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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Reactant | (R)-5-(5-bromo-2-fluoro-phenyl)-5-difluoromethyl-morpholin-3-one | HCID 66665720 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-5-(5-Bromo-2-fluoro-phenyl)-5-difluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338413B1 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-4360a20cd5be4990b7b760cd91ff3656 |
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| Source note | uspto-grants-2012_12 |
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