HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 2(1H)-Quinolinone, 1-butyl-4-(methylamino)-3-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2(1H)-Quinolinone, 1-butyl-4-chloro-3-nitro- | HCID 9970925 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2(1H)-Quinolinone, 1-butyl-4-(methylamino)-3-nitro- | HCID 10084780 | 87% |
Reaction Steps
11 g (0.039 mole) of Compound d obtained in Reference Example 4 was dissolved in 100 ml of tetrahydrofuran, and 30 ml (0.39 mole) of 40% methylamine was added with ice cooling, followed by stirring at room temperature for one hour. Then, the solvent was evaporated under reduced pressure, and water was added to the residues. The precipitate was collected by filtration and dried, to afford 9.2 g of Compound w (yield: 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994468 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-f3f84304477a4b1daecbafdedaab4c43 |
| Source note | uspto-grants-1991_02 |