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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565748Generated: October 30, 2026

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

https://huagongshe.com/reaction/565748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorchlorcyclizineHCID 9340—
ReactantN-cyclopropyl-6-chlorohexanesulfonamideHCID 11010063—
SolventDiisopropylethylamineHCID 81531—
ProductN-cyclopropyl-6-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamideHCID 987018190.1%

Reaction Steps

1-[(4-Chlorophenyl)phenylmethyl]piperazine (3.00 g, 10.46 mmol) and N-cyclopropyl-6-chlorohexanesulfonamide (2.76 g, 11.51 mmol) were refluxed in N-ethyldiisopropylamine (8 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-cyclopropyl-6-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide (4.62 g) as an oil (yield based on 1-[(4-chlorophenyl)phenylmethyl]piperazine: 90.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-35ba207b2d3e49259db59c8071a7b479
Source noteuspto-grants-2001_01