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HRID 2064182作成日:2026年10月27日

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

https://huagongshe.com/reaction/2064182

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Bromo-2,5-difluoronitrobenzeneHCID 2736286—
反応物1-(Oxan-4-yl)piperidin-4-amine dihydrochlorideHCID 45156751—
溶媒DimethylformamideHCID 6228—
生成物N-(5-Bromo-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamineHCID 59850147107.7%

反応条件

温度200 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08288412B2
出典データセットuspto-grants-2012_10
ORD IDord-afd837f064b7470e8672d0888b02859a
出典メモuspto-grants-2012_10