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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870422Generated: October 25, 2026

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

https://huagongshe.com/reaction/870422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantIodo benzene diacetateHCID 12217721—
Reactant4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2,3-difluorophenoxy)picolinamideHCID 73053264—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-(4-((2-aminopyridin-4-yl)oxy)-2,3-difluorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 7305361032.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)-2,3-difluorophenoxy)picolinamide (108 mg, 0.22 mmol) in EtOAc (2.5 mL), CH3CN (2.5 mL) and H2O (1.5 mL) was added iodobenzene diacetate (96 mg, 0.30 mmol) at 0° C. The reaction was stirred at 0° C. for 30 minutes, then warmed up to rt and continued to stir for 4 hours. The mixture was concentrated in vacuo, and the residue was purified by a silica gel column chromatography (EtOAc/CH3OH (v/v)=10/1) to give the title compound as a pale yellow solid (32 mg, 32.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969388B1
Source datasetuspto-grants-2015_03
ORD IDord-e2afc043e6b44ac08e09bf439cf81287
Source noteuspto-grants-2015_03