Reacción #1543049

ord-9f03cfb4887d4ed08bac0b281ef45b49

Ecuación de reacción

O=C(O)CC(=O)O
malonic acid
O=Cc1ccccn1
pyridine-carboxaldehyde
CC(=O)[O-].[NH4+]
ammonium acetate
NC(CC(=O)O)c1cccnc1
3-amino-3-(3-pyridyl)propionic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto synthesize compounds of the present invention wherein R1
  2. 2
    OtroThe reaction
  3. 3
    Temperaturaat reflux
  4. 4
    Filtraciónthe resulting precipitate filtered
  5. 5
    Lavadowashed with hot isopropanol
  6. 6
    Otrodried

Procedimiento

Scheme I describes a synthesis of a pyridyl β-amino acid which can be used to synthesize compounds of the present invention wherein R1 is pyridyl. The reaction can be modified using conventional methodology to prepare other aroma substituted or heterocyclic substituted β-amino acids by substitution of the pyridyl carboxaldehyde with any other appropriate aldehyde. Briefly, in Scheme I to pyridine-carboxaldehyde in isopropanol is added ammonium acetate followed by malonic acid. The reaction mixture is stirred at reflux, the resulting precipitate filtered and washed with hot isopropanol and dried to yield 3-amino-3-(3-pyridyl)propionic acid. The ethyl ester is synthesized by heating this acid in excess ethanol in the presence of excess HCl gas.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05843906uspto-grants-1998_12