Réaction #487543

ord-58ee575fb1c44abf9b534308bd2b810c

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe organic layer was collected
  2. 2
    Séchagedried over sodium sulfate
  3. 3
    Concentrationconcentrated under vacuum
  4. 4
    AutreThe crude product was purified by silica gel chromatography
  5. 5
    AutreThe product fractions were collected
  6. 6
    Concentrationconcentrated under vacuum

Mode opératoire

To a solution of 2,4-dichloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazine (770 mg, 2.79 mmol) in THF (10 mL) was added methyl 4-amino-2-(3-chloropropoxy)benzoate (681 mg, 2.79 mmol) and Hunig'sBase (1.464 mL, 8.38 mmol). The resulting mixture was stirred for 16 h. The reaction was diluted with DCM and water. The organic layer was collected and dried over sodium sulfate, and concentrated under vacuum. The crude product was purified by silica gel chromatography using 20-40% EtOAc/Hexanes. The product fractions were collected and concentrated under vacuum to give methyl 4-(4-chloro-6-(2,2,2-trifluoroethoxy)-1,3,5-triazin-2-ylamino)-2-(3-chloropropoxy)benzoate as a solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08741884B2uspto-grants-2014_06