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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 382263생성일: 2026년 10월 25일

4-(piperazin-1-yl)-1H-indole → 1-(4-Fluoro-phenoxy)-3-[4-(1H-indol-4-yl)piperazin-1-yl]-propan-2-ol

https://huagongshe.com/reaction/382263

반응식

참여 물질

역할이름HCID투입량
반응물4-(piperazin-1-yl)-1H-indoleHCID 594590—
반응물2-[(4-Fluorophenoxy)methyl]oxiraneHCID 2724792—
생성물1-(4-Fluoro-phenoxy)-3-[4-(1H-indol-4-yl)piperazin-1-yl]-propan-2-olHCID 984226699.3%

반응 단계

A methanolic solution (50 ml) of 1-(4-fluorophenoxy)-2,3-epoxypropane (0.50 g, 3.0 mmole) and 1-(indol-4yl)-piperazine (0.6 g, 3.0 mmole) was refluxed for 1 hr under an atmosphere of nitrogen. The mixture was concentrated in vacuo, and the product purified by silica gel chromatography (EtOAc) to afford a white solid (1.1 g, 99%). Treatment with a 0.25M ethanolic fumaric acid solution gave the required salt, which was recrystallized from ethanol to afford the title compound as a white solid. m.p. 234-235° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06310066B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-13295014b37a40e785b1c2f12f5270fa
출처 메모uspto-grants-2001_10