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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37180생성일: 2026년 10월 24일

Pyridine → 6-Nicotinoyloxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxin

https://huagongshe.com/ko/reaction/37180

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Nicotinoyl chlorideHCID 82604—
반응물6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxinHCID 9804471—
용매1,1-DichloroethaneHCID 6365—
생성물6-Nicotinoyloxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxinHCID 1103907195%

반응 단계

Heat at reflux for 8 hours, under a nitrogen atmosphere, a solution of 1.37 mmol of 6-hydroxy -2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxin, 4.5 mmol of nicotinoyl chloride and 3.42 mmol of anhydrous pyridine in 25 cm3 of dichloroethane. After cooling, the reaction mixture is washed with a saturated aqueous solution of sodium hydrogen carbonate, dried over magnesium sulfate and then concentrated under reduced pressure. The crude product is then purified by chromatography on a silica column (eluant:petroleum ether/ethyl acetate, 70:30). 6-Nicotinoyloxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxin is thereby obtained in a yield of 95%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420132
출처 데이터셋uspto-grants-1995_05
ORD IDord-b2ef0a3e5ed74fb8848f6f01b8d0192a
출처 메모uspto-grants-1995_05