Abstract
As the third step of a new general synthesis of pyrido[2,3‐d]pyrimidines, the substitution of the halogens by several nucleophiles has been carried out. Yields are between good and high in every case, even when 4‐halogenated compounds have a neighbouring methyl group in C5. Copyright © 1988 Journal of Heterocyclic Chemistry
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CITATION STYLE
Victory, P., Crespo, A., Garriga, M., & Nomen, R. (1988). New synthesis of pyrido[2,3‐d]pyrimidines. III. Nucleophilic substitution on 4‐amino‐2‐halo and 2‐amino‐4‐halo‐5,6‐dihydropyrido[2,3‐d]pyrimidin‐7(8H)‐ones. Journal of Heterocyclic Chemistry, 25(1), 245–247. https://doi.org/10.1002/jhet.5570250139
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