Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69872Generated: October 28, 2026

4-Nitro-3-(piperidin-1-yl)pyridine 1-oxide → 3-(Piperidin-1-yl)pyridin-4-amine

https://huagongshe.com/reaction/69872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitro-3-(piperidin-1-yl)pyridine 1-oxideHCID 14735913—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(Piperidin-1-yl)pyridin-4-amineHCID 6904736873%

Reaction Steps

To a solution of 4-nitro-3-(piperidin-1-yl)pyridine 1-oxide (1.0 equiv.) in ethanol, at a concentration of 0.1 M, was added 10% palladium on carbon (0.1 eq.). The resultant heterogeneous solution was put under an atmosphere of hydrogen and was stirred for 15 hours. At this time LC/MS analysis indicated that the nitro was reduced to the amine, but the N-oxide was remaining. More 10% palladium on carbon (0.2 eq.) was added and the mixture was resubmitted to a balloon atmosphere of hydrogen. After stirring for 24 hours, more 10% palladium on carbon (0.2 eq.) was added and the mixture was resubmitted to a balloon atmosphere of hydrogen. After stirring for an additional 3 days the mixture was filtered through a pad of celite eluting with methanol. The volatiles were removed in vacuo yielding 3-(piperidin-1-yl)pyridin-4-amine (73%). LCMS (m/z): 178.0 (MH+); LC Rt=1.66 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822497B2
Source datasetuspto-grants-2014_09
ORD IDord-88ea49dceea6479bb3324053034ea6bf
Source noteuspto-grants-2014_09