Syntheses and pharmacological properties of the histaminic H-1 antagonists sila-terfenadine-A, sila-terfenadine-B, disila-terfenadine, and sila-fexofenadine: A study on C/Si bioisosterism

摘要

Sila-substitution (C/Si exchange) of one or both of the two quaternary carbon atoms of the histaminic H-1 antagonist terfenadine (1a) leads to sila-terfenadine-A (1b; R3COH --> R3SiOH), sila-terfenadine-B (1c; R4C --> R4Si), or disila-terfenadine (1d; R3COH --> R3SiOH, R4C --> R4Si). Sila-substitution of the quaternary carbon atom of the histaminic H-1 antagonist fexofenadine (2a) affords sila-fexofenadine (2b; R3COH --> R3SiOH). The silicon compounds rac-1b, rac-1c, rac-1d, and rac-2b were synthesized in multistep syntheses, and the identities of these compounds and their precursors were established by elemental analyses and multinuclear NMR studies. Some of the precursors were additionally characterized by single-crystal X-ray diffraction. The pharmacological profiles of rac-1a, rac-1b, rac-1c, rac-1d, rac-2a, and rac-2b were assessed across a range of histaminic receptor binding assays (radioligand binding studies at histamine central H-1, peripheral H-1, H-2, and H-3 receptors). The silicon compounds, within experimental error, exhibited an affinity and selectivity profile similar to their corresponding carbon analogues.