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.

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Journal
Chemistry - An Asian Journal
Published
2025-01-27
DOI
https://doi.org/10.1002/asia.202401718
Primary Topic
Catalytic C–H Functionalization Methods
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article
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article

Ph3P‐I2‐mediated Syntheses of C‐12 Carboxamide Indoloquinazolines and 2‐Aminosubstituted‐indol‐3‐ones from Isatins and Amines

Mookda Pattarawarapan, Wong Phakhodee, Sirawit Wet‐osot, Surat Hongsibsong et al.
Chemistry - An Asian Journal
Catalytic C–H Functionalization Methods
article

Ph3P‐I2‐mediated Syntheses of C‐12 Carboxamide Indoloquinazolines and 2‐Aminosubstituted‐indol‐3‐ones from Isatins and Amines

Mookda Pattarawarapan, Wong Phakhodee, Sirawit Wet‐osot, Surat Hongsibsong, Nittaya Wiriya, Saranphong Yimklan
article en

Abstract

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.

Chemistry - An Asian JournalVol. 20(9)
Chiang Mai University (TH)
Openalex Percentile: Top 99%
Catalytic C–H Functionalization Methods
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