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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870434Generated: October 26, 2026

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

https://huagongshe.com/reaction/870434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantIodo benzene diacetateHCID 12217721—
Reactant4-(3-chloro-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamideHCID 73053263—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN-(4-((2-aminopyridin-4-yl)oxy)-2-chlorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 7305361267%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 4-(3-chloro-4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamide (160 mg, 0.33 mmol) in EtOAc (3 mL), CH3CN (2.5 mL) and H2O (1.3 mL) was added iodobenzene diacetate (130 mg, 0.40 mmol) at 0° C. The reaction was stirred at 0° C. for 30 minutes, then warmed up to rt and continued to stir for 3 hours. The mixture was concentrated in vacuo and the residue was purified by a silica gel column chromatography (DCM/MeOH (v/v)=25/1) to give the title compound as a beige solid (100 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969388B1
Source datasetuspto-grants-2015_03
ORD IDord-b60f84bf747543ae9d66f309974ea185
Source noteuspto-grants-2015_03