WO2009033704A1 - 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4'] bipyridinyl-2'-ones - Google Patents
1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4'] bipyridinyl-2'-ones Download PDFInfo
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- WO2009033704A1 WO2009033704A1 PCT/EP2008/007551 EP2008007551W WO2009033704A1 WO 2009033704 A1 WO2009033704 A1 WO 2009033704A1 EP 2008007551 W EP2008007551 W EP 2008007551W WO 2009033704 A1 WO2009033704 A1 WO 2009033704A1
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- 0 *=C1N(CC2CC2)C=CC(O)=C1C1CC1 Chemical compound *=C1N(CC2CC2)C=CC(O)=C1C1CC1 0.000 description 1
- OPMBNDHYGGYNMU-UHFFFAOYSA-N O=C1N(CC2CC2)C=CC(OCc2ccccc2)=C1C(F)(F)F Chemical compound O=C1N(CC2CC2)C=CC(OCc2ccccc2)=C1C(F)(F)F OPMBNDHYGGYNMU-UHFFFAOYSA-N 0.000 description 1
- ZVKALSOHGTUOCN-UHFFFAOYSA-N O=C1N(CC2CC2)C=CC(OCc2ccccc2)=C1C1CC1 Chemical compound O=C1N(CC2CC2)C=CC(OCc2ccccc2)=C1C1CC1 ZVKALSOHGTUOCN-UHFFFAOYSA-N 0.000 description 1
- ZQNDUHXKMNXYFS-UHFFFAOYSA-N OC(C=CN(Cc(cc1)ccc1OC(F)(F)F)C1=O)=C1Cl Chemical compound OC(C=CN(Cc(cc1)ccc1OC(F)(F)F)C1=O)=C1Cl ZQNDUHXKMNXYFS-UHFFFAOYSA-N 0.000 description 1
- NCVZTPPWLSWLCQ-UHFFFAOYSA-N OC(C=CN1CC2CC2)=C(C(F)(F)F)C1=O Chemical compound OC(C=CN1CC2CC2)=C(C(F)(F)F)C1=O NCVZTPPWLSWLCQ-UHFFFAOYSA-N 0.000 description 1
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Definitions
- the present invention relates to novel pyridinone-derivatives which are positive allosteric modulators of the metabotropic glutamate receptor subtype 2 ("mGluR2") and 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.
- Glutamate is the major amino acid neurotransmitter in the mammalian central nervous system. Glutamate plays a major role in numerous physiological functions, such as learning and memory but also sensory perception, development of synaptic plasticity, motor control, respiration, and regulation of cardiovascular function. Furthermore, glutamate is at the centre of several different neurological and psychiatric diseases, where there is an imbalance in glutamatergic neurotransmission.
- Glutamate mediates synaptic neurotransmission through the activation of ionotropic glutamate receptors channels (iGluRs), and the NMDA, AMPA and kainate receptors which are responsible for fast excitatory transmission.
- iGluRs ionotropic glutamate receptors channels
- glutamate activates metabotropic glutamate receptors (mGluRs) which have a more modulatory role that contributes to the fine-tuning of synaptic efficacy.
- mGluRs metabotropic glutamate receptors
- Glutamate activates the mGluRs through binding to the large extracellular amino-terminal domain of the receptor, herein called the orthosteric binding site. This binding induces a conformational change in the receptor which results in the activation of the G-protein and intracellular signaling pathways.
- the mGluR2 subtype is negatively coupled to adenylate cyclase via activation of G ⁇ i-protein, and its activation leads to inhibition of glutamate release in the synapse.
- mGluR2 receptors are abundant mainly throughout cortex, thalamic regions, accessory olfactory bulb, hippocampus, amygdala, caudate-putamen and nucleus accumbens.
- Activating mGluR2 was shown in clinical trials to be efficacious to treat anxiety disorders.
- activating mGluR2 in various animal models was shown to be efficacious, thus representing a potential novel therapeutic approach for the treatment of schizophrenia, epilepsy, addiction/drug dependence, Parkinson's disease, pain, sleep disorders and Huntington's disease.
- a new avenue for developing selective compounds acting at mGluRs is to identify compounds that act through allosteric mechanisms, modulating the receptor by binding to a site different from the highly conserved orthosteric binding site.
- WO2001/56990 (Eli Lilly) and WO2006/030032 (Addex & Janssen Pharmaceutica) describe respectively phenyl sulfonamide, acetophenone, indanone, pyridylmethyl sulfonamide and pyridinone derivatives as mGluR2 positive allosteric modulators.
- Allosteric modulators of mGluR2 have effects in anxiety and psychosis models similar to those obtained with orthosteric agonists.
- Allosteric modulators of mGluR2 were shown to be active in fear-potentiated startle, and in stress-induced hyperthermia models of anxiety. Furthermore, such compounds were shown to be active in reversal of ketamine- or amphetamine-induced hyperlocomotion, and in reversal of amphetamine-induced disruption of prepulse inhibition of the acoustic startle effect models of schizophrenia. (J. Pharmacol. Exp. Ther. 2006, 318, 173-185; Psychopharmacology 2005, 179, 271-283).
- BINA metabotropic glutamate receptor subtype 2 biphenyl-indanone
- Positive allosteric modulators enable potentiation of the glutamate response, but they have also been shown to potentiate the response to orthosteric mGluR2 agonists such as LY379268 or DCG-IV. These data provide evidence for yet another novel therapeutic approach to treat above mentioned neurological and psychiatric diseases involving mGluR2, which would use a combination of a positive allosteric modulator of mGluR2 together with an orthosteric agonist of mGluR2.
- the present invention relates to compounds having metabotropic glutamate receptor 2 modulator activity, said compounds having the Formula (I)
- R is Ci -6 alkyl; or Ci -3 alkyl substituted with C 3-7 cycloalkyl, phenyl, or phenyl substituted with halo, trifluoromethyl or trifluoromethoxy;
- R 2 is halo, trifluoromethyl, Ci ⁇ alkyl or cyclopropyl
- R 3 is hydrogen, fluoro, hydroxyl, hydroxyCi- 3 alkyl, hydroxyCi. 3 alkyloxy, fluoroCi. 3 alkyl, fluoroC 1-3 alkyloxy or cyano;
- Ar is unsubstituted phenyl; or phenyl substituted with n radicals R 4 , wherein n is 1, 2 or 3;
- R 4 is selected from the group consisting of hydrogen, halo, C 1 . 3 a.kyl, hydroxyCi -3 alkyl, polyhaloCi ⁇ alkyl , cyano, hydroxyl, amino, carboxyl, Ci -3 alkyloxyCi -3 alkyl, Ci -3 alkyloxy, polyhaloCi -3 alkyloxy, Cj -3 alkylcarbonyl, mono- and di(Ci -3 alkyl)amino, and mo ⁇ holinyl; or two vicinal R 4 radicals taken together form a bivalent radical of formula
- the invention relates to a compound of Formula (I) or a stereochemically isomeric form thereof wherein
- R 1 is C 1-6 alkyl; or Ci -3 alkyl substituted with C 3-7 cycloalkyl, phenyl, or phenyl substituted with halo, trifluoromethyl or trifluoromethoxy;
- R 2 is halo, trifluoromethyl, Ci -3 alkyl or cyclopropyl;
- R 3 is hydrogen, fluoro, hydroxyl, hydroxyCi -3 alkyl, hydroxyCi -3 alkyloxy, fluoroCi -3 alkyl, fluoroCi -3 alkyloxy or cyano; and
- Ar is unsubstituted phenyl, or phenyl substituted with n radicals R 4 , wherein n is 1, 2 or 3;
- the invention relates to a compound according to Formula (I) or a stereochemically isomeric form thereof, wherein R 1 is 1 -butyl, 2-methyl-l -propyl, 3-methyl-l -butyl, (cyclopropyl)methyl or 2-
- R 2 is chloro, bromo, cyclopropyl or trifluoromethyl
- R 3 is hydrogen, fluoro or cyano
- Ar is unsubstituted phenyl; or phenyl substituted with halo, trifluoromethyl, morpholinyl or hydroxyCi -3 alkyl; or a pharmaceutically acceptable salt or solvate thereof.
- the invention relates to a compound according to Formula
- R 1 is 1-butyl, 3-methyl-l -butyl, (cyclopropyl)methyl or 2-(cyclopropyl)-l -ethyl;
- R 2 is chloro;
- R is hydrogen or fluoro; and Ar is unsubstituted phenyl; or phenyl substituted with hydroxyCj. 3 alkyl; or a pharmaceutically acceptable salt or solvate thereof.
- the notation Ci -3 alkyl as a group or part of a group defines a saturated, straight or branched, hydrocarbon radical having from 1 to 3 carbon atoms, such as methyl, ethyl, 1 -propyl and 1 -methyl ethyl; e.g. hydroxyCi ⁇ alkyl for example defines hydroxymethyl, 2-hydroxyethyl, 3-hydroxypropyl and 1 -hydroxy- 1 -methyl ethyl.
- Ci -6 alkyl as a group or part of a group defines a saturated, straight or branched, hydrocarbon radical having from 1 to 6 carbon atoms such as methyl, ethyl, 1 -propyl, 1 -methyl ethyl, 1-butyl, 2 -methyl- 1 -propyl, 3-methyl-l -butyl, 1-pentyl, 1-hexyl and the like.
- the notation C 3-7 cycloalkyl defines a saturated, cyclic hydrocarbon radical having from 3 to 7 carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl.
- the notation halo or halogen as a group or part of a group is generic for fluoro, chloro, bromo, iodo.
- salts of the compounds of formula (I) are those wherein the counterion is pharmaceutically acceptable.
- salts of acids and bases which are non-pharmaceutically acceptable may also find use, for example, in the preparation or purification of a pharmaceutically acceptable compound. All salts, whether pharmaceutically acceptable or not, are included within the ambit of the present invention.
- the pharmaceutically acceptable salts are defined to comprise the therapeutically active non-toxic acid addition salt forms that the compounds according to Formula (I) are able to form.
- Said salts can be obtained by treating the base form of the compounds according to Formula (I) with appropriate acids, for example inorganic acids, for example hydrohalic acid, in particular hydrochloric acid, hydrobromic acid, sulphuric acid, nitric acid and phosphoric acid ; organic acids, for example acetic acid, hydroxyacetic acid, propanoic acid, lactic acid, pyruvic acid, oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid, malic acid, tartaric acid, citric acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, cyclamic acid, salicylic acid, p-aminosalicylic acid and pamoic acid.
- acids for example in
- salt forms can be converted into the free base form by treatment with an appropriate base .
- the compounds according to Formula (I) containing acidic protons may also be converted into their therapeutically active non-toxic base salt forms by treatment with appropriate organic and inorganic bases.
- Appropriate base salt forms comprise, for example, the ammonium salts, the alkaline and earth alkaline metal salts, in particular lithium, sodium, potassium, magnesium and calcium salts, salts with organic bases, e.g. the benzathine, N-methyl-D-glucamine, hybramine salts, and salts with amino acids, for example arginine and lysine.
- salt forms can be converted into the free acid forms by treatment with an appropriate acid.
- solvate comprises the solvent addition forms as well as the salts thereof, which the compounds of formula (I) are able to form.
- solvent addition forms are e.g. hydrates, alcoholates and the like.
- stereochemically isomeric forms as used hereinbefore defines all the possible isomeric forms that the compounds of Formula (I) may possess. Unless otherwise mentioned or indicated, the chemical designation of compounds denotes the mixture of all possible stereochemically isomeric forms, said mixtures containing all diastereomers and enantiomers of the basic molecular structure.
- the invention also embraces each of the individual isomeric forms of the compounds of Formula (I) and their salts and solvates, substantially free, i.e. associated with less than 10%, preferably less than 5%, in particular less than 2% and most preferably less than 1% of the other isomers.
- an R or S descriptor is assigned (based on Cahn-Ingold-Prelog sequence rule) to the lowest-numbered chiral center, the reference center.
- the configuration of the second stereogenic center is indicated using relative descriptors [R*, R*] or [R*, S*], where R* is always specified as the reference center and [R*,R*] indicates centers with the same chirality and [/?*,5*] indicates centers of unlike chirality.
- R*, R*] indicates centers with the same chirality
- [/?*,5*] indicates centers of unlike chirality.
- the stereo descriptor would be specified as S-[R*,S*].
- the position of the highest priority substituent on the asymmetric carbon atom in the ring system having the lowest ring number is arbitrarily always in the " ⁇ " position of the mean plane determined by the ring system.
- the position of the highest priority substituent on the other asymmetric carbon atom in the ring system (hydrogen atom in compounds according to Formula (I)) relative to the position of the highest priority substituent on the reference atom is denominated " ⁇ ", if it is on the same side of the mean plane determined by the ring system, or " ⁇ ", if it is on the other side of the mean plane determined by the ring system.
- Radiolabeled compounds of Formula (I) may comprise a radioactive isotope selected from the group of 3 H, 11 C, 18 F, 122 I, 123 I, 125 I, 131 I, 75 Br, 76 Br, 77 Br and 82 Br.
- the radioactive isotope is selected from the group of 3 H, 1 1 C and 18 F.
- the compounds according to the invention can generally be prepared by a succession of steps, each of which is known to the skilled person.
- the compounds can be prepared according to the following synthesis methods.
- the compounds of Formula (I) may be synthesized in the form of racemic mixtures of enantiomers which can be separated from one another following art-known resolution procedures.
- the racemic compounds of Formula (I) may be converted into the corresponding diastereomeric salt forms by reaction with a suitable chiral acid. Said diastereomeric salt forms are subsequently separated, for example, by selective or fractional crystallization and the enantiomers are liberated therefrom by alkali.
- An alternative manner of separating the enantiomeric forms of the compounds of Formula (I) involves liquid chromatography using a chiral stationary phase. Said pure stereochemical ⁇ isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecifically.
- the compounds according to Formula (I), in the case of R 2 being halogen, can be prepared by reacting an intermediate of Formula (II) with an N-halosuccinimide reagent, such as N-chlorosuccinimide, N-bromosuccinimide or iV-iodosuccinimide, according to reaction scheme (1).
- This reaction is performed in a suitable reaction-inert and aprotic solvent, such as, for example, dichloromethane or 1 ,2-dichloroethane, stirring the reaction mixture at a suitable temperature, typically at room temperature, for the required time to achieve completion of the reaction, usually 1 hour.
- R 2 is halogen and all other variables are defined as in Formula (I).
- R2 halogen
- reaction-inert solvent such as, for example, toluene
- a suitable base such as, for example, sodium tert-butoxide
- a metal -based catalyst specifically a palladium catalyst, such as palladium(II) acetate
- a suitable ligand such as for example [l,r-binaphthalene]-2,2'-diylbis[diphenylphosphine] (B MAP), heating for a suitable period of time that allows the completion of the reaction, for example at 100 0 C for 16 hours in a sealed tube.
- Z a is a group suitable for Pd mediated coupling with amines, such as, for example, a halogen or triflate. All other variables are defined as in Formula (I).
- Such intermediates of Formula (II) and Formula (III) may be prepared according to reaction schemes (3) to (11) (see below).
- the transformations of different functional groups present in the final compounds, into other functional groups according to Formula (I), can be performed by synthesis methods well known by the person skilled in the art.
- Intermediates of Formula (II) can be prepared by reacting an intermediate of Formula (V) with an intermediate of Formula (IV) according to reaction scheme (3).
- This reaction is performed in a suitable reaction-inert solvent such as, for example, toluene, in the presence of a suitable base such as, for example, sodium tert-butoxide, a metal- based catalyst, specifically a palladium catalyst, such as palladium(II) acetate, and a suitable ligand, such as for example [l,r-binaphthalene]-2,2'- diylbis[diphenylphosphine] (BINAP), heating for a suitable period of time that allows the completion of the reaction, for example at 100 0 C for 16 hours in a sealed tube.
- a suitable reaction-inert solvent such as, for example, toluene
- a suitable base such as, for example, sodium tert-butoxide
- a metal- based catalyst specifically a palladium catalyst, such as palla
- Intermediates of Formula (III-a) and (III-b) can be prepared by reacting an intermediate of Formula (VI), wherein Y is H or R 2 (as defined as in Formula I), with a suitable halogenating agent such as, for example, phosphorus oxybromide.
- This reaction may be performed in a suitable reaction-inert solvent such as, for example, DMF, at a moderately elevated temperature such as, for example, 110 0 C, for a suitable period of time that allows the completion of the reaction, for instance 1 hour.
- a suitable reaction-inert solvent such as, for example, DMF
- a moderately elevated temperature such as, for example, 110 0 C
- variable R 1 is defined as in Formula (I).
- Intermediates of Formula (III-c) can be prepared by reacting an intermediate of Formula (VI-a) with triflic anhydride (also called trifloromethanesulfonic anhydride).
- the reaction may be performed in a suitable reaction-inert solvent such as, for example, dichloromethane, in the presence of a base such as, for example, pyridine at a low temperature such as, for example, -78 0 C.
- a suitable reaction-inert solvent such as, for example, dichloromethane
- a base such as, for example, pyridine
- a low temperature such as, for example, -78 0 C.
- Intermediates of Formula (VI) can be prepared by hydrogenolysis of intermediates of Formula (VII-a, VII-b or VII-c), in a suitable reaction-inert solvent such as, for example, ethanol, in the presence of a catalyst such as, for example, 10 % palladium on activated carbon, for a period of time that ensures the completion of the reaction, typically at room temperature and 1 atmosphere of hydrogen for 2 hours.
- a suitable reaction-inert solvent such as, for example, ethanol
- a catalyst such as, for example, 10 % palladium on activated carbon
- intermediates of Formula (VI), wherein Y - halogen can be prepared by reacting an intermediate of Formula (VII-d) in a mixture of acetic acid and hydrobromic acid, and heating the mixture at a temperature and for the time required to allow completion of the reaction, typically at 130 0 C for 30 minutes under microwave irradiation.
- variable R 1 is defined as in Formula (I).
- Intermediates of Formula (VII-b) can be prepared by reacting an intermediate of Formula (VII-e), wherein Y is iodine, with commercially available methyl 2,2-difiuoro- 2-(fluorosulfonyl)acetate, in a suitable reaction-inert solvent such as, for example, DMF, in presence of a suitable copper salt such as copper(I) iodide, heating for a suitable period of time that allows the completion of the reaction, for example at 100 0 C for 5 hours.
- a suitable reaction-inert solvent such as, for example, DMF
- a suitable copper salt such as copper(I) iodide
- Intermediates of Formula (VII-d) can be prepared by reacting an intermediate of Formula (VII-a) with a commercially available N-halosuccinimide, such as N-chloro- ( ⁇ CS), N-bromo- ( ⁇ BS) or N-iodosuccinimide ( ⁇ IS), in a suitable reaction-inert solvent such as, for example, DMF, dichloromethane or acetic acid, typically at room temperature for 1 to 24 hours.
- a suitable reaction-inert solvent such as, for example, DMF, dichloromethane or acetic acid
- Intermediates of Formula (VII-c) can be prepared by reacting an intermediate of Formula (VII-d) with a Ci -3 alkyl- or cyclopropyl-boronic acid derivative, such as 5 cyclopropyl- boronic acid or methyl- boronic acid, in a suitable reaction-inert solvent such as, for example, 1 ,4-dioxane, in the presence of a suitable palladium catalyst- complex such as, for example, [l,l '-bis(diphenylphosphino)-ferrocene]- dichloropalladium(II) - DCM complex, and in the presence of a suitable base such as sodium hydrogencarbonate, heating for a suitable period of time that allows the 10 completion of the reaction, for example at 175 0 C for 20 minutes under microwave irradiation.
- a suitable reaction-inert solvent such as, for example, 1 ,4-dioxane
- a suitable palladium catalyst- complex such as, for example
- Intermediates of formula (IV) can be prepared by deprotection of the piperidine nitrogen in an intermediate of formula (IX) wherein L is a suitable protecting group for 20 the nitrogen atom of a piperidine derivative, such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl, applying art known procedures, according to reaction scheme (12).
- L is a suitable protecting group for 20 the nitrogen atom of a piperidine derivative, such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl, applying art known procedures, according to reaction scheme (12).
- reaction scheme (12) all variables are defined as in formula (I).
- Intermediates of formula (IX-a) can be prepared by hydrogenation of an intermediate of formula (XI) wherein L is a suitable protecting group for the nitrogen atom of a tetrahydropyridine derivative, such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl, applying art known procedures, according to reaction scheme (14).
- L is a suitable protecting group for the nitrogen atom of a tetrahydropyridine derivative, such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl, applying art known procedures, according to reaction scheme (14).
- Ar is defined as in Formula (I).
- Intermediates of formula (X) can be prepared by deprotection of the tetrahydropyridine nitrogen in an intermediate of formula (XI) wherein L is a suitable protecting group for the nitrogen atom of a tetrahydropyridine derivative, such as for example tert- butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl, applying art known procedures, according to reaction scheme (15).
- Ar is defined as in formula (I).
- Intermediates of formula (XI) can be prepared by reacting an intermediate of formula (XII) with an intermediate of formula (XIII) according to reaction scheme (16).
- the reaction may be performed in a suitable reaction-inert solvent, such as, for example, 1,4-dioxane, or mixtures of inert solvents such as, for example, 1 ,4-dioxane/DMF, in the presence of a suitable base, such as, for example, aqueous NaHCO 3 or Na 2 CO 3 , a suitable catalyst, such as for example a Pd-complex catalyst such as, for example,
- reaction scheme (16) all variables are defined as in formula (I); Z c is a group suitable for Pd mediated coupling with boronic acids or boronic esters, such as, for example, a halo or triflate; L is a suitable protecting group for the nitrogen atom of a tetrahydropyridine derivative, such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl and R 4 and R 5 are hydrogen or or may be taken together to form for example a bivalent radical of formula -CH 2 CH 2 -, -CH 2 CH 2 CH 2 -, or -C(CH 3 ) 2 C(CH 3 ) 2 -.
- Intermediates of formula (IV) wherein R 3 represents fluoro or Ci -3 alkyl substituted with fluoro, said R 3 being represented by -Li-F wherein Li represents Ci -3 alkyl or a covalent bond, and said intermediates being represented by formula (IV-b), can be prepared by art known procedures by reacting an intermediate of formula (IX-b) wherein L is a suitable protecting group for the nitrogen atom of the piperidine moiety, such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl, with a suitable fluorinating agent such as for example (diethylamino)sulfur trifluoride , resulting in an intermediate of formula (IX-c) according to reaction scheme (17) step (a).
- a suitable protecting group for the nitrogen atom of the piperidine moiety such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl
- the reaction may be performed in a suitable reaction-inert solvent, such as, for example, dichloromethane.
- the reaction may be performed under a moderately low temperature such as, for example, a temperature ranging from -78 0 C to 30 0 C during for example 0.5 to 12 hours.
- the resulting intermediate of formula (IX-c) can then be transformed according to reaction scheme (17) step (b), in an intermediate of Formula (IV-b) by deprotection of the piperidine nitrogen applying art known procedures, such as for example those described in experimental procedure 15 herein above.
- Ar is defined as in formula (I).
- reaction can be performed in a suitable reaction-inert solvent, such as, for example, dichloromethane, under a moderately low temperature such as, for example, a temperature ranging from -78 0 C to 30 0 C during for example 0.5 to 12 hours.
- a suitable reaction-inert solvent such as, for example, dichloromethane
- a moderately low temperature such as, for example, a temperature ranging from -78 0 C to 30 0 C during for example 0.5 to 12 hours.
- the intermediate of Formula (IX-e) can then be transformed according to reaction scheme (18) step (b) in an intermediate of Formula (IV-d) by deprotection of the piperidine nitrogen applying art known procedures, such as for example those described in experimental procedure 17 hereinabove.
- Ar is defined as in formula (I).
- Intermediates of formula (IX-b) wherein Ll represents CH 2 can be prepared by reacting an intermediate of formula (XIV) wherein L is a suitable protecting group for the nitrogen atom of the piperidine moiety, such as for example tert-butoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, benzyl and methyl, with a suitable reducing agent, such as for example, lithium aluminium hydride, according to reaction scheme (19).
- the reaction may be performed in a suitable solvent, such as for example tetrahydrofuran, at a moderately low temperature such as, for example from -20 0 C.
- Ar is defined as in formula (I)
- the compounds provided in this invention are positive allosteric modulators of metabotropic glutamate receptors, in particular they are positive allosteric modulators of mGluR2.
- the compounds of the present invention do not appear to bind to the glutamate recognition site, the orthosteric ligand site, but instead to an allosteric site within the seven transmembrane region of the receptor.
- the compounds of this invention increase the mGluR2 response.
- the compounds provided in this invention are expected to have their effect at mGluR2 by virtue of their ability to increase the response of such receptors to glutamate or mGluR2 agonists, enhancing the response of the receptor.
- the present invention relates to a compound according to the present invention for use as a medicine, as well as to the use of a compound according to the invention or a pharmaceutical composition according to the invention for the manufacture of a medicament for treating or preventing, in particular treating, a condition in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect of allosteric modulators of mGluR2, in particular positive allosteric modulators thereof.
- the present invention also relates to a compound according to the present invention or a pharmaceutical composition according to the invention for use in the manufacture of a medicament for treating or preventing, in particular treating, a condition in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect of allosteric modulators of mGluR2, in particular positive allosteric modulators thereof.
- the present invention also relates to a compound according to the present invention or a pharmaceutical composition according to the invention for treating or preventing, in particular treating, a condition in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect of allosteric modulators of mGluR2, in particular positive allosteric modulators thereof.
- the present invention relates to the use of a compound according to the invention or a pharmaceutical composition according to the invention for the manufacture of a medicament for treating, preventing, ameliorating, controlling or reducing the risk of various neurological and psychiatric disorders associated with glutamate dysfunction in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect of positive allosteric modulators of mGluR2.
- the invention is said to relate to the use of a compound or composition according to the invention for the manufacture of a medicament for e.g. the treatment of a mammal, it is understood that such use is to be interpreted in certain jurisdictions as a method of e.g.
- the neurological and psychiatric disorders associated with glutamate dysfunction include one or more of the following conditions or diseases: acute neurological and psychiatric disorders such as, for example, cerebral deficits subsequent to cardiac bypass surgery and grafting, stroke, cerebral ischemia, spinal cord trauma, head trauma, perinatal hypoxia, cardiac arrest, hypoglycemic neuronal damage, dementia (including AIDS-induced dementia), Alzheimer's disease, Huntington's Chorea, amyotrophic lateral sclerosis, ocular damage, retinopathy, cognitive disorders, idiopathic and drug-induced Parkinson's disease, muscular spasms and disorders associated with muscular spasticity including tremors, epilepsy, convulsions, migraine (including migraine headache), urinary incontinence, substance tolerance, substance withdrawal (including substances such as, for example, opiates, nicotine, tobacco
- condition or disease is a central nervous system disorder selected from the group of anxiety disorders, psychotic disorders, personality disorders, substance-related disorders, eating disorders, mood disorders, migraine, epilepsy or convulsive disorders, childhood disorders, cognitive disorders, neurodegeneration, neurotoxicity and ischemia.
- the central nervous system disorder is an anxiety disorder, selected from the group of agoraphobia, generalized anxiety disorder (GAD), obsessive-compulsive disorder (OCD), panic disorder, posttraumatic stress disorder (PTSD), social phobia and other phobias.
- GAD generalized anxiety disorder
- OCD obsessive-compulsive disorder
- PTSD posttraumatic stress disorder
- social phobia other phobias.
- the central nervous system disorder is a psychotic disorder selected from the group of schizophrenia, delusional disorder, schizoaffective disorder, schizophreniform disorder and substance-induced psychotic disorder
- the central nervous system disorder is a personality disorder selected from the group of obsessive-compulsive personality disorder and schizoid, schizotypal disorder.
- the central nervous system disorder is a substance-related disorder selected from the group of alcohol abuse, alcohol dependence, alcohol withdrawal, alcohol withdrawal delirium, alcohol-induced psychotic disorder, amphetamine dependence, amphetamine withdrawal, cocaine dependence, cocaine withdrawal, nicotine dependence, nicotine withdrawal, opioid dependence and opioid withdrawal.
- the central nervous system disorder is an eating disorder selected from the group of anorexia nervosa and bulimia nervosa.
- the central nervous system disorder is a mood disorder selected from the group of bipolar disorders (I & II), cyclothymic disorder, depression, dysthymic disorder, major depressive disorder and substance-induced mood disorder.
- bipolar disorders I & II
- cyclothymic disorder depression
- dysthymic disorder major depressive disorder
- substance-induced mood disorder substance-induced mood disorder
- the central nervous system disorder is migraine.
- the central nervous system disorder is epilepsy or a convulsive disorder selected from the group of generalized nonconvulsive epilepsy, generalized convulsive epilepsy, petit mal status epilepticus, grand mal status epilepticus, partial epilepsy with or without impairment of consciousness, infantile spasms, epilepsy partialis continua, and other forms of epilepsy.
- the central nervous system disorder is attention-deficit/hyperactivity disorder.
- the central nervous system disorder is a cognitive disorder selected from the group of delirium, substance-induced persisting delirium, dementia, dementia due to HIV disease, dementia due to Huntington's disease, dementia due to Parkinson's disease, dementia of the Alzheimer's type, substance-induced persisting dementia and mild cognitive impairment.
- DSM-IV Diagnostic & Statistical Manual of Mental Disorders
- DSM-IV Diagnostic & Statistical Manual of Mental Disorders
- the person skilled in the art will recognize that alternative nomenclatures, nosologies, and classification systems for neurological and psychiatric disorders described herein exist, and that these evolve with medical and scientific progresses. Because such positive allosteric modulators of mGluR2, including compounds of Formula (I), enhance the response of mGluR2 to glutamate, it is an advantage that the present methods utilize endogenous glutamate.
- positive allosteric modulators of mGluR2, including compounds of Formula (I) enhance the response of mGluR2 to agonists
- the present invention extends to the treatment of neurological and psychiatric disorders associated with glutamate dysfunction by administering an effective amount of a positive allosteric modulator of mGluR2, including compounds of Formula (I), in combination with an mGluR2 agonist.
- the compounds of the present invention may be utilized in combination with one or more other drugs in the treatment, prevention, control, amelioration, or reduction of risk of diseases or conditions for which compounds of Formula (I) or the other drugs may have utility, where the combination of the drugs together are safer or more effective than either drug alone.
- the invention also relates to a pharmaceutical composition
- a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and, as active ingredient, a therapeutically effective amount of a compound according to the invention, in particular a compound according to Formula (I), a pharmaceutically acceptable salt thereof, a solvate thereof or a stereochemically isomeric form thereof.
- the compounds according to the invention in particular the compounds according to Formula (I), the pharmaceutically acceptable salts thereof, the solvates and the stereochemically isomeric forms thereof, or any subgroup or combination thereof may be formulated into various pharmaceutical forms for administration purposes.
- compositions there may be cited all compositions usually employed for systemically administering drugs.
- compositions of this invention an effective amount of the particular compound, optionally in salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier or diluent, which carrier or diluent may take a wide variety of forms depending on the form of preparation desired for administration.
- a pharmaceutically acceptable carrier or diluent which carrier or diluent may take a wide variety of forms depending on the form of preparation desired for administration.
- These pharmaceutical compositions are desirable in unitary dosage form suitable, in particular, for administration orally, rectally, percutaneously, by parenteral injection or by inhalation.
- any of the usual pharmaceutical media may be employed such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as, for example, suspensions, syrups, elixirs, emulsions and solutions; or solid carriers such as, for example, starches, sugars, kaolin, diluents, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets.
- solid pharmaceutical media such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as, for example, suspensions, syrups, elixirs, emulsions and solutions; or solid carriers such as, for example, starches, sugars, kaolin, diluents, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets.
- oral administration is preferred, and tablets and capsules represent the most advantageous oral dosage unit forms in which
- the carrier will usually comprise sterile water, at least in large part, though other ingredients, for example, to aid solubility, may be included.
- injectable solutions for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution.
- injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed.
- solid form preparations that are intended to be converted, shortly before use, to liquid form preparations.
- the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not introduce a significant deleterious effect on the skin.
- Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions.
- These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment.
- Unit dosage form refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier.
- unit dosage forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, suppositories, injectable solutions or suspensions and the like, and segregated multiples thereof.
- the exact dosage and frequency of administration depends on the particular compound of formula (I) used, the particular condition being treated, the severity of the condition being treated, the age, weight, sex, extent of disorder and general physical condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art. Furthermore, it is evident that said effective daily amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention.
- the pharmaceutical composition will comprise from 0.05 to 99 % by weight, preferably from 0.1 to 70 % by weight, more preferably from 0.1 to 50 % by weight of the active ingredient, and, from 1 to 99.95 % by weight, preferably from 30 to 99.9 % by weight, more preferably from 50 to 99.9 % by weight of a pharmaceutically acceptable carrier, all percentages being based on the total weight of the composition.
- the invention also relates to a pharmaceutical composition
- a pharmaceutical composition comprising the compounds according to the invention and one or more other drugs in the treatment, prevention, control, amelioration, or reduction of risk of diseases or conditions for which compounds of Formula (I) or the other drugs may have utility as well as to the use of such a composition for the manufacture of a medicament.
- the present invention also relates to a combination of a compound according to the present invention and a mGluR2 orthosteric agonist.
- the present invention also relates to such a combination for use as a medicine.
- the present invention also relates to a product comprising (a) a compound according to the present invention, a pharmaceutically acceptable salt thereof or a solvate thereof, and (b) a mGluR2 orthosteric agonist, as a combined preparation for simultaneous ⁇ separate or sequential use in the treatment or prevention of a condition in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect of mGluR2 allosteric modulators, in particular positive mGluR2 allosteric modulators.
- the different drugs of such a combination or product may be combined in a single preparation together with pharmaceutically acceptable carriers or diluents, or they may each be present in a separate preparation together with pharmaceutically acceptable carriers or diluents.
- THF tetrahydrofiiran
- DMF means NJV- dimethylformamide
- EtOAc means ethyl acetate
- DCM means dichloromethane
- DME means 1 ,2-dimethoxyethane
- DCE means 1 ,2-dichloroethane
- DIPE means diisopropylether
- DMSO means dimethylsulfoxide
- BINAP means[l,l'- binaphthalene]-2,2'-diylbis[diphenylphosphine]
- DBU means l,8-diaza-7- bicyclo[5.4.0]undecene
- Xantphos means (9,9-dimethyl-9//-xanthene-4,5- diyl)bis[diphen
- Microwave assisted reactions were performed in a single-mode reactor:
- intermediate D4 (2.01 g, 7.83 mmol) and a catalytic amount of 10% palladium on activated carbon in ethanol (300 ml) was stirred under a hydrogen atmosphere for two hours. The mixture was filtered through diatomaceous earth and the solvent was evaporated in vacuo to yield intermediate D5 (1.3 g, 100 %) that was used without further purification.
- N-Chlorosuccinimide (1.6 g, 11.96 mmol) was added to a solution of intermediate D5 (2.0 g, 11.96 mmol) in DMF (30 ml). The reaction was stirred at room temperature overnight and then it was concentrated in vacuo. The crude product was purified by column chromatography (silica gel; 0-5% methanol / DCM as eluent) to yield intermediate D8 (2.0 g, 83 %).
- N-Iodosuccinimide (2.64 g, 11.74 mmol) was added to a solution of intermediate Dl (3.0 g, 11.74 mmol) in acetic acid (40 ml). The reaction mixture was stirred at room temperature for 1 hour, after which it was concentrated in vacuo, purified by flash chromatography (silica gel; 0-3% methanol / DCM as eluent) and finally recrystallized from diethyl ether to afford intermediate DlO (4.12 g, 92 %) as a solid.
- N-Chlorosuccinimide (1.68 g, 12.61 mmol) was added to a solution of intermediate D14 (4.31 g, 11.47 mmol) in DMF (30 ml) and the mixture was stirred at room temperature for 24 hours. The solvent was evaporated and the solid residue was washed with water (4 x 25 ml). The crude solid was washed with DIPE to yield intermediate D15 (4.5 g, 95 %) as a white solid.
- Methyl 2-bromobenzoate (1.816 ml, 12.936 mmol) [CAS 610-94-6] was added to a solution of 1 ,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-l ,3,2-dioxaborolan-2-yl)-pyridine (4 g, 12.936 mmol) [CAS 375853-82-0] (synthesis described in WO 2004072025 A2 20040826) in 1,4-dioxane (28 ml) and an aqueous saturated solution OfNaHCO 3 (24 ml).
- the resulting solution was degassed using a stream of nitrogen and Pd(PPh 3 ) 4 (0.747 g, 0.647 mmol) was added to this solution.
- the reaction was then microwaved in a sealed tube at 140 0 C for 5 minutes.
- the resulting cooled reaction mixture was then diluted with EtOAc and filtered through a pad of diatomaceous earth.
- the filtrate was collected, dried over Na 2 SO 4 and concentrated in vacuo.
- the crude reaction mixture was then purified by column chromatography (silica gel; DCM to DCM/EtOAc up to 6% as eluent). The desired fractions were collected and evaporated in vacuo to yield D21 (4.04 g, 98 %).
- Methyl 4-bromo-3-fluorobenzoate (2.261 g, 9.702 mmol) [CAS 849758-12-9] was added to a solution of l,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)-pyridine (3 g, 9.702 mmol) [CAS 375853-82-0] (synthesis described in WO 2004072025 A2 20040826) in 1,4-dioxane (21 ml) and an aqueous saturated solution of NaHCO 3 (18 ml).
- the resulting solution was degassed using a stream of nitrogen and Pd(P Ph 3 ) 4 (0.561 g, 0.485 mmol) was added to this solution.
- the reaction was then microwaved in a sealed tube at 150 0 C for 5 minutes.
- the resulting cooled reaction mixture was then diluted with EtOAc and filtered through a pad of diatomaceous earth.
- the filtrate was collected, dried over Na 2 SO 4 and concentrated in vacuo.
- the crude reaction mixture was then purified by column chromatography (silica gel; DCM to DCM/EtOAc up to 6% as eluent). The desired fractions were collected and evaporated in vacuo to yield D22 (2.107 g, 65 %).
- intermediate D34 1.0 g, 3.38 mmol
- a catalytic amount of 10% palladium on activated carbon in ethanol (150 ml) was stirred under a hydrogen atmosphere for 2 hours.
- the mixture was filtered through diatomaceous earth and the solvent was evaporated in vacuo to yield intermediate D35 (0.69 g, 100 %) that was used without further purification.
- HPLC measurement was performed using a HP 1100 from Agilent
- a pump quadrature or binary
- degasser a pump with degasser, an autosampler, a column oven, a diode-array detector (DAD) and a column as specified in the respective methods below.
- Flow from the column was split to a MS spectrometer.
- the MS detector was configured with an electrospray ionization source. Nitrogen was used as the nebulizer gas. The source temperature was maintained at 140 0 C. Data acquisition was performed with MassLynx-Openlynx software.
- Reversed phase HPLC was carried out on an XDB-C18 cartridge (1.8 ⁇ m, 2.1 x 30 mm) from Agilent, with a flow rate of 1 ml/min, at 60 0 C.
- the gradient conditions used are: 90 % A (0.5 g/1 ammonium acetate solution), 5 % B (acetonitrile), 5 % C (methanol) to 50 % B and 50 % C in 6.5 minutes, to 100 % B at 7 minutes and equilibrated to initial conditions at 7.5 minutes until 9.0 minutes. Injection volume 2 ⁇ l.
- High-resolution mass spectra (Time of Flight, TOF) were acquired only in positive ionization mode by scanning from 100 to 750 in 0.5 seconds using a dwell time of 0.1 seconds.
- the capillary needle voltage was 2.5 kV and the cone voltage was 20 V.
- Leucine-Enkephaline was the standard substance used for the lock mass calibration.
- Reversed phase HPLC was carried out on an ACE-C 18 column (3.0 ⁇ m, 4.6 x 30 mm) from Advanced Chromatography Technologies, with a flow rate of 1.5 ml/min, at 40 0 C.
- the gradient conditions used are: 80 % A (0.5 g/1 ammonium acetate solution), 10 % B (acetonitrile), 10 % C (methanol) to 50 % B and 50 % C in 6.5 minutes, to 100 % B at 7 minutes and equilibrated to initial conditions at 7.5 minutes until 9.0 minutes. Injection volume 5 ⁇ l.
- High-resolution mass spectra (Time of Flight, TOF) were acquired only in positive ionization mode by scanning from 100 to 750 in 0.5 seconds using a dwell time of 0.1 seconds.
- the capillary needle voltage was 2.5 kV for positive ionization mode and the cone voltage was 20 V.
- Leucine-Enkephaline was the standard substance used for the lock mass calibration.
- XDB-Cl 8 cartridge (1.8 ⁇ m, 2.1 x 30 mm) from Agilent, with a flow rate of
- the gradient conditions used are: 90 % A (0.5 g/1 ammonium acetate solution), 10 % B (mixture of Acetonitrile/ Methanol, 1/1), to 100 % B in 6.0 minutes, kept till 6.5 minutes and equilibrated to initial conditions at 7.0 minutes until
- the capillary needle voltage was 3 kV and the cone voltage was 20 V.
- Reversed phase HPLC was carried out on a Sunfire-C18 column (2.5 ⁇ m, 2.1 x 30 mm) from Waters, with a flow rate of 1.0 ml/min, at 60 0 C.
- the gradient conditions used are: 95 % A (0.5 g/1 ammonium acetate solution + 5% of acetonitrile), 2.5 % B (acetonitrile), 2.5 % C (methanol) to 50 % B and 50 % C in 6.5 minutes, kept till 7 minutes and equilibrated to initial conditions at 7.3 minutes until 9.0 minutes. Injection volume 2 ⁇ l.
- High-resolution mass spectra (Time of Flight, TOF) were acquired by scanning from 100 to 750 in 0.5 seconds using a dwell time of 0.3 seconds.
- the capillary needle voltage was 2.5 kV for positive ionization mode and 2.9 kV for negative ionization mode.
- the cone voltage was 20 V for both positive and negative ionization modes.
- Leucine-Enkephaline was the standard substance used for the lock mass calibration.
- Reversed phase HPLC was carried out on a BEH- Cl 8 column (1.7 ⁇ m, 2.1 x 50 mm) from Waters, with a flow rate of 0.8 ml/min, at 6O 0 C without split to the MS detector.
- the gradient conditions used are: 95 % A (0.5 g/1 ammonium acetate solution + 5 % acetonitrile), 5 % B (mixture of acetonitrile / methanol, 1/1), to 20 % A, 80 % B in 4.9 minutes, to 100 % B in 5.3 minutes, kept till 5.8 minutes and equilibrated to initial conditions at 6.0 minutes until 7.0 minutes.
- Injection volume 0.5 ⁇ l.
- the gradient conditions used are: 90 % A (0.5 g/1 ammonium acetate solution), 5 % B (acetonitrile), 5 % C (methanol), kept 0.2 minutes, to 50 % B, 50 % C in 3.5 minutes, kept till 3.65 minutes and equilibrated to initial conditions at 3.8 minutes until 5.0 minutes. Injection volume 2 ⁇ l.
- High-resolution mass spectra (Time of Flight, TOF) were acquired by scanning from 100 to 750 in 0.5 seconds using a dwell time of 0.3 seconds.
- the capillary needle voltage was 2.5 kV for positive ionization mode and 2.9 kV for negative ionization mode.
- the cone voltage was 20 V for both positive and negative ionization modes.
- Leucine-Enkephaline was the standard substance used for the lock mass calibration.
- melting points For a number of compounds, melting points were determined in open capillary tubes on a Mettler FP62 apparatus. Melting points were measured with a temperature gradient of 3 or 10 °C/minute. Maximum temperature was 300 0 C. The melting point was read from a digital display and were obtained with experimental uncertainties that are commonly associated with this analytical method.
- Table 1 lists compounds of Formula (I) that were prepared according to one of the above Examples.
- the compounds provided in the present invention are positive allosteric modulators of mGluR2. These compounds appear to potentiate glutamate responses by binding to an allosteric site other than the glutamate binding site.
- the response of mGluR2 to a concentration of glutamate is increased when compounds of Formula (I) are present.
- Compounds of Formula (I) are expected to have their effect substantially at mGluR2 by virtue of their ability to enhance the function of the receptor.
- Table 3 The behaviour of positive allosteric modulators tested at mGluR2 using the [ 35 S]GTPyS binding assay method described below and which is suitable for the identification of such compounds, and more particularly the compounds according to Formula (I), are shown in Table 3.
- the [ 35 S]GTPyS binding assay is a functional membrane-based assay used to study G-protein coupled receptor (GPCR) function whereby incorporation of a non-hydrolysable form of GTP, [ 35 S]GTPyS (guanosine 5 '-triphosphate, labelled with gamma-emitting 35 S), is measured.
- GPCR G-protein coupled receptor
- the G-protein ⁇ subunit catalyzes the exchange of guanosine 5 '-diphosphate (GDP) by guanosine triphosphate (GTP) and on activation of the GPCR by an agonist, [ 35 S]GTP ⁇ S, becomes incorporated and cannot be cleaved to continue the exchange cycle (Harper (1998) Current Protocols in Pharmacology 2.6.1-10, John Wiley & Sons, Inc.).
- the amount of radioactive [ 35 S]GTPyS incorporation is a direct measure of the activity of the G-protein and hence the activity of the agonist can be determined.
- MGluR2 receptors are shown to be preferentially coupled to G ⁇ l-protein, a preferential coupling for this method, and hence it is widely used to study receptor activation of mGluR2 receptors both in recombinant cell lines and in tissues (Schaffhauser et al 2003, Pinkerton et al, 2004, Mutel et al (1998) Journal of Neurochemistry. 71 :2558-64; Schaffhauser et al (1998) Molecular Pharmacology 53:228-33).
- CHO-cells were cultured to pre-confluence and stimulated with 5 mM butyrate for 24 hours, prior to washing in PBS, and then collected by scraping in homogenisation buffer (50 mM Tris-HCl buffer, pH 7.4, 4°C).
- homogenisation buffer 50 mM Tris-HCl buffer, pH 7.4, 4°C.
- Cell lysates were homogenized briefly (15s) using an ultra- turrax homogenizer. The homogenate was centrifuged at 23 500 x g for 10 minutes and the supernatant discarded. The pellet was resuspended in 5 mM Tris-HCl, pH 7.4 and centrifuged again (30 000 x g, 20 min, 4°C).
- the final pellet was resuspended in 50 mM HEPES, pH 7.4 and stored at— 80°C in appropriate aliquots before use. Protein concentration was determined by the Bradford method (Bio-Rad, USA) with bovine serum albumin as standard.
- Measurement of mGluR2 positive allosteric modulatory activity of test compounds in membranes containing human mGluR2 was performed using frozen membranes that were thawed and briefly homogenized prior to pre-incubation in 96-well microplates (15 ⁇ g/assay well, 30 minutes, 30°C) in assay buffer (50 mM HEPES pH 7.4, 100 mM NaCl, 3 mM MgCl 2 , 50 ⁇ M GDP, 10 ⁇ g/ml saponin,) with increasing concentrations of positive allosteric modulator (from 0.3 n ⁇ Vl to 50 ⁇ M) and either a minimal pre-determined concentration of glutamate (PAM assay), or no added glutamate.
- assay buffer 50 mM HEPES pH 7.4, 100 mM NaCl, 3 mM MgCl 2 , 50 ⁇ M GDP, 10 ⁇ g/ml saponin
- membranes were pre-incubated with glutamate at EC 25 concentration, i.e. a concentration that gives 25 % of the maximal response glutamate, and is in accordance to published data (Pin et al. (1999) Eur. J. Pharmacol. 375:277-294).
- EC 25 concentration i.e. a concentration that gives 25 % of the maximal response glutamate
- microplates were shaken briefly and further incubated to allow [ 35 S]GTPyS incorporation on activation (30 minutes, 30 0 C).
- the EC 50 is the concentration of a compound that causes a half-maximal potentiation of the glutamate response.
- Potato starch ad 200 mg active ingredient can be replaced with the same amount of any of the compounds according to the present invention, in particular by the same amount of any of the exemplified compounds.
- An aqueous suspension is prepared for oral administration so that each 1 milliliter contains 1 to 5 mg of one of the active compounds , 50 mg of sodium carboxymethyl cellulose, 1 mg of sodium benzoate, 500 mg of sorbitol and water ad 1 ml.
- a parenteral composition is prepared by stirring 1.5 % by weight of active ingredient of the invention in 10% by volume propylene glycol in water.
- active ingredient can be replaced with the same amount of any of the compounds according to the present invention, in particular by the same amount of any of the exemplified compounds.
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Abstract
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MX2010002536A MX2010002536A (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4'] bipyridinyl-2'-ones. |
US12/677,618 US9114138B2 (en) | 2007-09-14 | 2008-09-12 | 1′,3′-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1′H-[1,4′] bipyridinyl-2′-ones |
AT08802105T ATE496906T1 (en) | 2007-09-14 | 2008-09-12 | 1',3'-DISUBSTITUTED 4-PHENYL-3,4,5,6-TETRAHYDRO-2H,1'H-Ä1,4'ÜBIPYRI INYL-2'-ONE |
NZ584145A NZ584145A (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1,4'] bipyridinyl-2'-ones |
DE602008004794T DE602008004794D1 (en) | 2007-09-14 | 2008-09-12 | 1 ', 3'-DISUBSTITUTED 4-PHENYL-3,4,5,6-TETRAHYDRO-2H, 1'H-Ä1,4'-UPBIPYRIDINYL-2'-ONE |
EA201000314A EA017648B1 (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones |
SI200830204T SI2203439T1 (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-y1, 4' bipyridinyl-2'-ones |
DK08802105.0T DK2203439T3 (en) | 2007-09-14 | 2008-09-12 | 1 ', 3'-disubstituted 4-phenyl-3,4,5,6-tetrahydro-2H, 1'H- [1,4'] - bipyridinyl-2'-one |
KR1020107008034A KR101533440B1 (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1'H-[1,4']bipyridinyl-2'-ones |
BRPI0816767A BRPI0816767B8 (en) | 2007-09-14 | 2008-09-12 | compound 4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-disubstituted 1',3'-ones, pharmaceutical composition and use of same |
AU2008297878A AU2008297878B2 (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H, 1'H-[1, 4'] bipyridinyl-2'-ones |
JP2010524405A JP5133416B2 (en) | 2007-09-14 | 2008-09-12 | 1 ', 3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H, 1'H- [1,4'] bipyridinyl-2'-one |
CA2696948A CA2696948C (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones |
CN2008801071350A CN101801951B (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4'] bipyridinyl-2'-ones |
KR1020147000745A KR101520086B1 (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1'H-[1,4']bipyridinyl-2'-ones |
PL08802105T PL2203439T3 (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-ý1, 4'¨bipyridinyl-2'-ones |
EP08802105A EP2203439B1 (en) | 2007-09-14 | 2008-09-12 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-ý1, 4'¨bipyridinyl-2'-ones |
ZA2010/01151A ZA201001151B (en) | 2007-09-14 | 2010-02-17 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h-1'h-[1,4']bipyridinyl-2'-ones |
IL204032A IL204032A (en) | 2007-09-14 | 2010-02-18 | Compounds of 1',3' - disubstituted - 4 - phenyl- 3, 4, 5, 6 - tetrahydro - 2h, 1'h - [1, 4'] bipyridinyl - 2' - ones, compositions comprising them and uses thereof |
HK10110487.7A HK1143820A1 (en) | 2007-09-14 | 2010-11-10 | |
HR20110278T HRP20110278T1 (en) | 2007-09-14 | 2011-04-15 | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4']bipyridinyl-2'-ones |
US13/827,198 US20130196992A1 (en) | 2007-09-14 | 2013-03-14 | 1',3'-disubstituted-4-pheny-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones |
US13/803,267 US9132122B2 (en) | 2007-09-14 | 2013-03-14 | 1′,3′-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1′H-[1,4′]bipyridinyl-2′-ones |
IL229304A IL229304A (en) | 2007-09-14 | 2013-11-07 | 1',3'-disubstituted- 4- phenyl- 3, 4, 5, 6 -tetrahydro-2h, 1'h - [1, 4'] bipyridinyl- 2'-ones, pharmaceutical compositions comprising them and uses thereof |
US14/817,676 US20150336930A1 (en) | 2007-09-14 | 2015-08-04 | 1',3'-Disubstituted-4-Phenyl-3,4,5,6-Tetrahydro-2H,1'H-[1,4']Bipyridinyl-2'-Ones |
US16/601,431 US11071729B2 (en) | 2007-09-14 | 2019-10-14 | 1′,3′-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1′H-[1,4′]bipyridinyl-2′-ones |
US17/354,194 US20220000856A1 (en) | 2007-09-14 | 2021-06-22 | 1',3'-Disubstituted-4-Phenyl-3,4,5,6-Tetrahydro-2H,1'H-[1,4']Bipyridinyl-2'-Ones |
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US12/677,618 A-371-Of-International US9114138B2 (en) | 2007-09-14 | 2008-09-12 | 1′,3′-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1′H-[1,4′] bipyridinyl-2′-ones |
US13/827,198 Continuation US20130196992A1 (en) | 2007-09-14 | 2013-03-14 | 1',3'-disubstituted-4-pheny-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones |
US13/803,267 Continuation US9132122B2 (en) | 2007-09-14 | 2013-03-14 | 1′,3′-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1′H-[1,4′]bipyridinyl-2′-ones |
US13/803,267 Division US9132122B2 (en) | 2007-09-14 | 2013-03-14 | 1′,3′-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2H,1′H-[1,4′]bipyridinyl-2′-ones |
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