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HRID 49783作成日:2026年10月25日

4-Fluorophenyl isocyanate → N-(1-acetylpiperidin-4-yl)-N'-(4-fluorophenyl)urea

https://huagongshe.com/reaction/49783

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluorophenyl isocyanateHCID 70955—
反応物DiisopropylethylamineHCID 81531—
反応物1-Acetyl-4-aminopiperidine hydrochlorideHCID 17221642—
溶媒DichloromethaneHCID 6344—
生成物N-(1-acetylpiperidin-4-yl)-N'-(4-fluorophenyl)ureaHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710043B1
出典データセットuspto-grants-2004_03
ORD IDord-791c61bd4d46488d9cd3f88bc69b7774
出典メモuspto-grants-2004_03