Synthesis and α-adrenergic and I1-imidazoline activity of 3- phenylpiperidines dimethyl-substituted on the phenyl ring

Article abstract of DOI:10.1016/S0223-5234(99)80016-6

In a previous study we found that certain 3-phenylpiperidines (PPEs, 5) display a good activity at α₂-adrenergic receptors (α₂-AR), whereas they are completely inactive at α₁-AR. The PPEs 5 are conformationally restricted analogs of the corresponding adrenergic drug with a phenylethylamine structure (PAEs, 4) in which the benzylic hydroxyl group characteristic of the adrenergic catecholamines is not present. The most interesting of the PPEs proved to be the 3-(3,4-dimethylphenyl) substituted compound (5a) which had been found to be essentially inactive at β₁- and β₂-AR. The methyl groups present on the aromatic ring of 5a are found, albeit in a different position, on the phenyl of α₂-adrenergic agonists with arylimidazolidine and arylimidazole structures. As such PPE 5a provided a unique template for the design of α₂-AR ligands. On the basis of these premises, we synthesized all the possible dimethylphenyl-substituted isomers of PPE 5a. Their activity on α₁- and α₂-AR and on I₁-imidazoline receptors (IR) was evaluated in vitro both by radioligand binding assays and by functional tests on isolated preparation. Two selected PPEs, 5a and 5f, were also tested for their affinity on α₂-AR subtypes. Conformational studies were carried out by means of theoretical calculations, in order to rationalise the results of pharmacological tests at the molecular level.