Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615678Generated: November 2, 2026

HCID 68089343, compound → HCID 68089393, compound

https://huagongshe.com/reaction/1615678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68089343HCID 68089343—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 68089393HCID 6808939379.1%

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of tert-butyl 5-(benzylamino)-2,3-dihydropyrido[3,4-b][1,4]oxazine-1-carboxylate (3.6 g, 10.56 mmol) and 10% Pd on carbon (1.12 g, 1.06 mmol) in MeOH (100 mL) was stirred under hydrogen atmosphere (2 L) at 35° C. for 48 h. The mixture was then filtered through Celite and washed with MeOH (3×25 mL). The combined organic layer was concentrated under reduced pressure. The residue was re-dissolved in EtOAc (100 mL) and washed with brine (2×50 mL). The combined organic layer was dried over sodium sulfate, filtered, and the solvent removed under reduced pressure. The residue was purified by reverse phase column chromatography (eluting with 22% acetonitrile in water, with 0.1% NH3.H2O) to give tert-butyl 5-amino-2,3-dihydropyrido[3,4-b][1,4]oxazine-1-carboxylate (2.1 g, 79% yield) as a yellow solid. ESI MS: m/z 252 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-f0ae61b7378c43e9b8711af949490c04
Source noteuspto-grants-2014_07