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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2294835생성일: 2026년 10월 26일

Potassium Iodide → 6-Acetyl-3-(2-(4-(5-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/2294835

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물5-Fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochlorideHCID 2794754—
반응물6-Acety-3-(2-bromoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 21471935—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물6-Acetyl-3-(2-(4-(5-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridineHCID 2147203420.5%

반응 조건

온도90 °C

반응 단계

A mixture of 334 mg of 6-acetyl-3-(2-bromoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine, 308 mg of 4-(5-fluoro-1,2-benzisoxazol-3-yl)piperidine hydrochloride, 500 mg of potassium carbonate and 220 mg of potassium iodide in 10 ml of dimethylformamide and 10 ml of toluene was stirred at 90° C. for 25 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 100 mg of 6-acetyl-3-(2-(4-(5-fluoro-1,2-benzisoxazol-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine as an oil, m.p. 167°-172° C. as oxalate thereof.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05691330
출처 데이터셋uspto-grants-1997_11
ORD IDord-cb45a60e67c24fa19c67eb7b5f99763e
출처 메모uspto-grants-1997_11