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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105480Generated: October 30, 2026

O-ethylhydroxylamine hydrochloride → 1-ethoxy-1H-imidazo[4,5-c]quinoline

https://huagongshe.com/reaction/2105480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ethylhydroxylamine hydrochlorideHCID 76850—
ReactantN-(4-chloroquinolin-3-yl)formamideHCID 86227468—
SolventIsopropanolHCID 3776—
Product1-ethoxy-1H-imidazo[4,5-c]quinolineHCID 6750695547.9%

Reaction Steps

A solution of 4-chloroquinolin-3-ylformamide (5.0 g, 24 mmol), O-ethylhydroxylamine hydrochloride (2.95 g, 30.2 mmol), and isopropanol (75 mL) was heated at reflux overnight, allowed to cool to room temperature, and concentrated under reduced pressure. The residue was stirred with dichloromethane (150 mL) and saturated aqueous sodium carbonate (50 mL) for 15 minutes. The organic layer was separated and dried over potassium carbonate, filtered, and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel (eluting with 2% methanol in dichloromethane containing 5 mL of aqueous ammonium hydroxide per liter of eluent) to provide 2.45 g of 1-ethoxy-1H-imidazo[4,5-c]quinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579359B2
Source datasetuspto-grants-2009_08
ORD IDord-a91af1a69f174bea8db4f7f02889b41c
Source noteuspto-grants-2009_08