Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799231Generated: October 31, 2026

Ethyl Acetate → 4-(2-Cyclopropylethoxy)-n-[2-[(2-hydroxyethyl)amino]-2-oxo-1-(4-propylbenzyl)ethyl]benzamide

https://huagongshe.com/reaction/1799231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMeOH tetrahydrofuranHCID 21899815—
Reactant4-(2-Cyclopropylethoxy)-N-((Z)-2-(4-cyclopropylphenyl)-1-{[(2-hydroxyethyl)amino]carbonyl}vinyl)benzamideHCID 57684560—
CatalystHCID 178418390HCID 178418390—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product4-(2-Cyclopropylethoxy)-n-[2-[(2-hydroxyethyl)amino]-2-oxo-1-(4-propylbenzyl)ethyl]benzamideHCID 5797215048%

Reaction Steps

To a methanol:THF (2:1, V/V, 6 mL) solution of 4-(2-cyclopropylethoxy)-N-((Z)-2-(4-cyclopropylphenyl)-1-{[(2-hydroxyethyl)amino]carbonyl}vinyl)benzamide (215 mg, 0.495 mmol) prepared in Example (1 (1d) was added 10% palladium-carbon (wet, 100 mg). The mixture was stirred under a hydrogen atmosphere (rubber balloon) at room temperature for 2 hours. To the reaction solution was added ethyl acetate (10 mL), and the mixture was filtered. The solvent was evaporated, and the residue was purified by thin layer chromatography for separation (ethyl acetate, developed once) to give a white solid. This solid was suspended in acetonitrile:water (1:1, V/V, 4 mL), and the insoluble substance was collected by filtration, washed with water, and dried under reduced pressure to give 104 mg of the title compound (white powder, yield: 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344029B2
Source datasetuspto-grants-2013_01
ORD IDord-ae221d732ef046aa8db736f06f6c914f
Source noteuspto-grants-2013_01