HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethylmorpholine → N-ethoxycarbonyl-L-alanyl-L-proline ethylamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethylmorpholine | HCID 7525 | — |
| Edukt | Ethyl chloroformate | HCID 10928 | — |
| Edukt | L-alanyl-L-proline ethylamide hydrobromide | HCID 70602162 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-ethoxycarbonyl-L-alanyl-L-proline ethylamide | HCID 54402446 | 47% |
Reaktionsschritte
2 g (0.0066 mol) of L-alanyl-L-proline ethylamide hydrobromide were suspended in 20 ml of dry tetrahydrofuran, 1.84 ml (0.0145 mol) of N-ethylmorpholine and 0.76 ml (0.0079 mol) of ethyl chloroformate were added and the mixture was stirred at room temperature for 2 hours. The solvent was evaporated off and the residue dissolved in 100 ml of chloroform and washed successively with 2-N hydrochloric acid in brine, brine, saturated sodium bicarbonate solution and brine, dried over magnesium sulphate and evaporated to an oil which soon crystallised. Recrystallisation from chloroform/petrol yielded 0.88 g (47%) of N-ethoxycarbonyl-L-alanyl-L-proline ethylamide of melting point 126°-128° C.; [α]D20 =-117.6° (c=1.02% in methanol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04176116 |
| Quelldatensatz | uspto-grants-1979_11 |
| ORD ID | ord-3b7eb8016c7d444da66bd7e1e242c8e2 |
| Quellennotiz | uspto-grants-1979_11 |