HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine amide → N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine n-propylamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine amide | HCID 22796331 | — |
| Edukt | L-methionyl-L-aspartyl-D-alanine n-propylamide hydrochloride | HCID 22796356 | — |
| Produkt | N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine n-propylamide | HCID 22796332 | — |
Reaktionsschritte
When an equivalent quantity of L-methionyl-L-aspartyl-D-alanine n-propylamide hydrochloride is substituted for the L-methionyl-L-aspartyl-D-alanine amide hydrochloride of Example 6, and the procedure detailed therein substantially repeated, there is obtained N-t-butoxycarbonyl-L-tryptophanyl-L-methionyl-L-aspartyl-D-alanine n-propylamide. This compound melts at about 143.5°-148° C. with decomposition and is represented by the following formula.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04012367 |
| Quelldatensatz | uspto-grants-1977_03 |
| ORD ID | ord-7c2617dbcc114a10ab5bb5e45f67f47f |
| Quellennotiz | uspto-grants-1977_03 |