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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 510856Erstellt: 26. Oktober 2026

Nitrogen → 1-[4-Chloro-6-(2,6-difluoropyridin-4-yl)-5-methylbiphenyl-2-yl]ethanone

https://huagongshe.com/reaction/510856

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitrogenHCID 947—
EduktWaterHCID 962—
Edukt2,6-Difluoropyridine-4-boronic acidHCID 2762747—
Edukt1-(6-Bromo-4-chloro-5-methylbiphenyl-2-yl)ethanoneHCID 86666787—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelSodium CarbonateHCID 10340—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-[4-Chloro-6-(2,6-difluoropyridin-4-yl)-5-methylbiphenyl-2-yl]ethanoneHCID 8666678830%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A biphasic solution of 1-(6-bromo-4-chloro-5-methylbiphenyl-2-yl)ethanone (0.20 g, 0.62 mmol) and (2,6-difluoropyridin-4-yl)boronic acid (0.12 g, 0.74 mmol) in 1,4-dioxane (2.0 mL) and 10% Na2CO3 in water (0.98 mL, 0.93 mmol)) was bubbled with N2 to degas. After tetrakis(triphenylphosphine)palladium(0) (29 mg, 0.025 mmol) was added the mixture was bubbled with N2 for 5 min. and heated at 100° C. overnight. The mixture was cooled to room temperature and diluted with ethyl acetate. The layers were separated and the aq. layer was extracted with more ethyl acetate. The combined extracts were washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified on silica gel column, eluting with 0-30% of ethyl acetate in hexane, to give the desired product (60 mg, 30%). LCMS calculated for C20H15ClF2NO (M+H)+: m/z=358.1. found: 358.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096600B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-5c02a9856bba4c47b9bc7ab66ea54f41
Quellennotizuspto-grants-2015_08