Sodium → 1-[4-(3-Amino-1,2,4-oxadiazol-5-yl)phenyl]ethylamine

HRID 1729191

Reaktionsgleichung

Reaktionsgleichung von HRID 1729191
[Na].[OH:2][NH:3][C:4]([NH2:6])=[NH:5].[C:7]([C:10]1[CH:15]=[CH:14][C:13]([CH:16]([NH2:18])[CH3:17])=[CH:12][CH:11]=1)(O)=O>C(O)C>[NH2:5][C:4]1[N:6]=[C:7]([C:10]2[CH:15]=[CH:14][C:13]([CH:16]([NH2:18])[CH3:17])=[CH:12][CH:11]=2)[O:2][N:3]=1

Komponenten

5

Edukt 3

HCID 5360545SodiumHCID 125682714-(1-Aminoethyl)benzoic acidHCID 178513189HCID 178513189, Verbindung

Produkt 1

HCID 199334461-[4-(3-Amino-1,2,4-oxadiazol-5-yl)phenyl]ethylamine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

0.8 g of sodium is dissolved in 60 ml of absolute ethanol, and 12 g of molecular sieve (4Å) and 2.63 g of N-hydroxyguanidine are added. The batch is stirred for 1 hour at room temperature and then 1.14 g of 1-(4-carboxyphenyl)ethylamine are added. The resulting turbid yellowish solution is heated under reflux for 2 hours after which time it can be established by thin layer chromatography that the reaction is complete. The batch is filtered and the solvent is removed under reduced pressure. The residue is digested in water and cooled in an ice bath, and then the precipitate is isolated by filtration, washed with a small amount of water and dried under reduced pressure to give 1-[4-(3-amino-1,2,4-oxadiazol-5-yl)phenyl]ethylamine having a melting point of 150°-151°.

Aufarbeitung

  1. temperatureThe resulting turbid yellowish solution is heated
  2. temperatureunder reflux for 2 hours after which time it
  3. filtrationThe batch is filtered
  4. customthe solvent is removed under reduced pressure
  5. temperaturecooled in an ice bath
  6. customthe precipitate is isolated by filtration
  7. washwashed with a small amount of water
  8. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e04455e8649d43bea3fe0a3657a88c87
Quelldatensatz
uspto-grants-1994_07
Patentnummer
US05332729

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