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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459402Generated: October 31, 2026

Methyl iodide → HCID 53985471, compound

https://huagongshe.com/reaction/1459402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 53924158HCID 53924158—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53985471HCID 5398547138.1%

Reaction Steps

To a well-stirred suspension of N-adamantan-1-yl-2-hydroxymethyl-3-pyridin-4-yl-2-pyridin-4-ylmethyl-propionamide (40 mg, 0.1 mmol) in anhydrous tetrahydrofuran (0.50 ml), sodium hydride (7.8 mg of 60% mineral oil dispersion; 0.2 mmol of sodium hydride) was added. After stirring at ambient temperature for 30 minutes, methyl iodide (12.5 μl, 0.2 mmol) was added. After stirring for 2 hours at ambient temperature, the reaction was quenched by the addition of water/methylene chloride (10 ml of each). The mixture was then extracted twice with 10 ml portions of methylene chloride. The combined organic extracts were dried (anhydrous sodium sulfate) and concentrated in vacuo to an oil (60 mg). Flash chromatography of the entire sample (silica gel, 40 micron mesh; elution with methanol/ethyl acetate=1:9 in volume) afforded the title compound (free base) as an amorphous solid (16 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854232
Source datasetuspto-grants-1998_12
ORD IDord-c24baa278c494a269b425deb81489b62
Source noteuspto-grants-1998_12