5-(5-(6-[11C]methyl-3,6-diazabicyclo[3.2.0]heptan-3-yl)pyridin-2-yl)-1H-indole as a potential PET radioligand for imaging cerebral α7-nAChR in mice
2012
Abstract The radiosynthesis and in vivo evaluation of 5-(5-(6-[ 11 C]methyl-3,6-diazabicyclo[3.2.0]heptan-3-yl)pyridin-2-yl)-1 H -indole [ 11 C]rac-( 1 ), a potential PET tracer for α7 nicotinic acetylcholine receptors (α7-nAChR), are described. Syntheses of the nonradioactive standard rac- 1 and corresponding desmethyl precursor 7 were achieved in several reaction steps. Radiomethylation of 7 with [ 11 C]CH 3 I afforded [ 11 C]rac- 1 in an average radiochemical yield of 30 ± 5% ( n = 5) with high radiochemical purity and an average specific radioactivity of 444 ± 74 GBq/μmol ( n = 5). The total synthesis time was 30 min from end-of-bombardment. Biodistribution studies in mice showed that [ 11 C]rac- 1 penetrates the blood–brain barrier and specifically labels neuronal α7-nAChRs.
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