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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291293Generated: October 31, 2026

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

https://huagongshe.com/reaction/1291293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-Fluorobenzoyl)benzyl bromideHCID 4729013—
Reactant2,3,5-Trimethyl-1H-pyrrolo[2,3-d]pyridazin-4(5H)-oneHCID 135667599—
SolventDimethylformamideHCID 6228—
Product1-[4-(4-Fluorobenzoyl)benzyl]-2,3,5-trimethyl-1H-pyrrolo [2,3-d]pyridazin-4(5H)-oneHCID 6996125981%

Reaction Steps

A solution of 2,3,5-trimethyl-1H-pyrrolo[2,3-d]-pyridazin-4(5H)-one (354 mg) in DMF (30 ml) was dripped into a suspension of 60% sodium hydride-oil (96 mg) in DMF (8 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 (645 mg) in DMF (15 ml) was added and the mixture was further stirred at room temperature for 2 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; n-hexane: ethyl acetate=1:1) to provide the title compound as white powder (628 mg, yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-11514966b7124f7f9fabb2a694528997
Source noteuspto-grants-1998_05