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Indole → 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Indole | HCID 798 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Piperonylamine | HCID 2723901 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(1,2,3,6-Tetrahydropyridin-4-yl)-1H-indole | HCID 2761023 | — |
反応手順
30 g (0.26 mol) of indole were dissolved in a solution of potassium hydroxide (77.6 g, 1.38 mol) in methanol (692 ml). 4-piperidone monohydrate hydrochloride (102.3 g, 0.66 mol) was added in one portion and the mixture was heated to reflux for 5 h. Potassium chloride precipitated upon cooling at room temperature and it was filtered off. The liquid phase was concentrated until only one third of the liquid remained in the round-bottom flask. The solid formed during the concentration of the liquid phase was filtered and washed thoroughly with ethanol and, finally, with ethyl ether. 31.9 g (63% of yield) of the final product were obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07560471B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-5d424983c19e4484a8c8c5c927e205be |
| 出典メモ | uspto-grants-2009_07 |