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HRID 512029생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/512029

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물Methanesulfonyl chlorideHCID 31297—
반응물(5-Chloropyridin-2-yl)methanolHCID 20537893—
반응물2,5-difluoro-4-hydroxy-N-(methylsulfonyl)benzamideHCID 58042416—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-[(5-Chloropyridin-2-yl)methoxy]-2,5-difluoro-N-(methylsulfonyl)benzamide diethylamine saltHCID 86682567—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102621B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-3f891cc096084a35aafa378cfe49e8d8
출처 메모uspto-grants-2015_08