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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1009083Erstellt: 26. Oktober 2026

Triethylamine → Cbz-aminoglutarimide

https://huagongshe.com/reaction/1009083

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-Amino-2,6-piperidinedioneHCID 134508—
Edukt1H,3H-furo(3,4-c)pyridine-1,3-dioneHCID 278398—
ProduktCbz-aminoglutarimideHCID 6701796417%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973057B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-f516af7b368c44cfb603e9e95043cd8b
Quellennotizuspto-grants-2011_07