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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291286Generated: October 31, 2026

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

https://huagongshe.com/reaction/1291286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-Trifluoromethylbenzoyl)benzyl bromideHCID 18919118—
Reactant2,3-Dichloro-5-methyl-1H-pyrrolo[2,3-d]pyridazin-4(5H)-oneHCID 135667580—
SolventDimethylformamideHCID 6228—
Product2,3-Dichloro-5-methyl-1-[4-(4-trifluoromethylbenzoyl) benzyl]-1H-pyrrolo[2,3-d]pyridazin-4(5H)-oneHCID 6995998250.3%

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-trifluoromethylbenzoyl)benzyl bromide (754 mg) in DMF (15 ml) was added and the mixture was further stirred at room temperature for 15 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 (448 mg, yield 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753664
Source datasetuspto-grants-1998_05
ORD IDord-09b9f93a96f743018ef58d67cde920e1
Source noteuspto-grants-1998_05