Production Of <sup>11</sup> C‐Labeled Amides Via “In‐Loop” <sup>11</sup> C‐Carbonylation

The carbon-11 (<sup>11</sup>C) labeling of benzamides holds great promise in the development of PET radiotracers given the prevalence of benzamides in bioactive molecules. This work establishes an improved automated route to carbon-11 labeled primary benzamides through carbonylative cross-coupling of aryl halides with carbon-11 carbon monoxide using electrophilic aroyl dimethylaminopyridinium salts as an intermediate. The methodology uses GE TRACERLab FX automated radiochemistry synthesis modules and allows for the synthesis of a variety of benzamide containing compounds, including known PET imaging agent [<sup>11</sup>C]LY2795050, a KOR antagonist, in moderate to excellent radiochemical yields. This not only provides a practical means of synthesizing primary [<sup>11</sup>C]benzamides, but it sets the stage for potential future applications in PET tracer synthesis. Overall, this development offers a versatile tool for generating <sup>11</sup>C-labeled compounds for PET imaging applications, thus opening new avenues in the field of molecular imaging and advancing our understanding of various biological processes.

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Publication Details

Journal
Asian Journal of Organic Chemistry
Published
2025-03-27
DOI
https://doi.org/10.1002/ajoc.202500121
Primary Topic
Chemical Synthesis and Analysis
Type
article
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article

Production Of 11 C‐Labeled Amides Via “In‐Loop” 11 C‐Carbonylation

Peter J. H. Scott, Xia Shao, A. F. Brooks, Tanpreet Kaur
Asian Journal of Organic Chemistry
Chemical Synthesis and Analysis
article

Production Of 11 C‐Labeled Amides Via “In‐Loop” 11 C‐Carbonylation

Peter J. H. Scott, Xia Shao, A. F. Brooks, Tanpreet Kaur
article en

Abstract

The carbon-11 (<sup>11</sup>C) labeling of benzamides holds great promise in the development of PET radiotracers given the prevalence of benzamides in bioactive molecules. This work establishes an improved automated route to carbon-11 labeled primary benzamides through carbonylative cross-coupling of aryl halides with carbon-11 carbon monoxide using electrophilic aroyl dimethylaminopyridinium salts as an intermediate. The methodology uses GE TRACERLab FX automated radiochemistry synthesis modules and allows for the synthesis of a variety of benzamide containing compounds, including known PET imaging agent [<sup>11</sup>C]LY2795050, a KOR antagonist, in moderate to excellent radiochemical yields. This not only provides a practical means of synthesizing primary [<sup>11</sup>C]benzamides, but it sets the stage for potential future applications in PET tracer synthesis. Overall, this development offers a versatile tool for generating <sup>11</sup>C-labeled compounds for PET imaging applications, thus opening new avenues in the field of molecular imaging and advancing our understanding of various biological processes.

Asian Journal of Organic ChemistryVol. 14(6)
University of Michigan (US)
Openalex Percentile: Top 95%
Chemical Synthesis and Analysis
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Production Of <sup>11</sup> C‐Labeled Amides Via “In‐Loop” <sup>11</sup> C‐Carbonylation — Peter J. H. Scott, Xia Shao, et al. · Asian Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS