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HRID 1843244Erstellt: 25. Oktober 2026
Potassium Acetate → 2-Bromo-4-fluoro-6-(1-oxo-6,7,8,9-tetrahydropyrazino[1,2-a]indol-2(1H)-yl)benzaldehyde
https://huagongshe.com/reaction/1843244
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Acetate | HCID 517044 | — |
| Edukt | 4,7-Dimethoxy-1,10-phenanthroline | HCID 10462298 | — |
| Edukt | 2,6-Dibromo-4-fluorobenzaldehyde | HCID 44474666 | — |
| Edukt | 6,7,8,9-Tetrahydropyrazino[1,2-a]indol-1(2H)-one | HCID 86683755 | — |
| Produkt | 2-Bromo-4-fluoro-6-(1-oxo-6,7,8,9-tetrahydropyrazino[1,2-a]indol-2(1H)-yl)benzaldehyde | HCID 86683756 | 49,3% |
Reaktionsschritte
A 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 121e (500 mg, 2.66 mmol), 2,6-dibromo-4-fluorobenzaldehyde (1.50 g, 5.32 mmol), and potassium acetate (521 mg, 5.32 mmol). After bubbling argon through the suspension for 30 minutes, 4,7-dimethoxy-1,10-phenanthroline (638.4 mg, 2.66 mmol) and cuprous iodide (506 mg, 2.66 mmol) were added. The system was subjected to three cycles of vacuum/argon flush and then heated at 100° C. for 16 h. It was then cooled to room temperature and filtered. The solid was washed with dichloromethane (2×100 ml). The combined filtrate was concentrated under reduced pressure and the residue was purified by silica-gel column chromatography eluting with petroleum ether/ethyl acetate (10:1 to 3:1) to afford 121f (510 mg, 49%) as a yellow solid. MS: [M+H]+ 389.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08946213B2 |
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| Quelldatensatz | uspto-grants-2015_02 |
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| ORD ID | ord-3fb9c591517140d28502beca5091938b |
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| Quellennotiz | uspto-grants-2015_02 |
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