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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2064182생성일: 2026년 10월 26일

Diisopropylethylamine → N-(5-Bromo-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamine

https://huagongshe.com/reaction/2064182

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Bromo-2,5-difluoronitrobenzeneHCID 2736286—
반응물1-(Oxan-4-yl)piperidin-4-amine dihydrochlorideHCID 45156751—
용매DimethylformamideHCID 6228—
생성물N-(5-Bromo-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamineHCID 59850147107.7%

반응 조건

온도200 °C

반응 단계

A mixture of 4-bromo-2,5-difluoro-1-nitrobenzene (1 g, 4.2 mmol), 1-(tetrahydro-2H-pyran-4yl)piperidin-4-amine dihydrochloride salt (D40, 1.08 g, 4.2 mmol), and di-iso-propylethylamine (2.2 ml, 1.26 mmol) in dimethylformamide (10 ml) was heated in microwave reactor for 5 min at 200° C. The mixture was washed with water, then extracted with dichloromethane and the extract dried over MgSO4 and concentrated under vacuum. The crude material was purified on silica column (100 g of silica, ethyl acetate/methanol: 1.0% to 0%, 3CV; 2.0% to 100% 2CV 3. 100% to 100% 5CV) to leave 1.82 g (96%) of a mixture of title compound and an unknown impurity (˜3:1 by HPLC).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08288412B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-afd837f064b7470e8672d0888b02859a
출처 메모uspto-grants-2012_10