Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223905Generated: October 29, 2026

4-Chlorobenzenesulfonyl chloride → HCID 69146664, compound

https://huagongshe.com/reaction/2223905

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantDabcoHCID 9237—
ReactantHCID 23109894HCID 23109894—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 69146664HCID 6914666465%

Reaction Steps

To a solution of N-[1-[2-[1-(2-aminoethyl)cyclohexyl]ethyl]piperidin-4-yl]-N-(p-tolyl)-2-furancarboxamide (synthesized in Example 18) (199 mg) in dichloromethane (3 mL) were added 1,4-diazabicyclo[2.2.2]octane (100 mg) and p-chlorobenzenesulfonyl chloride (100 mg) successively. The solution was stirred at room temperature for 2 hours. The reaction solution was diluted with chloroform, washed in turn with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The resulting residue was purified by chromatography [NH silica gel, hexane-ethyl acetate (7:3)] to give the title compound (181 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375115B2
Source datasetuspto-grants-2008_05
ORD IDord-3a0cb6c1827e45f693c66d2ea93240ef
Source noteuspto-grants-2008_05