Реакция #3547

ord-72ff6e6fed6a469e82049eb403a60197

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеfollowed by purification on flash silica gel chromatography
  2. 2
    Промывкаeluting sequentially with 100:0, 3:1, 1:1, and 0:100 dichloromethane
  3. 3
    Другоеethyl acetate gave a solid
  4. 4
    Другоеthat was triturated in 2-propanol

Методика

1-[2-Amino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-7-yl]-3-tert-butylurea from Example 3 was reacted with DMF dimethyl acetal for 13.5 hours as described in Example 78. Workup as described above, followed by purification on flash silica gel chromatography eluting sequentially with 100:0, 3:1, 1:1, and 0:100 dichloromethane:ethyl acetate gave a solid that was triturated in 2-propanol to afford the title compound N'-[7-(3-tert-butylureido)-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidin-2-yl]-N,N-dimethylformamidine, mp 190°-193° C.

Источник

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