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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392379생성일: 2026년 10월 24일

Potassium Carbonate → N-pyrimidinyl piperidine sulfonamide

https://huagongshe.com/ko/reaction/392379

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-PiperidinesulfonamideHCID 276741—
반응물Ammonium formateHCID 2723923—
반응물2-Chloro-4-(trifluoromethyl)pyrimidineHCID 2773912—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물N-pyrimidinyl piperidine sulfonamideHCID 2205266276%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06800646B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-ec745acc8ef74ee1a328678c818da859
출처 메모uspto-grants-2004_10