Reacción #2835
ord-9ca3b20357e643e9bc74d3800e3ccc9e
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroThe compound ([9]-(94)-467') (2.4610 g) prepared in Example 98
- 2FiltraciónThe insolubles were filtered out
- 3Concentraciónthe filtrate was concentrated
- 4workup.DISSOLUTIONThe resulting residue was dissolved in chloroform
- 5Lavadowashed with water and saturated brine
- 6Secadodried over anhydrous sodium sulfate
- 7Concentraciónconcentrated
Procedimiento
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.