HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-cyclopropyl-6-[4-[(3-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-[(3-Chlorophenyl)phenylmethyl]piperazine | HCID 4564525 | — |
| Reactant | N-cyclopropyl-6-chlorohexanesulfonamide | HCID 11010063 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-cyclopropyl-6-[4-[(3-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide | HCID 15895709 | 51.8% |
Reaction Steps
1-[(3-Chlorophenyl)phenylmethyl]piperazine (543.7 mg, 1.90 mmol) and N-cyclopropyl-6-chlorohexanesulfonamide (500 mg, 2.09 mmol) were refluxed in toluene (15 ml) in the presence of triethylamine (211 mg, 2.09 mmol) for 48 hours. The reaction mixture was washed with water, and the organic layer was 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-[(3-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide (482.7 mg) as an oil (yield based on 1-[(3-chlorophenyl)phenylmethyl]piperazine: 52.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172228B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-14110c8072074ccda7f89bcaddc1e73c |
| Source note | uspto-grants-2001_01 |