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HRID 50658作成日:2026年10月27日

Diisopropylethylamine → 1-[1-(4-Chloro-phenyl)-cyclopropanecarbonyl]-piperidine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/50658

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物1-(p-Chlorophenyl)cyclopropanecarboxylic acidHCID 98606—
反応物Ethyl nipecotateHCID 98969—
反応物PyBroPHCID 2733179—
溶媒DichloromethaneHCID 6344—
生成物1-[1-(4-Chloro-phenyl)-cyclopropanecarbonyl]-piperidine-3-carboxylic acid ethyl esterHCID 21303200167.5%

反応手順

A solution of piperidine-3-carboxylic acid ethyl ester (10.0 g, 0.032 mol), 1-(4-chloro-phenyl)-cyclopropylcarboxylic acid (9.57 g, 0.049 mol), diisopropylethyl amine (21.0 g, 0.16 mol) in dichloromethane (160 mL) was stirred at room temperature. PyBroP (22.6 g, 0.49 mol) was added and the reaction mixture continued stirring at room temperature. After 12 h the reaction mixture was quenched with 10% KOH. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated to yield a crude oil. The crude material was purified using silica gel chromatography (80:20 hexane:ethyl acetate) to yield the amide (18.0 g).

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-25ed3f05cf2c4ab4bc562403d65e3039
出典メモuspto-grants-2004_03