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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417970생성일: 2026년 10월 27일

1-(3-(Trifluoromethyl)phenyl)piperazine → 2-(4-Methylpiperazin-1-yl)ethyl 4-(3-trifluoromethyl-phenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/417970

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
반응물TriethylamineHCID 8471—
반응물2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
용매DimethylformamideHCID 6228—
생성물AmmoniaHCID 222—
생성물2-(4-Methylpiperazin-1-yl)ethyl 4-(3-trifluoromethyl-phenyl)piperazine-1-carboxylateHCID 42635623126.1%

반응 단계

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 761 mg, 2.5 mmol) was dissolved in DMF (20 mL). NEt3 (0.4 mL, 2.9 mmol) and 4-(3-trifluoromethyl-phenyl)piperazine (583 mg, 2.5 mmol) were added and the reaction mixture was stirred at room temperature for 24 hours, the reaction mixture was then concentrated in vacuo. The resulting residue was dissolved in EtOAc (50 mL) and washed with 1 M aq Na2CO3 solution (5×50 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by normal phase column chromatography (eluting with DCM, followed by a 100:8:1 mixture of DCM:EtOH:NH3) to give 2-(4-methylpiperazin-1-yl)ethyl 4-(3-trifluoromethyl-phenyl)piperazine-1-carboxylate (631 mg, 64%) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093248B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-8139c60e46dd481ba056a1403dd7669b
출처 메모uspto-grants-2012_01