<p>New amino(phenylsulfonyl)dihydropyrido[2,3-<i>d</i>]pyrimidinedione derivatives were synthesized using a three-component reaction involving the starting materials aryl aldehydes, (phenylsulfonyl)acetonitrile, and 6-aminouracil or 6-amino-1,3-dimethyluracil in the presence of a Fe<sub>3</sub>O<sub>4</sub>@vitamin B<sub>1</sub> nanocatalyst. The present method was very efficient and synthesized various amino(phenylsulfonyl)dihydropyrido[2,3-<i>d</i>]pyrimidinedione derivatives in a short reaction times and with good yields. Green solvent, high yield of products, easy separation and purification, and synthesis of various dihydropyrido[2,3-<i>d</i>]pyrimidinedione derivatives are the advantages of the present work. In work-up procedure, the Fe<sub>3</sub>O<sub>4</sub>@vitamin B<sub>1</sub> nanocatalyst was simply separated from the reaction medium by an external magnet and reused for similar reactions without losing catalytic properties.</p> Graphical Abstract <p></p>

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Synthesis of new amino(phenylsulfonyl)dihydropyrido[2,3-d]pyrimidinedione derivatives using Fe3O4@vitamin B1 as a nanocatalyst

  • Farhad Shirzaei,
  • Hamid Reza Shaterian

摘要

New amino(phenylsulfonyl)dihydropyrido[2,3-d]pyrimidinedione derivatives were synthesized using a three-component reaction involving the starting materials aryl aldehydes, (phenylsulfonyl)acetonitrile, and 6-aminouracil or 6-amino-1,3-dimethyluracil in the presence of a Fe3O4@vitamin B1 nanocatalyst. The present method was very efficient and synthesized various amino(phenylsulfonyl)dihydropyrido[2,3-d]pyrimidinedione derivatives in a short reaction times and with good yields. Green solvent, high yield of products, easy separation and purification, and synthesis of various dihydropyrido[2,3-d]pyrimidinedione derivatives are the advantages of the present work. In work-up procedure, the Fe3O4@vitamin B1 nanocatalyst was simply separated from the reaction medium by an external magnet and reused for similar reactions without losing catalytic properties.

Graphical Abstract