반응 #48558

ord-233a4d5fb9204759a0274c00e9660869

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the reaction was heated
  2. 2
    온도at reflux for 22 hours
  3. 3
    기타The cooled mixture was partitioned between ethyl acetate (300 mL) and 20% aqueous 0.88 ammonia (120 mL)
  4. 4
    기타the layers were separated
  5. 5
    건조The organic phase was dried over MgSO4
  6. 6
    기타evaporated under reduced pressure
  7. 7
    기타The residue was triturated with ether

실험 절차

Trifluoroacetic acid (600 μL, 8.1 mmol) was added to a suspension of 4-chloroaniline (2.1 g, 16.2 mmol) and 4-(5-methyl-1,3,4-oxadiazol-2-yl)benzonitrile (Journal für Praktische Chemie, 1994; 336(8); 678-85) (3.0 g, 16.2 mmol) in tetrahydrofuran (50 mL) and the reaction was heated at reflux for 22 hours. The cooled mixture was partitioned between ethyl acetate (300 mL) and 20% aqueous 0.88 ammonia (120 mL), and then the layers were separated. The organic phase was dried over MgSO4 and evaporated under reduced pressure. The residue was triturated with ether and a minimum volume of ethyl acetate to afford the title compound as a white crystalline solid, 2.82 g.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745630B2uspto-grants-2010_06