Réaction #607439

ord-aea9ed20245b468d91b8e950bb3d1780

Solvants

Conditions de réaction

Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction was quenched by addition of water
  2. 2
    Extractionextracted with EtOAc
  3. 3
    Séchagedried over MgSO4
  4. 4
    Concentrationconcentrated
  5. 5
    AutreThe residue was purified by chromatography on silica gel

Mode opératoire

To a solution of 2-phenylethyl (4-{[({(1Z,2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate (160 mg, 71% purity, 0.24 mmol, 1 eq.) in acetonitrile (3 ml), was added 1,1′-carbonyldiimidazole (555 mg, 0.342 mmol, 1.4 eq.). After stirring at 80° C. for 6 hour, the reaction was quenched by addition of water and extracted with EtOAc. The organics were combined, dried over MgSO4 and concentrated. The residue was purified by chromatography on silica gel to give 3-[(Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-ethyl-1,2,4-oxadiazol-5(2H)-one (70 mg, 55% yield).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09326515B2uspto-grants-2016_05