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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340258Erstellt: 25. Oktober 2026

Potassium Phosphate, Tribasic → 2-((4-Ethoxyphenyl)ethynyl)-8-methylbenzo[f][1,7]naphthyridin-5-amine

https://huagongshe.com/reaction/340258

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Edukttert-Butyl (5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamateHCID 46737997—
Edukt3-Chloro-5-((4-ethoxyphenyl)ethynyl)picolinonitrileHCID 66875303—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Lösungsmittel1-ButanolHCID 263—
LösungsmittelWaterHCID 962—
Produkt2-((4-Ethoxyphenyl)ethynyl)-8-methylbenzo[f][1,7]naphthyridin-5-amineHCID 66874905—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a round bottom flask with refluxing condenser were added 3-chloro-5-((4-ethoxyphenyl)ethynyl)picolinonitrile (from the previous step) (1 eq.), tert-butyl 5-methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (from Example 5/Step 2) (1.25 eq.), K3PO4 (2 eq.), tris(dibenzylideneacetone)dipalladium(0) (0.05 eq.), and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.1 eq.). n-Butanol and water (5:2, 0.2 M) were added, and the content were degassed (vacuum followed by nitrogen flush) for three times. The reaction mixture was stirred vigorously under nitrogen at 100° C. overnight in an oil bath. The content were cooled down and were taken up in 200 mL of water followed by extraction with methylene chloride. Combined organic layers were dried (Na2SO4) and concentrated. Flash chromatography (silica gel, 0-50% EtOAc in CH2Cl2) afforded the product 2-((4-ethoxyphenyl)ethynyl)-8-methylbenzo[f][1,7]naphthyridin-5-amine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895577B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-87c02ad19429400eb7a2f52941318e11
Quellennotizuspto-grants-2014_11