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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | Ethyl 6-Iodoimidazo[1,2-b]pyridazine-2-carboxylate | HCID 51063906 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 6-(3-aminophenoxy)imidazo[1,2-b]pyridazine-2-carboxylate | HCID 57385786 | 39.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034812B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-dfe8ecbb9b9d46ba8dfcc003fb112aca |
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| Source note | uspto-grants-2011_10 |
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