Reaction #607439

ord-aea9ed20245b468d91b8e950bb3d1780

Reaction equation

[H]/N=C(/C(=N\OCc1csc(NC(=O)OCCc2ccccc2)n1)c1ccccc1)N(O)CC
2-phenylethyl (4-{[({(1Z,2Z)-2-[ethyl(hydroxy)amino]-2-imino-1-phenylethylidene}amino)oxy]methyl}-1,3-thiazol-2-yl)carbamate
O=C(n1ccnc1)n1ccnc1
1,1′-carbonyldiimidazole
CCn1oc(=O)nc1/C(=N\OCc1csc(N)n1)c1ccccc1
3-[(Z)-{[(2-amino-1,3-thiazol-4-yl)methoxy]imino}(phenyl)methyl]-2-ethyl-1,2,4-oxadiazol-5(2H)-one
Yield 84.4%

Solvents

Conditions

Temperature
80°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.v1Patent: US09326515B2uspto-grants-2016_05