HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668044Generated: October 26, 2026
Water → N-[6-(3-amino-4-fluorophenoxy)imidazo[1,2-b]pyridazin-2-yl]acetamide
https://huagongshe.com/reaction/1668044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Amino-4-fluorophenol | HCID 13519180 | — |
| Reactant | N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamide | HCID 57441059 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[6-(3-amino-4-fluorophenoxy)imidazo[1,2-b]pyridazin-2-yl]acetamide | HCID 57505595 | 79.4% |
Reaction Steps
To a solution of N-(6-iodoimidazo[1,2-b]pyridazin-2-yl)acetamide (12 g, 39.7 mmol) in N,N-dimethylformamide (120 mL) were added 3-amino-4-fluorophenol (7.6 g, 59.6 mmol) and potassium carbonate (11.0 g, 79.5 mmol), and the mixture was stirred at 140° C. for 12 hr. After cooling the mixture to room temperature, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate/tetrahydrofuran, washed with saturated brine, dried over anhydrous sodium sulfate, and filtrated. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=3/1→ethyl acetate alone) to give the title compound (9.5 g, 79%) as a brown powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044049B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-6d13bca9574146efa10ef35b46d80946 |
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| Source note | uspto-grants-2011_10 |
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