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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593956Erstellt: 25. Oktober 2026

2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl → N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazin-1-amine

https://huagongshe.com/reaction/593956

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
EduktSodium t-butoxideHCID 23676156—
Edukt4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amineHCID 66735161—
Edukt1-Chloro-6,7-dihydro-4-phenyl-5H-cyclopenta[d]pyridazineHCID 86614164—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
ProduktN-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazin-1-amineHCID 57756249—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A resealable reaction tube was charged with tris(dibenzylideneacetone)dipalladium (0) (0.012 g, 0.013 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxy-1,1′-biphenyl (0.021 g, 0.051 mmol), 4-(2-(4-aminophenoxy)pyridin-3-yl)-N-methylpyridin-2-amine (0.075 g, 0.257 mmol), 1-chloro-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazine (0.059 g, 0.257 mmol), and sodium tert-butoxide (0.035 g, 0.359 mmol). This mixture was purged with nitrogen for several minutes, followed by addition of 0.780 mL of toluene. The vial was capped and heated at 100° C. for 1.5 h. Upon cooling, ethyl acetate was added and a precipitate formed. After filtration and washing with EtOAc, the crude material was purified by ISCO silica gel chromatography (90/10/1 DCM/MeOH/NH4OH, 12 g column), to provide N-(4-(3-(2-(methylamino)pyridin-4-yl)pyridin-2-yloxy)phenyl)-4-phenyl-6,7-dihydro-5H-cyclopenta[d]pyridazin-1-amine as a tan solid. MS m/z=487 [M+H]+. Calc'd for C30H26N6O: 486.57.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242961B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-0a1e5b278abe4ef89c9597d01ecd7bac
Quellennotizuspto-grants-2016_01