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HRID 547984作成日:2026年10月27日

Piperazine → 2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester

https://huagongshe.com/reaction/547984

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物1-PhenylpiperazineHCID 7096—
反応物TriethylamineHCID 8471—
反応物Sodium IodateHCID 23675764—
反応物5-Bromo-2-(4-bromophenyl)-2-isopropylpentanoic acid methyl esterHCID 46855860—
溶媒AcetonitrileHCID 6342—
生成物2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl esterHCID 46186740—

反応手順

After the 5-bromo-2-(4-bromophenyl)-2-isopropylpentanoic acid methyl ester (200 mg, 1 eq) was dissolved in acetonitrile, 4-phenylpiperazine (70 mg, 1 eq) as a piperazine derivative, Et3N (0.06 ml, 1.2 eq), and sodium iodate were added into the solution and heated and refluxed for 3 hours. When the reaction was completed, the precipitate was filtrated and the mixture was vacuum distilled and extracted with ethyl acetate and water. After the organic layer was washed with 1N HCl and saturated NaHCO3, the target compound 2-(4-bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl ester was obtained by drying the mixture with anhydrous sodium sulfate and removing the solvent at low pressures (69 mg, 42%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07939672B2
出典データセットuspto-grants-2011_05
ORD IDord-5be30e553d664163ac3b72e36c175460
出典メモuspto-grants-2011_05