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HRID 49961作成日:2026年10月26日

4-Butyloxyaniline → N-(4-n-butoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamide

https://huagongshe.com/reaction/49961

反応式

関与物質

役割名称HCID仕込み量
反応物4-ButyloxyanilineHCID 20352—
反応物Phosphorus oxychlorideHCID 24813—
反応物Sodium BicarbonateHCID 516892—
反応物(1-Benzyl-4-hydroxypiperidin-4-yl) acetic acid lithium saltHCID 69894340—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物N-(4-n-butoxyphenyl)-2-(1-benzyl-4-hydroxypiperidin-4-yl)acetamideHCID 1782386524%

反応条件

温度7.5 °C

反応手順

To a solution of (1-benzyl-4-hydroxypiperidin-4-yl) acetic acid lithium salt (3.09 g) in methylene chloride (60 mL) were added 4-n-butoxyaniline (2.0 g) and pyridine (2.14 mL). Phosphorous oxychloride (1.19 mL) was added dropwise to the solution under cooling with an ice-sodium chloride, followed by stirring at 5 to 10° C. for 1 hour. The mixture was made alkaline with saturated aqueous sodium bicarbonate under cooling with an ice-water, and the solution was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over anhydrous sodium sulfate, and then, the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography (elution solvent; methylene chloride:methanol=19:1 to 9:1) to obtain the titled compound (1.15 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710060B2
出典データセットuspto-grants-2004_03
ORD IDord-23334740640f45f081f14beef34c204b
出典メモuspto-grants-2004_03