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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411883Generated: November 1, 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/1411883

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 numberUS08921353B2
Source datasetuspto-grants-2014_12
ORD IDord-8ada197a7e044fca8c322bd95a1d8b9a
Source noteuspto-grants-2014_12