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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895783Generated: October 30, 2026

Thionyl Chloride → HCID 22381773, compound

https://huagongshe.com/reaction/895783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13007357HCID 13007357—
ReactantEthylacetate methanolHCID 21584119—
SolventWaterHCID 962—
ProductHCID 22381773HCID 22381773—

Reaction Steps

Thionyl chloride (5 mL) and 4-amino-2-ethoxymethyl-1H-imidazo[4,5-c]quinoline1-ethanol (1 g) were combined and heated on a steam bath until thin layer chromatography (20% methanol/ethyl acetate) showed the disappearance of starting material. The reaction mixture was cooled to ambient temperature and then slowly poured into a mixture of ice and water. The mixture was neutralized with sodium bicarbonate and then extracted 3 times with dichloromethane. The extracts were combined, washed 3 times with aqueous sodium bicarbonate, dried with magnesium sulfate, filtered and then concentrated under vacuum. Acetone (about 10 mL) was added to the residue followed by methanolic hydrogen chloride (about 1 mL). The mixture was refluxed and a precipitate formed. The reaction mixture was cooled to ambient temperature. The precipitate was isolated by filtration and then washed with acetone. The solid was dissolved in hot methanol and then precipitated by the addition of acetone. The precipitate was isolated by filtration, washed with water and then dried to provide 1-(2-chloroethyl)-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-4-amine hydrochloride. Analysis:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916925B1
Source datasetuspto-grants-2005_07
ORD IDord-4ed2f667d2fb45b2ae55f6405ed30b7a
Source noteuspto-grants-2005_07