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HRID 50646作成日:2026年10月27日

Diisopropylethylamine → 1-[1-(4-Chloro-phenyl)-cyclobutanecarbonyl]-piperidin-3-ylmethyl alcohol

https://huagongshe.com/reaction/50646

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Piperidin-3-ylmethanolHCID 107308—
反応物1-(p-Chlorophenyl)cyclobutanecarboxylic acidHCID 602761—
反応物PyBroPHCID 2733179—
溶媒DichloromethaneHCID 6344—
生成物1-[1-(4-Chloro-phenyl)-cyclobutanecarbonyl]-piperidin-3-ylmethyl alcoholHCID 2190203543.4%

反応条件

温度0 °C

反応手順

To a solution of 3-piperidinemethanol (5.0 g, 43.4 mmol), 1-(4-chlorophenyl)-1-cyclobutanecarboxylic acid (9.14 g, 43.4 mmol), and diisopropylethylamine (11.22 g, 86.8 mmol) in dichloromethane (100 mL) at 0° C. was added PyBroP® (22.26 g, 47.8 mmol). The reaction was stirred at 0° C. for 1 h and then at room temperature for 4 h. The reaction mixture was washed successively with water, 1 N HCl, water, sat. sodium bicarbonate solution, and water (100 mL each). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated by rotary evaporation. The residue was purified by chromatography on silica gel, eluting with dichloromethane/methanol (96:4) to give 5.8 g of the amide 1 as a thick gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713479B2
出典データセットuspto-grants-2004_03
ORD IDord-6469e73dfeb34cdd8edaa7e1eb69d9b9
出典メモuspto-grants-2004_03