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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1963881Erstellt: 26. Oktober 2026

Sodium Carbonate → 5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-5-carbonitrile

https://huagongshe.com/reaction/1963881

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt(5-Chloro-2-fluoropyridin-4-yl)boronic acidHCID 44754822—
EduktHCID 86650611HCID 86650611—
KatalysatorHCID 178418807HCID 178418807—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-5-carbonitrileHCID 6693715333%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

6-chloro-2-(3-fluorobenzylamino)nicotinonitrile (0.602 g, 2.30 mmol), 5-chloro-2-fluoropyridin-4-ylboronic acid (1.21 g, 6.91 mmol), and sodium carbonate (2.99 mL, 5.99 mmol, 2M in H2O) were dissolved in DME (10.5 mL). The resulting solution was then degassed by sparging with argon for 5 min. It was then treated with PdCl2(dppf) CH2Cl2 adduct (0.376 g, 0.460 mmol). The resulting reaction mixture was heated in the microwave at 120° C. for 10 min. It was then filtered through a pad of Celite. The filtrate was concentrated in vacuo. The resulting residue was subjected to silica gel column chromatography. Elution using 5 EtOAc/95 hexanes to 50 EtOAc/50 hexanes yielded 0.2689 g (33%) of 5′-chloro-2′-fluoro-6-(3-fluorobenzylamino)-2,4′-bipyridine-5-carbonitrile. LCMS (m/z): 357.2 (MH+), retention time=1.02 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08415381B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-cc9f1fe7b1e342d399118193725b94cb
Quellennotizuspto-grants-2013_04