HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromobenzene → 2-(3-Bromo-phenyl)-6-dimethylamino-2H-isoquinolin-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-(Dimethylamino)-1,2-dihydroisoquinolin-1-one | HCID 57424142 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(3-Bromo-phenyl)-6-dimethylamino-2H-isoquinolin-1-one | HCID 59216430 | 61.9% |
Reaction Conditions
| Temperature | 150 °C |
|---|
Reaction Steps
6-Dimethylamino-2H-isoquinolin-1-one (39 mg, 0.21 mmol), cuprous iodide (8.0 mg, 0.041 mmol), and potassium carbonate (29 mg, 0.21 mmol) were deposited in sealed vessel. 3 mL DMSO and 1,3-dibromobenzene (98 mg, 0.42 mmol) were added. Argon was bubbled through the mixture for 2 minutes and the lid was tightly closed. This was heated at 150° C. for 5 hours. The resulting mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, concentrated in vacuo, and purified by flash chromatography (25% ethyl acetate/hexanes) to yield 2-(3-Bromo-phenyl)-6-dimethylamino-2H-isoquinolin-1-one (45 mg, 0.13 mmol). MS (ESI) 345.0 (M+H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299077B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-bd46e15f052346c892daece9c9f2f2ea |
| Source note | uspto-grants-2012_10 |