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. A diazabicyclic biaryl compound represented by Formula I
any of its enantiomers or any mixture of its enantiomers, or a pharmaceutically acceptable salt thereof, wherein
n is 1, 2 or 3; and
′A″ represents a bivalent phenyl group of the formula
′A″ represents a bivalent 6-membered aromatic monocyclic carbocyclic or heterocyclic group selected from
(read in the direction represented by ′ and ″); and
B represents a phenyl group; or
B represents a 5-membered aromatic monocyclic heterocyclic group selected from
B represents a 6-membered aromatic monocyclic heterocyclic group selected from
B represents an indol-2-yl, an indol-3-yl, and indol-5-yl, or an indol-6-yl group.
2. The diazabicyclic biaryl compound of claim 1 , which is
4-(6-Thien-3-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Pyridin-3-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Selenophen-3-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6Furan-2-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Thien-2-yl-pyridazin-3-yl)-1,4-diazabicyelo[3.2.2]nonane;
4-(6-Furan-3-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6Thiazol-2-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Selenophen-2-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Indol-2-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Indol-3-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Indol-5-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-Indol-6-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-oxazol-2-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6-oxazol-5-yl-pyridazin-3-yl)-1,4-diazabicyclo[3.2.2]nonane;
4-(6thiazol-5-yl-pyridazin-3-yl)-1,4-diazabicycio[3.2.2]nonane;
4-[(6-(1,3,4)-thiadiazol-2-yl]-pyridazin-3-yl-1,4-diazabicyclo[3.2.2]nonane; or
4-[6-(1,3,4)-oxadiazol-2-yl]-pyridazin-3-yl-1,4-diazabieyelo[3.2.2]nonane;
or an enantiomer or a mixture of its enantiomers, or a pharmaceutically acceptable salt thereof.
3. 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.
4. A method of treatment of a disease or a disorder or a condition of a living animal body, including a human, wherein the disease, disorder or condition is responsive to modulation of cholinergic receptors and/or monoamine receptors and wherein the disease, disorder, or condition is selected from the group consisting of Alzheimer's disease and Parkinson's disease, which method comprises the step of administering to a living animal body in need thereof a therapeutically effective amount of a diazabicyclic biaryl compound of claim 1 .