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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238486Generated: October 25, 2026

Ethylmorpholine → 1-ethyl-5-oxo-N-[(2,3,4-trifluorophenyl)methyl]-prolinamide

https://huagongshe.com/reaction/2238486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2,3,4-TrifluorobenzylamineHCID 2777042—
ReactantL-Proline, 1-ethyl-5-oxo-HCID 18605196—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-ethyl-5-oxo-N-[(2,3,4-trifluorophenyl)methyl]-prolinamideHCID 6746182133.3%

Reaction Steps

1-Ethyl-5-oxo-proline (0.050 g, 0.32 mmol) was dissolved in anhydrous dichloromethane (˜7 ml) and dimethylformamide (1 ml) and to this was added 1-hydroxybenzotriazole (0.052 g, 0.38 mmol), [(2,3,4-trifluorophenyl)methyl]amine (0.103 g, 0.64 mmol), N-ethyl morpholine (0.151 ml, 0.95 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.073 g, 0.38 mmol). The mixture was shaken at room temperature over the weekend. A further aliquot of [(2,3,4-trifluorophenyl)methyl]amine (0.051 g, 0.32 mmol) was added to the mixture and stirring continued for a while longer until HPLC indicated that no further product was forming. The mixture was diluted with 2M aqueous hydrogen chloride (5 ml) and then filtered through a phase separator. The organic layer was then washed with saturated aqueous sodium hydrogen carbonate and again filtered through a phase separator. The organic layer was then evaporated to give the crude product. The crude material was purified by mass-directed automated HPLC to give pure 1-ethyl-5-oxo-N-[(2,3,4-trifluorophenyl)methyl]-prolinamide (0.032 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718693B2
Source datasetuspto-grants-2010_05
ORD IDord-9e915935638440ae85ec891ffaf87990
Source noteuspto-grants-2010_05