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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2232407생성일: 2026년 10월 26일

Potassium Carbonate → N-Methyl-4-[4-(4-pyridyl)piperazin-1-yl]benzenesulphonamide

https://huagongshe.com/reaction/2232407

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-(4-Pyridyl)piperazineHCID 70517—
반응물4-fluoro-N-methylbenzene-1-sulfonamideHCID 2440054—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물N-Methyl-4-[4-(4-pyridyl)piperazin-1-yl]benzenesulphonamideHCID 212835366.9%

반응 조건

온도100 °C

반응 단계

A mixture of 1-(4-pyridyl)piperazine (0.86 g), N-methyl-4-fluorobenzenesulphonamide (1.00 g) and potassium carbonate (2.00 g) in N-methylpyrrolidone was stirred at 100° C. for 24 hours and then evaporated. The residue was partitioned between dichloromethane and 2N hydrochloric acid. The acid layer was washed with dichloromethane, filtered and made basic with sodium bicarbonate solution. The mixture was extracted several times with chloroform, and the combined extracts were washed with water, dried over magnesium sulphate and evaporated. The residue was crystallised from ethanol/ethyl acetate to give the title compound (0.12 g), m.p. 204°-206° C. Found: C,57.55; H,6.13; N,16.62. C16H20N4O2S requires: C,57.81; H,6.06; N,16.85%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04788196
출처 데이터셋uspto-grants-1988_11
ORD IDord-542a1ec6e4ad4a5d9140fb585b095058
출처 메모uspto-grants-1988_11