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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238535Generated: October 26, 2026

Ethylmorpholine → 1-methyl-N-(1-naphthalenylmethyl)-5-oxoprolinamide

https://huagongshe.com/reaction/2238535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylmorpholineHCID 7525—
Reactant1-NaphthalenemethanamineHCID 8355—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(2S)-1-methyl-5-oxopyrrolidine-2-carboxylic acidHCID 18649403—
SolventDichloromethaneHCID 6344—
Product1-methyl-N-(1-naphthalenylmethyl)-5-oxoprolinamideHCID 67460091—

Reaction Steps

1-methyl-5-oxoproline (0.050 g, 0.35 mmol, prepared in a manner analogous to that described above for example 51), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.081 g, 0.42 mmol), 1-hydroxybenzotriazole (0.057 g, 0.42 mmol), N-ethyl morpholine (0.166 ml, 1.05 mmol) and (1-naphthalenylmethyl)amine were combined in dichloromethane (˜8 ml) and the mixture was stirred for ˜20 hrs at room temperature. The mixture was then washed with 2M aqueous hydrogen chloride (5 ml) and the organic layer was separated using a phase separator. The organic layer was washed with saturated aqueous sodium hydrogen carbonate, separated as before, and then evaporated. The residue was purified by mass-directed automated HPLC to give pure 1-methyl-N-(1-naphthalenylmethyl)-5-oxoprolinamide as a white solid (0.062 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718693B2
Source datasetuspto-grants-2010_05
ORD IDord-641891f2aa0e4f489e5d14fe06157023
Source noteuspto-grants-2010_05