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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493567Generated: October 30, 2026

Methyl iodide → 3-Fluoro-6-(methylamino)pyridine

https://huagongshe.com/reaction/493567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-5-fluoropyridineHCID 2737701—
SolventTetrahydrofuranHCID 8028—
Product3-Fluoro-6-(methylamino)pyridineHCID 5914966723%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a suspension of sodium hydride (60% dispersion in mineral oil, 117.8 mg, 4.91 mmol) in tetrahydrofuran (25 ml) was added a solution of 5-fluoropyridin-2-amine (500 mg, 4.46 mmol) in tetrahydrofuran (25 ml) at room temperature and the reaction mixture was stirred at 40° C. for 30 min. Then to the reaction mixture was added methyl iodide (696.9 mg, 4.91 mmol) at −40° C. and the resulting mixture was stand at room temperature overnight with stirring. The reaction was quenched by the addition of water and whole mixture was extracted with ethyl acetate. The organic extracts were dried over sodium sulfate and concentrated. The residue was purified by flush column chromatography on silica gel eluting with hexane/ethyl acetate (4/1) to afford 129 mg (23%) of the title compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534914B2
Source datasetuspto-grants-2009_05
ORD IDord-5683dfbb5d5c486ca1c7092525a6739e
Source noteuspto-grants-2009_05