HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 4-Methylamino-3-nitroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-Chloro-3-nitroquinoline | HCID 11275808 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Methylamino-3-nitroquinoline | HCID 13958321 | 93% |
Reaction Steps
To a suspension of 2.0 g of 4-chloro-3-nitroquinoline in 20 ml of dry ethanol is added 15 ml of 30% methylamine in ethanol. The mixture is stirred at room temperature for 30 minutes and concentrated in vacuo. The residue is triturated with excess water. The resulting crystals are collected by filtration and washed repeatedly with water. The crystals are dried over phosphorus pentoxide in vacuo to afford 1.82 g (93%) of 4-methylamino-3-nitroquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04753951 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-a0273dc5255247159c8d25faa317f8ae |
| Source note | uspto-grants-1988_06 |