化工社化工社 化学情報印刷レポート · 研究参考用
4-Fluorophenyl isocyanate → N-(1-acetylpiperidin-4-yl)-N'-(4-fluorophenyl)urea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Fluorophenyl isocyanate | HCID 70955 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 1-Acetyl-4-aminopiperidine hydrochloride | HCID 17221642 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(1-acetylpiperidin-4-yl)-N'-(4-fluorophenyl)urea | HCID 9860476 | — |
反応手順
To a suspension of 1-acetyl-4-aminopiperidine hydrochloride (536 mg) in dichloromethane (5 ml) were added 4-fluorophenyl isocyanate (375 μl) and diisopropylethylamine (575 μl ) at ambient temperature. After stirring for 3 hours, the reaction mixture was diluted with dichloromethane. An organic phase was separated and an aqueous phase was extracted with dichloromethane. A combined organic phase was dried over magnesium sulfate and the solvents were removed under reduced pressure. After crystallization from diisopropyl ether and n-hexane, N-(1-acetylpiperidin-4-yl)-N′-(4-fluorophenyl)urea (448 mg) was obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06710043B1 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-791c61bd4d46488d9cd3f88bc69b7774 |
| 出典メモ | uspto-grants-2004_03 |