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HRID 50656作成日:2026年10月26日

Diisopropylethylamine → [1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanone

https://huagongshe.com/reaction/50656

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-(4-Chlorophenyl)cyclopentanecarboxylic acidHCID 97447—
反応物Piperidin-3-ylmethanolHCID 107308—
反応物PyBroPHCID 2733179—
溶媒DichloromethaneHCID 6344—
生成物[1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanoneHCID 22335026156.9%

反応手順

A solution of piperdin-3-yl methanol (0.342 g, 2.97 mmol), 1-(4-chloro-phenyl)-cyclopentylcarboxylic acid (1.0 g, 4.45 mmol), diisopropylethyl amine (1.9, 15.00 mmol) in dichloromethane (7 mL) was stirred at room temperature. PyBroP (2.07 g, 4.45 mmol) 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 (95:5 hexane:ethyl acetate) to yield the desired compound (1.50 g). C18H24ClNO2, LRMS (m/z)=322 (MH+).

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-f01119f38d2b4a158dbe36d70edafa10
出典メモuspto-grants-2004_03