Chemical Transformation of Pyrido[2,3-d]Pyrimidin-4-ONES. 2. Selective Reduction of 2,3-Trimethylenepyrido[2,3-d]Pyrimidin-4-one by Sodium Borohydride.

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Kh Khodjaniyazov
A Mamadrakhimov
Kh Tadjimukhamedov
M Levkovich

Abstract

Reduction of 2,3-trimethylenepyrido[2,3-d]pyrimidin-4-one by sodium borohydride was investigated in an alcohol solution. Selective reduction of only a N1=C2 double bound of the initial compound was shown. The isomeric 2,3-trimethylene-1,2,3,4-tetrahydropyrido[2,3-d]-pyrimidin-4-ones are formed and quantitatively separated on HPLC with chiral adsorbent column. Theoretically formation of four optical isomers of 2,3-trimethylene-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-4-ones are discussed.

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How to Cite
Khodjaniyazov, K., Mamadrakhimov, A., Tadjimukhamedov, K., & Levkovich, M. (2022). Chemical Transformation of Pyrido[2,3-d]Pyrimidin-4-ONES. 2. Selective Reduction of 2,3-Trimethylenepyrido[2,3-d]Pyrimidin-4-one by Sodium Borohydride. Journal of Basic and Applied Research in Biomedicine, 2(2), 82–85. Retrieved from https://jbarbiomed.com/index.php/home/article/view/56
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