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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921352Generated: October 27, 2026

Sodium Iodide → 3-ethyl-6-methyl-5-(1,3,4-oxadiazol-2-yl)-1H-pyridin-2-one

https://huagongshe.com/reaction/1921352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3-Ethyl-2-methoxy-6-methyl-5-[1,3,4]oxadiazol-2-yl-pyridineHCID 11637132—
SolventAcetonitrileHCID 6342—
Product3-ethyl-6-methyl-5-(1,3,4-oxadiazol-2-yl)-1H-pyridin-2-oneHCID 13599098021.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 3-ethyl-2-methoxy-6-methyl-5-[1,3,4]oxadiazol-2-yl-pyridine (10 mg, 0.0457 mmol) and sodium iodide (19 mg, 0.127 mmol) under a nitrogen atmosphere is added anhydrous acetonitrile (2 mL) followed by chlorotrimethylsilane (16.4 μL, 0.131 mmol). The reaction mixture is stirred at 50° C. under nitrogen for 2.5 hr. The reaction mixture is allowed to cool and then quenched with water (0.1 mL). After stirring for 30 min, the mixture is evaporated. The crude residue is purified by flash chromatography on a 2-gram silica gel cartridge by elution with dichloromethane:methanol (49:1). The fraction containing the product is evaporated to give 3-ethyl-6-methyl-5-(1,3,4-oxadiazol-2-yl)-1H-pyridin-2-one (2 mg, 21% yield) as a white solid. LC/MS: RT: 1.98 min, MS: m/e=206 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173682B2
Source datasetuspto-grants-2012_05
ORD IDord-dd270799250b46bea2ae30fedaa4bb1e
Source noteuspto-grants-2012_05