HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Amino-3-chloropyridazine → 6-Chloro-2-phenyl-3-pyrid-4-ylimidazo[1,2-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Amino-3-chloropyridazine | HCID 21643 | — |
| Reactant | 2-Bromo-1-phenyl-2-pyrid-4-ylethanone | HCID 13466010 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Chloro-2-phenyl-3-pyrid-4-ylimidazo[1,2-b]pyridazine | HCID 59406954 | — |
Reaction Steps
A mixture of 13 g (36.5 mmol) of 2-bromo-1-phenyl-2-pyrid-4-ylethanone (CAS No.: 741633-76-1) and 18.9 g (146 mmol) of 6-chloropyridazin-3-ylamine in 200 mL of ethanol is maintained at 90° C. for 5 hours 30 minutes. After cooling, the solvent is evaporated off under reduced pressure, the medium is taken up in 50 mL of water and the product is extracted with ethyl acetate. The organic phases are dried over magnesium sulfate and then concentrated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846676B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-3197f8470dfc43b6a117c10cf499bc10 |
| Source note | uspto-grants-2014_09 |