This study describes the synthesis of a fluoroethylated derivative of [N-methyl-C-11]2-(4'-methylaminophenyl)-6-hydroxybenzothiazole ([C-11]6-OH-BTA-1; Pittsburgh Compound B (PIB)), an already established amyloid imaging agent. The [C-11]methylamino group of [C-11]6-OH-BTA-1 was formally replaced by a fluoroethyl group in a cold synthesis via N-alkylation of N-Boc-2-(4'-aminophenyl)-6-(methoxyethoxymethoxy)benzothiazole with fluoroethyl tosylate. Subsequent deprotection gave the target compound 2-[4'-(2-fluoroethyl)aminophenyl]-6-hydroxybenzothiazole (FBTA). In a radioligand competition assay on aggregated synthetic amyloid fibrils using N-[H-3-methyl]6-OH-BTA-1, 100 nM FBTA inhibited binding with 93 +/- 1 and 83 +/- 11% efficiency for A beta(1-40) and A beta(1-42), respectively. For the radiosynthesis a precursor carrying a tosylethyl moiety was prepared allowing the introduction of [F-18]fluoride via nucleophilic substitution with [F-18]tetra-n-butyl-ammonium fluoride (TBAF). Subsequent removal of all protecting groups was performed in a one-pot procedure followed by semi-preparative HPLC, delivering the target compound [F-18]FBTA in good radiochemical yield of 21% on average and radiochemical purity of >= 98% at EOS. In vitro autoradiography on human postmortem AD brain tissue slices showed intense cortical binding of [F-18]FBTA (11 nM), which was displaced in presence of 6-OH-BTA-1 (1 mu M). Brain up-take was evaluated in wild-type (wt) mice with microPET imaging. Based on these results, [F-18]FBTA appears to be a suitable candidate tracer for amyloid imaging in humans.     «

This study describes the synthesis of a fluoroethylated derivative of [N-methyl-C-11]2-(4'-methylaminophenyl)-6-hydroxybenzothiazole ([C-11]6-OH-BTA-1; Pittsburgh Compound B (PIB)), an already established amyloid imaging agent. The [C-11]methylamino group of [C-11]6-OH-BTA-1 was formally replaced by a fluoroethyl group in a cold synthesis via N-alkylation of N-Boc-2-(4'-aminophenyl)-6-(methoxyethoxymethoxy)benzothiazole with fluoroethyl tosylate. Subsequent deprotection gave the target compound...     »