Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725769Generated: October 26, 2026

tert-butyl 4-(1H-imidazol-2-yl)-3,6-dihydropyridine-1(2H)-carboxylate → tert-butyl 4-(1H-imidazol-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1725769

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(1H-imidazol-2-yl)-3,6-dihydropyridine-1(2H)-carboxylateHCID 69053296—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-butyl 4-(1H-imidazol-2-yl)piperidine-1-carboxylateHCID 1784001599.2%

Reaction Steps

A mixture of tert-butyl 4-(1H-imidazol-2-yl)-3,6-dihydropyridine-1(2H)-carboxylate (7.5 g) and palladium on carbon (10%, 1 g) in ethanol (150 mL) was hydrogenated at 30 psi overnight. The catalyst was removed by filtration through celite and the filtrate was evaporated to give tert-butyl 4-(1H-imidazol-2-yl)piperidine-1-carboxylate (7.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491737B2
Source datasetuspto-grants-2009_02
ORD IDord-b5455f3b58794e18851cd3d8ae8c03ae
Source noteuspto-grants-2009_02