Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417956생성일: 2026년 10월 25일
1-(4-Fluorophenyl)piperazine → (1-Methylpiperidin-4-yl)methyl 4-(4-fluorophenyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/417956
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-(4-Fluorophenyl)piperazine | HCID 75260 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | (1-Methylpiperidin-4-yl)methyl 4-nitrophenyl carbonate | HCID 57445006 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (1-Methylpiperidin-4-yl)methyl 4-(4-fluorophenyl)piperazine-1-carboxylate | HCID 42609860 | 11.8% |
반응 단계
(1-Methylpiperidin-4-yl)methyl 4-nitrophenyl carbonate (Intermediate 1; 4.99 g, 16.9 mmol) was dissolved in DMF (40 mL). DIPEA (5.90 mL, 33.9 mmol) and 4-(4-fluoro-phenyl)piperazine (3.21 g, 17.8 mmol) were added. The reaction mixture was stirred at room temperature for 3 h and then concentrated in vacuo. The residue was dissolved in EtOAc (400 mL) and then washed sequentially with 1 M aq NaOH solution (6×150 mL), brine (50 mL), dried (MgSO4) and concentrated in vacuo. The residue was dissolved in DCM (100 mL) and methyl isocyanate resin (1.0 g) was added. The reaction mixture was shaken for 14 h, filtered and then concentrated in vacuo. The residue was purified by reverse phase chromatography (gradient eluting with MeOH in water, with 1% formic acid in each solvent, 0-30%). The resulting residue was dissolved in DCM (70 mL) and stirred with solid K2CO3 for 20 minutes, filtered and concentrated in vacuo to give (1-methylpiperidin-4-yl)methyl 4-(4-fluorophenyl)piperazine-1-carboxylate (0.67 g, 11.8%) as a pale yellow oil.
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-2e1b090cf6c0463e87ea83d24c77f027 |
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| 출처 메모 | uspto-grants-2012_01 |
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