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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium AcetateHCID 517044—
Edukt4,7-Dimethoxy-1,10-phenanthrolineHCID 10462298—
Edukt2,6-Dibromo-4-fluorobenzaldehydeHCID 44474666—
Edukt6,7,8,9-Tetrahydropyrazino[1,2-a]indol-1(2H)-oneHCID 86683755—
Produkt2-Bromo-4-fluoro-6-(1-oxo-6,7,8,9-tetrahydropyrazino[1,2-a]indol-2(1H)-yl)benzaldehydeHCID 8668375649,3%

Reaktionsbedingungen

Temperatur100 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08946213B2
Quelldatensatzuspto-grants-2015_02
ORD IDord-3fb9c591517140d28502beca5091938b
Quellennotizuspto-grants-2015_02