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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56159Generated: October 29, 2026

2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)- → 3-(3-fluoro-4-((2-morpholinoethyl)amino)phenyl)-2,6-dimethyl pyrimidin-4(3H)-one

https://huagongshe.com/reaction/56159

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)-HCID 5705360—
ReactantTrimethylaluminumHCID 16682925—
Reactant2-fluoro-N1-(2-morpholinoethyl)benzene-1,4-diamineHCID 17609690—
SolventDichloromethaneHCID 6344—
Product3-(3-fluoro-4-((2-morpholinoethyl)amino)phenyl)-2,6-dimethyl pyrimidin-4(3H)-oneHCID 7294983369.1%

Reaction Steps

To a solution of 2-fluoro-N1-(2-morpholinoethyl)benzene-1,4-diamine (0.50 g, 2.09 mmol) in CH2Cl2 (20 mL) was added trimethylaluminum (3.2 mL, 6.40 mmol, 2 M in toluene) slowly at rt. The reaction mixture was stirred at rt for 0.5 h, followed by the addition of a solution of methyl 3-acetaminocrotonate (0.65 g, 4.13 mmol) in CH2Cl2 (5 mL). The reaction mixture was stirred at rt for 36 h, then quenched with saturated NH4Cl aqueous solution and extracted with CH2Cl2 (100 mL×3). The combined organic phases were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (EtOAc/MeOH (V/V)=30:1) to give the title compound as a white solid (0.50 g, 24%). 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-738b2cbda2a04d41a39f2d384bb3c46c
Source noteuspto-grants-2016_09