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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119877Generated: November 2, 2026

Methyl iodide → HCID 10268853, compound

https://huagongshe.com/reaction/2119877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 9996503HCID 9996503—
ProductHCID 10268853HCID 1026885316%

Reaction Steps

Sodium hydride (0.32 g; 10.1 mmol) was added to a suspension of 4-amino-α-butyl-1-(2-methylpropyl)-1H-imidazo[4,5-c]quinoline-2-methanol (3 g; 9.2 mmol, Example 60) and the resulting mixture was stirred for about 2 hours. Methyl iodide (0.82 mL; 13.8 mmol) was added to the mixture and stirring was continued overnight. Thin layer chromatography indicated that the reaction was incomplete so sodium hydride (0.25 g) was added followed two hours later by methyl iodide (1 mL). The reaction was stirred for several additional hours then quenched with water and diluted with ethyl acetate. The organic layer was separated, washed with water, dried over magnesium sulfate and concentrated under vacuum to provide an oil. The oil was purified by silica gel chromatography (1-3% methanol in methylene chloride as eluent) to provide 0.5 g of a solid, m.p. 125-128° C. Analysis: Calculated: C, 70.55; H, 8.3; %N, 16.5; Found: C, 70.2; H, 8.3; N, 16.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686472B2
Source datasetuspto-grants-2004_02
ORD IDord-41329b3ba48b41029c9aea4e29513793
Source noteuspto-grants-2004_02