Réaction #607436

ord-3d720effa36c447cb67946fef7771c95

Équation de réaction

CN(O)C(=N)/C(=N\OCc1csc(Br)n1)c1ccccc1
(2Z)-2-{[(2-bromo-1,3-thiazol-4-yl)methoxy]imino}-N-hydroxy-N-methyl-2-phenylethanimidamide
O=C(n1ccnc1)n1ccnc1
1,1′-carbonyldiimidazole
Cn1oc(=O)nc1/C(=N\OCc1csc(Br)n1)c1ccccc1
3-[(Z)-{[(2-bromo-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-methyl-1,2,4-oxadiazol-5(2H)-one
Rendement 103.9%

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 (100 ml)
  2. 2
    Extractionextracted with EtOAc (2×100 ml)
  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 (2Z)-2-{[(2-bromo-1,3-thiazol-4-yl)methoxy]imino}-N-hydroxy-N-methyl-2-phenylethanimidamide (1.8 g, 4.87 mmol, 1 eq.) in acetonitrile (120 ml), was added 1,1′-carbonyldiimidazole (1.58 g, 9.75 mmol, 2 eq.). After stirring at 80° C. for 1 hour, the reaction was quenched by addition of water (100 ml) and extracted with EtOAc (2×100 ml). The organics were combined, dried over MgSO4 and concentrated. The residue was purified by chromatography on silica gel to give 3-[(Z)-{[(2-bromo-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-methyl-1,2,4-oxadiazol-5(2H)-one (2 g, 100% yield).

Source

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