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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238513Generated: October 29, 2026

Ethylmorpholine → N-[(2-chloro-4-fluorophenyl)methyl]-1-ethyl-5-oxo-D-prolinamide

https://huagongshe.com/reaction/2238513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Chloro-4-fluorobenzylamineHCID 139909—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantL-Proline, 1-ethyl-5-oxo-HCID 18605196—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-[(2-chloro-4-fluorophenyl)methyl]-1-ethyl-5-oxo-D-prolinamideHCID 49865054—

Reaction Steps

1-ethyl-5-oxoproline (0.100 g, 0.64 mmol) was dissolved in a mixture of dichloromethane (3 ml) and dimethylformamide (0.5 ml) and to this was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.147 g, 0.77 mmol), 1-hydroxybenzotriazole (0.104 g, 0.77 mmol), and N-ethyl morpholine (0.244 ml, 1.92 mmol). The mixture was stirred for 10 minutes and then 2-chloro-4-fluorobenzylamine was added to the mixture and stirring continued overnight (˜16 hrs) at room temperature. The mixture was then treated with saturated aqueous sodium hydrogen carbonate (˜2 ml) and stirred vigorously for ˜10 minutes. The aqueous layer was removed using a phase separator and extracted with more dichloromethane (2×1 ml). The combined organic layers were concentrated to give a yellow oil and this was subsequently purified by mass-directed automated HPLC to give N-[(2-chloro-4-fluorophenyl)methyl]-1-ethyl-5-oxo-D-prolinamide (0.065 g) as a white solid. LC/MS [M+H]+=299, retention time=2.16 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718693B2
Source datasetuspto-grants-2010_05
ORD IDord-f6ae040a718147ba93a3ea64047bdcf3
Source noteuspto-grants-2010_05