HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 419610Erstellt: 24. Oktober 2026
Dimethyl Sulfoxide → 1-[2-Chloro-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine
https://huagongshe.com/de/reaction/419610
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-Chloro-2-fluoro-4-methoxy-5-nitrobenzene | HCID 53403289 | — |
| Edukt | 1-[2-(Methylsulfonyl)ethyl]piperazine hydrochloride | HCID 66649667 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-[2-Chloro-5-(methyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine | HCID 59452634 | 91,3% |
Reaktionsschritte
To 1-chloro-2-fluoro-4-(methyloxy)-5-nitrobenzene (Example 104, Step B) (0.822 g, 4.0 mmol), 4-[2-(methylsulfonyl)ethyl]piperazine hydrochloride (Example 148, Step B) (0.915 g, 4.0 mmol), and K2CO3 (1.7 g, 12 mmol) was added DMSO (8 mL). The reaction was heated to 100° C. for two days. The reaction was determined to be complete by TLC. The reaction mixture was diluted with H2O and extracted with DCM and EtOAc sequentially for two iterations. The organic was dried (MgSO4), filtered, and rotovapped down. Purification by flash chromatography provided the title compound of Step A (1.38 g, 91%). MS (M+H, ES+) 378.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08093239B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-86d4005b11134c4792f37dc014c8d999 |
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| Quellennotiz | uspto-grants-2012_01 |
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