HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)oxy]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromoacetamide | HCID 69632 | — |
| Reactant | 2-propyl-1H-imidazo[4,5-c]quinolin-1-ol | HCID 67506948 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)oxy]acetamide | HCID 67506980 | 83.9% |
Reaction Steps
A solution of 2-propyl-1H-imidazo[4,5-c]quinolin-1-ol (2.0 g, 8.8 mmol), bromoacetamide (1.9 g, 14 mmol), and triethylamine (2.8 mL, 0.020 mol) in THF (100 mL) was heated at reflux overnight. The solvent was removed under reduced pressure, and dichloromethane (75 mL) and saturated aqueous sodium bicarbonate (25 mL) were added to the residue. The resulting mixture was filtered to provide 2.1 g of 2-[(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)oxy]acetamide as a solid. The organic layer was separated, and methanol was added until all solids were dissolved. The solution was then dried over potassium carbonate, filtered, and concentrated under reduced pressure to provide an additional 0.13 g of material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579359B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-cb390c5089a544359f5c8a94ea2b5417 |
| Source note | uspto-grants-2009_08 |