Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428003Generated: October 31, 2026

Tert-butyl 4-(4-aminophenyl)-5,6-dihydropyridine-1(2H)-carboxylate → tert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1428003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-aminophenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 53415310—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 21940085105.5%

Reaction Steps

A solution of 4-(4-amino-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester (0.35 g, 1.2 mmol) (as prepared in the previous step) in methanol was hydrogenated over 10% Pd/C at 20 psi for 1 h. The solution was filtered and concentrated to give 0.35 g (100%) of the title compound as a yellow solid: Mass spectrum (ESI, m/z): Calcd. for C16H24N2O2, 277.2 (M+H). found 277.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933091B2
Source datasetuspto-grants-2015_01
ORD IDord-a9b5a17c808e46d08a92c988bd3feb4a
Source noteuspto-grants-2015_01