Réaction #66685

ord-a4f5717cb5c343979f87123a9d74984d

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe reaction mixture was partitioned between EtOAc and H2O
  2. 2
    ExtractionThe organic extract
  3. 3
    Séchagewas dried over Na2SO4
  4. 4
    Filtrationfiltered

Mode opératoire

To a solution of 4-(2,4-Diamino-pyrimidin-5-yloxy)-2-iodo-5-isopropyl-phenol (0.2 g, 0.52 mmol) in anhydrous DMF (2 ml) was added EtBr (57 mg, 0.52 mmol) in portions. The reaction mixture was partitioned between EtOAc and H2O. The organic extract was dried over Na2SO4, filtered and aconcentrated. Flash chromatography on silica (3% MeOH in methylene chloride with 1% NH4OH) gave 5-(4-Ethoxy-5-iodo-2-isopropyl-phenoxy)-pyrimidine-2,4-diamine (0.17 g, 28%) as a yellow solid. (M+H)=415.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08524725B2uspto-grants-2013_09