HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-{[(3-Nitroquinolin-4-yl)amino]methyl}cyclopentanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-3-nitroquinoline | HCID 11275808 | — |
| Reactant | 1-(Aminomethyl)cyclopentan-1-ol | HCID 13051202 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-{[(3-Nitroquinolin-4-yl)amino]methyl}cyclopentanol | HCID 57457809 | 65.1% |
Reaction Steps
To a solution of 1-(aminomethyl)cyclopentanol (approximately 55.2 mmol, prepared as described above) in dichloromethane (280 mL) was added triethylamine (7.76 mL, 55.7 mmol) and 4-chloro-3-nitroquinoline (9.22 g, 44.3 mmol). The mixture was allowed to stand at rt over the weekend. A solid formed that was isolated by filtration. Two more crops of solid were isolated from the mother liquor. The yellow solid was stirred in water and filtered. The solid was washed with water multiple times and was dried under vacuum with heat to give 1-{[(3-nitroquinolin-4-yl)amino]methyl}cyclopentanol as yellow crystals (8.29 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006264B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-eb3c6cd45ab84406ab7635dd36d81043 |
| Source note | uspto-grants-2015_04 |