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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 392374생성일: 2026년 10월 24일

Potassium Carbonate → HCID 22052572, 화합물

https://huagongshe.com/ko/reaction/392374

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Bromoethyl methyl etherHCID 80972—
반응물1-PiperidinesulfonamideHCID 276741—
반응물Ammonium formateHCID 2723923—
용매MethanolHCID 887—
생성물HCID 22052572HCID 2205257253%

반응 단계

To a slurry of the piperidine sulfonamide from part F (420 mg, 0.8 mmol) in methanol (15 mL) was added ammonium formate (147 mg, 2.3 mmol). The system was purged with nitrogen for 10 minutes. The nitrogen stream was removed and palladium on carbon (80 mg 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 was dissolved in dry dimethylformamide (5 mL) and potassium carbonate (150 mg, 1.07 mmol) and 2-bromoethyl methyl ether (100 mL, 1.07 mmol) were added. The reaction was stirred at thirty five degrees Celsius for thirty hours 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-methoxyethyl piperidine sulfonamide as an off-white solid (190 mg, 53%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06800646B1
출처 데이터셋uspto-grants-2004_10
ORD IDord-5ab576492c2d4687ae9f16af1b41da73
출처 메모uspto-grants-2004_10