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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 452633Erstellt: 24. Oktober 2026

2-Aminopyridine → Methyl 2-(2-pyridylamino)isonicotinate

https://huagongshe.com/de/reaction/452633

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminopyridineHCID 10439—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktMethyl 2-chloropyridine-4-carboxylateHCID 2736842—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Katalysator2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 2-(2-pyridylamino)isonicotinateHCID 6866423265%

Reaktionsschritte

A suspension of methyl 2-chloroisonicotinate (1.00 g, 5.83 mmol), 2-aminopyridine (658 mg, 6.99 mmol), tris(dibenzylideneacetone)dipalladium(0) (107 mg, 0.17 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (139 mg, 0.29 mmol) and tripotassium phosphate (3.09 g, 14.6 mmol) in toluene (30 mL) was heated under reflux under an argon atmosphere overnight. After cooling, the reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=9/1-2/3) and recrystallized from hexane/ethyl acetate to give the title compound (866 mg, yield 65%) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492378B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-5947a725ed7340a889cf8a5963cb710d
Quellennotizuspto-grants-2013_07