HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565768Generated: October 29, 2026
Norchlorcyclizine → HCID 69987898, compound
https://huagongshe.com/reaction/565768
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Norchlorcyclizine | HCID 9340 | — |
| Reactant | HCID 22111542 | HCID 22111542 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 69987898 | HCID 69987898 | 93.2% |
Reaction Steps
1-[(4-Chlorophenyl)phenylmethyl]piperazine (573.6 mg, 2.00 mmol) and N-(4-hydroxybutyl)-5-chloropentanesulfonamide (515.6 mg, 2.00 mmol) prepared in Preparation Example 23 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-(4-hydroxybutyl)-5-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]pentanesulfonamide (947.0 mg) as a pale yellow oil (yield: 93.2%).
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-7d3bb02f6cc841fb8361327f16c69661 |
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| Source note | uspto-grants-2001_01 |
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