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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542456Generated: October 25, 2026

5-(4-Nitrophenyl)pyrazin-2(1H)-one → 5-(4-Aminophenyl)pyrazin-2(1H)-one

https://huagongshe.com/reaction/542456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Nitrophenyl)pyrazin-2(1H)-oneHCID 13853573—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
Product5-(4-Aminophenyl)pyrazin-2(1H)-oneHCID 1235802881.2%

Reaction Steps

5-(4-Nitrophenyl)-2-(1H)-pyrazinone (0.1 g) was hydrogenated over 10% Palladium on Charcoal (0.01 g) at atmospheric pressure in 50% aqueous dimethylformamide containing 2N sodium hydroxide (0.46 ml). Once the theoretical quantity of hydrogen uptake had been observed, the reaction mixture was filtered and the filtrate treated with HCl to pH6 and evaporated. Trituration of the residue with water afforded the title compound 0.07 g, m.p. 269°-271.5° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04657906
Source datasetuspto-grants-1987_04
ORD IDord-9ea8fa7432e44b85bfda7e7ceeebd41a
Source noteuspto-grants-1987_04