Reacción #62689

ord-b135d78203c9446597fb1623655ecbc0

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturaat reflux for 8 hours
  3. 3
    FiltraciónThe resulting precipitate was filtered
  4. 4
    Lavadowashed with methanol
  5. 5
    Otrodried

Procedimiento

A mixture of 2-cyanoethy 3-oxobutanoate (83.3 g, 0.54 mol), methyl 3-aminocrotonate (61.9 g, 0.54 mol), and 3-nitrobenzaldehyde (81.3 g, 0.54 mol) in methanol (540 mL ) was heated at reflux for 8 hours, then stirred overnight. The resulting precipitate was filtered, washed with methanol, and dried to produce racemic 2,6-dimethyl-3-carbomethoxy-4-(3-nitrophenyl)-5-(2-cyano)ethoxycarbonyl-1,4-dihydropyridine (mp=123° C.).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04761420uspto-grants-1988_08