Reacción #3512

ord-66fceab868444128830a463ef7b06941

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas consumed
  2. 2
    OtroThe solvents were removed under reduced pressure
  3. 3
    workup.ADDITIONthe residue treated with 17 mL of concentrate HCl
  4. 4
    Filtraciónfiltered
  5. 5
    Lavadowashed with isopropyl alcohol
  6. 6
    Otrodried
  7. 7
    OtroCrystallization from ethanol

Procedimiento

A suspension of 13.4 g of 2,4-diamino-5-cyanopyridine from Example 14, 2 g of Raney nickel catalyst, 40 mL of 97-100% formic acid, and 80 mL of water were shaken in a Parr apparatus under an atmosphere of nitrogen until the requisite amount of hydrogen was consumed. The solvents were removed under reduced pressure and the residue treated with 17 mL of concentrate HCl. The resulting pink solid was slurried in a small amount of water, filtered, washed with isopropyl alcohol, followed by diethylether, and dried. Crystallization from ethanol afforded 6.5 g of the title compound 2,4-diaminonicotinaldehyde.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05733913uspto-grants-1998_03