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HRID 37164作成日:2026年10月25日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxin

https://huagongshe.com/reaction/37164

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
反応物6-Hydroxy-1,4-benzodioxin-2-carboxylic acidHCID 11063291—
反応物HCID 178418300HCID 178418300—
溶媒DimethylformamideHCID 6228—
生成物6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxinHCID 980447185%

反応条件

温度0 °C

反応手順

Under a nitrogen atmosphere, add 5.5 mmol of 1-[bis(4-fluorophenyl)methyl]piperazine, 5.5 mmol of EDCI (1-(3-dimethylaminopropyl)-3-ethylcarbodiimide) and 5.5 mmol of HOBt (hydroxybenzotriazole) in succession to a solution at 0° C. of 5 nmml of 6-hydroxy-1,4-benzodioxin -2-carboxylic acid in 25 cm3 of N,N-dimethylformamide. Stir for 2 hours at 0° C. and then for 12 hours at room temperature, and concentrate the reaction mixture under reduced pressure. Extract the resulting amide with diethyl ether and then, after concentration to dryness, purify the crude product by chromatography on a silica column (eluant:petroleum ether then an increasing gradient of ethyl acetate in petroleum ether). 6-Hydroxy-2-{4-[bis-(4-fluorophenyl)methyl]piperazin-1-ylcarbonyl}-1,4-benzodioxin is thereby obtained in a yield of 85%. The product obtained is precipitated from 10 ml of pentane and is then filtered and recrystallised from cyclohexane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420132
出典データセットuspto-grants-1995_05
ORD IDord-da61facdfcae4470a9b632686e8809ea
出典メモuspto-grants-1995_05