戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1913702作成日:2026年10月27日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3-tert-butoxycarbonylamino-N-[2-hydroxy-5-(trifluoromethyl)phenyl]isonicotinamide

https://huagongshe.com/reaction/1913702

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2-Amino-4-(trifluoromethyl)phenolHCID 120246—
反応物3-(((Tert-butoxy)carbonyl)amino)pyridine-4-carboxylic acidHCID 21201523—
溶媒PyridineHCID 1049—
生成物3-tert-butoxycarbonylamino-N-[2-hydroxy-5-(trifluoromethyl)phenyl]isonicotinamideHCID 6688025275.3%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08609705B2
出典データセットuspto-grants-2013_12
ORD IDord-620d426e3f76424a84deafb4e48224f6
出典メモuspto-grants-2013_12