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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660723Generated: November 1, 2026

HCID 59737058, compound → 1-[(Piperidin-3-yl)methyl]pyridin-2(1H)-one

https://huagongshe.com/reaction/1660723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59737058HCID 59737058—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-[(Piperidin-3-yl)methyl]pyridin-2(1H)-oneHCID 4441053385%

Reaction Steps

A mixture of 3-(2-oxo-2H-pyridin-1-ylmethyl)piperidine-1-carboxylic acid benzyl ester (100 mg) and 5% Pd—C (20 mg) in EtOH (15 mL) was stirred under H2 (1 atm). The reaction was traced by TLC. The catalyst was filtered and the filtration was concentrated and purified by chromatography with CH2Cl2-MeOH—NH3.H2O (10:1:0.1) to give a syrup (50 mg, 85%). 1H NMR (CDCl3) δ 7.31 (m, 1H), 7.21 (dd, 1H, J=6.9, 2.1 Hz), 6.56 (d, 1H, J=9.0 Hz), 6.14 (td, 1H, J=6.6, 1.5 Hz), 3.90 (dd, 1H, J=13.0, 8.1 Hz) 3.76 (dd, 1H, J=13.0, 6.7 Hz), 2.98 (m, 2H), 2.62 (t, 1H, J=9.8 Hz), 2.44 (t, 1H, J=11.2 Hz), 2.10-1.10 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030300B2
Source datasetuspto-grants-2011_10
ORD IDord-9fb9615441cc4fd0b91670ef5dd1348e
Source noteuspto-grants-2011_10