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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058631Generated: November 2, 2026

Hydrochloric Acid → 4-Amino-1-[2-(4-piperidyl)ethyl]-1h-imidazo[4,5-c]quinoline hydrochloride

https://huagongshe.com/reaction/1058631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 18668744HCID 18668744—
SolventWaterHCID 962—
Product4-Amino-1-[2-(4-piperidyl)ethyl]-1h-imidazo[4,5-c]quinoline hydrochlorideHCID 18668799—

Reaction Steps

A mixture of 1.57 g of tert-butyl 4-[2-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-1-piperidinecarboxylate and 40 ml of ethyl acetate solution of hydrogen chloride was stirred at room temperature for 5 hours. The reaction mixture was added with water, adjusted to pH 10 with 10% aqueous sodium hydroxide solution, and extracted with methylene chloride. The extract was dried, and the solvent was evaporated. The resulting residue was washed with ethyl acetate to give 1.01 g of pale brown crystals. The resulting crystals were purified by alumina column chromatography using methylene chloride—methanol (40:1 to 20:1) as eluting solvents, and washed with diisopropyl ether to give colorless crystals. Hydrochloride was prepared in a conventional method. Recrystallization from ethanol gave colorless crystals having the melting point of from 243 to 244° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518265B1
Source datasetuspto-grants-2003_02
ORD IDord-a1698816b7824719b956d51eafa72079
Source noteuspto-grants-2003_02