HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
3-Amino-1-adamantanol → (2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 3-Amino-1-adamantanol | HCID 658645 | — |
| Edukt | (2S,5R)-1-(2-chloroacetyl)-5-ethynylpyrrolidine-2-carbonitrile | HCID 16090854 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | (2S,5R)-5-ethynyl-1-{N-((5R,7S)-3-hydroxy-1-adamantyl)glycyl}pyrrolidine-2-carbonitrile | HCID 9973731 | — |
Reaktionsschritte
To a stirred solution of Example 8D (0.06 g, 0.305 mmol) in acetonitrile (3 mL) at room temperature under nitrogen, was added 3-amino-1-adamantanol (0.1 g, 0.61 mmol). The reaction mixture was stirred for two days and then concentrated under reduced pressure. The residue was flash chromatographed with 5-7% MeOH/CH2Cl2 to provide the desired compound as a pale yellow oil. MS (DCI) m/z 328 (M+H)+; 1H NMR (300 MHz, DMSO-d6) δ 1.5-2 (14H, m), 2.11-2.21 (2H, m), 2.45-2.48 (2H, m), 3.78 (1H, d), 3.8-4.5 (2H, m), 4.53-4.55 (1H, t), 5.01 (1H, m), 5.05 (1H, m).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08119664B2 |
| Quelldatensatz | uspto-grants-2012_02 |
| ORD ID | ord-4f9c4fcb7a744c7aa853e2f931febb9f |
| Quellennotiz | uspto-grants-2012_02 |