Reacción #215106

ord-987e068ecaa3415f802f3d359bf7b64e

Ecuación de reacción

COc1ccc(C(C#N)=CCNc2ccccc2)cc1OCc1ccccc1
3-benzyloxy-4-methoxy-β-cyano-N-phenylcinnamylamine
Cl.N=C(N)N
guanidine hydrochloride
C[O-].[Na+]
sodium methoxide
COc1ccc(Cc2cnc(N)nc2N)cc1OCc1ccccc1
2,4-diamino-5-(3-benzyloxy-4-methoxybenzyl)pyrimidine
Rendimiento 81.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturaat reflux for 1.5 hr
  3. 3
    Otrois continued for a total of 20 hr
  4. 4
    OtroMost of the ethanol is removed by vacuum distillation
  5. 5
    workup.STIRRINGthe resulting residue is stirred with 1500 ml of water
  6. 6
    Lavadowashed well with water
  7. 7
    Temperaturacooled
  8. 8
    Filtraciónfiltered
  9. 9
    Lavadowashed with ethanol and with water

Procedimiento

75 Grams (0.5 mole) of crude 3-benzyloxy-4-methoxy-β-cyano-N-phenylcinnamylamine is added to a suspension made by stirring 40 g (0.42 mole) of guanidine hydrochloride with 27.5 g (0.51 mole) of sodium methoxide in 320 ml of ethanol. The reaction mixture is stirred and heated at reflux for 1.5 hr., after which the mixture becomes quite thick. An additional 320 ml of ethanol is added, and the refluxing is continued for a total of 20 hr. Most of the ethanol is removed by vacuum distillation, the resulting residue is stirred with 1500 ml of water and washed well with water. The crude moist product is digested with 250 ml of hot ethanol, cooled, filtered, and washed with ethanol and with water to yield 55 g (81%) of 2,4-diamino-5-(3-benzyloxy-4-methoxybenzyl)pyrimidine, m.p. 210°-212°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04258045uspto-grants-1981_03