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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036118Generated: November 4, 2026

Potassium Carbonate → 1'-[6-(3-methyl-1,2,4-oxadiazol-5-yl)pyridazin-3-yl]spiro[indole-3,3'-pyrrolidin]-2(1H)-one

https://huagongshe.com/reaction/2036118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSpiro[3H-indole-3,3'-pyrrolidin]-2(1H)-oneHCID 10954296—
Reactant3-Chloro-6-(3-methyl-1,2,4-oxadiazol-5-yl)pyridazineHCID 16732294—
CatalystTetrabutylammonium IodideHCID 67553—
SolventEthyl AcetateHCID 8857—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product1'-[6-(3-methyl-1,2,4-oxadiazol-5-yl)pyridazin-3-yl]spiro[indole-3,3'-pyrrolidin]-2(1H)-oneHCID 6855460062%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-Chloro-6-(3-methyl-1,2,4-oxadiazol-5-yl)pyridazine (690 mg) obtained in Example 43(2), spiro[indole-3,3′-pyrrolidin]-2(1H)-one (800 mg), potassium carbonate (500 mg) and tetrabutylammonium iodide (130 mg) were suspended in N,N-dimethylformamide-tetrahydrofuran (1:1, v/v, 50 mL), and the suspension was stirred at 120° C. overnight. The mixture was cooled to room temperature, diluted with ethyl acetate, and washed with aqueous sodium carbonate solution. The organic layer was dried over sodium sulfate and the solvent was evaporated under reduced pressure. Ethyl acetate was added and the resulting precipitate was collected by filtration, and recrystallized from ethyl acetate to give the object product (750 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575167B2
Source datasetuspto-grants-2013_11
ORD IDord-8b967e958ac5430e88063481c8156955
Source noteuspto-grants-2013_11