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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl N-{[(3R)-4-(phenylmethyl)-3-morpholinyl]carbonyl}-D-serinateHCID 59215767—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product((7S,9aS)-Octahydropyrazino[2,1-c][1,4]oxazin-7-yl)methanolHCID 5921583135%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097618B2
Source datasetuspto-grants-2012_01
ORD IDord-0aee76bf66f745b093e47955588ee137
Source noteuspto-grants-2012_01