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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294814생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2294814

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물R-56109 hydrochlorideHCID 11334359—
반응물6-Acety-3-(2-bromoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 21471935—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물6-Acetyl-3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl) ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 21471925—

반응 조건

온도50 °C

반응 단계

A mixture of 5.9 g of 6-acetyl-3-(2-bromoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine, 5 g of 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine hydrochloride, 6.7 g of potassium carbonate and 3.2 g of potassium iodide in 50 ml of dimethylformamide and 50 ml of toluene was stirred at 50° C. for 7 hours and poured into water. The toluene layer was washed with water, dried over magnesium sulfate and concentrated. The residue was purified by column chromatography on a silica gel and crystallized from isopropyl ether. The resulting crystals were recrystallized from acetonitrile to give 6-acetyl-3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine, m.p. 70°-75° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05691330
출처 데이터셋uspto-grants-1997_11
ORD IDord-689f83469952498fbd33354ebb36e529
출처 메모uspto-grants-1997_11