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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105500Generated: October 30, 2026

Triethylamine → 2-[(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)oxy]acetamide

https://huagongshe.com/reaction/2105500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromoacetamideHCID 69632—
Reactant2-propyl-1H-imidazo[4,5-c]quinolin-1-olHCID 67506948—
SolventTetrahydrofuranHCID 8028—
Product2-[(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)oxy]acetamideHCID 6750698083.9%

Reaction Steps

A solution of 2-propyl-1H-imidazo[4,5-c]quinolin-1-ol (2.0 g, 8.8 mmol), bromoacetamide (1.9 g, 14 mmol), and triethylamine (2.8 mL, 0.020 mol) in THF (100 mL) was heated at reflux overnight. The solvent was removed under reduced pressure, and dichloromethane (75 mL) and saturated aqueous sodium bicarbonate (25 mL) were added to the residue. The resulting mixture was filtered to provide 2.1 g of 2-[(2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)oxy]acetamide as a solid. The organic layer was separated, and methanol was added until all solids were dissolved. The solution was then dried over potassium carbonate, filtered, and concentrated under reduced pressure to provide an additional 0.13 g of material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579359B2
Source datasetuspto-grants-2009_08
ORD IDord-cb390c5089a544359f5c8a94ea2b5417
Source noteuspto-grants-2009_08