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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1379188Generated: November 1, 2026

Ethyl Acetate → (2R)-4-benzyl-1-(3,5-dichlorobenzoyl)-2-(1H-indol-3-yl-methyl)piperazine

https://huagongshe.com/reaction/1379188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Dichlorobenzoyl chlorideHCID 76191—
Reactant(3R)-1-benzyl-3-(1H-indol-3-yl-methyl)piperazineHCID 53910379—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(2R)-4-benzyl-1-(3,5-dichlorobenzoyl)-2-(1H-indol-3-yl-methyl)piperazineHCID 54039029—

Reaction Steps

To an ice-cooled mixture of (3R)-1-benzyl-3-(1H-indol-3-yl-methyl)piperazine (305 mg) and potassium carbonate (207 mg) in dimethylformamide (1 ml) was added 3,5-dichlorobenzoyl chloride (210 mg). The mixture was stirred at room temperature for 1 hour. Ethyl acetate and water were added. The organic layer was washed successively with aqueous sodium bicarbonate solution and brine and dried over magnesium sulfate. After evaporation of the solvent, the residue was dissolved in ethyl ether. After insoluble material was removed by filtration, the filtrate was concentrated under reduced pressure and the residue was triturated with diisopropyl ether, collected by filtration and dried to give (2R)-4-benzyl-1-(3,5-dichlorobenzoyl)-2-(1H-indol-3-yl-methyl)piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05670505
Source datasetuspto-grants-1997_09
ORD IDord-fe275ec4e18b4f1291b13ac100ee79a1
Source noteuspto-grants-1997_09