Azabicyclic aryl derivatives and their medical use
Azabicyclo pyridazinyl compounds including azabicyclooctyl-pyridazinyl-oxy compounds, 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 may be used for the treatment of various diseases or disorders, including 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 azabicyclic pyridazinyl 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;
X represents O, S, NR′, wherein R′ represents hydrogen or alkyl;
Y represents a pyridazinyl group;
L represents a linking group selected from —CH 2 —, —CH 2 —CH 2 —, —CH═CH—, and —C≡C—; and
Z represents an aromatic monocyclic or bicyclic carbocyclic or heterocyclic group selected from phenyl, naphthyl, thienyl, pyridyl, imidazolyl, and indolyl, which phenyl, naphthyl, thienyl, pyridyl, imidazolyl, and indolyl groups are optionally substituted one or more times with substituents selected from the group consisting of alkyl, cycloalkyl, cycloalkyl-alkyl, hydroxy, alkoxy, cyanoalkyl, halo, trihaloalkyl, trihaloalkoxy, cyano, nitro, amino and alkyl-carbonyl-amino.
2. The azabicyclic pyridazinyl compound of claim 1 , wherein n is 1 or 2.
3. The azabicyclic pyridazinyl compound of claim 2 , wherein n is 2.
4. The azabicyclic pyridazinyl compound of claim 1 , wherein X represents O or S.
5. The azabicyclic pyridazinyl compound of claim 4 , wherein X represents O.
6. The azabicyclic pyridazinyl compound of claim 1 , wherein L represents —CH═CH— or —C≡C—.
7. The azabicyclic pyridazinyl compound of claim 6 , wherein L represents —C≡C—.
8. The azabicyclic pyridazinyl compound of claim 1 , wherein Z represents phenyl or naphthyl, which carbocyclic groups are optionally substituted one or more times with substituents selected from the group consisting of alkyl, cycloalkyl, cycloalkyl-alkyl, hydroxy, alkoxy, cyanoalkyl, halo, trihaloalkyl, trihaloalkoxy, cyano, nitro, amino and alkyl-carbonyl-amino.
9. The azabicyclic pyridazinyl compound of claim 8 , wherein Z represents phenyl, which carbocyclic group is optionally substituted one or more times with substituents selected from the group consisting of alkyl, cycloalkyl, cycloalkyl-alkyl, hydroxy, alkoxy, cyanoalkyl, halo, trihaloalkyl, trihaloalkoxy, cyano, nitro, amino and alkyl-carbonyl-amino.
10. The azabicyclic pyridazinyl compound of claim 9 , wherein Z represents phenyl.
11. The azabicyclic pyridazinyl compound of claim 1 , wherein Z represents a 5- or 6-membered monocyclic heterocyclic group selected from thienyl, imidazolyl, and pyridyl, which heterocyclic group is optionally substituted one or more times with substituents selected from the group consisting of alkyl, cycloalkyl, cycloalkyl-alkyl, hydroxy, alkoxy, cyanoalkyl, halo, trihaloalkyl, trihaloalkoxy, cyano, nitro, amino and alkyl-carbonyl-amino.
12. The azabicyclic pyridazinyl compound of claim 11 , wherein Z represents a 5-membered monocyclic heterocyclic group selected from thienyl and imidazolyl, which heterocyclic group is optionally substituted one or more times with substituents selected from the group consisting of alkyl, cycloalkyl, cycloalkyl-alkyl, hydroxy, alkoxy, cyanoalkyl, halo, trihaloalkyl, trihaloalkoxy, cyano, nitro, amino and alkyl-carbonyl-amino.
13. The azabicyclic pyridazinyl compound of claim 11 , wherein Z represents pyridyl, optionally substituted one or more times with substituents selected from the group consisting of alkyl, cycloalkyl, cycloalkyl-alkyl, hydroxy, alkoxy, cyanoalkyl, halo, trihaloalkyl, trihaloalkoxy, cyano, nitro, amino and alkyl-carbonyl-amino.
14. The azabicyclic pyridazinyl compound of claim 1 , wherein Z represents indolyl, optionally substituted one or more times with substituents selected from the group consisting of alkyl, cycloalkyl, cycloalkyl-alkyl, hydroxy, alkoxy, cyanoalkyl, halo, trihaloalkyl, trihaloalkoxy, cyano, nitro, amino and alkyl-carbonyl-amino.
15. The azabicyclic pyridazinyl compound of claim 1 , wherein Z represents phenyl or thienyl, which phenyl and thienyl groups are optionally substituted one or two times with substituents selected from the group consisting of halo, alkoxy, amino and alkyl-carbonyl-amino.
16. The azabicyclic pyridazinyl compound of claim 1 , which is
(±)-3-(6-Phenylethynyl-pyridazin-3-yloxy)-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(4-Methoxy-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-N-{4-[6-(1-Aza-bicyclo[2.2.2]oct-3-yloxy)-pyridazin-3-ylethynyl]-phenyl}-acetamide;
(±)-3-[6-(1-Aza-bicyclo[2.2.2]oct-3-yloxy)-pyridazin-3-ylethynyl]-phenylamine;
(±)-4-[6-(1-Aza-bicyclo[2.2.2]oct-3-yloxy)-pyridazin-3-ylethynyl]-phenylamine;
(±)-N-{3-[6-(1-Aza-bicyclo[2.2.2]oct-3-yloxy)-pyridazin-3-ylethynyl]-phenyl}-acetamide;
(±)-3-(6-Thiophen-3-ylethynyl-pyridazin-3-yloxy)-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(2-Fluoro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(3-Fluoro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(4-Fluoro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(2,4-Difluoro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(2-Nitro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(3-Nitro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(4-Nitro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(2-Chloro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(3-Chloro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(4-Chloro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo [2.2.2]octane;
(±)-3-[6-(2-Trifluoromethyl-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(3-Trifluoromethyl-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(4-Trifluoromethyl-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-3[6-(3,5-Dimethoxy-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(3,5-Difluoro-phenylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-3-(6-Pyridin-2-ylethynyl-pyridazin-3-yloxy)-1-aza-bicyclo[2.2.2]octane;
(±)-3-(6-Pyridin-3-ylethynyl-pyridazin-3-yloxy)-1-aza-bicyclo[2.2.2]octane;
(±)-3-(6-Pyridin-4-ylethynyl-pyridazin-3-yloxy)-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(6-Methoxy-naphthalen-2-ylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]-octane;
(±)-3-(6-Naphthalen-2-ylethynyl-pyridazin-3-yloxy)-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(1H-Indol-5-ylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]octane;
(±)-3-[6-(3-Methyl-3H-imidazol-4-ylethynyl)-pyridazin-3-yloxy]-1-aza-bicyclo[2.2.2]-octane;
(±)-N-{2-[6-(1-Aza-bicyclo[2.2.2]oct-3-yloxy)-pyridazin-3-ylethynyl]-phenyl}-acetamide; or
(±)-2-[6-(1-Aza-bicyclo[2.2.2]oct-3-yloxy)-pyridazin-3-ylethynyl]-phenylamine;
or an enantiomer, or a mixture of its enantiomers, or a pharmaceutically acceptable salt thereof.
17. A pharmaceutical composition comprising a therapeutically effective amount of an azabicyclic pyridazinyl compound of claim 1 , or a pharmaceutically-acceptable addition salt thereof, together with at least one pharmaceutically-acceptable carrier or diluent.