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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524933Generated: October 30, 2026

Ethanol → (S)-tert-butyl 3-((3-aminopyridin-4-yl)oxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/524933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactanttert-butyl(3S)-3-[(3-nitro-4-pyridyl)oxy]piperidine-1-carboxylateHCID 86720990—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(S)-tert-butyl 3-((3-aminopyridin-4-yl)oxy)piperidine-1-carboxylateHCID 86720991102.3%

Reaction Steps

Pd on C, (10%, wet, Degussa) (1 g, 0.9397 mmol) was added to a stirred solution of tert-butyl (3S)-3-[(3-nitro-4-pyridyl)oxy]piperidine-1-carboxylate (2.65 g, 8.196 mmol) in EtOAc (30 mL)/EtOH (15 mL). The reaction was placed under an atmosphere of hydrogen and stirred at ambient temperature for 16 hours. The catalyst was removed by filtration through a pad of celite and the filtrate concentrated in vacuo to give the sub-title compound as an off-white solid (2.46 g, >100% Yield). MS (2ES+) 587.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-8b2bb26d32494b96a9a59da65df3c9f9
Source noteuspto-grants-2016_05