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Practical and Efficient Approach to Scalable Synthesis of Rucaparib

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Abstract

A scalable synthesis of rucaparib was developed from methyl 5-fluoro-2-methyl-3-nitrobenzoate and 4-cyanobenzaldehyde. Methyl 5-fluoro-2-methyl-3-nitrobenzoate was converted into a 2-aminocinnamonitrile derivative, which was subjected to the imino-Stetter reaction with 4-cyanobenzaldehyde to yield trisubstituted indole-3-acetonitrile. The reduction of both nitriles, followed by azepinone scaffold construction and selective monomethylation, completed the synthesis of rucaparib. This synthetic route features the use of inexpensive starting materials, scalability, and ease of purification through recrystallization.

Original languageEnglish
Pages (from-to)4392-4399
Number of pages8
JournalOrganic Process Research and Development
Volume28
Issue number12
DOIs
Publication statusPublished - 2024 Dec 20

Bibliographical note

Publisher Copyright:
© 2024 American Chemical Society.

Keywords

  • chemoselective reduction
  • imino-Stetter reaction
  • indole
  • PARP inhibitor
  • rucaparib

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

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