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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565782Generated: October 29, 2026

Norchlorcyclizine → N,N-diethyl-5-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamide

https://huagongshe.com/reaction/565782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorchlorcyclizineHCID 9340—
ReactantHCID 22111600HCID 22111600—
SolventDiisopropylethylamineHCID 81531—
ProductN,N-diethyl-5-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamideHCID 6998800292%

Reaction Steps

1-[(4-Chlorophenyl)phenylmethyl]piperazine (573.6 mg, 2.00 mmol) and N,N-diethyl-5-chloropentanesulfonamide (531.9 mg, 2.20 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 (50:1), to give N,N-diethyl-5-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamide (905.2 mg) as a yellow oil (yield based on 1-[(4-chlorophenyl)phenylmethyl]piperazine: 92.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-049ca5c65e9643d1b9d2571dbe168274
Source noteuspto-grants-2001_01