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HRID 1874409Erstellt: 24. Oktober 2026

Ethyl isocyanate → N-{3-[(2-{[(ethylamino)carbonyl]amino}imidazo[1,2-a]pyridin-6-yl) oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/de/reaction/1874409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl isocyanateHCID 8022—
EduktN-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 57749097—
LösungsmittelPyridineHCID 1049—
ProduktN-{3-[(2-{[(ethylamino)carbonyl]amino}imidazo[1,2-a]pyridin-6-yl) oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 5774921722%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]-5-methylphenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide (301 mg, 0.800 mmol), ethyl isocyanate (100 μL, 1.27 mmol) and pyridine (10 mL) was stirred at 50° C. for 18 hr. The mixture was concentrated under reduced pressure and ethyl acetate was added to the residue. The mixture was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (silica gel, hexane/ethyl acetate=100/0→0/100) and recrystallized from ethyl acetate-hexane to give the title compound (78.0 mg, 22%) as a pale-yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304557B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-9ca562863e3e4a59960e56df53cc40bd
Quellennotizuspto-grants-2012_11