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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 56243Erstellt: 24. Oktober 2026

3-Fluoro-4-morpholinoaniline → 2-((3,4-difluorophenoxy)methyl)-3-(3-fluoro-4-morpholinophenyl)-6-methyl-pyrimidin-4(3H)-one

https://huagongshe.com/de/reaction/56243

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Fluoro-4-morpholinoanilineHCID 1485330—
EduktTrimethylaluminumHCID 16682925—
Edukt(Z)-methyl 3-(2-(3,4-difluorophenoxy)acetamido)but-2-enoateHCID 90023321—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-((3,4-difluorophenoxy)methyl)-3-(3-fluoro-4-morpholinophenyl)-6-methyl-pyrimidin-4(3H)-oneHCID 7294929958%

Reaktionsschritte

To a solution of 3-fluoro-4-morpholinoaniline (0.39 g, 2.00 mmol) in DCM (15 mL) was added trimethylaluminium (3.5 mL, 7.0 mmol, 2 M in toluene) and the mixture was stirred at rt for 0.5 h. A solution of (Z)-methyl-3-(2-(3,4-difluorophenoxy)acetamido)but-2-enoate (0.57 g, 2.00 mmol) in DCM (5 mL) was added slowly and the resulting mixture was stirred further at rt for 12 h. The mixture was then quenched with saturated NH4Cl aqueous solution and extracted with CH2Cl2 (50 mL×2). The combined organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:1) to give the title compound as a pale brown solid (0.50 g, 58%). The compound was characterized by the following spectroscopic data:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434695B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-832caf4729fa4de5a129f76a30ddbb2d
Quellennotizuspto-grants-2016_09