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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7915생성일: 2026년 10월 23일

Water → 4-(4-tert-butoxycarbonyl-1-piperazinyl)-methyl-6-(3-fluoro-4-methylphenyl)-2-isobutyl-2H-pyridazin-3-one

https://huagongshe.com/ko/reaction/7915

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물6-(3-fluoro-4-methylphenyl)-2-isobutyl-4-methane-sulfonyloxymethyl-2H-pyridazin-3-oneHCID 21991531—
용매AcetonitrileHCID 6342—
생성물4-(4-tert-butoxycarbonyl-1-piperazinyl)-methyl-6-(3-fluoro-4-methylphenyl)-2-isobutyl-2H-pyridazin-3-oneHCID 6721409992.9%

반응 조건

온도80 °C

반응 단계

To a solution of 6-(3-fluoro-4-methylphenyl)-2-isobutyl-4-methanesulfonyloxy methyl-2H-pyridazin-3-one (100 mg, 0.27 mmol) in acetonitrile (1 mL) were added potassium carbonate (56.3 mg, 0.41 mmol) and tert-butyl 1-piperazine-carboxylate (60.7 mg, 0.33 mmol), and the mixture was stirred at 80° C. for 2 hours. The temperature of the reaction mixture was allowed to drop back to room temperature, and then, water was added. The mixture was extracted with chloroform. The extract was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel [chloroform/methanol (40/1)] to yield the title compound as a yellow oil (115 mg, 92.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087606B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-fe9e652ae9ab4faca893097b8edf8b1c
출처 메모uspto-grants-2006_08