Reacción #3510

ord-2f0d5340aaf840a58a389a03ef389f8c

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawere heated in a bomb on a steam bath for 4 hours
  2. 2
    TemperaturaAfter cooling
  3. 3
    Lavadothe suspension was washed out of the bomb with 50 mL of methanol/water (50:50)
  4. 4
    Otrothe solvents were evaporated in vacuo
  5. 5
    Filtraciónfiltered
  6. 6
    Otrocrystallized from ethanol

Procedimiento

A mixture of 3.4 g of 2-amino-7-chloro-6-(4-methoxyphenyl)-pyrido[2,3-d]pyrimidine from Example 12, 40 mL of anhydrous methylamine, and 10 mL of methanol were heated in a bomb on a steam bath for 4 hours. After cooling, the suspension was washed out of the bomb with 50 mL of methanol/water (50:50) and the solvents were evaporated in vacuo. The solid residue was slurried with 50 mL of water, filtered, and crystallized from ethanol to afford 2.2 g of the title compound 6-(4-methoxyphenyl)-N7 -methyl-pyrido[2,3-d]pyrimidine-2,7-diamine, mp 270°-275° C. dec.

Fuente

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