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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828541Generated: October 23, 2026

N-(4-methyl-5-nitropyridin-2-yl)acetamide → N-(5-Amino-4-methylpyridin-2-yl)acetamide

https://huagongshe.com/en/reaction/1828541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-methyl-5-nitropyridin-2-yl)acetamideHCID 13567013—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-(5-Amino-4-methylpyridin-2-yl)acetamideHCID 22063573103%

Reaction Steps

The N1-(4-methyl-5-nitro-2-pyridyl)acetamide (4.70 g, 24.1 mmol) obtained in (A) was dissolved in ethanol (150 ml), added with 10% palladium/carbon (0.95 g) and subjected to catalytic reduction overnight at 1 atm under hydrogen atmosphere. The catalyst was removed by filtration and washed with ethanol. The filtrate was concentrated and the resulting residue was purified by silica gel column chromatography (chloroform chloroform:methanol=100:5) to obtain the title compound (4.10 g, quantitative) as brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056917B2
Source datasetuspto-grants-2006_06
ORD IDord-ef9681cf549f4b29a9a1e54462238dc5
Source noteuspto-grants-2006_06