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HRID 60237Erstellt: 23. Oktober 2026

Potassium Fluoride → 6'-Chloro-2,5'-difluoro(3,4'-bipyridin)-3'-amine

https://huagongshe.com/de/reaction/60237

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium FluorideHCID 522689—
Edukt2-Fluoropyridine-3-boronic acidHCID 2783270—
Edukt6-Chloro-5-fluoro-4-iodopyridin-3-amineHCID 58365033—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt6'-Chloro-2,5'-difluoro(3,4'-bipyridin)-3'-amineHCID 5836500075,2%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A degassed mixture of 6-chloro-5-fluoro-4-iodopyridin-3-ylamine (98.7 g, 362 mmol), 2-fluoropyridine 3-boronic acid (68.3 g, 485 mmol), bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II) (7.7 g, 10.9 mmol) and potassium fluoride (63 g, 1.09 mol) in a mixture of acetonitrile (900 mL) and water (275 mL) was heated at 90° C. for 2 hours. The reaction mixture was allowed to cool to ambient temperature and filtered through Celite© and washed through with ethyl acetate. The filtrate was diluted with ethyl acetate and the organic layer collected, dried (Na2SO4), filtered and concentrated in-vacuo to afford a residue. The resultant residue was triturated with diethyl ether to afford the title compound as a grey solid (65.8 g, 75%). The trituration liquors were concentrated and purified by flash chromatography (silica: dichloromethane to 20% ethyl acetate/dichloromethane) to afford, after trituration with ether, an additional batch of the title compound as a grey solid (9.7 g, 11%). Total yield=75.5 g, 86%. 1H NMR (400 MHz, CDCl3): 8.39 (ddd, J=4.9, 2.0, 1.1 Hz, 1H), 7.86-7.84 (m, 2H), 7.39 (ddd, J=7.4, 4.9, 1.9 Hz, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440976B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-cf0f2ad0946a48268431403b500b8bb8
Quellennotizuspto-grants-2016_09