Réaction #49052

ord-e1a179c48aa24e148150009a12a9ba8b

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThen, the reaction vessel was equipped with a reflux condenser
  2. 2
    Températurethe mixture was heated at 60° C. for 2 days
  3. 3
    AutreAfter completion of the reaction
  4. 4
    Extractionthe reaction mixture was extracted with ethyl acetate
  5. 5
    Lavagethe organic layer was washed sequentially with water and saturated brine
  6. 6
    Séchagedried over anhydrous sodium sulfate
  7. 7
    Concentrationconcentrated under reduced pressure
  8. 8
    AutreThe resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 4% methanol/methylene chloride as an eluent)

Mode opératoire

Methyl 5-amino-pentanoate hydrochloride {see J. Org. Chem. (1968) 1581} (128 mg, 0.178 mmol) and sodium cyanoborohydride (45 mg, 0.718 mmol) were added to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (115 mg, 0.239 mmol) obtained in Step F of Example 1 in tetrahydrofuran (anhydrous, 4.0 mL). The mixture was stirred at room temperature for 1.5 hours. Then, the reaction vessel was equipped with a reflux condenser, and the mixture was heated at 60° C. for 2 days. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 4% methanol/methylene chloride as an eluent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin-1-ylmethyl)-benzamide (Compound H-4, 42.7 mg, 37%) as a white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07745663B2uspto-grants-2010_06