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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910394Generated: November 1, 2026

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

https://huagongshe.com/reaction/1910394

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(1-methyl-1H-imidazol-2-yl)-3,6-dihydropyridine-1(2H)-carboxylateHCID 68598207—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylateHCID 2308414532.9%

Reaction Steps

To a solution of tert-butyl 4-(1-methyl-1H-imidazol-2-yl)-3,6-dihydropyridine-1(2H)-carboxylate (398 mg) in MeOH (4.0 ml) was added 5% Pd/C (wet; 40 mg) and the mixture was stirred at room temperature for 7 hours under hydrogen atmosphere (1 atm). After removal of Pd/C with cerite, the filtrate was concentrated in vacuo. The resultant residue was purified by silica gel column (n-hexane:EtOAc=80:20 to EtOAc only) to give tert-butyl 4-(1-methyl-1H-imidazol-2-yl)piperidine-1-carboxylate (132 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08603975B2
Source datasetuspto-grants-2013_12
ORD IDord-ac6b4f827b0c43d397d22a3a4a6f7bc0
Source noteuspto-grants-2013_12