反应 #3555

ord-f181ec7fa91846eca2529e969dd97cf0

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The product was purified by MPLC
  2. 2
    洗涤eluting with a gradient of CHCl3 :EtOAc (1:1) to EtOAc
  3. 3
    其他to afford the pure product

实验过程

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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05733913uspto-grants-1998_03