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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992588Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 68536238, compound

https://huagongshe.com/reaction/1992588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium HydroxideHCID 14923—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68536377HCID 68536377—
SolventChloroformHCID 6212—
ProductHCID 68536238HCID 68536238—

Reaction Steps

To a solution of 2-{2-[2-(2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethoxy}-1H-isoindole-1,3(2H)-dione (11.0 g, 25.5 mmol) in chloroform (150 mL) was added mCPBA (11.4 g, 51.1 mmol). The solution was stirred at room temperature for 2 hours. Concentrated ammonium hydroxide (100 mL) was added, followed by p-toluenesulfonyl chloride (5.40 g, 28.1 mmol). The mixture was stirred overnight at room temperature. The mixture was transferred to a separatory funnel and was washed twice with 5% aqueous ammonium chloride and once with aqueous sodium carbonate solution, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude product was purified by flash chromatography (silica gel, gradient elution with 0-5% methanol in dichloromethane) to provide 6 g of 1-{2-[2-(aminooxy)ethoxy]ethyl}-2-ethyl-1H-imidazo[4,5-c]quinolin-4-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648997B2
Source datasetuspto-grants-2010_01
ORD IDord-dc2598efb33c4e3292f194f7e157550f
Source noteuspto-grants-2010_01