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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383157Generated: October 31, 2026

4-Toluenesulfonyl chloride → HCID 86626167, compound

https://huagongshe.com/reaction/2383157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium HydroxideHCID 14923—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 86626166HCID 86626166—
SolventChloroformHCID 6212—
ProductHCID 86626167HCID 86626167—

Reaction Steps

mCPBA (10.6 g, 33.7 mmol) was added in one portion to a solution of tert-butyl[4-(7-benzyloxy-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]carbamate (16.0 g, 33.7 mmol) in chloroform (270 mL). After the reaction was stirred for 1.5 hours, ammonium hydroxide (270 mL) was added. The mixture was stirred for 15 minutes, and p-toluenesulfonyl chloride (6.42 g, 33.7 mmol) was added in three portions. The reaction was stirred for 18 hours. The layers were separated, and the aqueous layer was extracted with dichloromethane. The combined organic fractions were washed with water and brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was recrystallized from acetonitrile to afford 9.73 g of tert-butyl[4-(4-amino-7-benzyloxy-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]carbamate as a gray powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263594B2
Source datasetuspto-grants-2012_09
ORD IDord-c0e3486ba407473caeece47b452ace24
Source noteuspto-grants-2012_09