4.8 Article

An Unprecedented Approach to 4,5-Disubstituted Pyrimidine Derivatives by a ZnCl2-Catalyzed Three-Component Coupling Reaction

Journal

ORGANIC LETTERS
Volume 11, Issue 10, Pages 2161-2164

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol900382j

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Funding

  1. Japan Private School Promotion Foundation
  2. MEXT [16550148]
  3. Grants-in-Aid for Scientific Research [16550148] Funding Source: KAKEN

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We have developed a ZnCl2-catatyzed three-component coupling reaction involving a variety of functionalized enamines, triethyl orthoformate, and ammonium acetate, which leads to the production of 4,5-disubstituted pyrimidine derivatives in a single step. The procedure can be successfully applied to the efficient synthesis of mono- and disubstituted pydmidine derivatives, using methyl ketone derivatives instead of enamines.

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