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HRID 1006059作成日:2026年10月27日

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

https://huagongshe.com/reaction/1006059

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物TriethylamineHCID 8471—
反応物Potassium CarbonateHCID 11430—
反応物Methanesulfonyl chlorideHCID 31297—
反応物1-(1-Naphthyl)ethanolHCID 98030—
反応物4-(2-Bromo-5-methoxybenzyl)piperidine hydrochlorideHCID 22675334—
溶媒DichloromethaneHCID 6344—
生成物N-(2-(1-naphthyl)ethyl)-4-(2-bromo-5-methoxybenzyl)piperidineHCID 1296887381%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06787560B2
出典データセットuspto-grants-2004_09
ORD IDord-42d154bb417940aa99b4d83fad8fa025
出典メモuspto-grants-2004_09