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HRID 1006059생성일: 2026년 10월 26일

Potassium Iodide → N-(2-(1-naphthyl)ethyl)-4-(2-bromo-5-methoxybenzyl)piperidine

https://huagongshe.com/reaction/1006059

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물Methanesulfonyl chlorideHCID 31297—
반응물1-(1-Naphthyl)ethanolHCID 98030—
반응물4-(2-Bromo-5-methoxybenzyl)piperidine hydrochlorideHCID 22675334—
용매DichloromethaneHCID 6344—
생성물N-(2-(1-naphthyl)ethyl)-4-(2-bromo-5-methoxybenzyl)piperidineHCID 1296887381%

반응 단계

Methanesulfonyl chloride (100 μl, 1.26 mmol) was added dropwise to a solution of 1-naphthylethanol (206 mg, 1.20 mmol) and triethylamine (350 μl, 2.40 mmol) in dichloromethane (2 ml) under ice-cooling and stirred for 3 hours. The solvent was distilled off and the resulting residue was dissolved in acetonitrile (3 ml) together with a base converted from 4-(2-bromo-5-methoxybenzyl)piperidine hydrochloride (384 mg, 1.20 mmol) according to the method described in Example 11, potassium iodide (199 mg, 1.20 mmol) and potassium carbonate (332 mg, 2.40 mmol). The resulting solution was heated under reflux for 3.5 hours and then allowed to cool. The precipitate was filtered off and the filtrate was concentrated, and then the residue was purified by a silica gel column chromatography (chloroform:methanol=20:1) to obtain the title compound (425 mg, 81%) as a light-brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06787560B2
출처 데이터셋uspto-grants-2004_09
ORD IDord-42d154bb417940aa99b4d83fad8fa025
출처 메모uspto-grants-2004_09