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Download fileSynthesis of 11C‑Labeled RXR Partial Agonist 1‑[(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)amino]benzotriazole-5-carboxylic Acid (CBt-PMN) by Direct [11C]Carbon Dioxide Fixation via Organolithiation of Trialkyltin Precursor and PET Imaging Thereof
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posted on 2017-07-28, 00:00 authored by Osamu Shibahara, Masaki Watanabe, Shoya Yamada, Masaru Akehi, Takanori Sasaki, Akiya Akahoshi, Takahisa Hanada, Hiroyuki Hirano, Shunsuke Nakatani, Hiromi Nishioka, Yasuo Takeuchi, Hiroki KakutaThe
retinoid X receptor (RXR) partial agonist 1-[(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydronaphthalen-2-yl)amino]benzotriazole-5-carboxylic
acid (1; CBt-PMN, Emax =
75%, EC50 = 143 nM) is a candidate for treatment of central
nervous system (CNS) diseases such as Alzheimer’s and Parkinson’s
diseases based on reports that RXR-full agonist 4-[1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)ethynyl]benzoic
acid (bexarotene) shows therapeutic effects on these disease in rodent
models. Here, we synthesized carbon-11-labeled ([11C]1) as a tracer for positron emission tomography (PET) and
used it in a PET imaging study to examine the brain uptake and biodistribution
of 1. We found that 11CO2 fixation
after tin–lithium exchange at −20 °C afforded [11C]1. This methodology may also be useful for
synthesizing 11CO2H-PET tracer derivatives of
other compounds bearing π-rich heterocyclic rings. A PET/CT
imaging study of [11C]1 in mice indicated 1 is distributed to the brain and is thus a candidate for
treatment of CNS diseases.