SYNTHESIS OF[C-11]DAPOXETINE-CENTER-DOT-HCL, A SEROTONIN REUPTAKE INHIBITOR - BIODISTRIBUTION IN RAT AND PRELIMINARY PET IMAGING IN THE MONKEY

[C-11]Dapoxetine . HCl, S-(+)-N,N-dimethyl-a-[2-(naphthalenyloxy)ethyl ] benzenemethanamine hydrochloride, a potent serotonin re-uptake inhib itor was prepared from its mono-methyl precursor, S-(+)-N-methyl-a-[2- (naphthalenyloxy)ethyl]benze methanamine hydrochloride. Biodistributio n was determined in rats at 5, 30 and 60 min after injection and preli minary PET studies were performed in a Rhesus monkey. (CH3I)-C-11 was bubbled into a solution of S-(+)-N-methyl-alpha-[2-(naphthalenyloxy)et hyl] methanamine hydrochloride (3.0 mg in DMSO) and the mixture was he ated at 110 degrees C for 8 min. [C-11]Dapoxetine . HCl was purified b y HPLC on a C-18 cartridge eluted with MeOH:phosphate buffer, pH 7.2 ( 75:25) with a 10% yield (end of synthesis). The time required for the synthesis was 40 min, from the end of bombardment. Radiochemical purit y of the final product was > 99% and specific activity was routinely > 400 mCi/mu mol [EOS]. In the biodistribution studies the highest conc entration (%ID/g +/- SEM) of dapoxetine . HCl was detected in lung: 4. 56 +/- 0.27 (5 min), 1.28 +/- 0.18 (30 min) and 0.67 +/- 0.04 (60 min) . Brain accumulation was 0.76 +/- 0.02 (5 min), 0.46 +/- 0.04 (30 min) and 0.27 +/- 0.01 (60 min). Preliminary PET studies demonstrated sign ificant displaceable binding in the cerebral cortex and subcortical gr ey matter. These results demonstrate that [C-11]dapoxetine . HCl can b e prepared in high purity and may be useful for the in vivo evaluation of serotonin re-uptake mechanisms.