Reacción #2829

ord-d4473f302a7441cbb178c086184f7270

Ecuación de reacción

CCCCCCc1ccc(C(=O)N2CCOCC2)cc1[N+](=O)[O-]
compound ( [5]-(54)-75 )
CCCCCCc1ccc(C(=O)N2CCOCC2)cc1[N+](=O)[O-]
4-hexyl-3-nitrobenzoic acid morpholide
NN.O
hydrazine monohydrate
CCCCCCc1ccc(C(=O)N2CCOCC2)cc1N
compound ( [5]-(55)-75 )
Rendimiento 99.4%
CCCCCCc1ccc(C(=O)N2CCOCC2)cc1N
3-amino-4-hexylbenzoic acid morpholide
Rendimiento 99.4%

Disolventes

Condiciones de reacción

Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    Filtraciónthe solution was filtered through celite 545
  3. 3
    Otroto remove the catalyst
  4. 4
    OtroThe solvent was evaporated under reduced pressure
  5. 5
    OtroThe residue was purified by silica gel column chromatography (Kieselgel 60=20 g, ethyl acetate)

Procedimiento

The compound ([5]-(54)-75) (700 mg) prepared in Example 62 was dissolved in ethanol (35 ml). After the solution was heated to 50° C., a suspension of 10% Pd/C (70 mg) in ethanol was added, and hydrazine monohydrate (0.35 ml) was added to the solution. The solution was stirred at 50° C. for 30 minutes. After the reaction was completed, the solution was filtered through celite 545 to remove the catalyst. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (Kieselgel 60=20 g, ethyl acetate) to obtain the above-captioned compound ([5]-(55)-75) (631 mg) as colorless oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05731310uspto-grants-1998_03