Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218113Generated: October 29, 2026

HCID 11596355, compound → HCID 59769615, compound

https://huagongshe.com/reaction/2218113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11596355HCID 11596355—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 59769615HCID 5976961563%

Reaction Steps

A mixture of 3-(benzyloxy)-N-(cyclohexylmethyl)-1-cyclopropyl-6-methyl-4-oxo-1,4-dihydropyridine-2-carboxamide (2.0 g, 4.8 mmol), Pd/C (10% wet, 0.45 g) in ethanol (150 mL) was hydrogenated in a Parr apparatus at 50 psi of hydrogen pressure for 16 h. The reaction mixture was filtered over a pad of celite and the celite was thoroughly washed with EtOH (25 mL). Evaporation of the solvent afforded a pale pink solid. The solid was dissolved in hot methanol, then cooled to RT as solid product precipitated out. The solid was collected by suction filtration. The mother liquor was concentrated in vacuo and the residual solid was again dissolved in hot methanol and cooled to RT to precipitate out the product, which was then collected. This process was repeated one more time. The three combined white solid fractions weighed 0.95 g (63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410985B2
Source datasetuspto-grants-2008_08
ORD IDord-50ab3eac84e34680b9719b2cd1056888
Source noteuspto-grants-2008_08