Reacción #63959

ord-bf027ace75584b7f8c1ba5e6491e15a1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroevaporated in vacuo
  2. 2
    LavadoThe residual solid was washed with water
  3. 3
    Otrodried
  4. 4
    Otrorecrystallized from a mixture of chloroform and methanol

Procedimiento

Chloroform (50 ml) was added to a mixture of 3-dimethylaminomethylene-6-nitro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline (3.03 g), hydrazine hydrate (0.6 g), and acetic acid (0.78 g) in methanol (50 ml) and stirred at room temperature for 8 hours. To the mixture was added acetic acid (2 ml) and evaporated in vacuo. The residual solid was washed with water, dried, and recrystallized from a mixture of chloroform and methanol to give 4,5-dihydro-8-nitro-5-propionyl-1H-pyrazolo[4,3-c]quinoline (2.53 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04767780uspto-grants-1988_08