反应详情

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. CIMS (1% ammonia in methane): m/z (relative intensity) 462 (MH+ +2, 0.78), 460 (MH+, 0.93).

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2. washeluting sequentially with 100:0, 3:1, 1:1, and 0:100 dichloromethane
3. customethyl acetate gave a solid
4. customthat was triturated in 2-propanol