HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-8-ethoxalylamino-7-nitroquinoline → 1,4,7,8,9,10-Hexahydro-pyrido[2,3-f]quinoxaline-2,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-8-ethoxalylamino-7-nitroquinoline | HCID 11726498 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,4,7,8,9,10-Hexahydro-pyrido[2,3-f]quinoxaline-2,3-dione | HCID 11820647 | 44.3% |
Reaction Steps
A solution of the product from Example 83 (1 g, 2.7 mmol) in 250 mL acetic acid was treated with 20% Pd/C (0.1 g) and shaken on a Parr apparatus under 52 psi hydrogen gas for 21 hours. After removal of the catalyst, the solvent was evaporated but gave negligible material. The catalyst/celite was washed two times with 1 N HCl, and the aqueous solution was basified with sodium bicarbonate. The precipitate was collected by filtration, dried and then recrystallized from methanol/dimethylformamide to give the title compound (0.26 g, 44% yield) mp>300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703391B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-53b4c64284844d0e9ceff9418e683dc7 |
| Source note | uspto-grants-2004_03 |