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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 547984생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/547984

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물1-PhenylpiperazineHCID 7096—
반응물TriethylamineHCID 8471—
반응물Sodium IodateHCID 23675764—
반응물5-Bromo-2-(4-bromophenyl)-2-isopropylpentanoic acid methyl esterHCID 46855860—
용매AcetonitrileHCID 6342—
생성물2-(4-Bromophenyl)-2-isopropyl-5-(4-phenylpiperazine-1-yl)pentanoic acid methyl esterHCID 46186740—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939672B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-5be30e553d664163ac3b72e36c175460
출처 메모uspto-grants-2011_05