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HRID 884939作成日:2026年10月25日
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3-tert-butoxycarbonylamino-N-[2-hydroxy-5-(trifluoromethyl)phenyl]isonicotinamide
https://huagongshe.com/reaction/884939
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| 反応物 | 2-Amino-4-(trifluoromethyl)phenol | HCID 120246 | — |
| 反応物 | 3-(((Tert-butoxy)carbonyl)amino)pyridine-4-carboxylic acid | HCID 21201523 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 3-tert-butoxycarbonylamino-N-[2-hydroxy-5-(trifluoromethyl)phenyl]isonicotinamide | HCID 66880252 | 75.3% |
反応手順
To a mixture of 1.15 g of WSC and 8 ml of pyridine, 1.43 g of 3-tert-butoxycarbonylamino isonicotinic acid was added and stirred at room temperature for 15 minutes. To the reaction mixture, 1.06 g of 2-amino-4-(trifluoromethyl)phenol was added and stirred while heating at 60° C. for two hours. Thereafter, the mixture reaction was cooled to room temperature, and then concentrated under reduced pressure. Water was added to the residue, followed by extraction with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to give 1.79 g of 3-tert-butoxycarbonylamino-N-[2-hydroxy-5-(trifluoromethyl)phenyl]isonicotinamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08242133B2 |
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| 出典データセット | uspto-grants-2012_08 |
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| ORD ID | ord-5427e9634e0a41ef8ae381d1b4fac1bf |
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| 出典メモ | uspto-grants-2012_08 |
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