Parp inhibitor containing piperazine structure, preparation method therefor and pharmaceutical use thereof
US-2024336624-A1 · Oct 10, 2024 · US
US8993591B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-8993591-B2 |
| Application number | US-201113883818-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 8, 2011 |
| Priority date | Nov 8, 2010 |
| Publication date | Mar 31, 2015 |
| Grant date | Mar 31, 2015 |
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The present invention relates to novel triazolo[4,3-a]pyridine derivatives of Formula (I) wherein all radicals are as defined in the claims. The compounds according to the invention are positive allosteric modulators of the metabotropic glutamate receptor subtype 2 (“mGluR2”), which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes to prepare such compounds and compositions, and to the use of such compounds for the prevention or treatment of neurological and psychiatric disorders and diseases in which mGluR2 is involved.
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The invention claimed is: 1. A compound of formula (I) or a stereochemically isomeric form thereof, wherein R 1 is selected from the group consisting of C 1-6 alkyl, (C 3-8 cycloalkyl)C 1-3 alkyl, (C 1-3 alkyloxy)C 1-3 alkyl, and C 1-3 alkyl substituted with 1, 2 or 3 fluoro substituents; R 2 is selected from the group consisting of Cl, CF 3 , —C…
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