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Water → 2-(4-Methoxyphenyl)imidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| 反応物 | 2-Aminopyridine | HCID 10439 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-(4-Methoxyphenyl)imidazo[1,2-a]pyridine | HCID 694963 | — |
反応手順
A mixture of 25.2 g. of sodium bicarbonate, 12.3 g. of 2-aminopyridine and 30 g. of α-bromo-p-methoxyacetophenone in 100 ml. of water and 550 ml. of absolute ethanol is heated at reflux temperatures for 1.5 hrs. The reaction mixture is concentrated under reduced pressure to a yellow solid, which is partitioned between chloroform and water. The organic layer is separated, dried over sodium sulfate. Removal of the chloroform in vacuo leaves the crude intermediate as a yellow solid. Recrystallization from ethanol-water give 15.2 g. of the desired material, m.p. 131°-134° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04044015 |
| 出典データセット | uspto-grants-1977_08 |
| ORD ID | ord-0fb6f9d9758d4b97941d706b085eb6fe |
| 出典メモ | uspto-grants-1977_08 |