Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388197Generated: November 2, 2026

Ethyl Acetate → Ethyl 4-(((2,4-dimethoxybenzyl)(2-ethoxy-2-oxoethyl)amino)methyl)-3-(pyridin-4-yl)isoxazole-5-carboxylate

https://huagongshe.com/reaction/2388197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-(2,4-dimethoxybenzylamino)acetateHCID 19895532—
ReactantEthyl 4-(bromomethyl)-3-(pyridin-4-yl)isoxazole-5-carboxylateHCID 67531296—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(((2,4-dimethoxybenzyl)(2-ethoxy-2-oxoethyl)amino)methyl)-3-(pyridin-4-yl)isoxazole-5-carboxylateHCID 6753005821%

Reaction Steps

Ethyl 4-(bromomethyl)-3-(pyridin-4-yl)isoxazole-5-carboxylate (1.5 g, 4.82 mmol) was dissolved in 20 mL of DMF. N-(2,4-dimethoxybenzyl)glycine ethyl ester (1.22 g, 4.82 mmol) and potassium carbonate (1.33 g, 9.65 mmol) were added, and the mixture was stirred at room temperature for 16 h. EtOAc (100 mL) and water (100 mL) were added and the aqueous layer was extracted with additional EtOAc. The combined organic layer was washed with water and brine, and dried over MgSO4. After solvent was removed in vacuo, the crude was purified by flash chromatography (0-50% EtOAc/hexanes) to give 0.49 g of the title compound. MS: (+) m/z 484.48 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269008B2
Source datasetuspto-grants-2012_09
ORD IDord-67d97979f22944f1af7a5864c6d99e42
Source noteuspto-grants-2012_09