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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565768Generated: October 29, 2026

Norchlorcyclizine → HCID 69987898, compound

https://huagongshe.com/reaction/565768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorchlorcyclizineHCID 9340—
ReactantHCID 22111542HCID 22111542—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 69987898HCID 6998789893.2%

Reaction Steps

1-[(4-Chlorophenyl)phenylmethyl]piperazine (573.6 mg, 2.00 mmol) and N-(4-hydroxybutyl)-5-chloropentanesulfonamide (515.6 mg, 2.00 mmol) prepared in Preparation Example 23 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-(4-hydroxybutyl)-5-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamide (947.0 mg) as a pale yellow oil (yield: 93.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-7d3bb02f6cc841fb8361327f16c69661
Source noteuspto-grants-2001_01