戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 512029作成日:2026年10月27日

Triethylamine → 4-[(5-Chloropyridin-2-yl)methoxy]-2,5-difluoro-N-(methylsulfonyl)benzamide diethylamine salt

https://huagongshe.com/reaction/512029

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Potassium CarbonateHCID 11430—
反応物Methanesulfonyl chlorideHCID 31297—
反応物(5-Chloropyridin-2-yl)methanolHCID 20537893—
反応物2,5-difluoro-4-hydroxy-N-(methylsulfonyl)benzamideHCID 58042416—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物4-[(5-Chloropyridin-2-yl)methoxy]-2,5-difluoro-N-(methylsulfonyl)benzamide diethylamine saltHCID 86682567—

反応手順

To a solution of (5-chloropyridin-2-yl)methanol (15 mg, 0.105 mmol), in dichloromethane (5 mL) and triethylamine (0.02 mL, 0.157 mmol) was added methanesulfonyl chloride (0.01 mL, 0.115 mmol). The reaction was stirred at room temperature for 2 hours. The solvent was removed in vacuo to afford a residue, which was taken up in DMSO (5 mL). Potassium carbonate (43 mg, 0.315 mmol) was added, followed by 2,5-difluoro-4-hydroxy-N-(methylsulfonyl)benzamide (Preparation 110, 29 mg, 0.115 mmol) and the reaction was heated to 50° C. overnight. The reaction mixture was cooled to room temperature, diluted with water (10 mL) and extracted with ethyl acetate (3×10 mL). The combined organic layers were dried over sodium sulphate, filtered and concentrated in vacuo. The resulting residue was purified by preparative HPLC to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102621B2
出典データセットuspto-grants-2015_08
ORD IDord-3f891cc096084a35aafa378cfe49e8d8
出典メモuspto-grants-2015_08