Реакция #3555

ord-f181ec7fa91846eca2529e969dd97cf0

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe product was purified by MPLC
  2. 2
    Промывкаeluting with a gradient of CHCl3 :EtOAc (1:1) to EtOAc
  3. 3
    Другоеto afford the pure product

Методика

The title compound was prepared from 0.25 g of 6-(2,6-difluoro-phenyl)-pyrido[2,3-d]pyrimidine-2,7-diamine from Example 63 and 0.112 mL of tert-butyl isocyanate according to Example 2. The product was purified by MPLC eluting with a gradient of CHCl3 :EtOAc (1:1) to EtOAc to afford the pure product; mp >300° C., CIMS (1% ammonia in methane): m/z (relative intensity) 373 (MH+ +1, 60), 374 (MH+ +2, 10), 274 (100).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05733913uspto-grants-1998_03