HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 1-Chloro-7-fluoro-4-ethoxyisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Chloro-7-fluoroisoquinolin-4-OL | HCID 71742716 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Chloro-7-fluoro-4-ethoxyisoquinoline | HCID 86683267 | 70.1% |
Reaction Steps
To a solution of 1-chloro-7-fluoroisoquinolin-4-ol (0.5 g, 2.53 mmol) in acetonitrile (10 ml) was added K2CO3 (700 mg, 5.06 mmol) followed by ethyl iodide (475 mg, 3.04 mmol) at room temperature. The reaction mixture was stirred at room temperature for overnight. The solvent was evaporated under reduced pressure and the residue was diluted with water and extracted with ethyl acetate. The combined organic layer was dried over anhydrous Na2SO4 and evaporated under reduced pressure to get crude compound. The crude compound was purified by silica gel chromatography to get 1-chloro-7-fluoro-4-ethoxyisoquinoline (400 mg 70%) as off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957203B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-7a9115e8fdb0409d93bf4d00ba942886 |
| Source note | uspto-grants-2015_02 |