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HRID 40337Erstellt: 24. Oktober 2026

Dimethylformamide → 6-((5-(3,5-Difluorophenyl)isoxazolo[5,4-b]pyridin-3-yl)difluoromethyl)quinoline

https://huagongshe.com/de/reaction/40337

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktCesium carbonateHCID 10796—
Edukt(3,5-Difluorophenyl)boronic acidHCID 2734338—
Edukt1-(6-Chloro-3-fluoropyridin-2-yl)-2,2-difluoro-2-(quinolin-6-yl)ethanone oximeHCID 136387215—
KatalysatorHCID 178418807HCID 178418807—
LösungsmittelWaterHCID 962—
Produkt6-((5-(3,5-Difluorophenyl)isoxazolo[5,4-b]pyridin-3-yl)difluoromethyl)quinolineHCID 576912209%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a pressure vessel was added cesium carbonate (0.61 g, 1.9 mmol), PdCl2(dppf)-CH2Cl2 adduct (26 mg, 0.031 mmol), 1-(6-chloro-3-fluoropyridin-2-yl)-2,2-difluoro-2-(quinolin-6-yl)ethanone oxime (0.26 g, 0.63 mmol) and 3,5-difluorophenylboronic acid (0.15 g, 0.94 mmol) in anhydrous DMF (5 mL) and water (1 mL). The mixture flushed with argon, sealed and stirred at 80° C. for one hour. The suspension was concentrated, triturated with water and filtered to afford a tan solid, purification by MPLC (eluted with a gradient of 20 to 50% ethyl acetate in hexanes) afforded the product as a white solid (23 mg, 9%). MS m/z=410.0 [M+1]+ Calc'd for C22H11F4N3O: 409.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524900B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-e06e1bb530aa4feb9564f9f98730b2a1
Quellennotizuspto-grants-2013_09