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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294836생성일: 2026년 10월 26일

Potassium Iodide → 6-Acetyl-3-(2-(4-(6-fluorobenzo(b)thiophen-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine

https://huagongshe.com/reaction/2294836

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물6-Acety-3-(2-bromoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 21471935—
반응물4-(6-Fluorobenzo(b)thiophen-3-yl)piperidine hydrochlorideHCID 22649334—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물6-Acetyl-3-(2-(4-(6-fluorobenzo(b)thiophen-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 2147184450.4%

반응 조건

온도90 °C

반응 단계

A mixture of 210 mg of 6-acetyl-3-(2-bromoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine, 200 mg of 4-(6-fluorobenzo(b)thiophen-3-yl)piperidine hydrochloride, 250 mg of potassium carbonate and 140 mg of potassium iodide in 5 ml of dimethylformamide and 5 ml of toluene was stirred at 90° C. for 22 hours and concentrated in vacuo. To the residue were added ethyl acetate and water, and separated. The ethyl acetate layer was washed with water, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on a silica gel to give 160 mg of 6-acetyl-3-(2-(4-(6-fluorobenzo(b)thiophen-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05691330
출처 데이터셋uspto-grants-1997_11
ORD IDord-9bc56f9c34be44699094c0221c785768
출처 메모uspto-grants-1997_11