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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56243Generated: October 26, 2026

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

https://huagongshe.com/reaction/56243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-morpholinoanilineHCID 1485330—
ReactantTrimethylaluminumHCID 16682925—
Reactant(Z)-methyl 3-(2-(3,4-difluorophenoxy)acetamido)but-2-enoateHCID 90023321—
SolventDichloromethaneHCID 6344—
Product2-((3,4-difluorophenoxy)methyl)-3-(3-fluoro-4-morpholinophenyl)-6-methyl-pyrimidin-4(3H)-oneHCID 7294929958%

Reaction Steps

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:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434695B2
Source datasetuspto-grants-2016_09
ORD IDord-832caf4729fa4de5a129f76a30ddbb2d
Source noteuspto-grants-2016_09