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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1371905생성일: 2026년 10월 26일

Ethanol → Idalopirdine

https://huagongshe.com/reaction/1371905

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물2-(6-fluoro-1H-indol-3-yl)ethanamineHCID 854024—
반응물Sodium borohydrideHCID 4311764—
반응물2-(2,2,3,3-Tetrafluoropropoxy)benzaldehydeHCID 21071395—
생성물IdalopirdineHCID 21071390—

반응 단계

Combine 6-fluorotryptamine hydrochloride (90 g, 0.419 mol) and water (900 ml). Add an aqueous solution of NaOH (2N, 230 ml) and dichloromethane (900 ml). After 1 hour, separate the organic layer, extract the aqueous layer with dichloromethane, combine the organic layers, wash water, dry over MgSO4, and evaporate to a residue. Combine the residue and toluene (200 ml) and evaporate to give 78.45 g of a brown oil. Combine the above 78.5 g with another 41.4 g batch to provide 6-fluorotryptamine. Combine 6-fluorotryptamine (119.85) and ethanol (3.325 L), add 2,2,3,3-tetrafluoropropoxybenzaldehyde (176 g, 0.745 moles, 1.2 equiv.) and 150 g of molecular sleve 3 Å. Heat to reflux. After 2 hours, cool to RT room temperature and add NaBH4 (35.2 g, 0.93 mol, 1.5 equiv.). After 1 hour, filter through celite and wash with 500 ml of ethanol. Evaporate the filtrate under reduced pressure to give an oily residue. Partition the residue between water and dichloromethane. Separate the layers, extract the aqueous later with dichloromethane, combine organic layers, wash with brine and dry over MgSO4. Filter and evaporate under reduced pressure to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157488B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-1ee24821430c4021b582decf0c09565b
출처 메모uspto-grants-2007_01