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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274391Generated: October 31, 2026

Methyl iodide → HCID 15224434, compound

https://huagongshe.com/reaction/274391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15224433HCID 15224433—
SolventDimethylformamideHCID 6228—
ProductHCID 15224434HCID 1522443443.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

α-Methyl-1-(2-methylpropyl)-1H-imidazo[4,5c]quinoline-2-ethanol (6.5 g, 23 mmol, Example 74) was dissolved in N,N-dimethylformamide (50 mL) then cooled to 0° C. Sodium hydride (0.8 g, 25 mmol), 80% dispersion in mineral oil) was added and the resulting mixture was stirred at 0° C. for about 1 hour. Methyl iodide (2.2 mL, 34 mmol) was added and the resulting mixture was stirred at 0° C. for about 1 hour and then allowed to warm to room temperature. The reaction was quenched with water and then diluted with ethyl acetate. The organic layer was separated, washed several times with water, dried over magnesium sulfate then concentrated under vacuum. The resulting residue was purified by silica gel chromatography using 2-5% methanol in methylene chloride to give about 3 g of the desired product. The structure was confirmed by nuclear magnetic resonance spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389640
Source datasetuspto-grants-1995_02
ORD IDord-4c266a0363c74b289c65cea45d8999c0
Source noteuspto-grants-1995_02