HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130423Erstellt: 24. Oktober 2026
p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]benzenesulfonamide
https://huagongshe.com/reaction/130423
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Edukt | 5-(cis-3,5-Dimethyl-1-piperazinyl)-2-chloroaniline | HCID 59007078 | — |
| Lösungsmittel | Pyridine methylene chloride | HCID 21875418 | — |
| Produkt | 4-Bromo-N-[2-chloro-5-(cis-3,5-dimethyl-1-piperazinyl)phenyl]benzenesulfonamide | HCID 59007090 | — |
Reaktionsschritte
A solution of 5-(cis-3,5-dimethyl-1-piperazinyl)-2-chloroaniline (D34) (108 mg, 0.45 mmol) in pyridine:dichloromethane (1:1, 4 ml) was treated with 4-bromobenzenesulfonyl chloride (138 mg, 0.54 mmol). The solution was stirred at room temperature for 2 hours, quenched with methanol and concentrated in vacuo. The residue was applied to a SCX cartridge (Varian bond-elute, 5 g) and washed with methanol and 2M ammonia in methanol. The combined basic fractions were concentrated in vacuo and the resulting residue was purified by column chromatography (FlashMaster) (dichloromethane to 5% methanol:dichloromethane) to afford some pure product. The impure fractions were purified further by MDAP, and combined with the above pure product to afford the title product (D35). MS (ES+) m/e 458/460/462 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07381728B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-f07f4d9910774fc9810990896b77eba6 |
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| Quellennotiz | uspto-grants-2008_06 |
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