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HRID 60127Erstellt: 23. Oktober 2026

Methyl 2-aminopyridine-4-carboxylate → Methyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylate

https://huagongshe.com/de/reaction/60127

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 2-aminopyridine-4-carboxylateHCID 236984—
Edukt2-Bromo-1-(2,5-difluorophenyl)ethanoneHCID 2778264—
LösungsmittelEthanolHCID 702—
ProduktMethyl 2-(2,5-difluorophenyl)imidazo[1,2-a]pyridine-7-carboxylateHCID 90383269135,9%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

2-Bromo-1-(2,5-difluorophenyl)ethanone (1.5 g) was added to an ethanol (8.2 ml) solution of methyl 2-aminoisonicotinate (1.0 g), and the obtained mixture was then stirred in a nitrogen atmosphere at 60° C. for 18 hours. Thereafter, 2-bromo-1-(2,5-difluorophenyl)ethanone (0.77 g) was added to the reaction solution, and the obtained mixture was then stirred for 6 hours at the same temperature as described above. Thereafter, the reaction solution was concentrated under reduced pressure, and ethyl acetate (10 ml) was then added to the obtained residue. The precipitated solid was collected by filtration, and it was washed with ethyl acetate (15 ml) and heptane (6 ml) and was then dried, so as to obtain the title compound (2.5 g) in the form of a pink solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440970B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-1d414470be0b476fab1ac89e737035b4
Quellennotizuspto-grants-2016_09