Reaction #2835

ord-9ca3b20357e643e9bc74d3800e3ccc9e

Reaction equation

CN(C)C=O
dimethylformamide
On1nnc2ccccc21
1-hydroxybenzotriazole
C(=NC1CCCCC1)=NC1CCCCC1
N,N'-dicyclohexylcarbodiimide
C1COCCN1
morpholine
CCCCC(=O)Nc1cc(C(=O)N2CCOCC2)ccn1
oil
CCCCC(=O)Nc1cc(C(=O)N2CCOCC2)ccn1
2-valeramidoisonicotinic acid morpholide

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe 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
    Washwashed with water and saturated brine
  6. 6
    Dryingdried over anhydrous sodium sulfate
  7. 7
    Concentrationconcentrated

Procedure

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.v1Patent: US05731310uspto-grants-1998_03