Synthesis and binding of 6,7,8,9-tetrahydro-5H-pyrido[3,4-d]azepine and related ring-opened analogs at central nicotinic receptors

6,7,8,9-Tetrahydro-5H-pyrido[3,4-d]azepine (5a) and its N-7-methyl derivati ve 5b were synthesized and evaluated as potential nicotinic acetylcholinerg ic receptor (nAChR) ligands. On the basis that 6,7,8,9-tetrahydro-5H-pyrido [3,4-c]azepine (4a), which binds at nAChRs with low affinity (K-i = 1100 nM ), possesses an internitrogen distance (4.6 Angstrom) that may be less than optimal, we designed compound 5a due to its similar shape but longer inter nitrogen distance (5.5 Angstrom). Compound 5a (K-i = 45 nM) was found to bi nd with enhanced affinity. However, unlike what is seen with nornicotine/ni cotine, N-methylation of 5a reduced affinity (5b; K-i = 268 nM) rather than enhancing it. The results suggest that 5 may interact at nicotine receptor s in a manner that is somewhat different from that of nicotine. Ring-openin g of the pyrido[3,4-d]azepine ring led to a series of 3-(2-aminoethyl)pyrid ines 21 that retained the affinity of the cyclic compound. Subsequent modif ication, including further chain lengthening (e.g. aminopropylpyridines 22) and introduction of unsaturation, ultimately led to the development of a s eries of 3-(2-aminethoxy)pyridines 27. Simple N-substituted derivatives of 27 were found to bind with K-i values of 20 to 35 nM. Because parallel stru ctural changes in several series of related compounds did not result in par allel shifts in nAChR affinity, it is unlikely that all the investigated co mpounds bind in a similar fashion at these receptors. Nevertheless, some of these compounds represent novel classes of nAChR ligands. (C) Elsevier, Pa ris.