تفاعل #607436

ord-3d720effa36c447cb67946fef7771c95

معادلة التفاعل

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
المردود 103.9%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe reaction was quenched by addition of water (100 ml)
  2. 2
    استخلاصextracted with EtOAc (2×100 ml)
  3. 3
    تجفيفdried over MgSO4
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe residue was purified by chromatography on silica gel

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09326515B2uspto-grants-2016_05