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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2381053Erstellt: 27. Oktober 2026

Propylphosphonic anhydride → 2-[2-(Aminocarbonylmethoxy)-6-methoxyphenyl]-3-(2,6-dimethylphenylamino)-6-fluoroimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/2381053

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropylphosphonic anhydrideHCID 111923—
EduktN-(2,6-Dimethylphenyl)formamideHCID 345859—
Edukt2-Amino-5-fluoropyridineHCID 2737701—
EduktPropylphosphoric anhydrideHCID 16167369—
Edukt2-(2-Formyl-3-methoxyphenoxy)acetamideHCID 42604614—
LösungsmittelTriethylamineHCID 8471—
Produkt2-[2-(Aminocarbonylmethoxy)-6-methoxyphenyl]-3-(2,6-dimethylphenylamino)-6-fluoroimidazo[1,2-a]pyridineHCID 24854988—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

4.2 0.149 g of 12, 0.112 g of 2-amino-5-fluoropyridine 4, 0.209 g of 2-(2-formyl-3-methoxyphenoxy)acetamide 3, 0.286 ml of triethylamine and, dropwise, 2.5 ml of T3P® [=propylphosphonic anhydride (50% solution in ethyl acetate)] are introduced successively into a flask with ice-cooling and under an inert gas. The reaction mixture is stirred at 100° C. for 7 h. The mixture is subsequently subjected to conventional work-up, giving 0.2 g (40%) of “A1”.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08258151B2
Quelldatensatzuspto-grants-2012_09
ORD IDord-df4dd51a7ae14f998fd7e0c33560e0bc
Quellennotizuspto-grants-2012_09