Abstract The first reaction between 2, 4, 6-trichloropyrimidine 1 and anionic nitrogen nucleophiles is described. Treatment of 1 with one equivalent of sodium amide gave mixtures of 4-amino-2, 6-dichloropyrimidine 2 and 2-amino-4, 6-dichloropyrimidine 3. Additional quantities of sodium amide failed to provide either diamino-or triaminopyrimidines. Instead, the strongly basic nature of sodium amide led to higher ...
[Savall, Brad M.; Chavez, Frank; Tays, Kevin; Dunford, Paul J.; Cowden, Jeffery M.; Hack, Michael D.; Wolin, Ronald L.; Thurmond, Robin L.; Edwards, James P. Journal of Medicinal Chemistry, 2014 , vol. 57, # 6 p. 2429 - 2439]