Réaction #60106

ord-c67edb3d78f349c98442b881ba67f6db

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas added
  2. 2
    Concentrationconcentrated under reduced pressure
  3. 3
    AutreThe crude product was purified by flash chromatography
  4. 4
    Lavageeluting with 85% hexane

Mode opératoire

To a mixture of 2,6-dichloro-3-acetamidopyridine (6.3 g, 55% pure) and pyridine (4.93 ml, 61 mmole) in dichloromethane (100 ml), trifluoroacetic anhydride (4.23 ml, 30 mmole) was added. The reaction mixture was stirred at room temperature overnight and concentrated under reduced pressure. The crude product was purified by flash chromatography, eluting with 85% hexane: 15% ethyl acetate to give a pale yellow product (1.77 g, 90%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07425557B2uspto-grants-2008_09