Ph<sub>3</sub>P‐I<sub>2</sub>‐mediated Syntheses of C‐12 Carboxamide Indoloquinazolines and 2‐Aminosubstituted‐indol‐3‐ones from Isatins and Amines
The Ph<sub>3</sub>P-I<sub>2</sub>-mediated reactions between isatins and amines were extensively investigated leading to the discovery of highly selective and divergent routes toward the synthesis of two distinct classes of indole-based frameworks. Through a strategic design of the reaction paths, we overcome potential side reactions to achieve convenient and straightforward one-pot methods to access either indoloquinazolines with C-12 carboxamide or 2-aminosubstituted indol-3-ones using the same reagent system. Mechanistic studies reveal the role of Ph<sub>3</sub>P-I<sub>2</sub> in governing product selectivity, providing an efficient route to novel fused-indolone derivatives with promising applications in drug discovery and medicinal chemistry.
Authors
- Mookda Pattarawarapan (ORCID: https://orcid.org/0000-0002-7484-122X)
- Wong Phakhodee (ORCID: https://orcid.org/0000-0002-5489-9555)
- Sirawit Wet‐osot (ORCID: https://orcid.org/0000-0001-5244-3696)
- Surat Hongsibsong (ORCID: https://orcid.org/0000-0002-5510-5905)
- Nittaya Wiriya
- Saranphong Yimklan (ORCID: https://orcid.org/0000-0003-4008-0845)
Institutions
- Chiang Mai University (TH)
Publication Details
- Journal
- Chemistry - An Asian Journal
- Published
- 2025-01-27
- DOI
- https://doi.org/10.1002/asia.202401718
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00