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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565764Generated: October 29, 2026

Norchlorcyclizine → N-(2-hydroxyethyl)-5-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamide

https://huagongshe.com/reaction/565764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorchlorcyclizineHCID 9340—
ReactantN-(2-hydroxyethyl)-5-chloropentanesulfonamideHCID 22111547—
SolventDiisopropylethylamineHCID 81531—
ProductN-(2-hydroxyethyl)-5-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamideHCID 6998822791.4%

Reaction Steps

1-[(4-Chlorophenyl)phenylmethyl]piperazine (573.6 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-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamide (877.0 mg) as a pale yellow oil (yield: 91.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-fcf8fd4d669e4a38b8c4e2ed41530e17
Source noteuspto-grants-2001_01