Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
  • A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
  • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
  • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/50—Pyridazines; Hydrogenated pyridazines
  • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system

Definitions

• the present invention provides compounds of formula (I) having affinity and selectivity for the gamma-aminobutyric acid A receptor subunit alpha 5 (GABA a5) and act as GABA a5 positive allosteric modulators (GABAA a5 PAMS), thereby useful in the treatment or prevention of diseases related to the GABAA a5 receptor, process for the preparation and intermediates of the preparation process thereof, pharmaceutical compositions comprising them and their use as medicaments.
• GABA a5 gamma-aminobutyric acid A receptor subunit alpha 5
• GABAA a5 PAMS GABA a5 positive allosteric modulators
• GABA Gamma-aminobutyric acid
• Receptors sensitive for GABA are divided into two main families, the ligand gated GABAA receptors and the G-protein coupled GABAB receptors.
• the ligand gated GABAA receptor mediates the majority of inhibitory neurotransmission in the adult mammalian brain.
• the receptor is composed by the pentameric assembly of multiple subunits (a1-6, (31-3, y1-3, 5, E, TT, 0, p1-3) (Olsen and Sieghart, Pharmacol Rev 2008, 60:243-260) forming a ligand-gated chloride-channel.
• Subunit distribution varies developmentally and regionally in the brain. This high variability leads to broad variation in inhibitory and in certain conditions excitatory neural mechanisms and provides the possibility for specific therapeutic interventions (Fritschy and Mohler, J Comp Neurol 1995, 359:154-194; Jacob, Front Mol Neurosci 2019, 12: Art 179).
• the widely distributed a1- containing receptors mediate the sedative and amnesic effects, whereas the a2- and a3- containing receptors account for the anxiolytic, anticonvulsant and myorelaxant effects (Sieghart and Sperk, Curr Top Med Chem 2002, 2:795-816; Whiting et al, Drug Discov Today 2003, 8:445-450).
• a5 subunit containing receptors are preferentially expressed in the hippocampus, prefrontal cortex, amygdala and nucleus accumbens (Olsen and Sieghart, Neuropharmacology 2009, 56:141-148; Sur et al., Brain Res 1999, 822:265-270; Martin et al., Biochem Soc Trans 2009, 37:1334-1337) and thought to be involved in a variety of CNS disorders.
• a5-containing receptors are predominantly extrasynaptic and mediate tonic inhibition (Caraiscos et al., Proc Natl Acad Sci USA 2004, 101 :3662-3667).
• O5GABAARS can provoke excitation in early hippocampal circuit development (Marchionni et al., J Physiol. 2007, 581 :515-528).
• Their modulatory effect on the excitability of hippocampal and cortical principal neurons can explain the significant effect of O5GABAARS in neuronal development, cognition, learning and memory and their potential therapeutic usefulness in various disorders including stroke, mild cognitive impairment, schizophrenia, depression, dementia-related conditions or diseases related to impaired social cognition or neurodevelopmental disorders such as Down syndrome or autism spectrum disorder (ASD) (Jacob, Front Mol Neurosci 2019, 12: Art 179; Mohamad and Tarmizi Che Has, J Mol Neurosci 2019, 67:343-351 ; Soh and Lynch, CurrDrug Targets 20 5, 16:735- 746).
• ASD autism spectrum disorder
• Acute treatment with GL-ll-73 rescued chemogenetically induced behavioural deficits in a mouse model of depression (Fee et al., Int J Neuropsychopharmacol 2021 , 24:505-518), while chronic treatment with GL-ll-73 reversed age-related neuronal atrophy as well as impairment in working memory in adult mice (Sibille et al., Biol Psychiatry 2020, 87:Suppl1 , page S85).
• SH-053-2'F-R-CH3 and MP-lll-022 attenuated pathological changes of locomotor activity of rats in developmental models of schizophrenia (Gill et al., Neuropsychopharmacology 2011 , 36:1903-1911 ; Batinic et al. Int J Dev
• AgeneBio Inc. described imidazo[1 ,5-a][1 ,2,4]-triazolo[1 ,5-c(
• ASD autism spectrum disorder
• ASD is a complex, heterogeneous neurodevelopmental disorder characterized by a deterioration of social relationships, a decrease in communication, typical repetitive behaviours, and impairment in executive functions (Anagnostou et al., CMAJ 2014, 186:509-519; Diagnostic and statistical manual of mental disorders. 5th ed. Arlington, VA: American Psychiatric Association; 2013 - Diagnostic Criteria for 299.00 Autism Spectrum Disorder).
• ASD can be associated with genomic alterations coupled with GABAAR subunits.
• Chromosomal abnormalities namely duplication of copy number variations in the q11.2-13 region on chromosome 15 were reported in ASD patients. In humans, this region contains genes that encode the a5, p3 and y3 subunits of the GABAA receptor (Coghlan et al., Neurosci Biobehav Rev 2012, 36:2044-2055).
• a pilot PET study showed reduced binding of an O5GABAAR selective tracer [ 11 C]Ro154513 across multiple brain regions suggesting reduced level of O5GABAAR in ASD (Mendez at al., Neuropharmacology 2013, 68:195-201).
• Another study showed changes in a GABA-sensitive perceptual task in ASD patients (Horder et al., Sci Trans! Med 2018, pii: eaam8434).
• postmortem analyses revealed reduced expression of a5GABA A R (Blatt et al., J Autism Dev Disord 2001 , 31 :537-54; Fatemi et al. J Autism Dev Disord, 2010, 40:743-750).
• Impaired GABAergic function in ASD patients can be considered, thus facilitating cortical inhibition and restoring E/l balance by a5 PAMs can be a feasible therapeutic strategy in the treatment of the disease.
• the prenatal valproate model has excellent construct and face validity, therefore it is a widely accepted disease model of ASD (Christensen et al., JAMA 2013, 309:1696-1703; Roullet et al., Neurotox Teratoi. 2013, 36:45-56).
• ASD a widely accepted disease model of ASD
• time-mated female Wistar rats are administered a single dose of valproic acid on gestational day 12.5.
• offspring are examined behavioraLly in the social preference assay at postnatal day 59.
• the social preference test is a highly accepted assay to assess autistic behavior in rodents (Nadler et al., Genes Brain Behav 2007, 3:303-314; Bambini- Junior et al., Brain Res 2011 , 1408:8-16). Briefly, in this assay a test animal is allowed to investigate a conspecific separated by a dividing perforated wall or a similar area however, without a target conspecific. An autistic animal (such as a prenatally valproate-exposed rat) spends little time with social investigation during a test session.
• examples of the present invention may be of great behavioral benefit in this preclinical disease model that recapitulates the core symptoms of ASD. Therefore, it can be presented that the compounds of the invention, specifically GABA A a5 PAMs, may have therapeutic potential for the core symptoms of autism spectrum disorder in humans.
• GABA-A receptor positive modulators such as the non-selective clonazepam in low dose, have also proven to ameliorate symptoms in preclinical models of ASD (Han et al., Nature 2012, 489:385-390; Okamoto et al., J Neuroimmunol 2018, 321 :92-96) increasing the expectations that clinically used benzodiazepines could be used in extremely low doses for the treatment of the disease.
• a2/3 modulators such as a2/3 modulators (AZD7325; https://www.clinicaltrials.gov/ct2/show/NCT03678129) or a5 positive allosteric modulators may offer an alternative approach for the treatment of ASD possibly with an improved therapeutic window.
• the a5 selective PAM compound RG7816 (RO7017773) is in Phase II clinical development for the treatment of ASD (https://www.clinicaltrials.gov/ct2/show/NCT04299464).
• compounds having high affinity and selectivity for the ⁇ 5GABAARS, GABAA a5 PAMs respectively can be used, alone or in combination with one or more other active ingredients, for the treatment or prevention of disorders of the central nervous system where one of the symptoms and/or syndromes of the disease may be related to the GABAA a5 receptor.
• disorders of the central nervous system where one of the symptoms and/or syndromes of the disease may be related to the GABAA a5 receptor.
• GABAA a5 receptor include, but not limited to neurodevelopmental disorders such as autism spectrum disorder (ASD) (Mendez et al., Neuropharmacology 2013, 68:195-201), Fragile X disorder (Curia et al, Cereb.
• Modulating O5GABAA S may also be beneficial in treating diseases and conditions including, but not limited to bronchoconstrictive diseases such as, but not limited to asthma, chronic obstructive pulmonary disease, and bronchopulmonary dysplasia (Gallos et al., Am J Physiol Lung Cell Mol Physiol 2015, 308:L931-942; Mizuta et al., Am J Physiol Lung Cell Mol Physiol 2008, 294:L1206-1216) and obesity (Xia et al., Mol Psychiatry 2021, doi: 10.1038/s41380-021-01053-w).
• Compounds capable of modulating a5GABA Rs are in particular expected to be useful candidates for the treatment of neurodevelopmental disorders, neurocognitive disorders, mood disorders and schizophrenia.
• the present invention relates to compounds of formula (I) wherein
• A is represented by
• R 1 is an alkyl, an alkoxy, or a haloalkyl group
• R 2 is hydrogen; an alkyl group optionally substituted with -S(O)2-alkyl, a cycloalkyl or a heterocycle; a cycloalkyl group; a heterocycle group optionally substituted with an alkyl; or a heteroaryl group;
• X is CH or N; and/or salts thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof or diastereomers thereof and/or biologically active metabolites thereof or prodrugs thereof or solvates thereof or hydrates thereof and/or polymorphs thereof.
• the present invention provides a compound of formula (I), as defined above for use as medicament.
• the present invention provides a compound of formula (I), as defined above for use in the treatment or prevention of diseases related to the GABAA O5 receptor.
• the present invention provides the use of a compound of formula (I), as defined above, for the manufacture of a medicament for the treatment or prevention of diseases related to the GABAA O5 receptor.
• the present invention provides a method of treating or preventing a disease related to the GABAA O5 receptor comprising administering to a subject, including humans, in need of such treatment or prevention an effective amount of at least one compound of formula (I), as defined above.
• the present invention provides the combinational use of compounds of formula (I) as defined above, with one or more other active ingredients for the treatment or prevention of diseases related to the GABAA a5 receptor.
• the present invention provides pharmaceutical compositions containing the compound of formula (I), as defined above as active ingredients.
• the present invention provides medicaments (combinational pharmaceutical compositions) comprising a combination of the compound of formula (I), as defined above with one or more other active ingredients.
• the present invention provides pharmaceutical compositions containing the compound of formula (I), as defined above as active ingredients alone or in combination with one or more other active ingredients for use in the treatment or prevention of diseases related to the GABAA a5 receptor.
• the present invention provides a process for the manufacture of the compounds of formula (I), as defined above and intemediates of the preparation process as well.
• the present invention also provides preparation of pharmaceutical compositions containing the compounds of formula (I), as defined above alone, or in combination with one or more other active ingredients.
• the present invention provides compounds of formula (I) having affinity and selectivity for the alpha 5 subunit-containing gamma-aminobutyric acid A receptor (GABAA a5 receptor) and act as GABAA a5 receptor positive allosteric modulators, thereby useful in the treatment or prevention of diseases related to the GABAA a5 receptor, process for the preparation thereof, pharmaceutical compositions comprising them alone or in combination with one or more other active ingredients and their use as medicaments.
• GABAA a5 receptor alpha 5 subunit-containing gamma-aminobutyric acid A receptor
• A is represented by , group
• R 1 is an alkyl, an alkoxy, or a haloalkyl group
• R 2 is hydrogen; an alkyl group optionally substituted with -S(O)2-alkyl, cycloalkyl or heterocycle; a cycloalkyl group; a heterocycle group optionally substituted with an alkyl; or a heteroaryl group;
• X is CH or N; and/or salts thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof or diastereomers thereof and/or biologically active metabolites thereof or prodrugs thereof or solvates thereof or hydrates thereof and/or polymorphs thereof.
• substituted denotes an atom or a group of atoms replacing a hydrogen atom on the parent molecule.
• substituted denotes that a specified group bears one or more substituents.
• any atom of the specified group is unsubstituted or substituted by one or more substituents, independently chosen from the group of possible substituents.
• substituents independently chosen from the group of possible substituents.
• one or more means from one substituent to the highest possible number of substitutions, i.e., replacement of one hydrogen up to replacement of all hydrogens by substituents.
• the possible substituents include, but are not limited to Ci-4alkyl, oxo and the like.
• alkyl refers alone or in combination with other groups to a straight or branched, single or multiple branched, hydrocarbon radical and consists of 1 to 6 carbon atoms.
• an alkyl group consists of 1 to 4 carbon atoms. Examples include, but are not limited to methyl, ethyl, propyl, /-propyl (isopropyl), n-butyl, 2-butyl (sec-butyl) or t-butyl (tert-butyl) group.
• Ci-2alkyl groups are more preferred. Methyl group is most preferred.
• alkoxy refers alone or in combination with other groups to -O-alkyl group, wherein the alkyl is as defined above.
• an alkoxy group is a -O-alkyl group wherein the alkyl group consists of 1 to 4 carbon atoms. Examples include, but are not limited to methoxy, ethoxy, /-propoxy, n-propoxy or t-butoxy. Ci.2alkoxy groups are more preferred. Methoxy group is most preferred.
• halogen refers alone or in combination with other groups to fluoro (fluorine), chloro (chlorine), bromo (bromine) or iodo (iodine).
• the halogen is fluorine.
• haloalkyl refers alone or in combination with other groups to an alkyl as defined above substituted with one or more identical or different halogens on any carbon atoms of said alkyl, including vicinal and/or germinal halo-substitutions as well, such as perhaloalkyl groups.
• perhaloalkyl refers to an alkyl where all hydrogen atoms have been replaced by the same or different halogen atoms.
• Examples include, but are not limited to trihalo, dihalo-, or monohaloalkyl groups, for example 3,3,3-trifluoropropyl, 2- fluoroethyl, 2,2 ,2-trifluoroethyl , fluoromethyl, difluoromethyl or trifluoromethyl.
• the haloalkyl group is a halo-Ci.2alkyl group, more preferably difluoromethyl or trifluoromethyl, most preferably trifluoromethyl.
• cycloalkyl refers to monovalent monocyclic saturated carbocyclic groups comprising 3 to 7 carbon ring atoms. Examples include cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane. Preferably, the cycloalkyl group comprises 4 to 6 carbon ring atoms. Most preferably the cycloalkyl is cyclobutane or cyclopentane.
• heterocycle refers alone or in combination with other groups to a monovalent saturated or partly unsaturated monocyclic, bicyclic, fused, bridged or spiro ring system of 3 to 10 ring atoms comprising 1 , 2, 3 or 4 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon.
• Examples for monocyclic heterocycles are aziridine, 2H-azirine, oxirane, thiirane, azetidine, oxetane, thietane, azetidine-2-one, pyrrolidine, pyrrolidinone, pyrroline, pyrazolidine, imidazoline, pyrazoline, tetrahydrofuran, dihydrofuran, dioxolane, tetrahydrothiophene, oxazolidine, di hydro-oxazole, isoxazolidine, oxathiolane, sulfolane, thiazolidine, thiazolidinedione, succinimid, oxazolidone, hydantoin, piperidine, piperidinone, piperazine, tetrahydropyran, tetrahydrothiopyrane, dihydropyrane, tetrahydropyridine, dioxane, t
• the heterocycle refers alone or in combination with other groups to a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising 1 , or 2 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon. More preferably, the heterocycle refers alone or in combination with other groups to a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising one ring heteroatom selected from O and S, the remaining ring atoms being carbon.
• the heterocycle refers alone or in combination with other groups to a monovalent saturated monocyclic ring of 3 to 6 ring atoms comprising one ring heteroatom selected from O and S, the remaining ring atoms being carbon such as oxetane, tetrahydrofuran, tetrahydrothiophene, tetrahydropyran.
• heteroaryl refers alone or in combination with other groups to a monovalent, heterocyclic aromatic, mono- or bicyclic ring system of 5 to 10 ring atoms, comprising 1 , 2 or 3 heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon.
• heteroaryl examples include pyrrole, furan, thiophene, imidazole, oxazole, isoxazole, thiazole, isothiazole, triazole, tetrazole, oxadiazole, thiadiazole, tetrazole, pyridine, pyrazine, pyrazole, pyridazine, pyrimidine, triazine, azepine, diazepine, benzofuran, benzothiophene, indole, isoindole, isobenzofuran, benzimidazole, benzoxazole, benzoisoxazole, benzothiazole, benzoisothiazole, benzooxadiazole, benzothiadiazole, benzotriazole, purine, quinoline, isoquinoline, quinazoline, quinoxaline, carbazole, or acridine.
• the heteroaryl refers alone or in combination with other groups to a monovalent, heterocyclic aromatic, monocyclic ring system of 5 to 6 ring atoms, comprising 1 , or 2 heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon. More preferably, the heteroaryl refers alone or in combination with other groups to a monovalent, heterocyclic aromatic, monocyclic ring system of 6 ring atoms, comprising 1 , or 2 heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon.
• the heteroaryl refers alone or in combination with other groups to a monovalent, heterocyclic aromatic, monocyclic ring system of 6 ring atoms, comprising 1 , or 2 heteroatoms being N, the remaining ring atoms being carbon, such as pyridine, pyridazine, pyrimidine, pyrazine.
• compound(s) of this invention refers to compounds of formula (I) and/or salts thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof or diastereomers thereof and/or biologically active metabolites thereof or prodrugs thereof or solvates thereof or hydrates thereof and/or polymorphs thereof.
• salt refers to pharmaceutically acceptable or to pharmaceutically non- acceptable salts.
• pharmaceutically acceptable salt refers to a conventional acid addition or base addition salt which preserves the biological efficacy and properties of the compounds of formula (I) and which can be formed with suitable non-toxic organic or inorganic acids or organic or inorganic bases.
• acid addition salts include salts derived from inorganic acids, such as, but not limited to hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, sulphamic acid, phosphoric acid, nitric acid and perchloric acid and derived from various organic acids, such as, but not limited to acetic acid, propionic acid, benzoic acid, glycolic acid, phenylacetic acid, salicylic acid, malonic acid, maleic acid, oleic acid, pamoic acid, palmitic acid, benzenesulfonic acid, toluenesulfonic acid, methanesulfonic acid, oxalic acid, tartaric acid, naphthalenedisulfonic acid, succinic acid, citric acid, malic acid, lactic acid, glutamic acid, fumaric acid and the like.
• inorganic acids such as, but not limited to hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid,
• base addition salts are salts derived from ammonium-, potassium-, sodium- and quaternary ammonium hydroxides such as tetramethylammonium hydroxide.
• the “pharmaceutically non-acceptable salts” may be preferred for the purification or isolation of the compounds of formula (I) and are therefore also within the scope of the invention.
• prodrug refers to derivatives of compounds of formula (I) according to the invention which themselves have no therapeutic effect but containing such groups which, after in vivo chemical or metabolic degradation (biotransformation) become “biologically active metabolite” which is responsible for the therapeutic effect.
• Optical isomers can be prepared by resolving the racemic mixtures by known methods, for example, by using an optically active acid or base to form diastereoisomeric salts or by forming covalent diastereomers.
• Suitable acids include, for example, tartaric acid, diacetyltartaric acid, dibenzoyltartaric acid, ditoluoyltartaric acid and camphorsulfonic acid.
• Diastereoisomeric mixtures can be separated into individual diastereomers based on their physical and/or chemical differences, by methods known to those skilled in the art, such as chromatography or fractional crystallization. Subsequently, the optically active bases or acids are liberated from the separated diastereoisomeric salts.
• optically active compounds of general formula (I) can also be prepared using optically active starting materials using chiral synthesis without racemization reaction conditions.
• the absolute configuration of the chiral compounds can be determined e.g., by optical rotation, VCD (vibrational circular dichroism spectroscopy) and/or single crystal X-ray diffraction analysis, or 1 H NMR spectroscopic assays of the diastereomeric pair of compounds synthesized from chiral compounds.
• the compounds of formula (I) may exist in various polymorphic forms.
• polymorphism is the ability of a compound to crystallize in more than one crystalline form, i.e., in polymorphic form.
• Polymorphic forms of a particular compound can be defined by identical chemical formula or composition and differ in their chemical structure as crystalline structures of two different chemical compounds.
• solvates refers to non- covalent stoichiometric or nonstoichiometric combinations of solvent and solute.
• hydrate refers to non-covalent stoichiometric or nonstoichiometric combinations of water and solute.
• the present invention provides pharmaceutical compositions comprising at least one compound of formula (I), as defined above as active ingredient.
• the present invention provides pharmaceutical compositions comprising a combination of the compound of formula (I), as defined above with one or more other active ingredients.
• the pharmaceutical composition may comprise at least one compound of the invention together with one or more other active ingredients in a single dosage form or separately.
• the combinational composition may be administered simultaneously, separately or sequentially.
• composition refers to a mixture or solution comprising a therapeutically effective amount of an active ingredient together with pharmaceutically acceptable excipients to be administered to a subject, e.g., a human in need thereof.
• the present invention also relates to the preparation of pharmaceutical compositions.
• compositions of the present invention may be formulated in various pharmaceutical formulations, such as, but not limited to, solid oral dosage forms such as tablets (e.g., buccal, sublingual, effervescent, chewable, orally dispersible), capsules, pills, orally dispersible films, granules, powders; liquid formulations such as solutions, emulsions, suspensions, syrups, elixirs, drops; parenteral dosage forms such as intravenous injections, intramuscular injections, subcutaneous injections; other forms of medicine such as eye drops, semi-solid ophthalmic preparations, semi-solid dermal preparations (such as ointments, creams, pastes), transdermal therapeutic systems, suppositories, rectal capsules, rectal solutions, emulsions and suspensions, etc..
• solid oral dosage forms such as tablets (e.g., buccal, sublingual, effervescent, chewable, orally dispersible), capsules, pills, orally dispersible films,
• compositions of the present invention may be administered in various ways, such as, but not limited to oral, rectal, mucous, transdermal or intestinal administration; parenteral administration including intramuscular, subcutaneous, intravenous, intramedullary injections as well as intraarticular, intrathecal, direct intraventricular, intraperitoneal, intranasal or intraocular injections and eye drops.
• the compounds may be administered locally and not systemically, for example by direct injection of the compound to the kidney or the heart, often in a modified release formulation.
• the drug may be administered in a targeted carrier system, for example in a tissue-specific antibody encapsulated liposome.
• the pharmaceutical composition may be administered in various ways and in various pharmaceutical forms.
• the compound of the invention may be administered alone or in combination with pharmaceutically acceptable excipients, in single or multiple doses.
• the pharmaceutical compositions consist of dosage units that contain the amount of active ingredient(s) to be administered once, or a small number of multiple, or half, one third, a quarter.
• dosage units are, for example, tablets that can be provided with a half or quarter groove to facilitate half or quarter-splitting of the tablet in order to weigh the required amount of active ingredient(s).
• compositions containing the active ingredient(s) according to the invention generally contain from 0.001 to 500 mg of active ingredient(s) per dosage unit. It is of course also possible that the amount of active ingredient(s) in each formulation exceeds the above limit either up or down.
• the present invention relates also to pharmaceutical compositions for use in pediatric use such as, but not limited to, solutions, syrups, elixirs, suspensions, powders for the preparation of suspensions, dispersible or effervescent tablets, chewable tablets, orally disintegrating tablets or granules, tablets or coated tablets, sparkling powders or granules, capsules.
• compositions of the present invention may be prepared by methods known per se such as conventional mixing, dissolution, emulsification, suspending, microencapsulation, freeze drying, extrusion and spheronization, lamination, film coating, granulation, encapsulation, pelletization or pressing.
• compositions of the present invention may be formulated in the usual way using one or more physiologically or pharmaceutically acceptable excipients which promote the incorporation of the active ingredient into pharmaceutically acceptable pharmaceutical forms.
• physiologically or pharmaceutically acceptable excipient denotes any ingredient used in formulating pharmaceutical products which have no therapeutic activity and non-toxic. The proper formulation depends on the mode of administration chosen. Any of the techniques and excipients well known in the art can be used.
• excipients applicable in the preparation may be selected from the following categories, such as, but not limited to fillers of tablets and capsules, binders of tablets and capsules, drug release modifying agents, disintegrants, glidants, lubricants, sweeteners, taste-masking agents, flavorants, coating materials, surfactants, stabilizers, preservatives or antioxidants, buffering agents, complexing agents, wetting or emulsifying agents, salts for adjusting the osmotic pressure, lyophilization excipients, microencapsulating agents, ointment materials, penetration enhancers, solubilizers, solvents, suppository materials, suspending agents.
• other active ingredient refers to therapeutic agents including, but not limited to 5-HTIA antagonists or agonists (such as lecozotan, NLX 101 , sarizotan); 5-HTIB and 5-HTID agonists (such as rizatriptan, zolmitriptan, naratriptan and sumatriptan); 5-HT2 antagonists; 5- HT4 agonists (such as PRX-03140); 5-HTe antagonists (such as GSK 742467, SGS-518, FK- 962, SL-65.0155, SRA-333 and xaliproden); A2a adenosine receptor antagonists; acetylcholinesterase inhibitors (such as galantamine, rivastigmine, donepezil, tacrine, phenserine, ladostigil and ABT-089); ADAM-10 ligands; alpha adrenoceptor agonists; AMPA agonists or modulators (such as CX-7
• the other active ingredient refers to 5-HTIA antagonists or agonists (such as lecozotan, NLX 101 , sarizotan); atypical antipsychotics (such as aripiprazole, asenapine, brexpiprazole, brilaroxazine, cariprazine, iloperidone, loxapine, lumateperone tosylate, lurasidone hydrochloride, molindone, olanzapine, paliperidone, quetiapine, risperidone, sulpiride and ziprasidone); CB-1 receptor antagonists or inverse agonists (such as drinabant, cannabidiol); CB-2 agonists (such as GW-842166X and SAB378) or CB modulators (cannabidivarin, T1/C20, tetrahydrocannabinol conjugate, ZYN-002); DNA- directed DNA
• modulators refers to molecules interacting with the target receptor, wherein the interaction can be e.g., agonistic, antagonistic or inverse agonistic.
• inhibitors referes to molecules competing with, reducing or preventing the binding of a particular ligand to a particular receptor or reducing or preventing the inhibition of the function of a particular protein.
• agonists refers to compounds having affinity to a receptor binding site and enhancing the activity of the receptor-mediated response. “Full-agonists” effect a full response, “partial agonists” effects less than full activation even when occupying the total receptor population.
• inverse agonists refers to compounds producing an effect opposite to that of an agonist by binding to the same agonist binding site, or reducing the effect of an agonist by binding at a different allosteric binding site.
• antagonists refers to compounds diminishing or preventing the action of another compound or receptor site, or attenuating the effect of an agonist.
• Competitive antagonists bind to the same site as the agonist but does not activate it, thus blocks the agonists’ action.
• Non-competitive antagonists binds to an allosteric site on the receptor to prevent activation of the receptor. Binding of “reversible antagonists” to a receptor is non- covalent (can be washed out), while binding of “irreversible antagonists” is covalent (cannot be washed out).
• allosteric modulators refers to compounds binding to a receptor at a site distinct from the agonist binding site, i.e., to the allosteric site, wherein by inducing conformational change in the receptor, alter the affinity and/or activity of the receptor for the endogenous ligand or agonist.
• “Positive allosteric modulators” or “PAMs” increase the affinity and/or activity, whilst “negative allosteric modulators” or “NAMs” decrease the affinity and/or activity of a receptor.
• PAMs positive allosteric modulators.
• Kj inhibition constant
• Kj values can be converted logarithmically to pKj values (-logKj) in which higher values indicate exponentially greater potency.
• submaximal effective concentration refers to the concentration of a particular compound required for obtaining 10% of the maximum of a particular effect.
• condition means any disease, condition, symptom, syndrome, disorder or indication.
• the term ’’disease related to the GABAA a5 receptor refers to a disease, condition or disorder of the central nervous system where one of the symptoms and/or syndromes of the disease may be related to the GABAA a5 receptor.
• a disease includes, but not limited to a neurodevelopmental disorder, a neurodegenerative disorder, a neurocognitive disorder, schizophrenia, a mood disorder, a pain disorder, a substance-related and addictive disorder or other diseases.
• the diseases related to the GABAA a5 receptor may show comorbidity with each other.
• Comorbidity indicates a medical condition existing simultaneously but independently with another condition in a patient, or a medical condition in a patient that causes, is caused by, or is otherwise related to another condition in the same patient.
• comorbidity does not necessarily imply the presence of multiple diseases, but instead can reflect our current inability to supply a single diagnosis that accounts for all symptoms.
• neurodevelopmental disorder includes, but not limited to autism spectrum disorder (ASD), Angelman syndrome, Fragile X disorder, Prader-Willi syndrome, Rett syndrome or Down syndrome.
• ASD autism spectrum disorder
• Angelman syndrome Fragile X disorder
• Prader-Willi syndrome Rett syndrome or Down syndrome.
• neurodegenerative disorder includes, but not limited to Alzheimer's disease (AD), Huntington's disease (HD), Parkinson's disease (PD), or amyotrophic lateral sclerosis (ALS).
• neuropsychiatric symptoms mild cognitive impairment (MCI), vascular cognitive impairment (VCI), CNS conditions occurring after stroke, cognitive impairment associated with brain cancers (including, but not limited to medulloblastomas), cognitive decline in Down Syndrome (DS), cognitive dysfunction in major depressive disorder (MDD).
• pain disorder includes, but not limited to nociceptive, neuropathic or inflammatory pain.
• microood disorder includes, but not limited to depression-related disorders (such as major depressive disorder (MDD), dysthymia, cyclothymic disorder, seasonal affective disorder/seasonal depression, depression after traumatic brain injury (TBI), postpartum depression, premenstrual dysphoric disorder, depressive symptoms associated with menopause, depression following substance abuse/withdrawal, bipolar disorders (bipolar disorder in remission, or depressive episodes of bipolar disorder), substance (alcohol or drug) induced, or not otherwise specified mood disorders (MD-NOS).
• MDD major depressive disorder
• dysthymia dysthymia
• cyclothymic disorder seasonal affective disorder/seasonal depression
• TBI traumatic brain injury
• postpartum depression postpartum depression
• premenstrual dysphoric disorder depressive symptoms associated with menopause
• depression following substance abuse/withdrawal bipolar disorders (bipolar disorder in remission, or depressive episodes of bipolar disorder)
• substance alcohol or drug
• other disease includes, but not limited to attention deficit hyperactivity disorder and adult attention deficiency, other stress related conditions, stroke, neurofibromatosis type I, multiple sclerosis, acute meningitis, alcohol use disorder, fetal alcohol spectrum disorder, bronchoconstrictive diseases (such as asthma, chronic obstructive pulmonary disease, and bronchopulmonary dysplasia) or obesity.
• the disease related to the GABA a5 receptor refers to autism spectrum disorder (ASD); Angelman syndrome, Fragile X disorder, Prader-Willi syndrome, Rett syndrome, Down syndrome, Alzheimer's disease (AD), Huntington's disease (HD), Parkinson's disease, amyotrophic lateral sclerosis (ALS), cognition deficiency disorders, memory deficits, age-associated memory impairment or cognitive decline, dementia or different forms thereof such as dementia in Alzheimer’s disease, Niemann Pick-disease, Parkinson’s disease, or Huntington’s disease, dementia with Lewy bodies (DLB), frontotemporal dementia, vascular dementia (VaD), subcortical dementia, mixed vascular and subcortical dementia, multi-infarct dementia, post-operative dementia, or inflammation- induced dementia), Alzheimer’s disease related neuropsychiatric symptoms, mild cognitive impairment (MCI), vascular cognitive impairment (VCI), CNS conditions occurring after stroke, cognitive impairment associated with brain cancers (including but not limited to medulloblastomas),
• the disease related to the GABAA a5 receptor refers to autism spectrum disorder (ASD), Angelman syndrome, Fragile X disorder, Prader-Willi syndrome, Rett syndrome, Alzheimer's disease (AD), cognition deficiency disorders, memory deficits, age-associated memory impairment or cognitive decline, dementia, mild cognitive impairment (MCI), bipolar disorders, negative and/or cognitive symptoms associated with schizophrenia, epilepsy, post-traumatic stress disorder, amyotrophic lateral sclerosis.
• ASSD autism spectrum disorder
• Angelman syndrome Fragile X disorder
• Prader-Willi syndrome Prader-Willi syndrome
• Rett syndrome Alzheimer's disease
• AD cognition deficiency disorders
• memory deficits memory deficits
• age-associated memory impairment or cognitive decline dementia
• MCI mild cognitive impairment
• bipolar disorders negative and/or cognitive symptoms associated with schizophrenia
• epilepsy post-traumatic stress disorder
• amyotrophic lateral sclerosis amyotrophic lateral sclerosis.
• the present invention provides a method of treating or preventing a disease related to the GABAA a5 receptor comprising administering to a subject, preferably a mammal, more preferably a human being, in need of such treatment or prevention, therapeutically effective amount of a compound of formula (I), as defined above alone or with at least one pharmaceutically acceptable excipient in the form of a pharmaceutical formulation.
• the present invention provides a method of treating or preventing a disease related to the GABAA a5 receptor comprising administering to a subject, preferably a mammal, more preferably a human being, in need of such treatment or prevention, therapeutically effective amount of a compound of formula (I), as defined above in combination with one or more other active ingredients.
• the present invention provides a method of treating or preventing of a neurodevelopmental disorder, neurodegenerative disorder, neurocognitive disorder, schizophrenia, a mood disorder, a pain disorder, a substance-related and addictive disorder or other disease, or at least one of the symptoms and/or syndromes thereof, where one of the symptoms and/or syndromes of the disease may be related to the GABAA a5 receptor, in a subject, preferably a mammal, more preferably a human being, suffering therefrom.
• This method of treatment comprises administering to a subject, preferably a mammal, more preferably a human being, in need of such treatment or prevention, therapeutically effective amount of the compound of formula (I), as defined above.
• the method of treatment may include administering to a subject preferably a mammal, more preferably a human being, in need of such treatment therapeutically effective amount of a pharmaceutical composition comprising the compound of formula (I), as defined above.
• the present invention provides a method of treating or preventing autism spectrum disorder (ASD), Angelman syndrome, Fragile X disorder, Prader-Willi syndrome, Rett syndrome, Alzheimer's disease (AD), cognition deficiency disorders, memory deficits, age- associated memory impairment or cognitive decline, dementia, mild cognitive impairment (MCI), bipolar disorders, negative and/or cognitive symptoms associated with schizophrenia, epilepsy, post-traumatic stress disorder, amyotrophic lateral sclerosis, or at least one of the symptoms and/or syndromes thereof, in a subject, preferably a mammal, more preferably a human being, suffering therefrom comprising administering a therapeutically effective amount of the compound of formula (I), as defined above.
• the present invention provides the compound of formula (I), as defined above for use in the treatment or prevention of diseases related to the GABAA a5 receptor.
• the present invention provides the compound of formula (I), as defined above in combination with one or more other active ingredients for use in the treatment or prevention of diseases related to the GABAA a5 receptor.
• the present invention provides the compound of formula (I), as defined above for use in the treatment or prevention of a neurodevelopmental disorder, a neurodegenerative disorder, a neurocognitive disorder, schizophrenia, a mood disorder, a pain disorder, a substance-related and addictive disorder or other disease, or at least one of the symptoms and/or syndromes thereof.
• the present invention provides the compound of formula (I), as defined above for use in the treatment or prevention of autism spectrum disorder (ASD), Angelman syndrome, Fragile X disorder, Prader-Willi syndrome, Rett syndrome, Alzheimer's disease (AD), cognition deficiency disorders, memory deficits, age-associated memory impairment or cognitive decline, dementia, mild cognitive impairment (MCI), bipolar disorders, negative and/or cognitive symptoms associated with schizophrenia, epilepsy, post-traumatic stress disorder, amyotrophic lateral sclerosis, or at least one of the symptoms and/or syndromes thereof.
• ASSD autism spectrum disorder
• Angelman syndrome Fragile X disorder
• Prader-Willi syndrome Prader-Willi syndrome
• Rett syndrome Alzheimer's disease
• AD cognition deficiency disorders
• memory deficits memory deficits
• age-associated memory impairment or cognitive decline dementia
• MCI mild cognitive impairment
• bipolar disorders negative and/or cognitive symptoms associated with schizophrenia
• epilepsy post-traumatic stress disorder
• the present invention provides the use of the compound of formula (I), as defined above for the manufacture of a medicament for the treatment or prevention of diseases related to the GABAA a5 receptor.
• the present invention provides the use of the compound of formula (I), as defined above in combination with one or more other active ingredients, for the manufacture of a medicament for the treatment or prevention of diseases related to the GABAA a5 receptor.
• the present invention provides the use of the compound of formula (I), as defined above for the manufacture of a medicament for the treatment or prevention of a neurodevelopmental disorder, a neurodegenerative disorder, a neurocognitive disorder, schizophrenia, a mood disorder, a pain disorder, a substance-related and addictive disorders or other disease, or at least one of the symptoms and/or syndromes thereof.
• the present invention provides the use of the compound of formula (I), as defined above for the manufacture of a medicament for the treatment or prevention of autism spectrum disorder (ASD), Angelman syndrome, Fragile X disorder, Prader-Willi syndrome, Rett syndrome, Alzheimer's disease (AD), cognition deficiency disorders, memory deficits, age- associated memory impairment or cognitive decline, dementia, mild cognitive impairment (MCI), bipolar disorders, negative and/or cognitive symptoms associated with schizophrenia, epilepsy, post-traumatic stress disorder, amyotrophic lateral sclerosis, or at least one of the symptoms and/or syndromes thereof.
• ASSD autism spectrum disorder
• Angelman syndrome Fragile X disorder
• Prader-Willi syndrome Prader-Willi syndrome
• Rett syndrome Alzheimer's disease
• AD cognition deficiency disorders
• memory deficits memory deficits
• age-associated memory impairment or cognitive decline dementia
• MCI mild cognitive impairment
• bipolar disorders negative and/or cognitive symptoms associated with schizophrenia
• epilepsy post-traumatic stress disorder
• the present invention also relates to pharmaceutical composition
• pharmaceutical composition comprising the compound of formula (I), as defined above for use in the treatment or prevention of diseases related to the GABAA a5 receptor.
• the present invention also relates to pharmaceutical composition
• pharmaceutical composition comprising the compound of formula (I), as defined above with one or more other active ingredients for use in the treatment or prevention of diseases related to the GABAA a5 receptor.
• treatment refers to the alleviation of a specific pathological condition, the elimination or reduction of one or more of the symptoms of the condition, the slowing or elimination of the progression of the disease state, and the prevention or delay of recurrency of the pathological condition of a patient or subject already suffering from or diagnosed with the disease.
• prevention or prophylaxis or delay of action of the disease
• terapéuticaally effective amount refers to the amount of active ingredient - in comparison with the corresponding subject who did not receive such amount - which results in the treatment, cure, prevention or improvement of the disease or disease state or side effect, and reduces the progression of the disease or pathological condition.
• the term also includes effective amounts to enhance normal physiological function.
• the compound of formula (I), as defined above as well as any salts thereof and/or salts thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof or diastereomers thereof and/or biologically active metabolites thereof or prodrugs thereof or solvates thereof or hydrates thereof and/or polymorphs thereof may be administered in a therapeutically effective amount as a raw chemical.
• the active ingredient is available as a pharmaceutical formulation.
• the term “subject” refers to a vertebrate.
• the vertebrate is a mammal.
• Mammals include humans, non-human primates such as chimpanzees and other apes and monkey species, farm animals such as cattle, horses, sheep, goats, and swine, domestic animals such as rabbits, dogs, and cats, laboratory animals including rodents, such as rats, mice, and guinea pigs.
• a mammal is a human.
• the term subject does not denote a particular age or sex.
• the present invention relates to compounds of formula (I’) wherein A is represented by group, or group; wherein site “a1” of any ring A is attached to site “a2” and wherein site “b1” of any ring A is attached to site “b2”; R 1 , R 2 and X are as defined above for the compounds of formula (I) and/or salts thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof or diastereomers thereof and/or biologically active metabolites thereof or prodrugs thereof or solvates thereof or hydrates thereof and/or polymorphs thereof.
• the present invention relates to compounds of formula (l-a) wherein R 1 , R 2 and X are as defined above for the compounds of formula (I) and/or salts thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof or diastereomers thereof and/or biologically active metabolites thereof or prodrugs thereof or solvates thereof or hydrates thereof and/or polymorphs thereof.
• the present invention relates to compounds of formula (l-b)
• R 1 , R 2 and X are as defined above for the compounds of formula (I) and/or salts thereof and/or stereoisomers thereof and/or enantiomers thereof and/or racemates thereof or diastereomers thereof and/or biologically active metabolites thereof or prodrugs thereof or solvates thereof or hydrates thereof and/or polymorphs thereof.
• the present invention relates to compounds of formula (I) wherein R 1 is a Ci-ealkyl, a Ci-ealkoxy, or a halo-Ci-ealkyl group.
• the present invention relates to compounds of formula (I) wherein R 2 is hydrogen; a Ci-ealkyl group optionally substituted with -S(O)2-Ci-ealkyl, Cs-ycycloalkyl or a monovalent saturated or partly unsaturated monocyclic, bicyclic, fused, bridged or spiro ring system of 3 to 10 ring atoms comprising 1 , 2, 3 or 4 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon; a Cs-ycycloalkyl group; a monovalent saturated or partly unsaturated monocyclic, bicyclic, fused, bridged or spiro ring system of 3 to 10 ring atoms comprising 1 , 2, 3 or 4 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon optionally substituted with a Ci-ealkyl; or a monovalent, heterocyclic aromatic, mono- or bicyclic ring system of
• the present invention relates to compounds of formula (I) wherein
• R 1 is a Ci-ealkyl, a Ci-ealkoxy, or a halo-Ci-ealkyl group
• R 2 is hydrogen; a Ci-ealkyl group optionally substituted with -S(O)2-Ci-ealkyl, Cs-ycycloalkyl or a monovalent saturated or partly unsaturated monocyclic, bicyclic, fused, bridged or spiro ring system of 3 to 10 ring atoms comprising 1 , 2, 3 or 4 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon; a C ⁇ cycloalkyl group; a monovalent saturated or partly unsaturated monocyclic, bicyclic, fused, bridged or spiro ring system of 3 to 10 ring atoms comprising 1 , 2, 3 or 4 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon optionally substituted with a Ci-ealkyl; or a monovalent, heterocyclic aromatic, mono- or bicyclic ring system of 5 to 10 ring atoms, comprising 1 , 2 or 3 heteroatom
• the present invention relates to compounds of formula (I) wherein R 1 is a Ci-4alkyl, a Ci-4alkoxy, or a halo-Ci-4alkyl group.
• R 2 is hydrogen; a Ci-4alkyl group optionally substituted with -S(O)2-Ci-4alkyl, a C4-6cycloalkyl or a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising 1 , or 2 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon; a C4-ecycloalkyl group; a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising 1 , or 2 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon optionally substituted with a Ci-4alkyl; or a monovalent, heterocyclic aromatic, monocyclic ring system of
• the present invention relates to compounds of formula (I) wherein R 1 is a Ci-4alkyl, a Ci.4alkoxy, or a halo-Ci.4alkyl group;
• R 2 is hydrogen; a Ci-4alkyl group optionally substituted with -S(O)2-Ci-4alkyl, a C4-6cycloalkyl or a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising 1 , or 2 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon; a C4-ecycloalkyl group; a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising 1 , or 2 ring heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon optionally substituted with a Ci-4alkyl; or a monovalent, heterocyclic aromatic, monocyclic ring system of 5 to 6 ring atoms, comprising 1 , or 2 heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon.
• the present invention relates to compounds of formula (I) wherein R 1 is a Ci-2alkyl, a Ci.2alkoxy, or a halo-Ci.2alkyl group.
• the present invention relates to compounds of formula (I) wherein R 2 is hydrogen; a Ci-4alkyl group optionally substituted with -S(O)2-Ci-2alkyl, C4-ecycloalkyl or a a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising one ring heteroatom selected from O and S, the remaining ring atoms being carbon; a C4-6cycloalkyl group; a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising one ring heteroatom selected from O and S, the remaining ring atoms being carbon optionally substituted with a Ci-4alkyl; or a monovalent, heterocyclic aromatic, monocyclic ring system of 6 ring atoms, comprising 1 , or 2 heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon.
• the present invention relates to compounds of formula (I) wherein R 1 is a Ci-2alkyl, a Ci.2alkoxy, or a halo-Ci.2alkyl group;
• R 2 is hydrogen; a Ci-4alkyl group optionally substituted with -S(O)2-Ci-2alkyl, C4-6cycloalkyl or a a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising one ring heteroatom selected from O and S, the remaining ring atoms being carbon; a C4-6cycloalkyl group; a monovalent saturated monocyclic ring of 3 to 7 ring atoms comprising one ring heteroatom selected from O and S, the remaining ring atoms being carbon optionally substituted with a Ci-4alkyl; or a monovalent, heterocyclic aromatic, monocyclic ring system of 6 ring atoms, comprising 1 , or 2 heteroatoms independently selected from N, O and S, the remaining ring atoms being carbon.
• the present invention relates to compounds of formula (I) wherein X is CH.
• the present invention relates to compounds of formula (I) wherein X is N.
• the present invention relates to compounds of formula (I) wherein R 2 is hydrogen.
• the present invention relates to compounds of formula (I) wherein R 1 is an alkyl, an alkoxy, or a haloalkyl group; R 2 is hydrogen; and X is CH or N.
• the present invention relates to compounds of formula (I) wherein R 1 is a Ci-4alkyl, a Ci.4alkoxy, or a halo-Ci.4alkyl group; R 2 is hydrogen; and X is CH or N.
• the present invention relates to compounds of formula (l-a) wherein R 1 is a Ci-2alkyl, or a halo-Ci.2alkyl group; R 2 is hydrogen; and X is CH or N.
• the present invention relates to compounds of formula (I), as defined above selected from the group consisting of: 6- ⁇ [5-methyl-3-(6-methylpyridin-3-yl)-1 ,2-oxazol-4-yl]methoxy ⁇ -1 ,2,3,4-tetrahydro-2,7- naphthyridine,
• CS2CO3 cesium carbonate
• Na2SC sodium sulfate
• DIBAL-H diisobutylaluminium hydride
• POCI 3 phosphorus oxychloride
• DMSO dimethyl sulfoxide
• TBHP tert-butyl hydroperoxide
• K2CO3 potassium carbonate
• THF tetrahydrofuran
• Na2CC>3 sodium carbonate (usually sodium chloride)
• etherification between alcohols of formula (IV) and intermediates of formula (III) can be accomplished in the presence of a suitable base, such as K2CO3 in a suitable solvent, such as acetonitrile to form a compound of formula (V).
• a suitable base such as K2CO3
• a suitable solvent such as acetonitrile
• etherification between chloro derivatives of formula (VI) and hydroxy derivatives of formula (II) can be carried out by a palladium-mediated process in the presence of a suitable base, such as CS2CO3 to provide a compound of formula (VII).
• a suitable base such as CS2CO3
• a compound of formula (1) is reacted with ethyl acetoacetate in a suitable solvent, such as DMSO to give a compound of formula (2) which is coupled with N- tosyl hydrazide in the presence of KI and TBHP to give a compound of formula (3) (Huang et al. Adv. Synth. Catal. 2018, 360:3117-3123).
• a compound of formula (3) Treatment of a compound of formula (3) with a reducing agent such as DIBAL-H in a suitable solvent such as toluene gives a compound of formula (VIII).
• a compound of formula (1) is converted to a diazonium salt, which is further reacted with trimethylsilyl azide to give a compound of formula (4).
• Compounds of formula (4) reacted with 2-butyn-1-ol give a compound of formula (VIII).
• Scheme 5 According to Scheme 5, etherification between chloro derivatives of formula (VI) and hydroxy derivatives of formula (VIII) can be carried out by a palladium-mediated process in the presence of a suitable base, such as CS2CO3 to provide a compound of formula (IX).
• a suitable base such as CS2CO3
• the present invention thus relates to a process for the preparation of compounds of formula (I) as defined above, comprising step (i) a coupling reaction, selected from the group consisting of
• step (b) reacting a compound of formula (VI) with a compound of formula (VIII), to give a compound of formula (IX), wherein X, R 1 and R 2 are as defined above step (ii) deprotection of a compound of formula (V), (VII) or (IX) to obtain a compound of formula (I) wherein A, X, and R 1 are as defined above and R 2 is hydrogen, and step (iii) optionally transforming a compound of formula (I) wherein R 2 is hydrogen to a compound of formula (I) wherein A, X, and R 1 are as defined as above and R 2 is an alkyl group optionally substituted with -S(O)2-alkyl, a cycloalkyl or a heterocycle; a cycloalkyl group; a heterocycle group optionally substituted with an alkyl; or a heteroaryl group.
• the present invention provides novel intermediates of formula (I”) synthesised in the process for preparing the compound of general formula (I) wherein A, X, and R 1 are as defined above and R 2 is an amino protecting group (Peter G. M. Wuts: Greene’s Protective Groups in Organic Synthesis: Fifth Edition, Chapter 7.
• the present invention provides novel intermediates of formula (V) synthesised in the process for preparing the compound of general formula (I) wherein X is CH, R 1 and R 2 are as defined above with the proviso that the compound is not tert-butyl 6- ⁇ [5- methyl-3-(6-methylpyridin-3-yl)-1 ,2-oxazol-4-yl]methoxy ⁇ -1 ,2,3,4-tetrahydro-2,7- naphthyridine-2-carboxylate, or tert-butyl 6-( ⁇ 5-methyl-3-[6-(trifluoromethyl)pyridin-5 3-yl]-1 ,2- oxazol-4-yl ⁇ methoxy)-1 ,2,3,4-tetrahydro-2,7-naphthyridine-2-carboxylate.
• the present invention provides novel intermediates of formula (VII) synthesised in the process for preparing the compound of general formula (I) wherein X is N, R 1 and R 2 are as defined above.
• the present invention relates to the intermediates of formula (VII) selected from the group consisting of: tert-butyl 2-methyl-5-[5-methyl-4-( ⁇ 5H,6H,7H,8H-pyrido[3,4-c]pyridazin-3-yloxy ⁇ methyl)-1 ,2- oxazol-3-yl]pyridine-2-carboxylate, and tert-butyl 5-[5-methyl-4-( ⁇ 5H,6H,7H,8H-pyrido[3,4-c]pyridazin-3-yloxy ⁇ methyl)-1 ,2-oxazol-3- yl]-2-(trifluoromethyl)pyridine-2-carboxylate.
• the present invention provides novel intermediates of formula (IX) synthesised in the process for preparing the compound of general formula (I) wherein X, R 1 and R 2 are as defined above.
• the present invention relates to the intermediates of formula (IX) selected from the group consisting of: tert-butyl 6- ⁇ [4-methyl-1-(6-methylpyridin-3-yl)-1 H-1 ,2,3-triazol-5-yl]methoxy ⁇ -1 ,2,3,4- tetrahydro-2,7-naphthyridine-2-carboxylate, tert-butyl 6-( ⁇ 4-methyl-1-[6-(trifluoromethyl)pyridin-3-yl]-1 H-1 ,2,3-triazol-5-yl ⁇ methoxy)-
• the homogenate was centrifuged at 40,000 g for 30 minutes at 4 °C. Supernatant was discarded and the resulting pellet was washed in membrane preparation buffer. Pellet was resuspended in membrane preparation buffer and aliquots of 1.4 mL ampules were stored at -70 °C until use.
• IC50 and Kj determination a minimum of six drug concentrations in triplicate were used.
• IC50 values i.e., concentration of compound giving 50% inhibition of specific binding
• Kj values i.e., inhibition constants
• Kj ICso/[1 +(L/KD)]
• [L] is the radioligand concentration
• KD the affinity of the labelled ligand for receptor.
• KD was determined from the Saturation analyses.
• the compounds of the present invention were tested in the above described assay, and all were found to have high affinity for the GABAA a5 receptor (Kj ⁇ 150 nM).
• Human HEK293 cell lines expressing GABAA a5p3y2 receptors were used in functional assays using the QPatch automated patch clamp system.
• HEK293 cell lines stably expressing human recombinant GABA a5p3y2 receptor subunits were cultured in DM EM supplemented with 10% FBS (Gibco), passed two times per week and plated on Petri dishes previously coated with poly-d-lysine.
• the percentage modulation was calculated from the comparison of GABA-evoked peak current amplitudes in the presence and absence of the test compound.
• the compounds of the present invention were tested at 1 pM in the above described assay, and all were found to possess GABAA a5 positive allosteric modulator activity.
• Table 2 showing representative IIGABAA a5 functional efficacy test results, obtained by the above described assay:
• the compounds of formula (I) can be prepared according to the common general knowledge of the person skilled in the art and/or the methods described for the working examples and/or intermediates. Solvents, temperatures, pressures and other reaction conditions can be easily selected by the person skilled in the art. Starting materials are commercially available and/or can be easily prepared by the person skilled in the art according to literature procedure. During the preparation of compounds combinatorial techniques can be used, for example, where intermediates are suitable for the use of these methods.
• the obtained base was added to a stirred solution of 49 mg (0.36 mmol) of methanesulfonylacetone in 1 mL of methanol and 1 mL of 2,2,2-triluoroethanol at room temperature.
• the mixture was stirred for 1 h.
• 84 mg (0.72 mmol) of triethylsilicon was added by syringe and followed by 57 mg (0.26 mmol) of indium(lll) chloride (Lee et al., J. Org. Chem. 2008, 73, 22, 8829-8837).
• the reaction was allowed to stir at room temperature and was monitored by TLC. When the reaction was completed, the mixture was quenched by 1 mL of saturated K2CO3 solution.
• Active ingredient(s) 0.01 - 50%
• Liquid vehicle 10 99.9%
• Active ingredient(s) 0.01 - 50%
• Active ingredient(s) 0.01 - 50%
• Active ingredient(s) 0.01 - 50%

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Citations (24)

• 2021
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• 2022
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  • 2022-09-28 JP JP2024518133A patent/JP2024536039A/ja active Pending
  • 2022-09-28 CN CN202280074314.9A patent/CN118284606A/zh active Pending
  • 2022-09-28 GE GEAP202216510A patent/GEP20257812B/en unknown
  • 2022-09-28 WO PCT/IB2022/059214 patent/WO2023053015A1/en not_active Ceased
  • 2022-09-28 PE PE2024000597A patent/PE20240816A1/es unknown
  • 2022-09-28 IL IL311640A patent/IL311640A/en unknown
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  • 2022-09-28 MX MX2024003812A patent/MX2024003812A/es unknown
  • 2022-09-28 EP EP22783047.8A patent/EP4408842A1/en active Pending
  • 2022-09-28 CA CA3231776A patent/CA3231776A1/en active Pending
  • 2022-09-28 AU AU2022357572A patent/AU2022357572A1/en active Pending
  • 2022-09-28 KR KR1020247013656A patent/KR20240089056A/ko active Pending
  • 2022-09-28 GE GEAP202416510A patent/GEAP202416510A/en unknown
  • 2022-09-28 US US18/696,506 patent/US20250051323A1/en active Pending
  • 2022-09-29 AR ARP220102623A patent/AR127182A1/es unknown
• 2024
  • 2024-03-20 JO JOJO/P/2024/0057A patent/JOP20240057A1/ar unknown
  • 2024-03-27 CL CL2024000893A patent/CL2024000893A1/es unknown
  • 2024-04-25 ZA ZA2024/03230A patent/ZA202403230B/en unknown
  • 2024-04-26 EC ECSENADI202432316A patent/ECSP24032316A/es unknown
  • 2024-04-26 CO CONC2024/0005424A patent/CO2024005424A2/es unknown

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