In this grant application, we propose to develop and optimize two new fluorine-18 (18F) reactions for the synthesis of 18F-labeled small molecules as useful, generally available tools for positron emission tomography (PET). Our goal is to provide readily available reagents that can be used by the entire radiochemistry community for the robust and simple synthesis of 18F-fluorinated probes from readily available materials. Our preliminary data suggest that the proposed reactions combine the simplicity of conventional fluorination chemistry with the large substrate scope of modern late-stage fluorination reactions. Our approach is enabled by novel chemical reactivity that can convert available materials directly into the corresponding fluorinated analogs. Positron emission tomography (PET) is a non-invasive, high sensitivity imaging technology that can be used to diagnose and study human diseases. PET can provide information about normal or aberrant human physiology and is a powerful tool for monitoring disease progression and treatment response. Over the past decade, PET imaging has had an impact in studying several diseases, such as cancer and neurological diseases, and is also beginning to expedite the development of new pharmaceuticals. However, the vast majority of molecules (even those that contain fluorine) cannot currently be labeled with the positron-emitting 18F isotope necessary for imaging. A clear need exists for more versatile and robust radiochemistry methods for incorporation of the 18F isotope. Our lab has invented a new reagent and a new reaction to incorporate the positron-emitting nuclide 18F into molecules based on new chemical reactivity. We have already demonstrated that we can provide aryl and alkyl fluorides from readily available phenols and alcohols, respectively. We propose here reaction development to furnish practical, readily performed methods for the synthesis of PET probes. Reaction optimization will be guided by a mechanism-based approach. We will showcase the utility and generality of our new methods by preparing eight radiotracers that are challenging to prepare with conventional methods.

Public Health Relevance

Positron emission tomography (PET) is a non-invasive imaging technology used in clinical care. Many of the current technical difficulties associated with PET are rooted in its underlying technology, radiotracer synthesis. This grant proposal addresses the problem of developing novel chemical technology for a practical and general method to make PET tracers.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM088237-07
Application #
9020238
Study Section
Synthetic and Biological Chemistry A Study Section (SBCA)
Program Officer
Lees, Robert G
Project Start
2009-07-01
Project End
2017-02-28
Budget Start
2016-03-01
Budget End
2017-02-28
Support Year
7
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Harvard University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
082359691
City
Cambridge
State
MA
Country
United States
Zip Code
Strebl, Martin G; Campbell, Arthur J; Zhao, Wen-Ning et al. (2017) HDAC6 Brain Mapping with [18F]Bavarostat Enabled by a Ru-Mediated Deoxyfluorination. ACS Cent Sci 3:1006-1014
Hoover, Andrew J; Lazari, Mark; Ren, Hong et al. (2016) A Transmetalation Reaction Enables the Synthesis of [(18)F]5-Fluorouracil from [(18)F]Fluoride for Human PET Imaging. Organometallics 35:1008-1014
Goldberg, Nathaniel W; Shen, Xiao; Li, Jiakun et al. (2016) AlkylFluor: Deoxyfluorination of Alcohols. Org Lett 18:6102-6104
Shi, Hang; Braun, Augustin; Wang, Lu et al. (2016) Synthesis of (18) F-Difluoromethylarenes from Aryl (Pseudo) Halides. Angew Chem Int Ed Engl 55:10786-90
Boursalian, Gregory B; Ham, Won Seok; Mazzotti, Anthony R et al. (2016) Charge-transfer-directed radical substitution enables para-selective C-H functionalization. Nat Chem 8:810-5
Neumann, Constanze N; Hooker, Jacob M; Ritter, Tobias (2016) Concerted nucleophilic aromatic substitution with (19)F(-) and (18)F(-). Nature 534:369-73
D'Amato, Erica M; Neumann, Constanze N; Ritter, Tobias (2015) Selective Aromatic C-H Hydroxylation Enabled by ? (6)-Coordination to Iridium(III). Organometallics 34:4626-4631
Shen, Xiao; Neumann, Constanze N; Kleinlein, Claudia et al. (2015) Alkyl Aryl Ether Bond Formation with PhenoFluor. Angew Chem Int Ed Engl 54:5662-5
Campbell, Michael G; Ritter, Tobias (2014) Late-Stage Fluorination: From Fundamentals to Application. Org Process Res Dev 18:474-480
Campbell, Michael G; Ritter, Tobias (2014) Late-stage formation of carbon-fluorine bonds. Chem Rec 14:482-91

Showing the most recent 10 out of 28 publications