Diazabicyclic biaryl derivatives
This invention relates to novel diazabicyclic biaryl derivatives, which are found to be cholinergic ligands at the nicotinic acetylcholine receptors and modulators of the monoamine receptors and transporters. Due to their pharmacological profile the compounds of the invention may be useful for the treatment of diseases or disorders as diverse as those related to the cholinergic system of the central nervous system (CNS), the peripheral nervous system (PNS), diseases or disorders related to smooth muscle contraction, endocrine diseases or disorders, diseases or disorders related to neuro-degeneration, diseases or disorders related to inflammation, pain, and withdrawal symptoms caused by the termination of abuse of chemical substances.
1. An (R,R) or (S,S) diazabicyclic biaryl compound represented by Formula I
or an enantiomer thereof or a mixture of its enantiomers, or a pharmaceutically acceptable salt thereof, wherein
R represents hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl or benzyl; and
A represents a 5-membered aromatic monocyclic heterocyclic group selected from
wherein X represents O or S and R′ represents hydrogen or alkyl, or A represents a 6-membered aromatic monocyclic heterocyclic group selected from
which aromatic monocyclic heterocyclic group is optionally substituted with a substituent selected from the group consisting of halogen, CF 3 , CN, amino, and nitro, and B represents a 5-membered aromatic monocyctic heterocyclic group selected from
wherein X represents O or S and R′ represents hydrogen or methyl, which aromatic group may optionally be substituted one or two times with substituents selected from the group consisting of halogen, CF 3 , CN, amino and nitro; or
A represents a 5 -membered aromatic monocyclic heterocyclic group selected from
wherein X represents O or S and R′ represents hydrogen or alkyl, and B represents a phenyl or naphthyl group, which phenyl or naphthyl group may optionally be substituted one or two times with substituents selected from the group consisting of alkyl, cycloalkyl, alkoxy, cyano-alkyl, halogen, CF 3 , OCF 3 , CN, amino, and nitro, or B represents a 5-membered aromatic monocyclic heterocyclic group selected from
wherein X represents O or S and R′ represents hydrogen or methyl, which aromatic group may optionally be substituted one or two times with substituents selected from the group consisting of halogen, CF 3 , CN, amino and nitro.
2. The diazabicyclic biaryl compound of claim 1 , wherein R represents hydrogen, alkyl, cycloalkyl or cycloalkyl-alkyl.
3. The diazabicyclic biaryl compound of claim 1 , which is
2-[6-(3-Thienyl)-3-pyridazinyl]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane;
5-Methyl-2-[6-(3-tienyl)-3-pyridazinyl]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane;
2-[5-(3-Thienyl)-2-pyrazinyl]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane;
2-[2-(5-Phenyl)-1,3,4-thiadiazolyl)]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane;
2-[5-(3-Phenyl)-1,2,4-thiadiazolyl)]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane;
5-Methyl-2-[2-(5-phenyl)-1,3,4-thiadiazolyl)]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane;
5-Methyl-2-[5-(3-phenyl)-1,2,4-thiadiazolyl)]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane; or
5,5-Dimethyl-2-[2-(5-(5-Phenyl)-1,3,4-thiadiazolyl)]-(1S,4S)-2,5-diazabicyclo-[2.2.1]-heptane;
or an enantiomer or a mixture of its enantiomers, or a pharmaceutically acceptable salt thereof.
4. A pharmaceutical composition comprising a therapeutically effective amount of a diazabicyclic biaryl compound of claim 1 , or a pharmaceutically-acceptable addition salt thereof, together with at least one pharmaceutically-acceptable carrier or diluent.