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6-Amino-3-chloropyridazine → 6-Chloro-2-phenyl-3-pyrid-4-ylimidazo[1,2-b]pyridazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Amino-3-chloropyridazine | HCID 21643 | — |
| 反応物 | 2-Bromo-1-phenyl-2-pyrid-4-ylethanone | HCID 13466010 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-Chloro-2-phenyl-3-pyrid-4-ylimidazo[1,2-b]pyridazine | HCID 59406954 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846676B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-3197f8470dfc43b6a117c10cf499bc10 |
| 出典メモ | uspto-grants-2014_09 |