HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Vanillin → N-benzyloxycarbony-D-valine isopropylamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Vanillin | HCID 1183 | — |
| Edukt | Isopropylamine | HCID 6363 | — |
| Edukt | N-alpha-Benzyloxycarbonyl-D-valine | HCID 712434 | — |
| Lösungsmittel | Ethyl acetate hexane | HCID 21226206 | — |
| Produkt | N-benzyloxycarbony-D-valine isopropylamide | HCID 14723623 | — |
Reaktionsschritte
Reaction of N-benzyloxycarbonyl-D-valine with isopropylamine by the method of Example 20, Part A afforded a quantitative yield of N-benzyloxycarbonyl-D-valine isopropylamide of Rf 0.61 (TLC, ethyl acetate/hexane, 1:1, vanillin spray). Hydrogenolysis over Pd/C by the method of Example 20, Part B gave D-valine isopropylamide in 71% yield, Rf 0.50. Coupling with beta-benzyl N-Cbz-L-asparate provided the diblocked dipeptide amide (procedure of Example 20, Part C), Rf 0.40 (TLC, ethyl acetate/hexane, 1, vanillin spray), in 62% yield as an off-white solid. This was converted to the desired title compound by the procedure of Example 20, Part D, in 90.6% yield, M.P. 226°-227° C. (decomp.), Rf 0.44. Sweetness, 1-2 x sucrose.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04804782 |
| Quelldatensatz | uspto-grants-1989_02 |
| ORD ID | ord-c7b948592530464b9fc0f53a7f531629 |
| Quellennotiz | uspto-grants-1989_02 |