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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1-tert-Butoxycarbonyl-4-(4-fluorophenylcarbamoyl)-piperazine | HCID 9840182 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-(4-Fluorophenyl)piperazine-1-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06710043B1 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-53b38b681f054caaba873f6a82e40bc2 |
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| 出典メモ | uspto-grants-2004_03 |
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