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Acetonitrile → N-(1-hexylpiperidin-4-yl)xanthene-9-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-Iodohexane | HCID 12527 | — |
| 反応物 | N-(piperidin-4-yl)xanthene-9-carboxamide hydrochloride | HCID 23283003 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(1-hexylpiperidin-4-yl)xanthene-9-carboxamide | HCID 11794863 | — |
反応手順
60 mg of potassium carbonate and 25 ml of iodohexane were successively added to 5.0 ml of acetonitrile suspension having 50 mg of N-(piperidin-4-yl)xanthene-9-carboxamide hydrochloride, followed by reflux under heating for 4 hours. After cooled to room temperature, water was added to the reaction solution, followed by extraction with ethyl acetate and drying over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by preparative thin layer chromatography (Kieselgel™60F254, Art5744 produced by Merck Co.: chloroform/methanol=10/1), and 35 mg of the title compound as a white solid was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06140338 |
| 出典データセット | uspto-grants-2000_10 |
| ORD ID | ord-5d9b8530ec924490abf026fab400f5d0 |
| 出典メモ | uspto-grants-2000_10 |