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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877056Generated: November 3, 2026

beta-Alanine, ethyl ester, hydrochloride → HCID 59529514, compound

https://huagongshe.com/reaction/1877056

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
ReactantEthyl 3-(methylamino)propanoateHCID 541480—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 68512545HCID 68512545—
ReactantHCID 178526939HCID 178526939—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 59529514HCID 5952951469.2%

Reaction Steps

A solution of 4-[(cyclohexyl{2-(ethoxymethyl)-5-[4-(trifluoromethyl)phenyl]furan-3-yl}methyl)amino]benzoic acid (100 mg), ethyl β-alaninate hydrochloride (37 mg), ethyl 3-(methylamino)propanoate (31 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (46 mg), hydroxybenzotriazole monohydrate (37 mg) and triethylamine (33 μL) in N,N-dimethylformamide (10 mL) was stirred at room temperature for 4 hr. Ethyl acetate was added, the mixture was washed with saturated aqueous sodium hydrogen carbonate solution and water, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the organic layer was dried over magnesium sulfate. The solvent was evaporated under reduced pressure. To the residue were added ethanol (2 mL), tetrahydrofuran (2 mL) and 1N lithium hydroxide (0.4 mL), and the mixture was stirred at room temperature for 1 hr. The solvent was evaporated under reduced pressure, and water (10 mL) was added. The mixture was neutralized with 1N hydrochloric acid under ice-cooling, and stirred for 1 hr. The resulting precipitate was collected by filtration and dried to give the title compound (81 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-9e83384d97024c5ca1b45e08d094893a
Source noteuspto-grants-2012_11