HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1252813Erstellt: 25. Oktober 2026
4-Methylmorpholine → 1-[[3-(acetylmercapto)-1-oxopropyl]amino]-L-proline
https://huagongshe.com/reaction/1252813
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Dimethylacetamide | HCID 31374 | — |
| Edukt | Aminoproline | HCID 97357 | — |
| Edukt | 3-Acetylthiopropionyl chloride | HCID 20041315 | — |
| Produkt | 1-[[3-(acetylmercapto)-1-oxopropyl]amino]-L-proline | HCID 14181462 | — |
Reaktionsschritte
To a suspension of 3.9 g of N-amino-L-proline and 6.06 g of N-methylmorpholine in 200 ml of dimethylacetamide is added 4.98 g of 3-acetylthiopropionyl chloride. The temperature of the reaction mixture rises to 34° spontaneously. The reaction mixture is then heated at 90° for 5 hours and allowed to cool to room temperature overnight. The crystalline solid, N-methylmorpholine hydrochloride, is removed by filtration and the filtrate concentrated under reduced pressure. The residue is dissolved in a minimum amount of 20% hydrochloric acid and the aqueous solution is then extracted with 3×150 ml of ethyl acetate. The ethyl acetate extracts are combined, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to yield the desired N-[[3-(acetylmercapto)-1-oxopropyl]amino]-L-proline.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04745124 |
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| Quelldatensatz | uspto-grants-1988_05 |
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| ORD ID | ord-89d47a1d091044568678e7b9e3bc0505 |
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| Quellennotiz | uspto-grants-1988_05 |
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