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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 892446생성일: 2026년 10월 25일

Potassium Iodide → 4-(4-Methylsulfonylaminobenzoyl)-1-[2-(3-pyridyl)ethyl]piperidine dihydrochloride

https://huagongshe.com/reaction/892446

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물Pyridine, 3-(2-chloroethyl)-, hydrochlorideHCID 199465—
반응물N-[4-(piperidine-4-carbonyl)-phenyl]methanesulfonamide hydrochlorideHCID 14130042—
용매DimethylformamideHCID 6228—
생성물4-(4-Methylsulfonylaminobenzoyl)-1-[2-(3-pyridyl)ethyl]piperidine dihydrochlorideHCID 1413004628.8%

반응 조건

온도40 °C

반응 단계

35 g (0.101 mol) of 4-(4-methylsulfonylaminobenzoyl)piperidine hydrochloride and 55 g of potassium carbonate were suspended in 700 ml of dimethylformamide and the suspension was stirred at 40° C. for 20 min. 19.6 g (0.101 mol) of 3-(2-chloroethyl)pyridine hydrochloride and 6.0 g (0.036 mol) of potassium iodide were added to the suspension and the mixture was stirred at 90° C. for 3.5 h. The liquid reaction mixture was filtered and the filtrate was concentrated, while the residue was purified according to silica gel chromatography (chloroform:methanol=93.7). The purified product was converted into its hydrochloride with ethanolic hydrogen chloride and recrystallized from methanol/ispropanol to obtain 13.4 g of the intended compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05118689
출처 데이터셋uspto-grants-1992_06
ORD IDord-8c78914681234ccf8397e0e2837f7883
출처 메모uspto-grants-1992_06