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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1377024생성일: 2026년 10월 27일

Hydrochloric Acid → N-{1-[2-(6-Methyl-2-pyridyl)ethyl]-4-piperidyl}-4-(N-methylamino)benzenesulfonamide

https://huagongshe.com/reaction/1377024

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물2-Ethenyl-6-methylpyridineHCID 70735—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium AcetateHCID 517045—
반응물N-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetateHCID 67690431—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물N-{1-[2-(6-Methyl-2-pyridyl)ethyl]-4-piperidyl}-4-(N-methylamino)benzenesulfonamideHCID 2291893670%

반응 단계

The N-(4-piperidyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide acetate (3.71 g, 10.0 mmol), 6-methyl-2-vinylpyridine (1.43 g, 12.0 mmol) and sodium acetate (0.82 g) were dissolved in a mixture comprising methanol (20 ml) and water (20 ml). The obtained solution was heated under reflux for 5 hours, followed by the addition of sodium hydroxide (3.20 g). The obtained mixture was heated under reflux for additional three hours and acidified with 2N aqueous hydrochloric acid. The pH of the mixture was adjusted to about 8 with an aqueous solution of sodium hydrogencarbonate. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of common salt, dried over magnesium sulfate and concentrated. The obtained oily residue was purified by column chromatography (chloroform:methanol:aqueous ammonia=90:9:1) and recrystallized from ethyl acetate/ether to give the title compound as a white crystal (2.71 g, overall yield of two steps: 70%). m.p. (°C.): 80 to 84

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05663414
출처 데이터셋uspto-grants-1997_09
ORD IDord-a31a93ab971f4668b2de0a3fbc47d964
출처 메모uspto-grants-1997_09