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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877023Generated: November 2, 2026

Ethyl 3-(methylamino)propanoate → HCID 59529304, compound

https://huagongshe.com/reaction/1877023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(methylamino)propanoateHCID 541480—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 68509748HCID 68509748—
ReactantHCID 178526939HCID 178526939—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 59529304HCID 5952930488%

Reaction Steps

A solution of 4-({cyclohexyl[2-methyl-5-(pyridin-3-yl)furan-3-yl]methyl}amino)benzoic acid (586 mg), ethyl 3-(methylamino)propanoate (236 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (345 mg), hydroxybenzotriazole monohydrate (276 mg) and triethylamine (250 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 (3 mL), tetrahydrofuran (3 mL) and 1N lithium hydroxide (3.0 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 (544 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-c66f49d819ab4e16a5957b680ad4944f
Source noteuspto-grants-2012_11