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Gabapentin → Boc-Tyr Gabapentin

HRID 28766
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 28766
[NH:1]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[C@H:2]([C:11]([OH:13])=[O:12])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1.ONC(=O)CCC(N)=O.[CH2:30]1[CH2:35][CH2:34][C:33]([CH2:40][NH2:41])([CH2:36][C:37]([OH:39])=[O:38])[CH2:32][CH2:31]1.[OH-].[Na+]>C(#N)C>[NH:1]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[C@H:2]([C:11]([OH:13])=[O:12])[CH2:3][C:4]1[CH:5]=[CH:6][C:7]([OH:10])=[CH:8][CH:9]=1.[CH2:30]1[CH2:31][CH2:32][C:33]([CH2:40][NH2:41])([CH2:36][C:37]([OH:39])=[O:38])[CH2:34][CH2:35]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 3446GabapentinHCID 14798Sodium HydroxideHCID 117439L-Tyrosine, N-(1,1-dimethylethoxy)carbonyl-HCID 18381240N-hydroxysuccinamide

Produkt 1

HCID 131727014Boc-Tyr GabapentinAusbeute 106,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342
Acetonitrile
Lösungsmittel

Versuchsvorschrift

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).

Aufarbeitung

  1. stirringthe resulting mixture stirred at ambient temperature for 16 h
  2. concentrationThe reaction was concentrated under reduced pressure
  3. dissolutionthe residue was dissolved in ethyl acetate/diethyl ether (1/1, 200 mL)
  4. washwashed with 0.1M aqueous potassium hydrogensulfate (2×200 mL)
  5. customThe organic phase was separated
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated to dryness under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-d195102459e34c60aa3bc9d223c309ab
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07420002B2

Notizen zur Reaktion

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