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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663690Generated: October 30, 2026

Dimethylformamide → Ethyl 6-(3-aminophenoxy)imidazo[1,2-b]pyridazine-2-carboxylate

https://huagongshe.com/reaction/1663690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant3-AminophenolHCID 11568—
ReactantEthyl 6-Iodoimidazo[1,2-b]pyridazine-2-carboxylateHCID 51063906—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductEthyl 6-(3-aminophenoxy)imidazo[1,2-b]pyridazine-2-carboxylateHCID 5738578639.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of ethyl 6-iodoimidazo[1,2-b]pyridazine-2-carboxylate (951 mg, 3.00 mmol), 3-aminophenol (655 mg, 6.00 mmol), potassium carbonate (622 mg, 4.50 mmol) and N,N-dimethylformamide (9.0 mL) was stirred at 150° C. for 6 hr. After allowing the reaction mixture to cool to room temperature, ethyl acetate and water were added to the mixture and the insoluble material was filtered through celite. The organic layer was collected from the filtrate, washed with saturated aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/19→ethyl acetate alone) to give the title compound (350 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034812B2
Source datasetuspto-grants-2011_10
ORD IDord-dfe8ecbb9b9d46ba8dfcc003fb112aca
Source noteuspto-grants-2011_10