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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097499Generated: October 30, 2026

Butyl vinyl ether → 3-Acetyl-1-benzyloxymethyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one

https://huagongshe.com/reaction/2097499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl vinyl etherHCID 8108—
Reactant1-Benzyloxymethyl-3-iodo-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 66603008—
Catalyst1,3-Bis(diphenylphosphino)propaneHCID 81219—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product3-Acetyl-1-benzyloxymethyl-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 6660272740%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 43 ml of dehydrated N,N-dimethylformamide solution containing 6.48 g (17.0 mmol) of 1-benzyloxymethyl-3-iodo-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one obtained in Reference example 21-(b) were added 0.19 g (0.46 mmol) of 1,3-bis(diphenylphosphino)propane, 94 mg (0.42 mmol) of palladium acetate and 8.4 g (83.9 mmol) of butyl-vinyl ether, and after degassing under reduced pressure, 4.7 ml of triethylamine was further added to the mixture under nitrogen atmosphere, and the mixture was stirred at 100° C. for 7.5 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, the obtained residue was applied to silica gel column chromatography (Eluent; toluene:ethyl acetate=7:3 (V/V)), and the fractions containing the desired compound were concentrated under reduced pressure to obtain 2.02 g of the title compound as a pale yellowish solid. (Yield: 40%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-afec8a08fbb64fe599908a67edb95df5
Source noteuspto-grants-2013_05