Reacción #321819

ord-8512c949f59e488294e44de880c15aaa

Ecuación de reacción

COCc1ncnc(Cl)c1OC
4-chloro-5-methoxy-6-methoxymethylpyrimidine
CC(C)C=C1CCC(N)CC1
4-iso-butylidene-cyclohexylamine
CCN(CC)CC
triethylamine
COCc1ncnc(NC2CCC(=CC(C)C)CC2)c1OC
4-(4-Isobutylidenecyclohexylamino)-5-methoxy-6-methoxymethylpyrimidine

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling
  2. 2
    Otrothe organic phase was dried
  3. 3
    Otroevaporated on a rotary evaporator
  4. 4
    OtroPurification by chromatography (silica gel/ethyl acetate)
  5. 5
    Otrogave 2.2 g (36% of theory) of a virtually colorless oil

Procedimiento

3.8 g (20 mmol) of 4-chloro-5-methoxy-6-methoxymethylpyrimidine (DE-A 4 116 089), 3.1 g (20 mmol) of 4-iso-butylidene-cyclohexylamine and 3.0 g (30 mmol) of triethylamine were stirred for 3 hours without solvent at 80°-90° C. After cooling, the mixture was taken up in water/toluene, and the organic phase was dried and evaporated on a rotary evaporator. Purification by chromatography (silica gel/ethyl acetate) gave 2.2 g (36% of theory) of a virtually colorless oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05595992uspto-grants-1997_01