HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1868127Erstellt: 26. Oktober 2026
Diisopropylethylamine → (R)-4-(4-fluoro-2-(trifluoromethyl)phenyl)-1-(3-methoxyphenylsulfonyl)-2-methylpiperazine
https://huagongshe.com/reaction/1868127
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 3-Methoxybenzenesulfonyl chloride | HCID 2737504 | — |
| Edukt | (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine | HCID 68554948 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (R)-4-(4-fluoro-2-(trifluoromethyl)phenyl)-1-(3-methoxyphenylsulfonyl)-2-methylpiperazine | HCID 68551747 | — |
Reaktionsschritte
To a stirred solution of (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine (5.34 g, 21.86 mmol) in anhydrous dichloromethane (20 mL) was added diisopropylethylamine (10.3 mL, 59.1 mmol) at 0° C. The reaction mixture was stirred at room temperature for 15 minutes then 3-Methoxy benzene sulfonyl chloride (2.44 g, 11.82 mmol) dissolved in dichloromethane (10 mL) was introduced dropwise. The cooling bath was removed and the mixture was stirred at room temperature for 0.5 hour. Reaction was complete as determined by TLC. The reaction mixture was diluted with dichloromethane washed with saturated NaHCO3 (aqueous), dried over MgSO4 and concentrated. The crude product was purified via flash column chromatography to yield (R)-4-(4-fluoro-2-(trifluoromethyl)phenyl)-1-(3-methoxyphenylsulfonyl)-2-methylpiperazine in quantitative yield (5.10 g) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07632838B2 |
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| Quelldatensatz | uspto-grants-2009_12 |
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| ORD ID | ord-dfe0489e81be4f3fb842300481b6140d |
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| Quellennotiz | uspto-grants-2009_12 |
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