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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565762Generated: October 29, 2026

Norchlorcyclizine → N-(2-hydroxyethyl)-6-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide

https://huagongshe.com/reaction/565762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorchlorcyclizineHCID 9340—
ReactantN-(2-hydroxyethyl)-6-chlorohexanesulfonamideHCID 22111640—
SolventDiisopropylethylamineHCID 81531—
ProductN-(2-hydroxyethyl)-6-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamideHCID 2211162591.5%

Reaction Steps

1-[(4-Chlorophenyl)phenylmethyl]piperazine (573.6 mg, 2.00 mmol) and N-(2-hydroxyethyl)-6-chlorohexanesulfonamide (487.5 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)-6-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide (904.4 mg) as a pale yellow oil (yield: 91.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-548ed8fe35e142549263e53605d650aa
Source noteuspto-grants-2001_01