Réaction #2835

ord-9ca3b20357e643e9bc74d3800e3ccc9e

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe compound ([9]-(94)-467') (2.4610 g) prepared in Example 98
  2. 2
    FiltrationThe insolubles were filtered out
  3. 3
    Concentrationthe filtrate was concentrated
  4. 4
    workup.DISSOLUTIONThe resulting residue was dissolved in chloroform
  5. 5
    Lavagewashed with water and saturated brine
  6. 6
    Séchagedried over anhydrous sodium sulfate
  7. 7
    Concentrationconcentrated

Mode opératoire

The compound ([9]-(94)-467') (2.4610 g) prepared in Example 98 was dissolved in anhydrous dimethylformamide (DMF) (37 ml). Then, 1-hydroxybenzotriazole (1.9477 g), N,N'-dicyclohexylcarbodiimide (2.9739 g), and morpholine (1.3 ml) were added to the solution. The mixture was stirred at room temperature for 16 hours. The insolubles were filtered out, and the filtrate was concentrated. The resulting residue was dissolved in chloroform, washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain yellowish brown oil (7.4981 g). The crude oil was purified by silica gel column chromatography (Kieselgel 60=230 g, chloroform/acetone=5/1) to obtain the above-captioned compound ([9]-(94)-467") (3.1756 g) as white crystals.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05731310uspto-grants-1998_03