Expedited Aminoglutarimide C–N Cross-Coupling Enabled by High-Throughput Experimentation

A simple protocol for the Buchwald-Hartwig cross-coupling of (hetero)aryl halides with unprotected aminoglutarimide to afford diverse cereblon binding motifs is disclosed. The development of this C-N cross-coupling method was enabled by high-throughput combinatory screening of solvents, bases, temperatures, and ligands. Scope studies revealed generality across various heteroaryl and aryl halides with the reaction proceeding under mild conditions. In comparison, this method demonstrated strategic superiority over previously reported approaches, as evidenced by a significant decrease in step count from known syntheses in the patent literature.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-11-15
DOI
https://doi.org/10.1021/acs.joc.4c02536
Citations
3
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.70
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article

Expedited Aminoglutarimide C–N Cross-Coupling Enabled by High-Throughput Experimentation

Maximilian D. Palkowitz, F. E. ROBERTS, Jacob M. Ganley, Martins S. Oderinde et al.
3 citations
The Journal of Organic Chemistry
Chemical Synthesis and Analysis
0.70
article

Expedited Aminoglutarimide C–N Cross-Coupling Enabled by High-Throughput Experimentation

Maximilian D. Palkowitz, F. E. ROBERTS, Jacob M. Ganley, Martins S. Oderinde, Hui Li, Jacqueline W. Gu
article en
3 citations

Abstract

A simple protocol for the Buchwald-Hartwig cross-coupling of (hetero)aryl halides with unprotected aminoglutarimide to afford diverse cereblon binding motifs is disclosed. The development of this C-N cross-coupling method was enabled by high-throughput combinatory screening of solvents, bases, temperatures, and ligands. Scope studies revealed generality across various heteroaryl and aryl halides with the reaction proceeding under mild conditions. In comparison, this method demonstrated strategic superiority over previously reported approaches, as evidenced by a significant decrease in step count from known syntheses in the patent literature.

The Journal of Organic ChemistryVol. 89(23)
Analytical Services (US), Bristol-Myers Squibb (United States) (US), Université Bourgogne Franche-Comté (FR)
Openalex Percentile: Top 29%
Chemical Synthesis and Analysis
0.70
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