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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 520722Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/520722

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodo benzene diacetateHCID 12217721—
EduktEtOAc CH3CN waterHCID 86658869—
Edukt4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamidHCID 117842592—
ProduktN-(4-((2-aminopyridin-4-yl)oxy)phenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 7305360848%

Reaktionsschritte

To a solution of 4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamid (1.773 g, 3.998 mmol) in EtOAc/MeCN/H2O (20 mL/20 mL/10 mL) was added iodobenzene diacetate (1.6 g, 4.96 mmol) at 0° C. The reaction was stirred at rt overnight, then concentrated in vacuo and diluted with EtOAc (100 mL). The mixture was washed with saturated aq. NaHCO3 (60 mL), dried over Na2SO4, and concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/MeOH (v/v)=30/1) to give the title compound as a yellow solid (799 mg, 48%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09326975B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-6cd25f1834c745f98eb84ae3f774c80b
Quellennotizuspto-grants-2016_05