戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 49792作成日:2026年10月25日

1-tert-Butoxycarbonyl-4-(4-fluorophenylcarbamoyl)-piperazine → N-(4-Fluorophenyl)piperazine-1-carboxamide

https://huagongshe.com/reaction/49792

反応式

関与物質

役割名称HCID仕込み量
反応物1-tert-Butoxycarbonyl-4-(4-fluorophenylcarbamoyl)-piperazineHCID 9840182—
溶媒Hydrochloric AcidHCID 313—
溶媒Ethyl AcetateHCID 8857—
生成物N-(4-Fluorophenyl)piperazine-1-carboxamideHCID 16228149—

反応手順

1-tert-Butoxycarbonyl-4-(4-fluorophenylcarbamoyl)-piperazine (0.30 g) was dissolved in a solution of hydrogen chloride in ethyl acetate (4N, 2 ml), and the solution was stirred at ambient temperature for 1 hour. The solvent was removed by evaporation under reduced pressure to give 1-(4-fluorophenylcarbamoyl)piperazine as a white powder, which was taken up into dichloromethane (3 ml), and to the mixture were added in turn pyridine (0.25 ml), 4-trifluoromethoxybenzoyl chloride (0.146 ml), and catalytic amount of N,N-dimethylaminopyridine. After stirring at ambient temperature for 12 hours, the mixture was washed in turn with hydrochloric acid (0.5N), aqueous sodium hydrogen carbonate, and brine, dried over magnesium sulfate, and evaporated under reduced pressure. The residue was chromatographed on silica gel (50 ml) eluting with 0%-3% methanol in dichloromethane to give 1-(4-fluorophenylcarbamoyl)-4-(4-trifluoromethoxybenzoyl)-piperazine (0.19 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710043B1
出典データセットuspto-grants-2004_03
ORD IDord-53b38b681f054caaba873f6a82e40bc2
出典メモuspto-grants-2004_03