Reacción #9991

ord-cf753584cff448f29f411f9c50bea731

Reactivos

Ninguno

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling to room temperature
  2. 2
    workup.STIRRINGstirred at 10° C. for 90 minutes
  3. 3
    FiltraciónThe precipitate is filtered off
  4. 4
    Lavadorinsed with isopropanol and diethyl ether
  5. 5
    OtroThe crystals are partitioned between 50 ml of 2 N (two normal) sodium hydroxide solution, 100 ml of water and 700 ml of ethyl acetate
  6. 6
    ExtracciónThe aqueous phase is subsequently extracted twice with ethyl acetate
  7. 7
    LavadoThe combined organic extracts are washed twice with water and once with saturated sodium chloride solution
  8. 8
    Secadodried over sodium sulfate
  9. 9
    FiltraciónAfter filtration
  10. 10
    Concentraciónthe filtrate is concentrated under reduced pressure
  11. 11
    workup.STIRRINGThe crude product is stirred with diethyl ether
  12. 12
    Otrothe crystals are dried at 50° C. under an HV

Procedimiento

1.4 ml (13 mmol) of 3-chloro-aniline are added to a suspension of 650 mg (3.44 mmol) of 2,6-dichloro-purine in 5 ml of 1-pentanol. The reaction mixture is stirred at 100° C. (oil bath temperature) for 3 hours. After cooling to room temperature, the mixture is diluted with isopropanol and stirred at 10° C. for 90 minutes. The precipitate is filtered off and rinsed with isopropanol and diethyl ether. The crystals are partitioned between 50 ml of 2 N (two normal) sodium hydroxide solution, 100 ml of water and 700 ml of ethyl acetate. The aqueous phase is subsequently extracted twice with ethyl acetate. The combined organic extracts are washed twice with water and once with saturated sodium chloride solution and dried over sodium sulfate. After filtration, the filtrate is concentrated under reduced pressure. The crude product is stirred with diethyl ether and the crystals are dried at 50° C. under an HV. 2-Chloro-6-(3-chloro-phenyl-amino)-purine is obtained; Rf=0.47 (ethyl acetate:hexane=3:1); APCI-MS: (M+H)+=280; HPLC: tret(grad 20/1)=10.26 minutes.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091346B1uspto-grants-2006_08