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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160374Generated: November 1, 2026

3-(S)-Phenylcarbamoyl-piperidine-1-carboxylic acid benzyl ester → N-Phenylpiperidine-3-carboxamide

https://huagongshe.com/reaction/1160374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(S)-Phenylcarbamoyl-piperidine-1-carboxylic acid benzyl esterHCID 58737530—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-Phenylpiperidine-3-carboxamideHCID 1622711199%

Reaction Steps

A solution of 3-(S)-Phenylcarbamoyl-piperidine-1-carboxylic acid benzyl ester (1.80 mol, 608 mg) and Pd—C 30% (100 mg) in CH3OH (10 mL) at 25° C. were added to a Paar hydrogenator low pressure reaction vessel. The mixture was reacted at 55 psi with vigorous shaking until hydrogen uptake subsided (2 h). The catalyst was filtered through a pad of celite. The filtrate was concentrated in vacuo which provided piperidine-3-carboxylic acid phenylamide (367 mg, 367 mg theoretical, 99%) as a white foam: LRMS m/z 205 (M++1, C12H16N2O requires 205).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816375B2
Source datasetuspto-grants-2010_10
ORD IDord-f1fca06d3a8745099072c9f1ea31765e
Source noteuspto-grants-2010_10