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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877201Generated: October 30, 2026

Ethyl 3-(methylamino)propanoate → HCID 68516611, compound

https://huagongshe.com/reaction/1877201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(methylamino)propanoateHCID 541480—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 68511264HCID 68511264—
ReactantHCID 178526939HCID 178526939—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 68516611HCID 6851661178%

Reaction Steps

A solution of 4-(3-methyl-1-{3-methyl-5-[4-(trifluoromethyl)phenyl]thiophen-2-yl}butoxy)benzoic acid (179 mg), ethyl 3-(methylamino)propanoate (63 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (92 mg), hydroxybenzotriazole monohydrate (74 mg) 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 1N hydrochloric acid, 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 sodium hydroxide (1.0 mL), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water, and the mixture was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound (165 mg, 78%) as an amorphous compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-54f4581929c040528e6acf98d7f7333a
Source noteuspto-grants-2012_11