Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592944Generated: October 30, 2026

5-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-2-nitropyridine → 5-(1-Methylpiperidin-4-yl)pyridin-2-amine

https://huagongshe.com/reaction/592944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(1-Methyl-1,2,3,6-tetrahydropyridin-4-yl)-2-nitropyridineHCID 58044246—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product5-(1-Methylpiperidin-4-yl)pyridin-2-amineHCID 5804382092.9%

Reaction Steps

A 250-mL single-neck round-bottomed flask was purged with nitrogen and charged with 232b (2.0 g, 9.0 mmol), 10% palladium on carbon (50% wet, 200 mg), and methanol (40 mL). The flask was evacuated, charged with hydrogen gas, and stirred under hydrogen at room temperature for 12 h. The hydrogen was then evacuated and nitrogen was charged to the flask. The catalyst was removed by filtration through a pad of CELITE® and the filtrate was concentrated under reduced pressure to afford 232c (1.6 g, 92.5%), which was used directly in the next step without further purification. MS-ESI: [M+H]+ 192

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238655B2
Source datasetuspto-grants-2016_01
ORD IDord-2dac4173495d4c728c6e8ef77d201530
Source noteuspto-grants-2016_01