfb3d92b0e
Source noteuspto-grants-2005_04