Reacción #10350

ord-54c27a8b69d64090a7bc68f329ae5eb1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was evaporated
  2. 2
    workup.ADDITIONwater was added to the residue
  3. 3
    Filtraciónthe precipitate was filtered off
  4. 4
    OtroAfter drying at HV/50° C

Procedimiento

4,6-Dichloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidine (2.9 g, Referential Example 1d)) was suspended in dioxane (30 ml) and ammonia (gaseous) was introduced until the solution was saturated. Stirring was continued for 7 days while the saturation of the reaction mixture with ammonia (gaseous) was repeated every 16 to 20 h. The solvent was evaporated, water was added to the residue and the precipitate was filtered off. After drying at HV/50° C. 4-amino-6-chloro-5-(o-methoxyphenoxy)-2-(4-pyridyl)-pyrimidine (2.7 g) was obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07094781B2uspto-grants-2006_08