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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

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Fluorophenyl)piperazineHCID 75260—
반응물DiisopropylethylamineHCID 81531—
반응물(1-Methylpiperidin-4-yl)methyl 4-nitrophenyl carbonateHCID 57445006—
용매DimethylformamideHCID 6228—
생성물(1-Methylpiperidin-4-yl)methyl 4-(4-fluorophenyl)piperazine-1-carboxylateHCID 4260986011.8%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093248B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-2e1b090cf6c0463e87ea83d24c77f027
출처 메모uspto-grants-2012_01