Reacción #10014

ord-9d522069b2134617b6bccb18014497dc

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe crystal mass which precipitates out
  2. 2
    Temperaturaon cooling
  3. 3
    Filtraciónis filtered off
  4. 4
    Otrodried in vacuo

Procedimiento

1.9 g (10 mmol) of 2,6-dichloro-purine are stirred in 40 ml of DMF/n-butanol (1:3) with 4.1 g (30 mmol) of 4-nitro-aniline at 130° C. for 24 h and the crystal mass which precipitates out on cooling is filtered off and dried in vacuo. 2-Chloro-6-(4-nitro-phenyl-amino)-purine is obtained; m.p.>270° C.; FAB-MS: (M+H)+=291; Rf=0.6 (CH2Cl2:methanol=9:1).

Fuente

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