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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8037생성일: 2026년 10월 23일

1-(2-Hydroxyethyl)piperazine → 2-(4-chlorocinnamyl)-6-(3-fluoro-4-methoxyphenyl)-4-[4-(2-hydroxyethyl)-1-piperazinyl]methyl-2H-pyridazin-3-one

https://huagongshe.com/ko/reaction/8037

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Hydroxyethyl)piperazineHCID 7677—
반응물4-(4-tert-butoxycarbonyl-1-piperazinyl)-methyl-6-(3-fluoro-4-methylphenyl)-2-isobutyl-2H-pyridazin-3-oneHCID 67214099—
반응물2-(4-chlorocinnamyl)-6-(3-fluoro-4-methoxyphenyl)-4-methane sulfonyloxymethyl-2H-pyridazin-3-oneHCID 73858284—
생성물2-(4-chlorocinnamyl)-6-(3-fluoro-4-methoxyphenyl)-4-[4-(2-hydroxyethyl)-1-piperazinyl]methyl-2H-pyridazin-3-oneHCID 6721340065.1%

반응 단계

Following the procedure of Example 1 (10), 2-(4-chlorocinnamyl)-6-(3-fluoro-4-methoxyphenyl)-4-methanesulfonyloxymethyl-2H-pyridazin-3-one and 1-piperazineethanol were reacted to yield the title compound as slightly-yellow needles (yield: 65.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087606B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-05e673c9e6fa437aa9ab215ba6dafd87
출처 메모uspto-grants-2006_08