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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491638Generated: October 26, 2026

3-nitro-N-phenylpyridin-4-amine → 4-N-phenylpyridine-3,4-diamine

https://huagongshe.com/reaction/1491638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-nitro-N-phenylpyridin-4-amineHCID 612005—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product4-N-phenylpyridine-3,4-diamineHCID 1058367588.7%

Reaction Steps

4-Phenylamino-3-nitropyridine (1.40 g, 6.51 mmol) was dissolved in the mixed solvent of 15 ml of ethanol and 10 ml of dichloromethane. After the atmosphere was replaced with nitrogen, 0.10 g of 10% palladium-carbon was added thereto. After the atmosphere was replaced with hydrogen, hydrogen addition was conducted with stirring at room temperature for about 15 hours. Palladium-carbon was removed by filtration and the filtered cake was washed with ethanol. The filtrate and the washings were combined and then concentrated. The residue was purified by silica gel column chromatography [eluent: dichloromethane: methanol=2:1 (v/v)] to obtain 1.07 g of a light brown solid (yield: 88.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371086
Source datasetuspto-grants-1994_12
ORD IDord-37e8568da90f4bd09cec075a126afc53
Source noteuspto-grants-1994_12