Réaction #3565

ord-48bb0cbfb35c4f2d93ffd1055607d342

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe product was purified by medium pressure liquid chromatography
  2. 2
    Lavageeluting with 1:1 CHCl3

Mode opératoire

The title compound was prepared from 0.25 g of 6-(2,4,6-trimethyl-phenyl)-pyrido[2,3-d]pyrimidine-2,7-diamine from Example 96 and 0.109 mL of tert-butyl isocyanate according to Example 2. The product was purified by medium pressure liquid chromatography eluting with 1:1 CHCl3 :EtOAc; mp 281°-297° C.; CIMS (1% ammonia in methane): m/z (relative intensity) 379 (MH+ +1, 100), 380 (MH+ +2, 23).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05733913uspto-grants-1998_03