HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → Cbz-aminoglutarimide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 3-Amino-2,6-piperidinedione | HCID 134508 | — |
| Edukt | 1H,3H-furo(3,4-c)pyridine-1,3-dione | HCID 278398 | — |
| Produkt | Cbz-aminoglutarimide | HCID 67017964 | 17% |
Reaktionsschritte
With reference to Scheme 4 below, azathalidomide was prepared from aminoglutarimide and commercial pyridine-3,4-dicarboxylic anhydride. Cbz-aminoglutarimide was deprotected by hydrogenolysis with catalyst palladium hydroxide on carbon (10%) to form aminoglutarimide. Pyridine-3,4-dicarboxyic anhydride was refluxed with aminoglutarimide in the presence of triethylamine to yield azathalidomide 11 in the total yield of 17% from Cbz-aminoglutarimide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08853253B2 |
| Quelldatensatz | uspto-grants-2014_10 |
| ORD ID | ord-ce699545f7fa4c82baa51d40f8c107be |
| Quellennotiz | uspto-grants-2014_10 |