Synthesis of the racemate and individual enantiomers of [11C]methylphenidate for studying presynaptic dopaminergic neutron with positron emission tomography
AbstractAbstract
[en] Carbon-11 labeled dl-threo-methylphenidate (methyl-2-phenyl-2-(2-piperidyl)acetate, Ritalin), a psychostimulant drug widely used to treat attention deficit hyperactivity disorder, was prepared in two steps: O-methylation of the N-protected dl-threo-ritalinic acid derivative with [11C]methyl iodide followed by deprotection. The same strategy was applied for the preparation of C-11 labeled individual enantiomers of threo-methylphenidate from N-protected d-threo-l-threo-ritalinic acid. The subsequent C18 sep-pak and reverse-phase HPLC purification resulted in ca. 40% radiochemical yield with a total synthesis time of 40 minutes and an average specific activity of 1.5 Ci/μmole (at EOB). (author)
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Journal Article
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Journal of Labelled Compounds and Radiopharmaceuticals; ISSN 0362-4803; ; CODEN JLCRD4; v. 34(10); p. 989-997
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AMINES, AROMATICS, AUTONOMIC NERVOUS SYSTEM AGENTS, AZINES, BETA DECAY RADIOISOTOPES, BETA-PLUS DECAY RADIOISOTOPES, CARBON ISOTOPES, CARDIOTONICS, CARDIOVASCULAR AGENTS, CENTRAL NERVOUS SYSTEM AGENTS, COMPUTERIZED TOMOGRAPHY, DRUGS, EMISSION COMPUTED TOMOGRAPHY, EVEN-ODD NUCLEI, HETEROCYCLIC COMPOUNDS, HYDROXY COMPOUNDS, ISOTOPE APPLICATIONS, ISOTOPES, LABELLED COMPOUNDS, LIGHT NUCLEI, MATERIALS, MINUTES LIVING RADIOISOTOPES, NEUROREGULATORS, NUCLEI, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, PHENOLS, POLYPHENOLS, PYRIDINES, RADIOACTIVE MATERIALS, RADIOISOTOPES, SYMPATHOMIMETICS, SYNTHESIS, TOMOGRAPHY
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