4.8 Article

Synthesis of Anthranilic Acid Derivatives through Iron-Catalyzed Ortho Amination of Aromatic Carboxamides with N-Chloroamines

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 136, Issue 2, Pages 646-649

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja412521k

Keywords

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Funding

  1. MEXT [22000008, 25105711]
  2. Japan Society for the Promotion of Science through the Program for Leading Graduate Schools (MERIT)
  3. Japan Society for the Promotion of Science for Young Scientists [23-8207]
  4. Grants-in-Aid for Scientific Research [25105711, 11J08207, 22000008] Funding Source: KAKEN

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Arenes possessing an 8-quinolinylamide group as a directing group are ortho aminated with N-chloroamines and N-benzoyloxyamines in the presence of an iron/diphosphine catalyst and an organometallic base to produce anthranilic acid derivatives in high yield. The reaction proceeds via iron-catalyzed C H activation, followed by the reaction of the resulting iron intermediate with N-chloroamine. The choice of the directing group and diphosphine ligand is crucial for obtaining the anthranilic acid derivative with high yield and product selectivity.

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