戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1452318作成日:2026年10月25日

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

https://huagongshe.com/reaction/1452318

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物3-Methylflavone-8-carboxylic acidHCID 77016—
反応物1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
溶媒DimethylformamideHCID 6228—
生成物8-{3-[4-(2-Methoxyphenyl)-1-piperazinyl]-propoxycarbonyl}-3-methyl-4-oxo-2-phenyl-4H-1-benzopyran dihydrochlorideHCID 19972518—

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05605896
出典データセットuspto-grants-1997_02
ORD IDord-2e4fa8d28f9d4926887f7aec3539bd5e
出典メモuspto-grants-1997_02