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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2064182Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2064182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4-Bromo-2,5-difluoronitrobenzeneHCID 2736286—
Edukt1-(Oxan-4-yl)piperidin-4-amine dihydrochlorideHCID 45156751—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(5-Bromo-4-fluoro-2-nitrophenyl)-1-(tetrahydro-2H-pyran-4-yl)-4-piperidinamineHCID 59850147107,7%

Reaktionsbedingungen

Temperatur200 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08288412B2
Quelldatensatzuspto-grants-2012_10
ORD IDord-afd837f064b7470e8672d0888b02859a
Quellennotizuspto-grants-2012_10