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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 540974Erstellt: 23. Oktober 2026

1-Aminotetralin, (S)- → (s)-1,2,3,4-Tetrahydronaphthalen-1-aminium (1s,3ar,6as)-2-(t-butoxycarbonyl)octahydrocyclopenta[c]pyrrole-1-carboxylate

https://huagongshe.com/de/reaction/540974

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Aminotetralin, (S)-HCID 7058074—
Edukt2-(Tert-butoxycarbonyl)octahydrocyclopenta[C]pyrrole-1-carboxylic acidHCID 53249646—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(s)-1,2,3,4-Tetrahydronaphthalen-1-aminium (1s,3ar,6as)-2-(t-butoxycarbonyl)octahydrocyclopenta[c]pyrrole-1-carboxylateHCID 131731979—

Reaktionsbedingungen

Temperatur23.5 °C

Reaktionsschritte

The ethyl acetate solution of racemic N-t-butyloxycarbonyl-3-azabicyclo[3.3.0]octane-2-carboxylic acid from Example 2, Method 2, was added to a solution of (S)-1,2,3,4-tetrahydro-1-naphthylamine (56.7 g, 0.385 mol) in ethyl acetate (300 mL). The mixture was stirred for 3-4 hours at 22-25° C., then filtered, and the solids washed with ethyl acetate (200 mL). The product was dried at 20-30° C. under vacuum for 4 hours to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08871904B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-608fe0dfe61d43f6a5e1ded76efb526c
Quellennotizuspto-grants-2014_10