돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49783생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/49783

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluorophenyl isocyanateHCID 70955—
반응물DiisopropylethylamineHCID 81531—
반응물1-Acetyl-4-aminopiperidine hydrochlorideHCID 17221642—
용매DichloromethaneHCID 6344—
생성물N-(1-acetylpiperidin-4-yl)-N'-(4-fluorophenyl)ureaHCID 9860476—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710043B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-791c61bd4d46488d9cd3f88bc69b7774
출처 메모uspto-grants-2004_03