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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196355Generated: October 29, 2026

Phosphorus sulfide (P2S5) → (R)-5-(5-Bromo-2-fluoro-phenyl)-5-difluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine

https://huagongshe.com/reaction/2196355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantAzane;hydrateHCID 12896473—
Reactant(R)-5-(5-bromo-2-fluoro-phenyl)-5-difluoromethyl-morpholin-3-oneHCID 66665720—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(R)-5-(5-Bromo-2-fluoro-phenyl)-5-difluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamineHCID 66665548—

Reaction Steps

To a solution of (R)-5-(5-bromo-2-fluoro-phenyl)-5-difluoromethyl-morpholin-3-one (10 g, 30.86 mmol) in CH2Cl2 (100 mL) was added P2S5 (6.86 g, 30.86 mmol) at room temperature. The resulted yellow suspension was heated to reflux for 6.5 h. The reaction mixture was filtered through a pad of silica gel (200˜300 mesh), washed with CH2Cl2 for 3 times to get a brown solution. The solvent was removed to provide the crude product as a yellow solid, which was dispersed in THF (10 mL), then 25% NH3 water solution (60 mL) was added at room temperature. 20 hours later, the reaction mixture was extracted with IPAC. The combined organic phase was washed with brine, dried over Na2SO4, filtered and concentrated to provide the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338413B1
Source datasetuspto-grants-2012_12
ORD IDord-4360a20cd5be4990b7b760cd91ff3656
Source noteuspto-grants-2012_12