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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 520713Erstellt: 24. Oktober 2026

Iodo benzene diacetate → N-(4-((2-aminopyridin-4-yl)oxy)-3-fluorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-c arboxamide

https://huagongshe.com/de/reaction/520713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodo benzene diacetateHCID 12217721—
Edukt4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2-fluorophenoxy)picolinamideHCID 73053267—
EduktEtOAc CH3CN waterHCID 86658869—
ProduktN-(4-((2-aminopyridin-4-yl)oxy)-3-fluorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-c arboxamideHCID 7305365081%

Reaktionsschritte

To a solution of 4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2-fluorophenoxy)picolinamide (2.5 g, 6.0 mmol) in EtOAc/MeCN/H2O (60 mL/60 mL/30 mL) was added iodobenzene diacetate (2.9 g, 9.0 mmol) at 0° C. The reaction was stirred at rt for 2 hours, then concentrated in vacuo. The resulted residue was dissolved with EtOAc (150 mL), washed with saturated aq. NaHCO3 (80 mL), dried over anhydrous Na2SO4, and concentrated in vacuo. The residue was washed with DCM/ether (1/10, 22 mL) to give the title compound as a yellow solid (2.09 g, 81% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09326975B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-835a6f0ed3704225a84ec051756f8cc5
Quellennotizuspto-grants-2016_05