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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333727Generated: October 30, 2026

Water → 5-hydroxy-1-methyl-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one

https://huagongshe.com/reaction/333727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant5-methoxy-1-methyl-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-oneHCID 89586661—
SolventAcetonitrileHCID 6342—
Product5-hydroxy-1-methyl-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-oneHCID 8958673677%

Reaction Steps

To a solution of sodium iodide (3.75 g) in acetonitrile (150 mL) was added chlorotrimethylsilane (3.17 mL) with stirring at room temperature, and the mixture was stirred for min. Then, 5-methoxy-1-methyl-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one (1.41 g) was added, and the mixture was stirred for 30 min at the same temperature, and further refluxed for 3 hr. The reaction mixture was allowed to cool to room temperature, poured into water and the mixture was stirred for 30 min. The mixture was extracted with ethyl acetate, and the organic layer was washed successively with aqueous sodium thiosulfate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained residue was triturated with ethyl acetate-diisopropyl ether, collected by filtration, and dried to give the title compound (1.032 g) as white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883788B2
Source datasetuspto-grants-2014_11
ORD IDord-5099d1f4156645abae488f18998c305b
Source noteuspto-grants-2014_11