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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229657Generated: October 29, 2026

Sodium Iodide → 3-(2-Cyanophenyl)-5-(2-pyridyl)-2(1H)-pyridone

https://huagongshe.com/reaction/229657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(2-Cyanophenyl)-5-(2-pyridyl)-2-methoxypyridineHCID 22319089—
SolventAcetonitrileHCID 6342—
Product3-(2-Cyanophenyl)-5-(2-pyridyl)-2(1H)-pyridoneHCID 2231894557.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563811B2
Source datasetuspto-grants-2009_07
ORD IDord-c1166e3b660d48e5b6f263e265c9facd
Source noteuspto-grants-2009_07