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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1452318생성일: 2026년 10월 26일

Water → 8-{3-[4-(2-Methoxyphenyl)-1-piperazinyl]-propoxycarbonyl}-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran dihydrochloride

https://huagongshe.com/reaction/1452318

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물3-Methylflavone-8-carboxylic acidHCID 77016—
반응물1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
용매DimethylformamideHCID 6228—
생성물8-{3-[4-(2-Methoxyphenyl)-1-piperazinyl]-propoxycarbonyl}-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran dihydrochlorideHCID 19972518—

반응 조건

온도80 °C

반응 단계

A mixture of 4.24 g of 8-carboxy-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran and 6.3 g of anhydrous potassium carbonate in 60 ml of dimethylformamide was stirred at 80° C. for 30 minutes. 5.23 g of 1-(3-chloropropyl)-4-(2-methoxyphenyl)-piperazine was then added and stirring was continued at 80° C. for 3.5 hours. The reaction mixture was cooled to ambient temperature, poured on to iced water and extracted with ethyl acetate. The organic extracts were washed with aqueous sodium chloride solution, dried on anhydrous sodium sulfate, and evaporated to dryness in vacuo. The residue was taken up in ethanol and excess ethanolic hydrogen chloride was added to the solution. Yield: 8.16 g of the title compound, m.p. 198°-203° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05605896
출처 데이터셋uspto-grants-1997_02
ORD IDord-2e4fa8d28f9d4926887f7aec3539bd5e
출처 메모uspto-grants-1997_02