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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565775Generated: October 27, 2026

1-[Bis(4-chlorophenyl)methyl]piperazine → N-(2-hydroxyethyl)-5-[4-[bis(4-chlorophenyl)methyl]-1-piperazinyl]pentanesulfonamide

https://huagongshe.com/reaction/565775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[Bis(4-chlorophenyl)methyl]piperazineHCID 285510—
ReactantN-(2-hydroxyethyl)-5-chloropentanesulfonamideHCID 22111547—
SolventDiisopropylethylamineHCID 81531—
ProductN-(2-hydroxyethyl)-5-[4-[bis(4-chlorophenyl)methyl]-1-piperazinyl]pentanesulfonamideHCID 2211152997.5%

Reaction Steps

1-[Bis(4-chlorophenyl)methyl]piperazine (642.5 mg, 2.00 mmol) and N-(2-hydroxyethyl)-5-chloropentanesulfonamide (459.5 mg, 2.00 mmol) were refluxed in N-ethyldiisopropylamine (2 ml) for 6 hours. The reaction mixture was concentrated in vacuo, and water was added thereto. The mixture was extracted with chloroform. The chloroform layer was washed with water, and dried over anhydrous magnesium sulfate. Subsequently, the solvent was removed by evaporation in vacuo. The resulting crude product was purified by column chromatography on silica gel with chloroform-methanol (20:1), to give N-(2-hydroxyethyl)-5-[4-[bis(4-chlorophenyl)methyl]-1-piperazinyl]pentanesulfonamide (1003.0 mg) as a pale brown oil (97.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-3bc5285e719046eebe360e2e043ea2d6
Source noteuspto-grants-2001_01