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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16387Generated: October 29, 2026

Pyridine → (1S,6R,9aR)-6-(3,4-difluorophenyl)-1-methyltetrahydro-[1,4]oxazino[3,4-c][1,4]oxazine-3,4-dione

https://huagongshe.com/reaction/16387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOxalyl chlorideHCID 65578—
Reactant1-[(3R,5R)-5-(3,4-difluorophenyl)morpholin-3-yl]ethanolHCID 67375291—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(1S,6R,9aR)-6-(3,4-difluorophenyl)-1-methyltetrahydro-[1,4]oxazino[3,4-c][1,4]oxazine-3,4-dioneHCID 67372582—

Reaction Steps

To a solution consisting of 1-[(3R,5R)-5-(3,4-difluorophenyl)morpholine-3-yl]ethanol (424 mg) and pyridine (2 mL) in dichloromethane (8 mL) was dropwise added oxalyl chloride (417 μL) while cooling with ice. The resultant solution was stirred at the same temperature for 30 minutes. The reaction solution was diluted with water, and the organic layer was partitioned. The organic layer was then dried over magnesium sulfate. Solvent was removed by distillation under reduced pressure, and the resulting residue was purified by silica gel column chromatography (heptane/ethyl acetate 9/1→1/4), to thereby obtain the titled compound (353 mg). The physical properties of the compound were as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737141B2
Source datasetuspto-grants-2010_06
ORD IDord-257e7e727ab7428bbfc3c4d84c9c9624
Source noteuspto-grants-2010_06