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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Aminotetralin, (S)- | HCID 7058074 | — |
| Edukt | 2-(Tert-butoxycarbonyl)octahydrocyclopenta[C]pyrrole-1-carboxylic acid | HCID 53249646 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | (s)-1,2,3,4-Tetrahydronaphthalen-1-aminium (1s,3ar,6as)-2-(t-butoxycarbonyl)octahydrocyclopenta[c]pyrrole-1-carboxylate | HCID 131731979 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08871904B2 |
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| Quelldatensatz | uspto-grants-2014_10 |
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| ORD ID | ord-608fe0dfe61d43f6a5e1ded76efb526c |
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| Quellennotiz | uspto-grants-2014_10 |
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