戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 56038作成日:2026年10月25日

Ammonium Chloride → N-[2-(3,5-dibromopyridine-2-yl)-2-oxoethyl]-2-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/56038

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物3,5-DibromopyridineHCID 69369—
反応物Tetrahydrofuran tolueneHCID 22635083—
反応物N-[2-methoxy(methyl)amino-2-oxoethyl]-2-(trifluoromethyl)benzamideHCID 118071607—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物N-[2-(3,5-dibromopyridine-2-yl)-2-oxoethyl]-2-(trifluoromethyl)benzamideHCID 11807157813.7%

反応条件

温度-20 °C

反応手順

To 5.5 g of 3,5-dibromopyridine in 1 ml of tetrahydrofuran, 22.7 ml of a 1.0M tetrahydrofuran-toluene solution of 2,2,6,6-tetramethylpiperidinylmagnesium chloride-lithium chloride complex was added dropwise with stirring at −20° C., and after the addition, the mixture was stirred at the same temperature for 30 minutes. Then, to the reaction mixture, 3.0 g of the N-[2-methoxy(methyl)amino-2-oxoethyl]-2-(trifluoromethyl)benzamide prepared in Step 1 in Synthetic Example 17 in 17 ml of tetrahydrofuran was added dropwise, and after the addition, the mixture was stirred at the same temperature for another 1 hour. After completion of the reaction, the reaction mixture was mixed with 30 ml of saturated aqueous ammonium chloride and 20 ml of water and extracted with ethyl acetate (50 ml×2), the resulting organic layers were combined, washed with water (50 ml×1) and dried over saturated aqueous sodium chloride and then anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography using ethyl acetate-hexane (with a gradient of from 5:95 to 50:50) as the eluent to obtain 659 mg of the desired product as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434684B2
出典データセットuspto-grants-2016_09
ORD IDord-7a084dc2967e48f9a2e64d58421cc3cf
出典メモuspto-grants-2016_09