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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598329Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 86626167, compound

https://huagongshe.com/reaction/598329

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 numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-5202d788ee53422682cc7f6c08c5ed83
Source noteuspto-grants-2011_03