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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1042934Erstellt: 25. Oktober 2026

Ethyl Acetate → phosphoric acid di-tert-butyl ester 4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl ester

https://huagongshe.com/reaction/1042934

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
EduktPotassium di-tert-butyl phosphateHCID 23674467—
Edukt2,6-dichloro-N-[4-(1-chloromethyl-2-oxo-1,2-dihydro-pyridin-4-yl)-benzyl]-benzamideHCID 86675421—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelDimethylformamideHCID 6228—
Produktphosphoric acid di-tert-butyl ester 4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl esterHCID 71149943—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

2,6-Dichloro-N-[4-(1-chloromethyl-2-oxo-1,2-dihydro-pyridin-4-yl)-benzyl]-benzamide from the previous step was dissolved in 50 mL DMF. Potassium carbonate (1 g) was added followed by potassium di(t-butyl)phosphate (2 g) and tetrabutylammonium iodide (50 mg). The mixture was stirred at 70° C. for four hours after which it was poured into 300 mL ethyl acetate. The organic phase was washed with water and brine, dried with magnesium sulfate and evaporated under vacuum. The crude product was further purified by silica gel chromatography (eluent: ethyl acetate), giving phosphoric acid di-tert-butyl ester 4-{4-[(2,6-dichloro-benzoylamino)-methyl]-phenyl}-2-oxo-2H-pyridin-1-ylmethyl ester as a colorless oil which slowly crystallized.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08558001B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-e44cac3e8c1145db86fe9fb197a5c8e6
Quellennotizuspto-grants-2013_10