HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 652346Erstellt: 24. Oktober 2026
Sodium Iodide → (3S)-1-[N-[3-[[(t-Butyloxy)carbonyl]amino]-2-oxo-4-phenylbutyl]-N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-proline, t-butyl ester
https://huagongshe.com/de/reaction/652346
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | tert-Butyl L-alanyl-L-prolinate | HCID 12939800 | — |
| Edukt | N-[(t-Butyloxy)carbonyl]-L-phenylalanine chloromethyl ketone | HCID 88667995 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (3S)-1-[N-[3-[[(t-Butyloxy)carbonyl]amino]-2-oxo-4-phenylbutyl]-N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-proline, t-butyl ester | HCID 131714417 | 51,4% |
Reaktionsschritte
A solution of L-alanyl-L-proline t-butyl ester (1.0 g, 4.13 mmol), N-[(t-butyloxy)carbonyl]-L-phenylalanine chloromethyl ketone (1.2 g, 4.03 mmol), sodium bicarbonate (370 mg, 4.4 mmol) and sodium iodide (300 mg, 2 mmol) in dimethylformamide (7 ml) was stirred overnight at room temperature. The reaction mixture was evaporated. Dioxane (6 ml) was added to the residue followed by benzyloxycarbonyl chloride (0.75 ml, 5.24 mmol) and sodium bicarbonate (500 mg, 5.95 mmol). After stirring overnight, the reaction mixture was evaporated, the residue taken up in ethyl acetate and washed neutral (water, saturated sodium bicarbonate solution, water, 10% potassium bisulfate solution and water). The crude material (2.6 g) was chromatographed over silica gel (200 g) using the solvent system ethyl acetate:benzene-1:3 to obtain 1.32 g of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04670541 |
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| Quelldatensatz | uspto-grants-1987_06 |
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| ORD ID | ord-d770e609b9924213b201fbf0c6f09e4d |
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| Quellennotiz | uspto-grants-1987_06 |
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