Reacción #322061

ord-7a9f5c9d3ce34332972a7aa089723b7c

Ecuación de reacción

[K+].[OH-]
potassium hydroxide
Cc1ncc(C=O)c(N)n1
4-amino-5-formyl-2-methylpyrimidine
CC(=O)c1cccs1
2-acetylthiophene
Cc1ncc2ccc(-c3cccs3)nc2n1
2-Methyl-7-(2-thienyl)-pyrido[2,3-d]pyrimidine
Rendimiento 17.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas removed After the residue
  2. 2
    Lavadothe organic phase was washed with water
  3. 3
    Otrodried
  4. 4
    Otroevaporated down

Procedimiento

1 ml of 40% strength by weight aqueous potassium hydroxide solution was added to a suspension of 2.0 g (14.6 mmol) of 4-amino-5-formyl-2-methylpyrimidine and 1.93 g. (15.3 mmol) of 2-acetylthiophene in 25 ml of methanol. The reaction mixture was then stirred for 20 hours at 20°-25° C. after which the solvent was removed After the residue had been taken up in dichloromethane, the organic phase was washed with water, dried and evaporated down. Yield: 17%; mp.: 175°-180° C.

Fuente

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