HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-[(7-Bromo-3-nitroquinolin-4-yl)amino]propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | 7-Bromo-4-chloro-3-nitroquinoline | HCID 21984361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[(7-Bromo-3-nitroquinolin-4-yl)amino]propan-1-ol | HCID 66619878 | 129.3% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a round-bottomed flask containing 7-bromo-4-chloro-3-nitroquinoline (60 g, 209.1 mmol) was added DMF (390 mL) and triethylamine (44 mL, 313.6 mmol) and the solution was stirred at 0° C. in an ice-bath. To this cooled solution was added 3-aminopropan-1-ol (17.6 mL, 230.0 mmol) and the reaction was stirred at ambient temperature overnight. The solvent was removed under reduced pressure and the resultant orange solid was recrystallized from ethyl acetate (800 mL). The product was separated by filtration and the solids were washed with diethyl ether and dried under reduced pressure to afford crude 3-[(7-bromo-3-nitroquinolin-4-yl)amino]propan-1-ol (88.15 g) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088788B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-e30229a339e04112b68726aaf712bbc4 |
| Source note | uspto-grants-2012_01 |