Réaction #44629

ord-b821cd62ac954a23a425bea5b716d3b4

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe resulting reaction solution
  2. 2
    Températurecooling for 30 min
  3. 3
    Températureunder ice-cooling
  4. 4
    AutreThe resulting reaction solution
  5. 5
    workup.STIRRINGwas stirred under ice-
  6. 6
    Températurecooling for 1 hr
  7. 7
    AutreThe organic layer was separated
  8. 8
    Lavagewashed with saturated saline
  9. 9
    Séchagedried over magnesium sulfate
  10. 10
    Concentrationconcentrated under reduced pressure
  11. 11
    Autreto give a crude
  12. 12
    workup.ADDITIONwas added
  13. 13
    workup.STIRRINGThe resulting mixture was stirred at 120° C. for 2 hr
  14. 14
    Concentrationconcentrated under reduced pressure

Mode opératoire

In nitrogen atmosphere, trimethylsilyle iodide (0.188 mL) was added to a methylene chloride solution (6 mL) of (4R,9aS)-4-(3,4,5-trifluorophenyl)hexahydropyrido[2,1-c][1,4]oxazin-6-one (252 mg) and N,N,N′,N′-tetramethylethylenediamine (0.466 mL) at 0° C. The resulting reaction solution was stirred under ice-cooling for 30 min, and iodine (336 mg) was added thereto under ice-cooling. The resulting reaction solution was stirred under ice-cooling for 1 hr, and ethyl acetate and a saturated sodium thiosulfate aqueous solution were added thereto. The organic layer was separated, washed with saturated saline, dried over magnesium sulfate, and concentrated under reduced pressure to give a crude iodinated substance. To the given crude iodinated substance, triethyl phosphite (3 mL) was added. The resulting mixture was stirred at 120° C. for 2 hr, allowed to cool to room temperature, and then concentrated under reduced pressure to give 372 mg of the title compound. The physical property values of this compound were as follows:

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07737141B2uspto-grants-2010_06