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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227798Erstellt: 25. Oktober 2026

Sodium Carbonate → N-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine

https://huagongshe.com/reaction/227798

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Edukt2-Fluoropyridine-4-boronic acidHCID 2783396—
EduktN-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amineHCID 66731439—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktN-(4-(3-bromopyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amineHCID 66731439—
ProduktN-(4-(3-(2-fluoropyridin-4-yl)pyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amineHCID 66732281—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A resealable reaction tube was charged with tri-tert-butylphosphonium tetrafluoroborate (0.024 g, 0.082 mmol), palladium (II) acetate (0.009 g, 0.041 mmol), 2-fluoropyridine4-boronic acid (0.086 g, 0.614 mmol) and N-(4-(3-bromopyridin4-yloxy)phenyl)-4-phenylphthalazin-1-amine (0.192 mg, 0.409 mmol) and was purged with nitrogen for several minutes. 1.2 mL of dioxane and 2.0 M aqueous sodium carbonate (0.614 mL, 0.123 mmol) were added, the tube was sealed, and the reaction mixture was heated to 100° C. for 48 h. The mixture was diluted with EtOAc and washed with water. The organic portion was dried with MgSO4 and concentrated. Purification by Gilson reverse phase liquid chromatography (5-70% ACN/water/0.1% TFA over 14 min) provided N-(4-(3-(2-fluoropyridin-4-yl)pyridin-4-yloxy)phenyl)-4-phenylphthalazin-1-amine as a mixture with the hydrodehalogenation product of N-(4-(3-bromopyridin-4-yloxy)phenyl)4-phenylphthalazin-1-amine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560551B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-bfaff0fbea714597b399ff08fb409554
Quellennotizuspto-grants-2009_07