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
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2S)-2-aminobutyramide | HCID 7015191 | — |
| Reactant | Methyl 2-hydroxy-5-oxo-2,5-dihydrofuran-3-carboxylate | HCID 13401719 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2S)-2-(4-methoxycarbonyl-2-oxo-1-pyrrolidinyl)butanamide | HCID 44367383 | 43% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629474B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-b172ff3323014caaa8b91c2c9769bc64 |
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| Source note | uspto-grants-2009_12 |
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