HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930395Generated: October 29, 2026
HCID 86732227, compound → HCID 86732228, compound
https://huagongshe.com/reaction/930395
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86732227 | HCID 86732227 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86732228 | HCID 86732228 | — |
Reaction Steps
A mixture of (4S,6S)-4-(2,3-difluoro-5-nitrophenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (1.85 g, 5.18 mmol) and palladium 10 wt. % (dry basis) on activated carbon, wet (1.000 mL, 0.940 mmol) in EtOH (20 mL) was hydrogenated under a hydrogen balloon for 4 days until full conversion to the desired product. The reaction mixture was filtered through celite and the filter cake was rinsed with EtOAc followed by MeOH/DCM (10%). The filtrate was concentrated to dryness. The residue was triturated with DCM and the resulted suspension was filtered through filter paper. The filter cake was washed with DCM and dried in air to afford (4S,6S)-4-(5-amino-2,3-difluorophenyl)-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (1.2 g, 3.67 mmol, 70.8% yield) as off-white solid. MS m/z=328.1 [M+H]+. Calculated for C12H11F6N30: 327.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296734B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-00599ad4ea8d4d86984c4c8a1159300e |
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| Source note | uspto-grants-2016_03 |
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