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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565751Generated: October 28, 2026

1-(Bis(4-fluorophenyl)methyl)piperazine → N-cyclopropyl-6-[4-[bis(4-fluorophenyl)methyl]1-piperazinyl]hexanesulfonamide

https://huagongshe.com/reaction/565751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
ReactantN-cyclopropyl-6-chlorohexanesulfonamideHCID 11010063—
SolventDiisopropylethylamineHCID 81531—
ProductN-cyclopropyl-6-[4-[bis(4-fluorophenyl)methyl]1-piperazinyl]hexanesulfonamideHCID 1589571294.7%

Reaction Steps

1-[Bis(4-fluorophenyl)methyl]piperazine (8.92 g, 30.0 mmol) and N-cyclopropyl-6-chlorohexanesulfonamide (7.91 g, 33.0 mmol) were refluxed in N-ethyldiisopropylamine (20 ml) for 8 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 (50:3), to give N-cyclopropyl-6-[4-[bis(4-fluorophenyl)methyl]1-piperazinyl]hexanesulfonamide (13.97 g) as a crystalline substance (yield based on 1-[bis(4-fluorophenyl)methyl]piperazine: 94.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172228B2
Source datasetuspto-grants-2001_01
ORD IDord-4674244ea3fc4018a68902967da3090b
Source noteuspto-grants-2001_01