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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066076Generated: November 1, 2026

1-Tert-butoxycarbon-yl-4-(quinoxalin-2-yl)-1,2,5,6-tetrahydropyridine → 1-Tert-butoxycarbonyl-4-(quinoxalin-2-yl)piperidine

https://huagongshe.com/reaction/1066076

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butoxycarbon-yl-4-(quinoxalin-2-yl)-1,2,5,6-tetrahydropyridineHCID 21198060—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-Tert-butoxycarbonyl-4-(quinoxalin-2-yl)piperidineHCID 2119803584%

Reaction Steps

A mixture of 0.55 gm (1.8 mMol) 1-tert-butoxycarbon-yl-4-(quinoxalin-2-yl)-1,2,5,6-tetrahydropyridine and 0.1 gm 5% palladium on carbon in 10 mL methanol was stirred at room temperature for 45 minutes under a hydrogen atmosphere. The reaction mixture was then filtered and the filtrate concentrated under reduced pressure to provide 0.47 gm (84%) of 1-tert-butoxycarbonyl-4-(quinoxalin-2-yl)piperidine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242450B1
Source datasetuspto-grants-2001_06
ORD IDord-dcbf3659f9894d7daf2451b052f6c9b5
Source noteuspto-grants-2001_06