HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421192Generated: October 28, 2026
Methyl N-{[(3R)-4-(phenylmethyl)-3-morpholinyl]carbonyl}-D-serinate → ((7S,9aS)-Octahydropyrazino[2,1-c][1,4]oxazin-7-yl)methanol
https://huagongshe.com/reaction/421192
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl N-{[(3R)-4-(phenylmethyl)-3-morpholinyl]carbonyl}-D-serinate | HCID 59215767 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | ((7S,9aS)-Octahydropyrazino[2,1-c][1,4]oxazin-7-yl)methanol | HCID 59215831 | 35% |
Reaction Steps
Methyl N-{[(3R)-4-(phenylmethyl)-3-morpholinyl]carbonyl}-D-serinate (D48, 3.72 g, 11.55 mmol) was dissolved in EtOH (50 mL), treated with 10% Pd on C (450 mg) then placed under an atmosphere of hydrogen over the weekend. Left stirring for further 6 hours. Added 10% Pd on C (200 mg) and left under an atmosphere of hydrogen overnight. Catalyst removed by filtration through kieselguhr washed with acid, washing well with EtOH. Solvent removed under reduced pressure to afford a colourless oil. Oil dissolved in dry MeOH (15 mL) and heated at 50° C. overnight. Left heating for a further 3 hours before cooling to R.T. Solvent removed under reduced pressure. Residue triturated with DCM to afford the title compound as an off white solid in 35% yield over the 2 steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097618B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-0aee76bf66f745b093e47955588ee137 |
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| Source note | uspto-grants-2012_01 |
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