Reacción #62745

ord-817e59b075864a43ba1165743bca3c56

Ecuación de reacción

Cl.N=C(N)N
Guanidine hydrochloride
C[O-].[Na+]
sodium methoxide
N=C(N)N
guanidine
COCC(C#N)=Cc1cc(OC)c(OC)c2c1C=CCO2
3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)-2-methoxymethylpropenenitrile
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2
yellow solid
Rendimiento 42.8%
COc1cc(Cc2cnc(N)nc2N)c2c(c1OC)OCC=C2
2,4-Diamino-5-(7,8-dimethoxy-2H-1-benzopyran-5-ylmethyl)pyrimidine
Rendimiento 42.8%

Disolventes

Condiciones de reacción

Temperatura
3°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe resultant sodium chloride was filtered
  2. 2
    Lavadowashed with methanol (10 mL)
  3. 3
    Temperaturathe mixture heated
  4. 4
    Temperaturaat reflux for 2 hr

Procedimiento

Guanidine hydrochloride (11.46 g, 0.12 mole) in methanol (25 mL) was added to sodium methoxide (6.55 g, 0.12 mole) in methanol (40 mL) and the resultant sodium chloride was filtered and washed with methanol (10 mL). The guanidine solution was added to 3-(7,8-dimethoxy-2H-1-benzopyran-5-yl)-2-methoxymethylpropenenitrile (11.5 g, 0.04 mole) and the mixture heated at reflux for 2 hr. Cooling the mixture at 3° C. provided 5.38 g of yellow solid in two crops. HPLC assayed yield of 28.6%. A sample recrystallized from alcohol/water gave mp 232°-4° C.

Fuente

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