反応 #607439

ord-aea9ed20245b468d91b8e950bb3d1780

反応方程式

[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
収率 84.4%

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他the reaction was quenched by addition of water
  2. 2
    抽出extracted with EtOAc
  3. 3
    乾燥dried over MgSO4
  4. 4
    濃縮concentrated
  5. 5
    その他The residue was purified by chromatography on silica gel

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09326515B2uspto-grants-2016_05