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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021308Generated: November 3, 2026

Methyl iodide → HCID 68310279, compound

https://huagongshe.com/reaction/1021308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86686247HCID 86686247—
SolventDimethylformamideHCID 6228—
ProductHCID 68310279HCID 6831027963.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

5-({1-[2-Fluoro-3-(hydroxymethyl)phenyl]azetidin-3-yl}oxy)pyridin-2(1H)-one (160 mg) was mixed with DMF (3 ml), and methyl iodide (114 mg) and potassium carbonate (200 mg) were added thereto, followed by stirring at 60° C. for 2 hours. The reaction mixture was concentrated under reduced pressure, and to the residue were added CHCl3 and water. The organic layer was dried over Na2SO4 and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (CHCl3/MeOH) to obtain 5-({1-[2-fluoro-3-(hydroxymethyl)phenyl]azetidin-3-yl}oxy)-1-methylpyridin-2(1H)-one (106 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716470B2
Source datasetuspto-grants-2014_05
ORD IDord-7b633453f48246d99f592f761335c28f
Source noteuspto-grants-2014_05