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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291288Generated: November 1, 2026

Water → 1-[4-(4-Fluorobenzoyl)benzyl]-5-methyl-1H-pyrrolo-[2,3-d]pyridazin-4(5H)-one

https://huagongshe.com/reaction/1291288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-Fluorobenzoyl)benzyl bromideHCID 4729013—
Reactant5-Methyl-1H-pyrrolo[2,3-d]pyridazin-4(5H)-oneHCID 135667591—
SolventDimethylformamideHCID 6228—
Product1-[4-(4-Fluorobenzoyl)benzyl]-5-methyl-1H-pyrrolo-[2,3-d]pyridazin-4(5H)-oneHCID 1891925468.1%

Reaction Steps

A solution of 5-methyl-1H-pyrrolo[2,3-d]pyridazin-4(5H)-one (373 mg) in DMF (10 ml) was dripped into a suspension of 60% sodium hydride-oil (120 mg) in DMF (10 ml) on an ice-water bath. The mixture was stirred at room temperature for 1 hour, after which a solution of 4-(4-fluorobenzoyl)benzyl bromide (806 mg) in DMF (20 ml) was added and the mixture was further stirred at room temperature for 13 hours. The reaction was stopped by adding water and the reaction mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developer; dichloromethane: methanol=99:1) to provide the title compound as white powder (615 mg, yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-f001c9558a854b4790dc67f0b110d703
Source noteuspto-grants-1998_05