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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417977생성일: 2026년 10월 26일

1-Benzylpiperazine → 2-(4-Methylpiperazin-1-yl)ethyl 4-benzylpiperazine-1-carboxylate

https://huagongshe.com/reaction/417977

반응식

참여 물질

역할이름HCID투입량
반응물1-BenzylpiperazineHCID 75994—
반응물DiisopropylethylamineHCID 81531—
반응물2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
용매DimethylformamideHCID 6228—
생성물2-(4-Methylpiperazin-1-yl)ethyl 4-benzylpiperazine-1-carboxylateHCID 4263579860%

반응 단계

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 567 mg, 1.8 mmol) was dissolved in DMF (15 mL). DIPEA (0.52 mL, 3.0 mmol) and 4-benzyl-piperazine (0.296 mL, 1.7 mmol) were added. The reaction mixture was stirred at room temperature for 24 hours and then concentrated in vacuo. The residue was dissolved in EtOAc (40 mL) and washed with 1 M aq Na2CO3 solution (6×50 mL), dried (MgSO4) and concentrated in vacuo. The crude product was purified by reverse phase chromatography (gradient eluting with MeOH in water, 0-100%) to give 2-(4-methylpiperazin-1-yl)ethyl 4-benzylpiperazine-1-carboxylate (352 mg, 60% yield) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093248B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8af6a36b2aa94be18cd36b677ac064e1
출처 메모uspto-grants-2012_01