<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yuan G</submitter><funding>NIDA NIH HHS</funding><funding>National Institute on Drug Abuse</funding><pagination>4857-4860</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5018461</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(19)</volume><pubmed_abstract>To prompt the development of (18)F-labeled positron emission tomography (PET) tracers for the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor, we have prepared (18)F-labeled 2-(1-(3-fluorophenyl)-2-oxo-5-(pyrimidin-2-yl)-1,2-dihydropyridin-3-yl)benzonitrile ([(18)F]8). The radiosynthesis was achieved by a one-pot two-step method that utilized a spirocyclic hypervalent iodine(III) mediated radiofluorination to prepare the (18)F-labeled 1-bromo-3-fluorobenzene ([(18)F]15) intermediate with K(18)F. A subsequent copper(I) iodide mediated coupling reaction was carried out with 2-(2-oxo-5-(pyrimidin-2-yl)-1,2-dihydropyridin-3-yl)benzonitrile (10) to [(18)F]8 in 10±2% uncorrected radiochemical yield relative to starting (18)F-fluoride with >99% radiochemical purity and 29.6±7</pubmed_abstract><journal>Bioorganic &amp; medicinal chemistry letters</journal><pubmed_title>Radiosynthesis and preliminary PET evaluation of (18)F-labeled 2-(1-(3-fluorophenyl)-2-oxo-5-(pyrimidin-2-yl)-1,2-dihydropyridin-3-yl)benzonitrile for imaging AMPA receptors.</pubmed_title><pmcid>PMC5018461</pmcid><funding_grant_id>K01 DA038000</funding_grant_id><funding_grant_id>DA038000</funding_grant_id><pubmed_authors>Liang SH</pubmed_authors><pubmed_authors>Vasdev N</pubmed_authors><pubmed_authors>Jones GB</pubmed_authors><pubmed_authors>Yuan G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Radiosynthesis and preliminary PET evaluation of (18)F-labeled 2-(1-(3-fluorophenyl)-2-oxo-5-(pyrimidin-2-yl)-1,2-dihydropyridin-3-yl)benzonitrile for imaging AMPA receptors.</name><description>To prompt the development of (18)F-labeled positron emission tomography (PET) tracers for the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor, we have prepared (18)F-labeled 2-(1-(3-fluorophenyl)-2-oxo-5-(pyrimidin-2-yl)-1,2-dihydropyridin-3-yl)benzonitrile ([(18)F]8). The radiosynthesis was achieved by a one-pot two-step method that utilized a spirocyclic hypervalent iodine(III) mediated radiofluorination to prepare the (18)F-labeled 1-bromo-3-fluorobenzene ([(18)F]15) intermediate with K(18)F. A subsequent copper(I) iodide mediated coupling reaction was carried out with 2-(2-oxo-5-(pyrimidin-2-yl)-1,2-dihydropyridin-3-yl)benzonitrile (10) to [(18)F]8 in 10±2% uncorrected radiochemical yield relative to starting (18)F-fluoride with >99% radiochemical purity and 29.6±7</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Oct</publication><modification>2025-04-19T07:40:38.289Z</modification><creation>2019-03-27T02:23:54Z</creation></dates><accession>S-EPMC5018461</accession><cross_references><pubmed>27546294</pubmed><doi>10.1016/j.bmcl.2016.07.078</doi></cross_references></HashMap>