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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Bis(4-fluorophenyl)methyl)piperazine | HCID 152932 | — |
| Reactant | N-cyclopropyl-6-chlorohexanesulfonamide | HCID 11010063 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | N-cyclopropyl-6-[4-[bis(4-fluorophenyl)methyl]1-piperazinyl]hexanesulfonamide | HCID 15895712 | 94.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172228B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-4674244ea3fc4018a68902967da3090b |
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| Source note | uspto-grants-2001_01 |
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