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4-Methylmorpholine → Dextroamphetamine

HRID 500349
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 500349
C1CCC(N=C=NC2CCCCC2)CC1.S(O)(O)(=O)=O.[NH2:21][CH:22]([CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[CH3:23].CN1CCOCC1>CN(C=O)C.O1CCOCC1.O>[CH3:23][C@H:22]([NH2:21])[CH2:24][C:25]1[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 79724-MethylmorpholineHCID 10868DicyclohexylcarbodiimideHCID 222898Amphedrine

Produkt 1

HCID 5826Dextroamphetamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 86622776DMF dioxane waterLösungsmittel

Versuchsvorschrift

O-Acetyl-l-carnitine·Cl (1.000 g, 4.17 mmol) was dissolved in 12.5 mL of a mixture of DMF/dioxane/water (2:2:1). NHS (0.528 g, 4.59 mmol) and DCC (0.947 g, 4.59 mmol) were added and the mixture was stirred overnight at ambient temperature. Solvents were evaporated and the remaining residue was dried overnight in high vacuum. The crude succinimidyl ester intermediate was dissolved in 20 mL of anhydrous DMF. Amphetamine sulfate (0.700 g, 1.90 mmol) and NMM (0.92 mL, 8.34 mmol) were added and the mixture stirred overnight. Solvent was evaporated to dryness and the remaining residue was leached with IPA. Solvent was evaporated to yield Carn-d-amphetamine.

Aufarbeitung

  1. customSolvents were evaporated
  2. customthe remaining residue was dried overnight in high vacuum
  3. dissolutionThe crude succinimidyl ester intermediate was dissolved in 20 mL of anhydrous DMF
  4. stirringthe mixture stirred overnight
  5. customSolvent was evaporated to dryness
  6. customSolvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-684be369b7ea4f9bb6157c8fc9ed90a1
Quelldatensatz
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07772222B2

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