Reacción #62935

ord-999f0d60f88a46828744633fb78cedb5

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe resulting solution is evaporated in-vacuo
  2. 2
    Temperaturathe mixture is refluxed for 16 hours
  3. 3
    OtroThe solvent is evaporated
  4. 4
    Lavadothe yellow residue is washed with cold water
  5. 5
    Otrorecrystallized from absolute ethanol

Procedimiento

A solution of tris(dimethylamino)methane, 25.0 g (172 mmol), in 100 ml toluene is added dropwise, under nitrogen, to a solution of the monoethylene ketal of 1,4-cyclohexanedione, 25.0 g (160 mmol), in 300 ml of toluene. The resulting solution is evaporated in-vacuo and the residue is dissolved in 600 ml of methanol along with 38.72 g (320 mmol) of guanidine carbonate. The pH of the solution is adjusted to 9 with 15% hydrochloric acid and the mixture is refluxed for 16 hours. The solvent is evaporated and the yellow residue is washed with cold water and recrystallized from absolute ethanol to yield 11.0 g of 5,6,7,8-tetrahydro-6-ketoquinazolin-2-amine, ethylene ketal as yellow prisms; mp 214°-217° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04762843uspto-grants-1988_08