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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528081Generated: October 31, 2026

Potassium Carbonate → 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-pyrimidin-5-ylpyridazin-4(1H)-one

https://huagongshe.com/reaction/1528081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-BromopyrimidineHCID 78344—
ReactantSodium BicarbonateHCID 516892—
Reactant4,7-Dimethoxy-1,10-phenanthrolineHCID 10462298—
ReactantHCID 178493808HCID 178493808—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-pyrimidin-5-ylpyridazin-4(1H)-oneHCID 866865628.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4-ol (100 mg), 5-bromopyrimidine (119 mg), potassium carbonate (155 mg), copper(I) iodide (14 mg) and 4,7-dimethoxy-1,10-phenanthroline (20 mg) in DMSO (2 mL) was stirred at 110° C. for 40 hr under an argon atmosphere. To the reaction mixture was added aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate/methanol), and recrystallized from ethyl acetate/hexane to give the title compound (11 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090586B2
Source datasetuspto-grants-2015_07
ORD IDord-03ca3c2730494129871804e15e761e0c
Source noteuspto-grants-2015_07