HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280773Erstellt: 23. Oktober 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → dibenzylphosphoryl-L-alanyl-L-prolyl-D-alanine benzylester
https://huagongshe.com/de/reaction/280773
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | D-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1) | HCID 2802425 | — |
| Edukt | Dibenzylphosphory-L-alanyl-L-proline | HCID 53804723 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | dibenzylphosphoryl-L-alanyl-L-prolyl-D-alanine benzylester | HCID 70040519 | — |
Reaktionsschritte
Dibenzylphosphory-L-alanyl-L-proline (1.4 g, 3.2 m mole), HOBt (476 mg, 3.5 m mole) and D-alanine benzylester p-toluene sulfonic acid salt (1.3 g, 3.5 m mole) were dissolved in DMF (5 ml), and WSC (0.64 ml) was added thereto while cooling to -15° C. The reaction was carried out for 3 hours under cooling and then overnight at room temperature. To the reaction solution ethyl acetate (100 ml) was added and the mixture was washed with 1N hydrochloric acid, 5% sodium bicarbonate and water in order. The mixture was dried with anhydrous sodium sulfate and the thus obtained solution was distilled under reduced pressure to give an oily dibenzylphosphoryl-L-alanyl-L-prolyl-D-alanine benzylester material.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04590178 |
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| Quelldatensatz | uspto-grants-1986_05 |
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| ORD ID | ord-095c1e6ce3f2414fbfa1ba89dd751991 |
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| Quellennotiz | uspto-grants-1986_05 |
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