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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417968생성일: 2026년 10월 26일

1-Phenylpiperazine → 2-(4-Methyl-piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate formate

https://huagongshe.com/reaction/417968

반응식

참여 물질

역할이름HCID투입량
반응물1-PhenylpiperazineHCID 7096—
반응물DiisopropylethylamineHCID 81531—
반응물2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
용매DimethylformamideHCID 6228—
생성물2-(4-Methyl-piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate formateHCID 6665098811.7%

반응 단계

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 1.58 g, 5.1 mmol) was dissolved in DMF (25 mL). DIPEA (0.87 mL, 5.0 mmol) and 4-phenyl-piperazine (807 mg, 0.76 mL, 5.0 mmol) were added and the reaction mixture was stirred at room temperature for 14 hours. The reaction mixture was then concentrated in vacuo. The residue was purified by reverse phase column chromatography (gradient eluting with MeOH in water, with 1% formic acid in each solvent, 0-100%) to give 2-(4-methyl-piperazin-1-yl)ethyl 4-phenylpiperazine-1-carboxylate formate (113 mg, 6.7%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093248B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-e3baaee6b1f2426fad3952ca369662ae
출처 메모uspto-grants-2012_01