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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267118Generated: November 2, 2026

4-(4-Benzylamino-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester → tert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1267118

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Benzylamino-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl esterHCID 53748737—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 2194008587.9%

Reaction Steps

A solution of 4-(4-benzylamino-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (0.27 g) in EtOH (10 mL) containing Pd/C 10% (50 mg) was hydrogenated at room temperature. After 1 hour, the catalyst was removed by filtration and the filtrate was evaporated under reduced pressure to give the title compound (0.18 g) as a pale pink oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552022B1
Source datasetuspto-grants-2003_04
ORD IDord-8533461ffa7942efbaec63279dcd6cd2
Source noteuspto-grants-2003_04