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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611765Generated: November 1, 2026

Sodium hydride → 1-{2-[3-(benzyloxy)propoxy]ethyl}-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/1611765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzyl 3-Bromopropyl EtherHCID 2776064—
Reactant2-[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethanolHCID 13007355—
SolventDimethylformamideHCID 6228—
Product1-{2-[3-(benzyloxy)propoxy]ethyl}-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolineHCID 2225444129%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 2-[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethanol (1.0 g, 3.7 mmol) in N,N-dimethylformamide was added dropwise to a suspension of sodium hydride (0.19 g of a 60% dispersion in mineral oil, 4.8 mmol) in N,N-dimethylformamide (20 ml). The reaction was maintained for 2 hours followed by the dropwise addition of benzyl 3-bromopropyl ether (0.72 ml, 4.1 mmol). The reaction was stirred overnight at 100° C., quenched by pouring over ice, and extracted with ethyl acetate. The organic fractions were washed with water, dried (MgSO4), filtered, and concentrated. The crude product was purified by flash column chromatography (silica gel, 4:1 ethyl acetate/hexanes) to provide 0.45 g of 1-{2-[3-(benzyloxy)propoxy]ethyl}-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinoline as a brown oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06989389B2
Source datasetuspto-grants-2006_01
ORD IDord-90f63ad9da4f48d2bfe9f81ac277c810
Source noteuspto-grants-2006_01