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1H NMR spectra for all intermediates and final compounds were consistent with the assigned structures. All final compounds gave satisfactory C, H, N analyses. In case of compounds 4g and 4h, the purity was evaluated using separation methods of sequential gas chromatography/mass spectrometry measured in the EI mode at an ionization potential of 70 eV.
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It is interesting to note that some N-arylalkyl "chair" tropanes have been reported, and that in this case the highest affinity ligand, methyl N-(3-phenylpropyl)-3β-(4-fluorophenyl)tropane-2β-carboxylate possessed a propylene linker. Meltzer, P. C.; Blundell, P.; Madras, B. K. Med. Chem. Res. 1998, 8, 12-34.
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