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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1108208생성일: 2026년 10월 26일

Potassium Iodide → 5-Fluoro-3-(1-{2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl}piperidin-4-ylmethyl)-1H-indole

https://huagongshe.com/reaction/1108208

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1-(2-Chloroethyl)-4-(2-methoxyphenyl)piperazineHCID 595673—
반응물5-fluoro-3-[(4-piperidinyl)methyl]-1H-indoleHCID 11287716—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물5-Fluoro-3-(1-{2-[4-(2-methoxyphenyl)piperazin-1-yl]ethyl}piperidin-4-ylmethyl)-1H-indoleHCID 982501580%

반응 단계

Pulverized potassium carbonate (0.76 g, 5.5 mmole) and potassium iodide (0.97 g, 5.5 mmole) was added to a mixture of 4-(5-fluoro-1H-indol-3-ylmethyl)piperidine (1.16 g, 5.0 mmole) and 1-(2-chloroethyl)-4-(2-methoxyphenyl)piperazine (1.27 g, 5.0 mmole) in 25 ml of acetonitrile. The resulting mixture was heated to reflux under nitrogen for 5 hours. After cooling, it was diluted with water (150 ml) and the product extracted into ethyl acetate (50 ml). The organic layer was washed with water (50 ml), brine (50 ml), and after drying over sodium sulfate, filtration and concentration in vacuo afforded the required product as a white solid (1.8 g, 80%). Treatment with an excess of 1M etheral hydrochloric acid gave the acid addition salt, which was recrystallized from methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06066637
출처 데이터셋uspto-grants-2000_05
ORD IDord-c57ffb01e9a7445d9a831e48cdd8bab1
출처 메모uspto-grants-2000_05