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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547291Generated: October 30, 2026

m-Chloroperbenzoic acid → 2-butyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinoline 5-oxide

https://huagongshe.com/reaction/547291

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-butyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinolineHCID 67203643—
SolventChloroformHCID 6212—
Product2-butyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinoline 5-oxideHCID 67203499—

Reaction Steps

Solid 3-chloroperoxybenzoic acid (2.1 g of ˜60%) was added in portions over a period of 3 minutes to a solution of 2-butyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinoline (2.7 g, 7.2 mmol) in chloroform (72 μL). The reaction mixture was stirred at ambient temperature for 30 minutes then additional 3-chloroperoxybenzoic acid (0.4 g) was added. The reaction mixture was stirred at ambient temperature for 15 minutes and then partitioned between dichloromethane (100 mL) and saturated aqueous sodium carbonate (50 mL). The organic layer was washed sequentially with saturated aqueous sodium carbonate (50 mL) and brine (50 mL), dried over anhydrous sodium sulfate, filtered, and then concentrated under reduced pressure to provide 2-butyl-1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-1H-imidazo[4,5-c]quinoline 5-oxide as an orange foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939526B2
Source datasetuspto-grants-2011_05
ORD IDord-89708cfacac24778abb892d372d0c31c
Source noteuspto-grants-2011_05