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 language | English |
|---|---|
| Pages (from-to) | 4392-4399 |
| Number of pages | 8 |
| Journal | Organic Process Research and Development |
| Volume | 28 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 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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