Reacción #1847719

ord-91c93b4984184741933536acf0db4e14

Ecuación de reacción

CC(C)c1cc(Cl)nc(-c2ccc(Cl)cc2)n1
4-chloro-2-(4-chlorophenyl)-6-isopropylpyrimidine
CC1(C)CC(N)CC(C)(C)N1
4-amino-2,2,6,6-tetramethylpiperidine
CC(C)c1cc(NC2CC(C)(C)NC(C)(C)C2)nc(-c2ccc(Cl)cc2)n1.Cl.Cl
2-(4-Chlorophenyl)-6isopropyl-4-((2,2,6,6-tetramethylpiperidin-4-yl)amino)-pyrimidine dihydrochloride

Disolventes

Condiciones de reacción

Temperatura
150°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling
  2. 2
    workup.STIRRINGthe mixture was stirred at room temperature
  3. 3
    FiltraciónThe white precipitate was filtered off with suction
  4. 4
    Otrodried in vacuo
  5. 5
    workup.ADDITIONBy addition of hydrogen chloride
  6. 6
    Otrothe title compound was precipitated
  7. 7
    Filtraciónfiltered off with suction
  8. 8
    Otrodried in vacuo

Procedimiento

A mixture of 534 mg of 4-chloro-2-(4-chlorophenyl)-6-isopropylpyrimidine and 1.8 g of 4-amino-2,2,6,6-tetramethylpiperidine was heated at 150° C. for 2 hours with stirring. After cooling, 20 ml of water were added and the mixture was stirred at room temperature. The white precipitate was filtered off with suction, dried in vacuo and taken up in 20 ml of ethyl acetate. By addition of hydrogen chloride, the title compound was precipitated, filtered off with suction and dried in vacuo. Yield: 0.8 g.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06844347B1uspto-grants-2005_01