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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56176Generated: October 29, 2026

2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)- → 3-(4-(bis(2-propoxyethyl)amino)-3-fluorophenyl)-2,6-dimethyl pyrimidin-4(3H)-one

https://huagongshe.com/reaction/56176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butenoic acid, 3-(acetylamino)-, methyl ester, (2Z)-HCID 5705360—
ReactantTrimethylaluminumHCID 16682925—
Reactant2-fluoro-N1,N1-bis(2-propoxyethyl)benzene-1,4-diamineHCID 117966093—
SolventDichloromethaneHCID 6344—
Product3-(4-(bis(2-propoxyethyl)amino)-3-fluorophenyl)-2,6-dimethyl pyrimidin-4(3H)-oneHCID 7295000178%

Reaction Steps

To a solution of 2-fluoro-N1,N1-bis(2-propoxyethyl)benzene-1,4-diamine (0.50 g, 1.68 mmol) in CH2Cl2 (10 mL) was added trimethylaluminum (3.4 mL, 6.8 mmol, 2 M in toluene) slowly. The reaction mixture was stirred at rt for 0.5 h, followed by the addition of a solution of methyl 3-acetaminocrotonate (0.32 g, 2.02 mmol) in CH2Cl2 (2 mL). The reaction mixture was stirred at rt for 72 h, then quenched with saturated NH4Cl aqueous solution and extracted with CH2Cl2 (50 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 (PE/EtOAc (V/V)=2:1) to give the title compound as pale yellow oil (0.53 g, 78%). 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-7c3b65d676664db99dc9b02695df5e4e
Source noteuspto-grants-2016_09