HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 6-Bromo-3-methoxyisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 178515305 | HCID 178515305 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-3-methoxyisoquinoline | HCID 67491807 | 14% |
Reaction Steps
A mixture of 6-bromoisoquinolin-3-ol (606 mg, 2.70 mmol), silver carbonate (1.5 g, 5.3 mmol), and N,N-dimethylformamide (12 mL) was stirred at room temperature for 16 minutes. Methyl iodide (186 μL, 2.97 mmol) was added and the reaction was left stirring for 18 hours. The reaction was diluted with methanol and filtered through Celite. The filtrate was concentrated and purified by flash column chromatography to give the title compound (90 mg, 14%). +ESI (M+H+1) 240.0; 1H NMR (400 MHz, CDCl3, δ): 8.91 (s, 1H), 7.86 (d, J=1.8 Hz, 1H), 7.73 (d, J=8.8 Hz, 1H), 7.43 (dd, J=8.8, 1.8 Hz, 1H), 6.90 (s, 1H), 4.02 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859773B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-61986a3b268e42caa8bbcfa328359dbc |
| Source note | uspto-grants-2014_10 |