HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 3-(2-Cyanophenyl)-5-(2-pyridyl)-2(1H)-pyridone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(2-Cyanophenyl)-5-(2-pyridyl)-2-methoxypyridine | HCID 22319089 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-(2-Cyanophenyl)-5-(2-pyridyl)-2(1H)-pyridone | HCID 22318945 | 57.8% |
Reaction Steps
Chlorotrimethylsilane (0.1 ml) was added to a suspension of 0.20 g of 3-(2-cyanophenyl)-5-(2-pyridyl)-2-methoxypyridine and 0.12 g of sodium iodide in 10 ml of acetonitrile and the mixture was stirred at room temperature for 3 hours. A saturated sodium bicarbonate solution was added to the mixture followed by extracting with ethyl acetate. The ethyl acetate layer was washed with water and a saturated saline solution and dried over magnesium sulfate. The solvent was concentrated in vacuo and the residue was purified by a silica gel column chromatography (ethyl acetate:hexane=1:1) to give 0.11 g of the title compound in pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07563811B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-c1166e3b660d48e5b6f263e265c9facd |
| Source note | uspto-grants-2009_07 |