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HRID 392374作成日:2026年10月25日

Potassium Carbonate → HCID 22052572、化合物

https://huagongshe.com/reaction/392374

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2-Bromoethyl methyl etherHCID 80972—
反応物1-PiperidinesulfonamideHCID 276741—
反応物Ammonium formateHCID 2723923—
溶媒MethanolHCID 887—
生成物HCID 22052572HCID 2205257253%

反応手順

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%).

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-5ab576492c2d4687ae9f16af1b41da73
出典メモuspto-grants-2004_10