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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22345생성일: 2026년 10월 23일

1-(4-Fluorophenyl)piperazine → 8-{3-[4-(4-fluorophenyl)-1-piperazinyl]propoxy}-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one

https://huagongshe.com/ko/reaction/22345

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Fluorophenyl)piperazineHCID 75260—
반응물FumarateHCID 5460307—
반응물2,3-dihydro-8-[3-(methanesulfonyloxy)propoxy]-7-methoxy-cyclopenta[c][1]-benzopyran-4(1H)-oneHCID 19927662—
용매EthanolHCID 702—
생성물8-{3-[4-(4-fluorophenyl)-1-piperazinyl]propoxy}-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992771384%

반응 단계

Method B (12 h at 55° C.); starting materials: 2,3-dihydro-8-[3-(methanesulfonyloxy)propoxy]-7-methoxy-cyclopenta[c][1]-benzopyran-4(1H)-one (example 82) and 1-(4-fluorophenyl)piperazine; yield 84%; fusion point 139°-141° C. (from ethanol). Fumarate: method E; yield 90%; fusion point 195°-200° C. (from ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428038
출처 데이터셋uspto-grants-1995_06
ORD IDord-a9cd8dfe7fff459989a271e227763bd8
출처 메모uspto-grants-1995_06