Reacción #62740

ord-cee52d64b5dc4625a65ee23e86a5187e

Ecuación de reacción

COc1cc(CC(C#N)=CN2CCOCC2)c2c(c1OC)OCC=C2
2-(7,8-Dimethoxy-2H-1-benzopyran-5-ylmethyl)-3-morpholino acrylonitrile
Cl.Nc1ccccc1
aniline hydrochloride
Cl.N=C(N)N
guanidine hydrochloride
C[O-].[Na+]
sodium methoxide
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2
2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine
Rendimiento 42.7%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction was cooled
  2. 2
    TemperaturaAfter continued reflux
  3. 3
    Otrothe product crystallized from the cooled reaction mixture
  4. 4
    FiltraciónFiltration
  5. 5
    Lavadowash (2 L)

Procedimiento

2-(7,8-Dimethoxy-2H-1-benzopyran-5-ylmethyl)-3-morpholino acrylonitrile (562 g, 1.64 mol) and aniline hydrochloride (234 g, 1.80 mol) were refluxed in SD3A (2.4 L) for one hour. The reaction was cooled, and guanidine hydrochloride (313 g, 3.28 mol) and sodium methoxide (275 g, 5.08 mol) were added. After continued reflux, the product crystallized from the cooled reaction mixture. Filtration followed by water wash (2 L) gave 2,4-diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine (220 g, 42.7%). Crystallization from ethanol-water gave title compound, mp 235°-238°, identical to the product of Example 1C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04761475uspto-grants-1988_08