HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86626297, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Phenethylamine, (-)- | HCID 75818 | — |
| Reactant | 2,4-Dichloro-3-nitroquinoline | HCID 2785138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86626297 | HCID 86626297 | 97.6% |
Reaction Steps
The method described in Part A of Example 1 was used to treat 2,4-dichloro-3-nitroquinoline (19.4 g, 78.5 mmol) in DMF (100 mL) with triethylamine (32 mL, 0.235 mol) and (S)-(−)-α-methylbenzylamine (11.5 g, 94.2 mmol) with the modification that the reaction was allowed to warm to room temperature and stirred for two hours. After the isolated precipitate was washed with water, it was dried under high vacuum overnight to provide 25.1 g of 2-chloro-3-nitro-N-[(1S)-1-phenylethyl]quinolin-4-amine as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088790B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-1877ef14ecf84ef59806151e1462eeac |
| Source note | uspto-grants-2012_01 |