HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 419666Erstellt: 24. Oktober 2026
Potassium Carbonate → 1-[2-Methyl-5-(ethyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine
https://huagongshe.com/de/reaction/419666
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-Ethoxy-5-fluoro-4-methyl-2-nitrobenzene | HCID 59452883 | — |
| Edukt | 1-[2-(Methylsulfonyl)ethyl]piperazine hydrochloride | HCID 66649667 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-[2-Methyl-5-(ethyloxy)-4-nitrophenyl]-4-[2-(methylsulfonyl)ethyl]piperazine | HCID 59452734 | 90,6% |
Reaktionsschritte
1-Methyl-2-fluoro-4-(ethyloxy)-5-nitrobenzene (Example 215, step A) (5.74 g, 28.8 mmol) was dissolved in DMSO (60 mL). K2CO3 (11.9 g, 86.4 mmol) and 1-[2-(methylsulfonyl)ethyl]piperazine hydrochloride (Example 148, step B) (9.85 g, 43.2 mmol) were added and the reaction mixture was heated to 100° C. and allowed to stir overnight. The mixture was cooled to rt then diluted with DCM and filtered. The filtrate was poured into H2O and extracted with DCM. The combined organics were dried with MgSO4, filtered, and concentrated in vacuo to give the title compound of Step A (9.70 g, 26.1 mmol, 90%) as an orange solid. 1H NMR (400 MHz, CDCl3) δ 7.75 (s, 1H), 6.51 (s, 1H), 4.11 (q, J=7.0 Hz, 2H), 3.16 (t, J=6.5 Hz, 2H), 3.03 (s, 3H), 3.00-2.91 (m, 6H), 2.72-2.62 (m, 4H), 2.21 (s, 3H), 1.44 (t, J=7.0 Hz, 3H).
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-5c424a4468b349a1b55325fe61d26e26 |
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| Quellennotiz | uspto-grants-2012_01 |
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