Reacción #322060

ord-2ca04429d20f4a3d8462f3ae6d4cb2c2

Ecuación de reacción

[K+].[OH-]
potassium hydroxide
Cc1ncc(C=O)c(N)n1
4-amino-5-formyl-2-methylpyrimidine
CC(=O)c1ccc(F)cc1
4-fluoroacetophenone
Cc1ncc2ccc(-c3ccc(F)cc3)nc2n1
7-(4-Fluorophenyl)-2-methylpyrido[2,3-d]pyrimidine
Rendimiento 50.0%

Disolventes

Condiciones de reacción

Temperatura
20°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroa homogeneous solution being formed
  2. 2
    Otrothe solid formed
  3. 3
    Otrowas isolated
  4. 4
    Otrowas recrystallized from ethanol

Procedimiento

15 ml of 40% strength by weight aqueous potassium hydroxide solution were slowly added to a suspension of 30.1 g (0.22 mol) of 4-amino-5-formyl-2-methylpyrimidine and 31.7 g (0.23 mol) of 4-fluoroacetophenone in 395 ml of methanol at 20°-25° C., a homogeneous solution being formed. After the mixture had been stirred for 20 hours at about 20° C., the solid formed was isolated and was recrystallized from ethanol. Yield: 50%; mp.>200° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05597776uspto-grants-1997_01