HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1,2-Dihydro-5-methyl-2-oxo-1,6-naphthyridin-3-amidoxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 5-methyl-2-oxo-1H-1,6-naphthyridine-3-carbonitrile | HCID 5713068 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2-Dihydro-5-methyl-2-oxo-1,6-naphthyridin-3-amidoxime | HCID 136025279 | 96.3% |
Reaction Steps
To a solution of hydroxylamine hydrochloride (4.17 g) in water (50 ml) was added sodium carbonate (3.18 g) with stirring under ice cooling. To the solution were subsequently added ethanol (200 ml) and 1,2-dihydro-5-methyl-2-oxo-1,6-naphthyridine-3-carbonitrile (3.70 g), and the mixture was refluxed for 2 hours. After distilling off the solvent under reduced pressure, water was added to the residue, and the precipitated crystals were separated by filtration. The product was washed with water, isopropanol, diisopropyl ether in this order, and dried to give 1,2-dihydro-5-methyl-2-oxo-1,6-naphthyridin-3-amidoxime (4.2 g). This compound was used in the next reaction without being purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172079B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-579ef4d89f894f109ee1d96fbce47132 |
| Source note | uspto-grants-2001_01 |