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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291283Generated: October 30, 2026

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

https://huagongshe.com/reaction/1291283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-Fluorobenzoyl)benzyl bromideHCID 4729013—
Reactant2,3-Dichloro-5-methyl-1H-pyrrolo[2,3-d]pyridazin-4(5H)-oneHCID 135667580—
SolventDimethylformamideHCID 6228—
Product1-[4-(4-Fluorobenzoyl)benzyl]-2,3-dichloro-5-methyl-1H-pyrrolo [2,3-d]pyridazin-4(5H)-oneHCID 6996225746.5%

Reaction Steps

A solution of 2,3-dichloro-5-methyl-1H-pyrrolo [2,3-d]pyridazin-4(5H)-one (404 mg) in DMF (70 ml) was dripped into a suspension of 60% sodium hydride-oil (96 mg) in DMF (10 ml) on an ice-water bath. The mixture was stirred at room temperature for 2 hours, 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 16 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 (371 mg, yield 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-2d73bbae3b5544f18b6f700acd2769b9
Source noteuspto-grants-1998_05