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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(4-Fluorobenzoyl)benzyl bromide | HCID 4729013 | — |
| Reactant | 2,3,5-Trimethyl-1H-pyrrolo[2,3-d]pyridazin-4(5H)-one | HCID 135667599 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[4-(4-Fluorobenzoyl)benzyl]-2,3,5-trimethyl-1H-pyrrolo [2,3-d]pyridazin-4(5H)-one | HCID 69961259 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753664 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-11514966b7124f7f9fabb2a694528997 |
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| Source note | uspto-grants-1998_05 |
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