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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866779Generated: November 1, 2026

(2S)-2-aminobutyramide → (2S)-2-(4-methoxycarbonyl-2-oxo-1-pyrrolidinyl)butanamide

https://huagongshe.com/reaction/1866779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-aminobutyramideHCID 7015191—
ReactantMethyl 2-hydroxy-5-oxo-2,5-dihydrofuran-3-carboxylateHCID 13401719—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(2S)-2-(4-methoxycarbonyl-2-oxo-1-pyrrolidinyl)butanamideHCID 4436738343%

Reaction Steps

2-Hydroxy-5-oxo-2,5-dihydro-furan-3-carboxylic acid methyl ester (3.08 g) in methanol (40 ml) is added to a solution of (2S)-2-aminobutyramide (2.0 g) in methanol (30 ml) in a hydrogenation reactor and the mixture is maintained for at least 2 hours at room temperature. Then Pd/C catalyst (10 w/w %; Johnson Matthey 5% Pd on carbon—type 87L) is added and hydrogen introduced into the system under pressure. The temperature is kept at 40° C. maximum and the hydrogen pressure between 4 bar and 5 bar, followed by stirring for at least 20 hours following the initial reaction. The solution is then cooled between 15° C. and 25° C. and filtered to remove the catalyst. The solvent is evaporated under vacuum and the resulting yellow product is purified by preparative liquid chromatography (eluent: dichloromethane/methanol (95:5)) (Yield 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629474B2
Source datasetuspto-grants-2009_12
ORD IDord-b172ff3323014caaa8b91c2c9769bc64
Source noteuspto-grants-2009_12