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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051586Generated: 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/1051586

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 1784001599.5%

Reaction Steps

Palladium on carbon (10 wt %, 0.100 g) was added to a solution tert-butyl 4-(1H-imidazol-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (0.300 g, 1.20 mmol) in ethanol (20 mL), and the mixture stirred under a hydrogen atmosphere at room temperature for 2 h. The reaction mixture was filtered, and the filtrate was concentrated under vacuum to afford tert-butyl 4-(1H-imidazol-2-yl)piperidine-1-carboxylate (0.300 g, 99%) as an off-white solid. MS (ESI, pos. ion) m/z 252 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388161B2
Source datasetuspto-grants-2016_07
ORD IDord-59550fd5eec047f58045247dbdbcf8eb
Source noteuspto-grants-2016_07