HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1179607Erstellt: 23. Oktober 2026
Cesium carbonate → 2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinoline
https://huagongshe.com/de/reaction/1179607
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Edukt | 2-Methylquinolin-5-yl trifluoromethanesulfonate | HCID 49851899 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinoline | HCID 57444339 | 58% |
Reaktionsschritte
(2R)-2-Methylpiperazine (0.550 g; 2 eq), caesium carbonate (1.78 g; 2 eq), palladium acetate (0.123 g; 0.2 eq) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.513 g; 0.3 eq) were added to a solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1) (0.8 g; 1 eq) in toluene (30 mL) under an inert atmosphere. The reaction mixture was stirred at reflux under nitrogen for 3 hours. The reaction cooled to room temperature, quenched using saturated aqueous ammonium chloride solution (15 mL) and extracted with ethyl acetate (3×20 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica gel, eluting with dichloromethane-methanol (95:5) affording the title compound in 58% yield (0.383 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07279481B2 |
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| Quelldatensatz | uspto-grants-2007_10 |
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| ORD ID | ord-ff665965fea64949812a36f84c1c419f |
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| Quellennotiz | uspto-grants-2007_10 |
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