Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Gabapentin | HCID 3446 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | L-Tyrosine, N-(1,1-dimethylethoxy)carbonyl- | HCID 117439 | — |
| Edukt | N-hydroxysuccinamide | HCID 18381240 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Boc-Tyr Gabapentin | HCID 131727014 | 106,7% |
Reaktionsschritte
To a solution of Boc-Tyr-OH (4.2 g, 15 mmol) in acetonitrile (100 mL) was added N-hydroxysuccinamide (1.84 g, 16 mmol) and N,N-dicyclohexylcarbodiimide (3.3 g, 16 mmol). The reaction was stirred at ambient temperature for 2 h. The reaction mixture was filtered directly into an aqueous solution (100 mL) of gabapentin (2.7 g, 16 mmol) and sodium hydroxide (640 mg, 16 mmol), and the resulting mixture stirred at ambient temperature for 16 h. The reaction was concentrated under reduced pressure, the residue was dissolved in ethyl acetate/diethyl ether (1/1, 200 mL) and washed with 0.1M aqueous potassium hydrogensulfate (2×200 mL). The organic phase was separated, dried over Na2SO4, filtered, and concentrated to dryness under reduced pressure to afford Boc-Tyr-Gabapentin as a white solid (7.4 g, 16 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07420002B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-d195102459e34c60aa3bc9d223c309ab |
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| Quellennotiz | uspto-grants-2008_09 |
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