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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565765Generated: October 30, 2026

Norchlorcyclizine → HCID 69989469, compound

https://huagongshe.com/reaction/565765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorchlorcyclizineHCID 9340—
ReactantHCID 22111543HCID 22111543—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 69989469HCID 6998946991.6%

Reaction Steps

1-[(4-Chlorophenyl)phenylmethyl]piperazine (505.9 mg, 1.76 mmol) and N-(3-hydroxypropyl)-6-chlorohexanesulfonamide (500.0 mg, 1.94 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-(3-hydroxypropyl)-6-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide (819.3 mg) as a pale yellow oil (yield based on 1-[(4-chlorophenyl)phenylmethyl]piperazine: 91.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-9393937f1f9443cc869f678f9dc48b42
Source noteuspto-grants-2001_01