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HRID 392379作成日:2026年10月26日

Potassium Carbonate → N-pyrimidinyl piperidine sulfonamide

https://huagongshe.com/reaction/392379

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-PiperidinesulfonamideHCID 276741—
反応物Ammonium formateHCID 2723923—
反応物2-Chloro-4-(trifluoromethyl)pyrimidineHCID 2773912—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
生成物N-pyrimidinyl piperidine sulfonamideHCID 2205266276%

反応手順

To a slurry of the piperidine sulfonamide from part F (6.3 g, 12.0 mmol) in methanol (25 mL) was added ammonium formate (2.2 g, 34.5 mmol). The system was purged with nitrogen for 10 minutes. The nitrogen stream was removed and palladium on carbon (1.2 g of 10 weight % on activated carbon, 50% water) was added. The reaction was refluxed for forty five minutes, cooled, filtered through Celite under nitrogen, and concentrated in vacuo. The residue (4.5 g, 10 mmol) was dissolved in dry dimethylformamide (20 mL) and potassium carbonate (4.14 g, 30 mmol) and 2-chloro-4-trifluoromethylpyrimidine (2.4 mL, 20 mmol) were added. The reaction was stirred at seventy degrees Celsius for three hour and then concentrated in vacuo. The residue was taken up in ethyl acetate and filtered through Celite. The filtrate washed with water two times, saturated sodium chloride solution, dried over Na2SO4, filtered, and concentrated in vacuo. The product was recrystallized (methanol) to give the N-pyrimidinyl piperidine sulfonamide as a white solid (4.51 g, 76%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06800646B1
出典データセットuspto-grants-2004_10
ORD IDord-ec745acc8ef74ee1a328678c818da859
出典メモuspto-grants-2004_10