반응 #1976505

ord-eeb59400fc3d4efab9db9cf2f2f36d6d

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe mixture was further stirred at room temperature for 1 hr
  2. 2
    세척The reaction mixture was washed with water and saturated brine
  3. 3
    건조dried over anhydrous magnesium sulfate
  4. 4
    기타The solvent was evaporated under reduced pressure
  5. 5
    workup.DISSOLUTIONThe obtained residue was dissolved in methanol (40 mL)
  6. 6
    workup.ADDITIONsodium methoxide (28% methanol solution, 1.6 g) was added
  7. 7
    workup.STIRRINGthe mixture was stirred at 60° C. for 2 hr
  8. 8
    여과was filtered off
  9. 9
    기타the solvent was evaporated under reduced pressure
  10. 10
    여과The precipitated solid was collected by filtration

실험 절차

To a solution (40 mL) of methyl 2-amino-5-ethylthiophene-3-carboxylate (0.63 g) in methylene chloride were added triphosgene (0.44 g) and triethylamine (0.76 mL), and the mixture was stirred at room temperature for 2 hr. To the reaction mixture was added 5-methylisoxazol-3-amine (1 g), and the mixture was further stirred at room temperature for 1 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in methanol (40 mL), sodium methoxide (28% methanol solution, 1.6 g) was added, and the mixture was stirred at 60° C. for 2 hr. The reaction mixture was neutralized with hydrochloric acid (10% methanol solution), insoluble material was filtered off, and the solvent was evaporated under reduced pressure. The precipitated solid was collected by filtration to give the title compound as a colorless solid (0.94 g, 100%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08501750B2uspto-grants-2013_08