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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56246Generated: October 25, 2026

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

https://huagongshe.com/reaction/56246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-morpholinoanilineHCID 1485330—
ReactantTrimethylaluminumHCID 16682925—
Reactant(Z)-methyl-3-(2-((3-fluorophenyl)thio)acetamido)but-2-enoateHCID 90023425—
SolventDichloromethaneHCID 6344—
Product2-(((3-fluorophenyl)thio)methyl)-3-(3-fluoro-4-morpholinophenyl)-6-methyl-pyrimidin-4(3H)-oneHCID 7294947667%

Reaction Steps

To a solution of 3-fluoro-4-morpholinoaniline (0.54 g, 2.75 mmol) in DCM (15 mL) was added trimethylaluminium (4.8 mL, 9.60 mmol, 2 M in toluene) and the mixture was stirred at rt for 0.5 h. A solution of (Z)-methyl-3-(2-((3-fluorophenyl)thio)acetamido)but-2-enoate (0.78 g, 2.75 mmol) in DCM (5 mL) was added slowly and the resulting mixture was stirred at rt for 12 h. The mixture was 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 (0.79 g, 67%). 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-a1a856c2d4bd40c18ab594b1ed2baece
Source noteuspto-grants-2016_09