HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Propanol, 1-amino-2-methyl- | HCID 95102 | — |
| Reactant | 7-Benzyl-4-chloro-3-nitroquinoline | HCID 21984193 | — |
| Reactant | 6-Benzyl-4-chloro-3-nitroquinoline | HCID 21984226 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 21984410 | — |
| Product | 1-(7-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol | HCID 21984452 | — |
Reaction Steps
Under a nitrogen atmosphere, 1-amino-2-methylpropan-2-ol (1.2 equivalents) was added to a 0.2 M solution of 7-benzyl-4-chloro-3-nitroquinoline or 6-benzyl-4-chloro-3-nitroquinoline (1 equivalent) and triethylamine (3 equivalents) in dichloromethane, and the reaction was stirred overnight at ambient temperature. The volatiles were removed under reduced pressure, and the residue was stirred with water (50 mL) for one hour. The resulting yellow solid was isolated by filtration and washed with water to provide 1-(7-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol or 1-(6-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091214B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-a26247a753df407cb8aa5733bcc350c4 |
| Source note | uspto-grants-2006_08 |