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filingDate 2015-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b1f6d691097c07f27dbe3231f833ade4
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publicationDate 2020-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-10597340-B2
titleOfInvention Synthesis of fluorinated radiopharmaceuticals via electrochemical fluorination
abstract Provided herein are methods and compositions for the electrochemical selective radiofluorination of aromatic molecules. The resulting fluorine-18 labeled compounds are ideal radionuclides for use in Positron Emission Tomography (PET); they are also difficult to radiolabel efficiently and with high specific activity using existing approaches. For example, radiopharmaceuticals such as [F18]L-DOPA, which is indispensable in PET brain disease imaging, may be made electrochemically with high radiochemical yield and high specific activity using 18F-. The invention process described herein opens new possibilities and provides wider access to PET tracers such as 18F-L-Dopa, since 18F- is much more widely available than the 18F2, currently used for synthesis of electron rich substrates.
priorityDate 2013-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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