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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Piperazine, 1-(4-chlorophenyl)-, hydrochloride (1:2) | HCID 12212341 | — |
| 반응물 | 2-(4-Methylpiperazin-1-yl)ethyl 4-nitrophenyl carbonate | HCID 57445007 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Ammonia | HCID 222 | — |
| 생성물 | 2-(4-Methylpiperazin-1-yl)-ethyl 4-(4-chlorophenyl)piperazine-1-carboxylate | HCID 42635622 | 158.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08093248B2 |
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| 출처 데이터셋 | uspto-grants-2012_01 |
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| ORD ID | ord-f07f9e367e1041eab2c25ceface38d43 |
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| 출처 메모 | uspto-grants-2012_01 |
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