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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203488Generated: November 2, 2026

Triethylamine → 8-benzyloxy-2-ethoxymethyl-1-propyl-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/2203488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(6-benzyloxy-4-propylaminoquinolin-3-yl)-2-ethoxyacetamide hydrochlorideHCID 67051145—
SolventEthanolHCID 702—
Product8-benzyloxy-2-ethoxymethyl-1-propyl-1H-imidazo[4,5-c]quinolineHCID 67051127101.8%

Reaction Steps

Triethylamine (22.16 mL, 159.0 mmol) was added to a solution of N-(6-benzyloxy-4-propylaminoquinolin-3-yl)-2-ethoxyacetamide hydrochloride (16.1 g) in ethanol (265 mL), and the reaction mixture was heated at reflux and stirred for 3 hours. The reaction mixture was allowed to cool to ambient temperature. The ethanol was removed under reduced pressure and the residue dissolved in chloroform. The resulting solution was washed sequentially with water and brine, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting oil was dissolved in acetonitrile and concentrated under reduced pressure to yield 14.32 g of 8-benzyloxy-2-ethoxymethyl-1-propyl-1H-imidazo[4,5-c]quinoline as a brown, crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365567B2
Source datasetuspto-grants-2016_06
ORD IDord-0abb015f48b241aead03b29cb755c79c
Source noteuspto-grants-2016_06