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2-Bromo-4'-methylacetophenone → 2-(p-Tolyl)-6-(trifluoromethyl)imidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Bromo-4'-methylacetophenone | HCID 69272 | — |
| 反応物 | 2-Amino-5-(trifluoromethyl)pyridine | HCID 735862 | — |
| 溶媒 | 1-Propanol | HCID 1031 | — |
| 生成物 | 2-(p-Tolyl)-6-(trifluoromethyl)imidazo[1,2-a]pyridine | HCID 13938037 | 70.2% |
反応手順
10 g (0.0616 mole) of 2-amino-5-trifluoromethylpyridine and 17.5 g (0.0616 mole) of 1-bromo-2-(4-methylphenyl)-2-ethanone are mixed in 200 ml of n-propanol and the solution is heated to reflux. At the end of the reaction, the reaction mixture is concentrated under reduced pressure and the evaporation residue taken up with water and treated with an excess of ammonia solution until the pH is basic. The imidazopyridine is extracted with dichloromethane and purified by chromatography. 11.95 g (56%) of white solid are obtained. M.p. 187°-188° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04767755 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-20bd24ff2e884f868dd93e00939014f6 |
| 出典メモ | uspto-grants-1988_08 |