HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 7-Acetyl-1-butyl-1,4,7,8,9,10-hexahydro-pyrido[3,2-f]quinoxaline-2,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20633122 | HCID 20633122 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 7-Acetyl-1-butyl-1,4,7,8,9,10-hexahydro-pyrido[3,2-f]quinoxaline-2,3-dione | HCID 22742485 | 19% |
Reaction Steps
The product from Example 89 (0.14 g, 0.5 mmol) was solubilized in a minimal amount of dimethylformamide and then treated with 2 mL dichloromethane, acetic anhydride (0.15 g) and triethylamine (0.15 g). After the mixture stirred at room temperature for 18 h, it was poured onto dichloromethane/water. The aqueous layer was washed with dichloromethane and the combined organic layers over sodium sulfate, filtered and evaporated to give a dark syrup. The syrup was purified by silica gel chromatography (ethyl acetate as eluant) to give the title compound (30 mg, 19% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703391B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-2dc6125b3e9a45578597a614e14802c7 |
| Source note | uspto-grants-2004_03 |