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Abstract Synthesis and physicochemical characterization of all possible cis ‐ and trans ‐1,3‐disubstituted cyclobutane‐derived amines and carboxylic acids bearing mono‐, di‐ and trifluoromethyl groups at the C‐3 position is disclosed. Tetramethylammonium fluoride (TMAF)‐ or morpholinosulfur trifluoride (Morph‐DAST)‐mediated nucleophilic fluorination of appropriate cis ‐ and trans ‐diastereomeric substrates was used as the key step for the preparation of CH 2 F‐ and CHF 2 ‐substituted derivatives. To obtain the corresponding cis ‐ and trans ‐isomeric CF 3 ‐substituted derivatives, resolution of known 3‐(trifluoromethyl)cyclobutanecarboxylic acid (obtained as a mixture of diastereomers) was applied. The proposed procedures were suitable for the preparation of corresponding fluoroalkyl‐substituted cyclobutane‐derived amines and carboxylic acids on up to 50 g scale. All 12 building blocks obtained were characterized by measuring dissociation constants (p K a ) and lipophilicities (Log P , for model derivatives) to evaluate the effect of the fluoroalkyl substituents on their physicochemical properties relevant to further drug discovery applications.
Demchuk et al. (Tue,) studied this question.