Réaction #3563

ord-f03d647d1d394659beb1e6de74a454ce

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe product is purified by MPLC
  2. 2
    Lavageeluting with 1:1 CHCl3

Mode opératoire

The title compound was prepared from 0.3 g of 6-(3,5-dimethyl-phenyl)-pyrido[2,3-d]pyrimidine-2,7-diamine from Example 94 and 0.14 mL of tert-butyl isocyanate according to Example 2. The product is purified by MPLC eluting with 1:1 CHCl3 :EtOAc; mp 180°-182° C., CIMS (1% ammonia in methane): m/z (relative intensity) 365 (MH+ +1, 16), 366 (MH+ +2, 3), 84 (100).

Source

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