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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423896Generated: November 1, 2026

4-Pyridinecarboxaldehyde → HCID 57571261, compound

https://huagongshe.com/reaction/1423896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PyridinecarboxaldehydeHCID 13389—
Reactant(R)-5-phenylmorpholin-2-oneHCID 11126817—
SolventTolueneHCID 1140—
ProductHCID 57571261HCID 5757126146%

Reaction Steps

A solution of (R)-5-phenylmorpholinon-2-one EBE 06134 (3.0 g, 16.9 mmol) and pyridine-4-carboxaldehyde (5.43 g, 50.7 mmol) in toluene (75 mL) was refluxed in a soxhlet extractor filled with molecular sieves 4A (25 g) for 16 hours. All the volatiles were evaporated and the desired product was purified by column chromatography (SiO2) using a gradient of 80% to 100% [v/v] EtOAc in cyclohexane to give after evaporation (1S,3R,5R,8aR)-tetrahydro-5-phenyl-1,3-di(pyridin-4-yl)oxazolo[4,3-c][1,4]oxazin-8(311)-one EBE 06136 (1.7 g, 46% yield) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927589B2
Source datasetuspto-grants-2015_01
ORD IDord-d81a157c436a4553aeec977ada4e789a
Source noteuspto-grants-2015_01