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Practical synthesis of precursor of [N-methyl-11C]vorozole, an efficient PET tracer targeting aromatase in the brain
Authors:Takahashi Kayo  Yamagishi Gen  Hiramatsu Toshiyuki  Hosoya Ayako  Onoe Kayo  Doi Hisashi  Nagata Hiroko  Wada Yasuhiro  Onoe Hirotaka  Watanabe Yasuyoshi  Hosoya Takamitsu
Institution:RIKEN Center for Molecular Imaging Science, 6-7-3 Minatojima-minamimachi, Chuo-ku, Kobe 650-0047, Japan.
Abstract:A practical method to prepare precursor of N-methyl-(11)C]vorozole ((11)C]vorozole), an efficient positron emission tomography (PET) tracer for imaging aromatase in the living body, was established. Sufficient amount of the racemate including norvorozole, a demethylated vorozole derivative used as a precursor of (11)C]vorozole, became available by means of high-yield eight-step synthesis. The enantiomers were separated by preparative HPLC using a chiral stationary phase column to give optically pure norvorozole and its enantiomer. From the latter, ent-(11)C]vorozole, an enantiomer of (11)C]vorozole, was prepared and used in the PET study for the first time, which was shown to bind very weakly to aromatase in rhesus monkey brain supporting the previous pharmacological results. The stable supply of norvorozole will facilitate further researches on aromatase in the living body including brain by the PET technique.
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