HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 6-Chloro-2-(furan-2-yl)imidazo[1,2-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 6-Amino-3-chloropyridazine | HCID 21643 | — |
| Reactant | 2-Bromo-1-(furan-2-yl)ethan-1-one | HCID 2795076 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Chloro-2-(furan-2-yl)imidazo[1,2-b]pyridazine | HCID 11746128 | — |
Reaction Steps
A solution of 2-bromo-1-(2-furyl)ethanone (220 mg, 1.16 mmol) and 6-chloropyridazin-3-amine (150 mg, 1.16 mmol) in dioxane (4 ml) was stirred at room temperature for 1.5 hours, and at 65° C. for 16 hours. The reaction mixture was then cooled to ambient temperature, diluted with 3:1 (chloroform:isopropanol) and water. The layers were separated and the organic layer was concentrated under reduced pressure. Silica gel chromatography (0-15% methanol in dichloromethane) afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344144B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-77b86ddbb8dc4b2ea93310589e089a64 |
| Source note | uspto-grants-2013_01 |