HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565765Generated: October 30, 2026
Norchlorcyclizine → HCID 69989469, compound
https://huagongshe.com/reaction/565765
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Norchlorcyclizine | HCID 9340 | — |
| Reactant | HCID 22111543 | HCID 22111543 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 69989469 | HCID 69989469 | 91.6% |
Reaction Steps
1-[(4-Chlorophenyl)phenylmethyl]piperazine (505.9 mg, 1.76 mmol) and N-(3-hydroxypropyl)-6-chlorohexanesulfonamide (500.0 mg, 1.94 mmol) 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-(3-hydroxypropyl)-6-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]hexanesulfonamide (819.3 mg) as a pale yellow oil (yield based on 1-[(4-chlorophenyl)phenylmethyl]piperazine: 91.4%).
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-9393937f1f9443cc869f678f9dc48b42 |
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| Source note | uspto-grants-2001_01 |
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