HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allylamine → N-allyl-2-chloro-3-nitroquinolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloro-3-nitroquinoline | HCID 2785138 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-allyl-2-chloro-3-nitroquinolin-4-amine | HCID 59007293 | 105.2% |
Reaction Steps
Triethylamine (17.0 mL, 123 mmol) was added to a 0° C. solution of 2,4-dichloro-3-nitroquinoline (20.0 g, 82.3 mmol) in dichloromethane (350 mL) followed by the dropwise addition of allylamine (5.90 mL, 78.2 mmol). The solution was allowed to stir and warm to room temperature overnight. The solvent was evaporated under reduced pressure and the resulting orange solid was suspended in water (300 mL). Solid sodium carbonate was added to adjust the pH to 10-11 and the suspension was stirred for 2 hours at 0° C. A yellow solid was isolated by filtration and dried under vacuum overnight to yield N-allyl-2-chloro-3-nitroquinolin-4-amine (21.7 g) that contained small amounts of an impurity and water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915281B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-7533faf04dc6419f89e9b1ab9f5be9e6 |
| Source note | uspto-grants-2011_03 |