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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540890Generated: October 31, 2026

4-Toluenesulfonyl chloride → HCID 58833631, compound

https://huagongshe.com/reaction/540890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium HydroxideHCID 14923—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68972752HCID 68972752—
SolventChloroformHCID 6212—
ProductHCID 58833631HCID 58833631—

Reaction Steps

A stirred solution of tert-butyl 4-{[2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}piperidine-1-carboxylate (9.77 g, 20.8 mmol) in chloroform (175 mL) at room temperature was treated with mCPBA (55% pure, 6.54 g, 20.8 mmol). After 45 minutes, concentrated ammonium hydroxide (175 mL) was added, followed by p-toluenesulfonyl chloride (3.97 g, 20.8 mmol). The mixture was stirred for 62 hours, then the layers were separated and the aqueous layer was extracted with chloroform. The combined organic layers were washed with water and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The crude product was purified by flash chromatography (silica gel, gradient elution with 1.5-12.5% CMA in chloroform) followed by recrystallization from acetonitrile to afford 6.3 g of tert-butyl 4-{[4-amino-2-(2-methoxyethyl)-1-propyl-1H-imidazo[4,5-c]quinolin-7-yl]oxy}piperidine-1-carboxylate as tan crystals, mp 173-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871782B2
Source datasetuspto-grants-2014_10
ORD IDord-d8b1429c4bd346dbb0dd09f397537df4
Source noteuspto-grants-2014_10