A Design of Experiments (DoE) Approach Accelerates the Optimization of Copper-Mediated 18F-Fluorination Reactions of Arylstannanes

被引:124
作者
Bowden, Gregory D. [1 ]
Pichler, Bernd J. [1 ,2 ]
Maurer, Andreas [1 ,2 ]
机构
[1] Eberhard Karls Univ Tubingen, Werner Siemens Imaging Ctr, Dept Preclin Imaging & Radiopharm, Tubingen, Germany
[2] Eberhard Karls Univ Tubingen, iFIT Cluster Excellence, Tubingen, Germany
关键词
LATE-STAGE; RADIOFLUORINATION; FLUORINATION; F-18; ESTERS;
D O I
10.1038/s41598-019-47846-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent advancements in F-18 radiochemistry, such as the advent of copper-mediated radiofluorination (CMRF) chemistry, have provided unprecedented access to novel chemically diverse PET probes; however, these multicomponent reactions have come with a new set of complex optimization problems. Design of experiments (DoE) is a statistical approach to process optimization that is used across a variety of industries. It possesses a number of advantages over the traditionally employed "one variable at a time" (OVAT) approach, such as increased experimental efficiency as well as an ability to resolve factor interactions and provide detailed maps of a process's behavior. Here we demonstrate the utility of DoE to the development and optimization of new radiochemical methodologies and novel PET tracer synthesis. Using DoE to construct experimentally efficient factor screening and optimization studies, we were able to identify critical factors and model their behavior with more than two-fold greater experimental efficiency than the traditional OVAT approach. Additionally, the use of DoE allowed us to glean new insights into the behavior of the CMRF of a number of arylstannane precursors. This information has guided our decision-making efforts while developing efficient reaction conditions that suit the unique process requirements of F-18 PET tracer synthesis.
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页数:10
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共 35 条
[1]   Copper-Mediated Radiofluorination of Aryl Pinacolboronate Esters: A Straightforward Protocol by Using Pyridinium Sulfonates [J].
Antuganov, Dmitrii ;
Zykov, Michail ;
Timofeev, Vasilii ;
Timofeeva, Ksenija ;
Antuganova, Yulija ;
Orlovskaya, Victoriya ;
Fedorova, Olga ;
Krasikova, Raisa .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2019, 2019 (05) :918-922
[2]   18F-Deoxyfluorination of Phenols via Ru π-Complexes [J].
Beyzavi, M. Hassan ;
Mandal, Debashis ;
Strebl, Martin G. ;
Neumann, Constanze N. ;
D'Amato, Erica M. ;
Chen, Junting ;
Hooker, Jacob M. ;
Ritter, Tobias .
ACS CENTRAL SCIENCE, 2017, 3 (09) :944-948
[3]   Late-stage [18F]fluorination: new solutions to old problems [J].
Brooks, Allen F. ;
Topczewski, Joseph J. ;
Ichiishi, Naoko ;
Sanford, Melanie S. ;
Scott, Peter J. H. .
CHEMICAL SCIENCE, 2014, 5 (12) :4545-4553
[4]   Bridging the gaps in 18F PET tracer development [J].
Campbell, Michael G. ;
Mercier, Joel ;
Genicot, Christophe ;
Gouverneur, Veronique ;
Hooker, Jacob M. ;
Ritter, Tobias .
NATURE CHEMISTRY, 2017, 9 (01) :1-3
[5]   Modern Carbon-Fluorine Bond Forming Reactions for Aryl Fluoride Synthesis [J].
Campbell, Michael G. ;
Ritter, Tobias .
CHEMICAL REVIEWS, 2015, 115 (02) :612-633
[6]   Experimental designs and their recent advances in set-up, data interpretation, and analytical applications [J].
Dejaegher, Bieke ;
Vander Heyden, Yvan .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2011, 56 (02) :141-158
[7]   Copper-Catalyzed [18F]Fluorination of (Mesityl)(aryl)iodonium Salts [J].
Ichiishi, Naoko ;
Brooks, Allen F. ;
Topczewski, Joseph J. ;
Rodnick, Melissa E. ;
Sanford, Melanie S. ;
Scott, Peter J. H. .
ORGANIC LETTERS, 2014, 16 (12) :3224-3227
[8]   Kinetic and Spectroscopic Studies of Aerobic Copper(II)-Catalyzed Methoxylation of Arylboronic Esters and Insights into Aryl Transmetalation to Copper(II) [J].
King, Amanda E. ;
Ryland, Bradford L. ;
Brunold, Thomas C. ;
Stahl, Shannon S. .
ORGANOMETALLICS, 2012, 31 (22) :7948-7957
[9]   Experimental design in chemistry: A tutorial [J].
Leardi, Riccardo .
ANALYTICA CHIMICA ACTA, 2009, 652 (1-2) :161-172
[10]   A Fluoride-Derived Electrophilic Late-Stage Fluorination Reagent for PET Imaging [J].
Lee, Eunsung ;
Kamlet, Adam S. ;
Powers, David C. ;
Neumann, Constanze N. ;
Boursalian, Gregory B. ;
Furuya, Takeru ;
Choi, Daniel C. ;
Hooker, Jacob M. ;
Ritter, Tobias .
SCIENCE, 2011, 334 (6056) :639-642