HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(4-Nitrophenyl)pyrazin-2(1H)-one → 5-(4-Aminophenyl)pyrazin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(4-Nitrophenyl)pyrazin-2(1H)-one | HCID 13853573 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Aminophenyl)pyrazin-2(1H)-one | HCID 12358028 | 81.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04657906 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-9ea8fa7432e44b85bfda7e7ceeebd41a |
| Source note | uspto-grants-1987_04 |