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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417969생성일: 2026년 10월 26일

Triethylamine → 2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/417969

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Piperazine, 1-(4-chlorophenyl)-, hydrochloride (1:2)HCID 12212341—
반응물2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonateHCID 57445007—
용매DimethylformamideHCID 6228—
생성물AmmoniaHCID 222—
생성물2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylateHCID 42635622158.1%

반응 단계

2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate (Intermediate 4; 740 mg, 2.4 mmol) was dissolved in DMF (20 mL). NEt3 (1.2 mL, 8.6 mmol) and 4-(4-chlorophenyl)piperazine dihydrochloride (691 mg, 2.6 mmol) were added and the reaction mixture was stirred at room temperature for 24 hours, and the reaction mixture was then concentrated in vacuo. The resulting residue was dissolved in EtOAc (50 mL) and washed with 1M 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-(4-chlorophenyl)piperazine-1-carboxylate (696 mg, 79%) as a colourless oil which crystallized on standing to give a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093248B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-f07f9e367e1041eab2c25ceface38d43
출처 메모uspto-grants-2012_01