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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910616Generated: November 2, 2026

HCID 57584081, compound → HCID 57584031, compound

https://huagongshe.com/reaction/910616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57584081HCID 57584081—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 57584031HCID 5758403150%

Reaction Steps

10% Pd—C (360 mg) was added to an ethanol (30 ml) solution of ethyl 1-{2-[3-{4-[(benzyloxy)carbonyl]phenyl}-2-oxopyridin-1(2H)-yl]ethyl}piperidin-4-carboxylate (1.647 g), followed by stirring in a hydrogen atmosphere under normal pressure at room temperature for 27 hours. The reaction mixture was filtered through Celite, washed with THF and ethanol, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform:methanol=100:0 to 80:20) to obtain 4-(1-{2-[4-(ethoxycarbonyl)piperidin-1-yl]ethyl}-2-oxo-1,2-dihydropyridin-3-yl)benzoic acid (671 mg) as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022208B2
Source datasetuspto-grants-2011_09
ORD IDord-4257a6288107498ca1b6dd4ab69fe87e
Source noteuspto-grants-2011_09