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 PDF

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Publication number
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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WIPO (PCT)
Prior art keywords
disorder
disorders
mmol
formula
nervous system
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PCT/EP2008/007551
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French (fr)
Inventor
José Maria Cid-Nunez
Andrés Avelino TRABANCO-SUAREZ
Gregor James Macdonald
Guillaume Albert Jacques Duvey
Robert Johannes LÜTJENS
Terry Patrick Finn
Original Assignee
Ortho-Mcneil-Janssen Pharmaceuticals, Inc.
Addex Pharma S.A.
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Priority to CN2008801071350A priority Critical patent/CN101801951B/en
Priority to DE602008004794T priority patent/DE602008004794D1/en
Priority to KR1020147000745A priority patent/KR101520086B1/en
Priority to NZ584145A priority patent/NZ584145A/en
Priority to PL08802105T priority patent/PL2203439T3/en
Priority to EA201000314A priority patent/EA017648B1/en
Priority to SI200830204T priority patent/SI2203439T1/en
Priority to DK08802105.0T priority patent/DK2203439T3/en
Priority to KR1020107008034A priority patent/KR101533440B1/en
Priority to BRPI0816767A priority patent/BRPI0816767B8/en
Priority to AU2008297878A priority patent/AU2008297878B2/en
Priority to EP08802105A priority patent/EP2203439B1/en
Priority to CA2696948A priority patent/CA2696948C/en
Application filed by Ortho-Mcneil-Janssen Pharmaceuticals, Inc., Addex Pharma S.A. filed Critical Ortho-Mcneil-Janssen Pharmaceuticals, Inc.
Priority to AT08802105T priority patent/ATE496906T1/en
Priority to US12/677,618 priority patent/US9114138B2/en
Priority to JP2010524405A priority patent/JP5133416B2/en
Priority to MX2010002536A priority patent/MX2010002536A/en
Publication of WO2009033704A1 publication Critical patent/WO2009033704A1/en
Priority to ZA2010/01151A priority patent/ZA201001151B/en
Priority to IL204032A priority patent/IL204032A/en
Priority to HK10110487.7A priority patent/HK1143820A1/xx
Priority to HR20110278T priority patent/HRP20110278T1/en
Priority to US13/827,198 priority patent/US20130196992A1/en
Priority to US13/803,267 priority patent/US9132122B2/en
Priority to IL229304A priority patent/IL229304A/en
Priority to US14/817,676 priority patent/US20150336930A1/en
Priority to US16/601,431 priority patent/US11071729B2/en
Priority to US17/354,194 priority patent/US20220000856A1/en

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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

The present invention relates to novel compounds, in particular novel pyridinone derivatives according to Formula (I) wherein all radicals are as defined in the application and claims. The compounds according to the invention are positive allosteric modulators of metabotropic receptors - subtype 2 ('mGluR2') which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. In particular, such diseases are central nervous system disorders selected from the group of anxiety, schizophrenia, migraine, depression, and epilepsy. The invention is also directed to pharmaceutical compositions and processes to prepare such compounds and compositions, as well as to the use of such compounds for the prevention and treatment of such diseases in which mGluR2 is involved.

Description

lS3'-DISUBSTITUTED-4-PHENYL-3,4,5,6-TETRAHYDRO-2#,777- /1,41IBIPYRIDINYL-I1 ONES
Field of the Invention
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.
Background of the Invention
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.
In addition, glutamate activates metabotropic glutamate receptors (mGluRs) which have a more modulatory role that contributes to the fine-tuning of synaptic efficacy.
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 Gαi-protein, and its activation leads to inhibition of glutamate release in the synapse. In the central nervous system (CNS), 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. In addition, 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.
To date, most of the available pharmacological tools targeting mGluRs are orthosteric ligands which activate several members of the family as they are structural analogs of glutamate.
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.
Positive allosteric modulators of mGluRs have emerged recently as novel pharmacological entities offering this attractive alternative. Various compounds have been described as mGluR2 positive allosteric modulators. WO2004/092135 (NPS &
Astra Zeneca), WO2004/018386, WO2006/014918 and WO2006/015158 (Merck),
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.
None of the specifically disclosed compounds therein are structurally related to the compounds of the present invention.
It was demonstrated that such compounds do not activate the receptor by themselves. Rather, they enable the receptor to produce a maximal response to a concentration of glutamate which by itself induces a minimal response. Mutational analysis has demonstrated Unequivocally that the binding of mGluR2 positive allosteric modulators does not occur at the orthosteric site, but instead at an allosteric site situated within the seven transmembrane region of the receptor.
Animal data are suggesting that positive 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).
Recent animal studies further reveal that the selective positive allosteric modulator of metabotropic glutamate receptor subtype 2 biphenyl-indanone (BINA) blocks a hallucinogenic drug model of psychosis, supporting the strategy of targeting mGluR2 receptors for treating glutamatergic dysfunction in schizophrenia. (MoI.
Pharmacol. 2007, 72, 477-484).
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.
Detailed description of the Invention
The present invention relates to compounds having metabotropic glutamate receptor 2 modulator activity, said compounds having the Formula (I)
Figure imgf000004_0001
and the stereochemically isomeric forms thereof, wherein
R is Ci-6alkyl; or Ci-3alkyl substituted with C3-7cycloalkyl, phenyl, or phenyl substituted with halo, trifluoromethyl or trifluoromethoxy;
R2 is halo, trifluoromethyl, Ci^alkyl or cyclopropyl;
R3 is hydrogen, fluoro, hydroxyl, hydroxyCi-3alkyl, hydroxyCi.3alkyloxy, fluoroCi.3alkyl, fluoroC1-3alkyloxy or cyano; and
Ar is unsubstituted phenyl; or phenyl substituted with n radicals R4, wherein n is 1, 2 or 3;
R4 is selected from the group consisting of hydrogen, halo, C1.3a.kyl, hydroxyCi-3alkyl, polyhaloCi^alkyl , cyano, hydroxyl, amino, carboxyl, Ci-3alkyloxyCi-3alkyl, Ci-3alkyloxy, polyhaloCi-3alkyloxy, Cj-3alkylcarbonyl, mono- and di(Ci-3alkyl)amino, and moφholinyl; or two vicinal R4 radicals taken together form a bivalent radical of formula
-N-CH-NH- (a), -CH=CH-NH- (b), or
-0-CH2-CH2-NH- (c); or R and a R4 radical in ortho position taken together form a bivalent radical of formula
-CH2-O- (d), or
-0-CH2- (e); and the pharmaceutically acceptable salts and solvates thereof.
In one embodiment, the invention relates to a compound of Formula (I) or a stereochemically isomeric form thereof wherein
R1 is C1-6alkyl; or Ci-3alkyl substituted with C3-7cycloalkyl, phenyl, or phenyl substituted with halo, trifluoromethyl or trifluoromethoxy; R2 is halo, trifluoromethyl, Ci-3alkyl or cyclopropyl; R3 is hydrogen, fluoro, hydroxyl, hydroxyCi-3alkyl, hydroxyCi-3alkyloxy, fluoroCi-3alkyl, fluoroCi-3alkyloxy or cyano; and
Ar is unsubstituted phenyl, or phenyl substituted with n radicals R4, wherein n is 1, 2 or 3;
R4 is selected from the group consisting of hydrogen, halo ; Ci-3alkyl ; hydroxyCi-3alkyl, polyhaloC].3alkyl ; cyano ; hydroxy ; amino ; carboxyl ; Ci-3alkyloxyCi-3alkyl ; C)-3alkyloxy ; polyhaloCi-3alkyloxy; Ci-3alkylcarbonyl ; mono- and di(Ci-3alkyl)amino, and morpholinyl ; or two vicinal R4 radicals taken together form a bivalent radical of formula -N=CH-NH- (a), -CH=CH-NH- (b), or
-0-CH2-CH2-NH- (c); and the pharmaceutically acceptable salts and solvates thereof.
In one embodiment, the invention relates to a compound according to Formula (I) or a stereochemically isomeric form thereof, wherein R1 is 1 -butyl, 2-methyl-l -propyl, 3-methyl-l -butyl, (cyclopropyl)methyl or 2-
(cyclopropyl)- 1 -ethyl ; R2 is chloro, bromo, cyclopropyl or trifluoromethyl; R3 is hydrogen, fluoro or cyano; and Ar is unsubstituted phenyl; or phenyl substituted with halo, trifluoromethyl, morpholinyl or hydroxyCi-3alkyl; or a pharmaceutically acceptable salt or solvate thereof.
In one embodiment, the invention relates to a compound according to Formula
(I) or a stereochemically isomeric form thereof, wherein
R1 is 1-butyl, 3-methyl-l -butyl, (cyclopropyl)methyl or 2-(cyclopropyl)-l -ethyl; R2 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.
In one embodiment the invention relates to the compound
3'-Chloro-r-cyclopropylmethyl-4-phenyl-3,4,5,6-tetrahydro-2H,i 'H-[l,4']bipyridinyl- 2'-one (El) or l'-Butyl-3'-chloro-4-phenyl-3,4,5,6-tetrahydro-2H,; 'H-[l,4l]bipyridinyl-2'-one (E2).
The notation Ci-3alkyl 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.
The notation Ci-6alkyl 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 C3-7cycloalkyl 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.
For therapeutic use, salts of the compounds of formula (I) are those wherein the counterion is pharmaceutically acceptable. However, 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.
Conversely said 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.
Conversely, said salt forms can be converted into the free acid forms by treatment with an appropriate acid.
The term solvate comprises the solvent addition forms as well as the salts thereof, which the compounds of formula (I) are able to form. Examples of such solvent addition forms are e.g. hydrates, alcoholates and the like.
The term "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. Thus, when a compound of formula (I) is for instance specified as (R), this means that the compound is substantially free of the (S) isomer. Stereogenic centers may have the R- or S-configuration; substituents on bivalent cyclic (partially) saturated radicals may have either the cis- or trans-configuration.
Following CAS nomenclature conventions, when two stereogenic centers of known absolute configuration are present in a compound, 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. For example, if the lowest-numbered chiral center in the compound has an S configuration and the second center is R, the stereo descriptor would be specified as S-[R*,S*]. If "α" and "β" are used : 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 "α" 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 "α", if it is on the same side of the mean plane determined by the ring system, or "β", if it is on the other side of the mean plane determined by the ring system.
In the framework of this application, an element, in particular when mentioned in relation to a compound according to Formula (I), comprises all isotopes and isotopic mixtures of this element, either naturally occurring or synthetically produced, either with natural abundance or in an isotopically enriched form. Radiolabeled compounds of Formula (I) may comprise a radioactive isotope selected from the group of 3H, 11C, 18F, 122I, 123I, 125I, 131I, 75Br, 76Br, 77Br and 82Br. Preferably, the radioactive isotope is selected from the group of 3H, 1 1C and 18F.
Preparation The compounds according to the invention can generally be prepared by a succession of steps, each of which is known to the skilled person. In particular, 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.
A. Preparation of the final compounds
Experimental procedure 1
The compounds according to Formula (I), in the case of R2 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. In reaction scheme (1), R2 is halogen and all other variables are defined as in Formula (I).
Reaction Scheme 1
Λ/-halosuccinimide
Figure imgf000009_0002
R2 = halogen
Experimental procedure 2 Alternatively, compounds according to Formula (I) can be prepared by reacting an intermediate of Formula (III) with an intermediate of Formula (IV), which can be either commercially available or may be synthesized by procedures well known to anyone skilled in the art, according to reaction scheme (2). 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] (B MAP), heating for a suitable period of time that allows the completion of the reaction, for example at 100 0C for 16 hours in a sealed tube. In reaction scheme (2), Za 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).
Reaction Scheme 2
Figure imgf000010_0001
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.
Additionally, compounds according to Formula (I) can be prepared by a skilled person using art known procedures by further modifications of compounds of Formula (I):
- Alkylation of compounds of Formula (I) that contain in their structure one or more hydroxy-substituents with a suitable alkylating agent such as for example 2- fluorethyl tosylate under thermal conditions using a suitable base such as for example sodium hydride, in a suitable reaction-inert solvent such as, for example
1 ,2-dimethoxyethane or dimethylformamide.
- Fluorination of compounds of Formula (I) that contain in their structure one or more hydroxy-substituents with a suitable fluorinating agent, such as for example (diethylamino)sulfur trifluoride. This reaction may 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 0C to 30 0C during, for example, 0.5 to 12 hours. - Reaction of compounds of Formula (I) that contain in their structure one or more hydroxy-substituents with an alcohol derivative by using a suitable coupling system such as, for example, di-tert-butylazodicarboxylate/triphenylphosphine under thermal conditions.
B. Preparation of the intermediates
Experimental procedure 3
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 1000C for 16 hours in a sealed tube. In reaction scheme (3), all variables are defined as in Formula (I).
Reaction Scheme 3
Figure imgf000011_0001
Experimental procedure 4
Intermediates of Formula (III-a) and (III-b) can be prepared by reacting an intermediate of Formula (VI), wherein Y is H or R2 (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 0C, for a suitable period of time that allows the completion of the reaction, for instance 1 hour. In reaction scheme (4), variable R1 is defined as in Formula (I). Reaction Scheme 4
"halogenating agent"
Figure imgf000012_0001
Figure imgf000012_0002
(lll-a): Y = R2
(Vl) (Ml-b): Y = H
Experimental procedure 5
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 0C. In reaction scheme (5), all variables are defined as in Formula (I).
Reaction Scheme 5
Figure imgf000012_0003
(V'-a) (III-c)
Experimental procedure 6
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. In reaction scheme (6), variable R1 is defined as in Formula (I). Reaction Scheme 6
Figure imgf000013_0001
(Vll-a): Y = H, Y = H, CF3, C^alkyl or cyclopropyl (Vll-b): Y = CF3,
(Vll-c): Y = C^alkyl or cyclopropyl
Experimental procedure 7
Alternatively, 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 0C for 30 minutes under microwave irradiation. In reaction scheme (7), variable R1 is defined as in Formula (I).
Reaction Scheme 7
Figure imgf000013_0002
(VII-d): Y = Halogen Y = Halogen
Experimental procedure 8
Intermediates of Formula (VII-a) can be prepared by art known procedures by reacting commercially available 4-benzyloxy-iH-pyridin-2-one with a commercially available alkylating agent of Formula (VIII), in which Zb is a suitable leaving group, using a base such as, for example, K2CO3, and, optionally an iodine salt such as, for example, KI, in an inert solvent such as, for example, acetonitrile or DMF, at a moderately high temperature such as, for example, 80-120 0C, for a suitable period of time that allows the completion of the reaction, for example 16 hours. In reaction scheme (8), variable R1 is defined as in Formula (I) and Zb is a suitable leaving group such as, for example, halogen. Reaction Scheme 8
Figure imgf000014_0001
Experimental procedure 9
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 1000C for 5 hours. In reaction scheme (9), variable R1 is defined as in Formula (I).
Reaction Scheme 9
Figure imgf000014_0002
(VII-e), wherein Y = I
Experimental procedure 10
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- (ΝCS), N-bromo- (ΝBS) or N-iodosuccinimide (ΝIS), in a suitable reaction-inert solvent such as, for example, DMF, dichloromethane or acetic acid, typically at room temperature for 1 to 24 hours. In reaction scheme (10), variable R1 is defined as in Formula (I).
Reaction Scheme 10
Figure imgf000014_0003
Experimental procedure 11
Intermediates of Formula (VII-c) can be prepared by reacting an intermediate of Formula (VII-d) with a Ci-3alkyl- 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 0C for 20 minutes under microwave irradiation. In reaction scheme (11), variable R1 is defined as in Formula (I).
Reaction Scheme 11
Figure imgf000015_0001
, r (VII-d) (VII-c): Y = C^alkyl or cyclopropyl
Experimental procedure 12
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). In reaction scheme (12), all variables are defined as in formula (I).
Reaction Scheme (12)
"acidic hydrolysis" or basic hydrolysis or "hydrogenation"
Figure imgf000015_0002
Figure imgf000015_0003
25 (IX) (IV) Experimental procedure 13
Intermediates of formula (IV-a) can be prepared by hydrogenation of an intermediate of formula (X) applying art known procedures, according to reaction scheme (13). In reaction scheme (13), Ar is defined as in formula (I).
Reaction Scheme (13)
"hydrogenation"
Figure imgf000016_0002
Figure imgf000016_0001
(X) (IV-a)
Experimental procedure 14
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). In reaction scheme (14), Ar is defined as in Formula (I).
Reaction Scheme (14) "hydrogenation"
Figure imgf000016_0004
Figure imgf000016_0003
(Xl) (IX-a)
Experimental procedure 15
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). In reaction scheme (15), Ar is defined as in formula (I). Reaction Scheme (15)
"acidic hydrolysis" or basic hydrolysis" or X "hydrogenation"
Figure imgf000017_0002
Figure imgf000017_0001
(Xl) (X)
Experimental procedure 16
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 NaHCO3 or Na2CO3, a suitable catalyst, such as for example a Pd-complex catalyst such as, for example,
Pd(PPh3)4i under thermal conditions such as, for example, heating the reaction mixture at 150 0C under microwave irradiation, during, for example, 10 minutes. In reaction scheme (16), all variables are defined as in formula (I); Zc 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 R4 and R5 are hydrogen or
Figure imgf000017_0003
or may be taken together to form for example a bivalent radical of formula -CH2CH2-, -CH2CH2CH2-, or -C(CH3)2C(CH3)2-.
Reaction Scheme (16)
Figure imgf000017_0004
(XIIi) (Xi)
Experimental procedure 17
Intermediates of formula (IV) wherein R3 represents fluoro or Ci-3alkyl substituted with fluoro, said R3 being represented by -Li-F wherein Li represents Ci-3alkyl 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). 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 0C to 30 0C 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. In reaction scheme (17), Ar is defined as in formula (I).
Reaction Scheme (17)
H
Figure imgf000018_0001
(IX-b) (IX-c) (IV-b)
Experimental procedure 18
Intermediates of formula (IV) wherein R3 represents C1-3alkyloxy substituted with fluoro, said Ci-3alkyloxy being represented by Q, said R3 being represented by -Q-F, and said intermediates being represented by formula (IV-d), can be prepared by art known procedures by reacting a hydroxyl-substituted intermediate of formula (IX-d) 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 (diethylamino)sulfur trifluoride , resulting in an intermediate of formula (IX-e) according to reaction scheme (18) step (a). The 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 0C to 30 0C 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. In reaction scheme (18), Ar is defined as in formula (I).
Reaction Scheme (18)
Figure imgf000019_0001
(IX-d) (IX-e) (IV-d)
Experimental procedure 19
Intermediates of formula (IX-b) wherein Ll represents CH2, said intermediates being represented by formula (IX-f), 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 0C. In reaction scheme (19) Ar is defined as in formula (I)
Reaction Scheme (19)
Figure imgf000019_0002
(XIV)
The starting materials according to Formulas (VIII), (IX-b), (IX-d), (XII), (XIII) and XIV are either commercially available or may be prepared according to conventional reaction procedures generally known by those skilled in the art. Pharmacology
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. In the presence of glutamate or an agonist of mGluR2, 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. Hence, 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.
Also, 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. Where 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. treatment of a mammal, comprising administering to a mammal in need of such e.g. treatment, an effective amount of a compound or composition according to the invention. In particular, 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 products, alcohol, benzodiazepines, cocaine, sedatives, hypnotics, etc.), psychosis, schizophrenia, anxiety (including generalized anxiety disorder, panic disorder, and obsessive compulsive disorder), mood disorders (including depression, mania, bipolar disorders), trigeminal neuralgia, hearing loss, tinnitus, macular degeneration of the eye, emesis, brain edema, pain (including acute and chronic states, severe pain, intractable pain, neuropathic pain, and post-traumatic pain), tardive dyskinesia, sleep disorders (including narcolepsy), attention deficit/hyperactivity disorder, and conduct disorder.
In particular, the 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.
Preferably, 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.
Preferably, 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 Preferably, the central nervous system disorder is a personality disorder selected from the group of obsessive-compulsive personality disorder and schizoid, schizotypal disorder.
Preferably, 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.
Preferably, the central nervous system disorder is an eating disorder selected from the group of anorexia nervosa and bulimia nervosa.
Preferably, 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.
Preferably, the central nervous system disorder is migraine. Preferably, 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. Preferably, the central nervous system disorder is attention-deficit/hyperactivity disorder.
Preferably, 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.
Of the disorders mentioned above, the treatment of anxiety, schizophrenia, migraine, depression, and epilepsy are of particular importance.
At present, the fourth edition of the Diagnostic & Statistical Manual of Mental Disorders (DSM-IV) of the American Psychiatric Association provides a diagnostic tool for the identification of the disorders described herein. 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.
Because positive allosteric modulators of mGluR2, including compounds of Formula (I), enhance the response of mGluR2 to agonists, it is understood that 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.
Pharmaceutical compositions
The invention also relates to 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. As appropriate compositions there may be cited all compositions usually employed for systemically administering drugs.
To prepare the pharmaceutical 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. These pharmaceutical compositions are desirable in unitary dosage form suitable, in particular, for administration orally, rectally, percutaneously, by parenteral injection or by inhalation. For example, in preparing the compositions in oral dosage form, 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. Because of the ease in administration, oral administration is preferred, and tablets and capsules represent the most advantageous oral dosage unit forms in which case solid pharmaceutical carriers are obviously employed. For parenteral compositions, 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. Also included are solid form preparations that are intended to be converted, shortly before use, to liquid form preparations. In the compositions suitable for percutaneous administration, 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.
It is especially advantageous to formulate the aforementioned pharmaceutical compositions in unit dosage form for ease of administration and uniformity of dosage. Unit dosage form as used herein 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. Examples of such 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.
Depending on the mode of administration, 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.
As already mentioned, the invention also relates to 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.
The following examples are intended to illustrate but not to limit the scope of the present invention.
Chemistry
Several methods for preparing the compounds of this invention are illustrated in the following Examples. Unless otherwise noted, all starting materials were obtained from commercial suppliers and used without further purification. Hereinafter, "THF" means 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[diphenylphosphine]; MeOH means methanol; "q.s." means quantum sufficit; "M.P." means melting point;
Microwave assisted reactions were performed in a single-mode reactor:
IInniittiiaattoorr™™ SSiixxttyy EEXXPP mmiiccrroowwaavvee rreeaaccttoorr (Biotage AB), or in a multimode reactor: MicroSYNTH Labstation (Milestone, Inc.).
Description 1 4-Benzyloxy-l-cyclopropylmethyl-i/y-pyridin-2-one (Dl)
Figure imgf000026_0001
Bromomethyl-cyclopropane (3.68 g, 27.33 mmol) and potassium carbonate (10.3 g, 74.52 mmol) were added to a solution of 4-benzyloxy-/H-pyridin-2-one (5.0 g, 24.84 mmol) in acetonitrile (200 ml) and the mixture was heated at reflux for 16 hours. The reaction mixture was filtered through diatomaceous earth and concentrated in vacuo. The crude residue was then triturated with diethylether to yield pure Dl (6.32 g, 98 %) as a white solid.
Description 2 l-Cyclopropylmethyl-4-hydroxy-7//-pyridin-2-one (D2)
Figure imgf000026_0002
A mixture of intermediate Dl (2.0 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 D2 (1.3 g, 100 %) that was used without further purification.
Description 3 4-Bromo-l-cyclopropylmethyl-i//-pyridin-2-one (D3)
Figure imgf000027_0001
Phosphorus oxybromide (5.4 g, 18.9 mmol) was added to a solution of intermediate D2 (1.42 g, 8.6 mmol) in DMF (140 ml) and the mixture was heated at 110 0C for 1 hour. After cooling in an ice bath the solution was partitioned between water and EtOAc. After three extractions with EtOAc, the combined organic fractions were dried (Na2SO4) and the solvent was evaporated in vacuo. The crude product was purified by column chromatography (silica gel; DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D3 (1.82 g, 93 %).
Description 7
4-Bromo-l-(3-methylbutyl)-i//-pyridin-2-one (D7)
Figure imgf000027_0002
Intermediate D7 was prepared following the same procedure implemented for the synthesis of D3, using 4-hydroxy-l-(3-methylbutyl)-7H-pyridin-2-one as starting material, which was prepared by the same method used for the synthesis of intermediate D2, by reaction of 4-benzyloxy-7//-pyridin-2-one with l-bromo-3- methylbutane. Description 4 4-BenzyIoxy-l-butyl-iH-pyridin-2-one (D4)
Figure imgf000028_0001
1-Bromobutane (3.75 g, 27.33 mmol) and potassium carbonate (10.3 g, 74.52 mmol) were added to a solution of 4-benzyloxy-7H-pyridin-2-one (5.0 g, 24.84 mmol) in acetonitrile (200 ml) and the mixture was heated at reflux for 16 hours. The reaction mixture was filtered through diatomaceous earth and concentrated in vacuo. The crude residue was then triturated with diethylether to yield pure D4 (6.26 g, 98 %) as a white solid.
Description 5 l-Butyl-4-hydroxy-///-pyridin-2-one (D5)
Figure imgf000028_0002
A mixture of 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.
Description 6
4-Bromo-l-butyl-.Z//-pyridin-2-one (D6)
Figure imgf000028_0003
Phosphorus oxybromide (5.4 g, 18.9 mmol) was added to a solution of intermediate D5 (1.44 g, 8.6 mmol) in DMF (140 ml) and the mixture was heated at 110 0C for 1 hour. After cooling in an ice bath, the solution was partitioned between water and EtOAc. After three extractions with EtOAc, the combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D6 (1.82 g, 93 %).
Description 8 l-Butyl-3-chloro-4-hydroxy-i//-pyridin-2-one (D8)
Figure imgf000029_0001
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 %).
Description 9
Trifluoro-methanesulfonic acid l-butyI-3-chloro-2-oxo-l,2-dihydropyridin-4-yl ester (D9)
Figure imgf000029_0002
Pyridine (1.60 ml, 19.8 mmol) was added to a cooled (- 78 0C) solution of intermediate D8 (2.0 g, 9.92 mmol) in DCM (80 ml). The resulting solution was stirred for 10 minutes after which trifloromethanesulfonic anhydride (1.90 ml, 10.9 mmol) was added, and the resulting solution was stirred at -78 0C for 3 hours. Then the mixture was warmed to room temperature and was quenched by the addition of aqueous saturated ammonium chloride. The mixture was diluted with water,extracted with DCM, dried (Na2SO4) and the solvent evaporated in vacuo, yielding intermediate D9 (3.31 g, 100 %) as a crude that was used without further purification. Description 10
4-Benzyloxy-l-cyclopropylmethyl-3-iodo-7//-pyridin-2-one (DlO)
Figure imgf000030_0001
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.
Description 11
4-Benzyloxy-l-cyclopropylmethyl-3-trifluoromethyl-/H-pyridin-2-one (DIl)
Figure imgf000030_0002
Methyl 2,2-difluoro-2-(fluorosulfonyl)acetate (0.67 ml, 5.24 mmol) and intermediate DlO (1.0 g, 2.63 mmol) were added to a solution of copper(I) iodide (0.99 g, 5.24 mmol) in DMF (30 ml). The mixture was then heated at 100 0C for 5 hours, after which it was filtered through diatomaceous earth and the filtrate was concentrated in vacuo. The residue was purified by column chromatography (silica gel; DCM as eluent) to yield intermediate DIl (0.76 g, 89 %).
Description 12 l-Cyclopropylmethyl-4-hydroxy-3-trifluoromethyl-7//-pyridin-2-one (D12)
Figure imgf000030_0003
A mixture of intermediate DIl (2.0 g, 6.19 mmol), a catalytic amount of 10% palladium on activated carbon and ethanol (60 ml) was stirred under hydrogen atmosphere for 2 hours. The mixture was filtered through diatomaceous earth and the solvent was evaporated in vacuo to yield crude intermediate D12 (1.45 g, 100 %) that was used without further purification.
Description 13 4-Bromo-l-cyclopropylmethyl-3-trifluoromethyl-i/7-pyridin-2-one (D13)
Figure imgf000031_0001
Phosphorus oxybromide (7.03 g, 24.5 mmol) was added to a solution of intermediate D12 (2.60 g, 11.1 mmol) in DMF (50 ml) and the mixture was heated at 110 0C for 1 hour. After cooling in an ice bath the solution was partitioned between water and EtOAc. After three extractions with EtOAc, the combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D13 (1.38 g, 42 %).
Description 14
4-Benzyloxy-l-(4-trifluoromethoxy-benzyl)-7/-r-pyridin-2-one (D14)
Figure imgf000031_0002
l-Bromomethyl-4-trifluoromethoxybenzene (3.32 g, 13.04 mmol) and potassium carbonate (3.51 g, 25.46 mmol) were added to a mixture of 4-benzyloxy-i//-pyridin-2- one (2.5 g, 12.42 mmol) in acetonitrile (10 ml). The reaction mixture was heated at reflux temperature for 24 hours. After cooling to room temperature, it was filtered through diatomaceous earth, the solid residues were washed with methanol and the combined organic extracts were evaporated in vacuo. The crude residue thus obtained was precipitated with DIPE to yield intermediate D14 (4.5 g, 96%) as a white solid. Description 15 4-Benzyloxy-3-chloro-l-(4-trifluoromethoxy-benzyl)-///-pyridin-2-one (D15)
Figure imgf000032_0001
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.
Description 16
3-Chloro-4-hydroxy-l-(4-trifluoromethoxy-benzyl)-i//-pyridin-2-one (D16)
Figure imgf000032_0002
Hydrobromic acid (0.1 ml) was added to a mixture of intermediate D15 (4.5 g, 10.98 mmol) in acetic acid (20 ml). The solution was heated at 130 0C for 30 minutes under microwave irradiation. After cooling to room temperature, the solvent was evaporated in vacuo and the residue was treated with an aqueous saturated solution of NaHCO3 until the solution reached a pH of approximately 8. The white solid that precipitated was collected by filtration and washed with cold DIPE to yield intermediate D16 (1.1 g, 31 %).
Description 17 4-Bromo-3-chloro-l-(4-trifluoromethoxy-benzyl)-/JΪ-pyridin-2-one (D17)
Figure imgf000032_0003
Phosphorus oxybromide (1.05 g, 3.75 mmol) was added to a solution of intermediate D16 (1.0 g, 3.13 mmol) in DMF (5 ml) and the mixture was heated at 115 0C for 4 hours. The solvent was evaporated in vacuo and the crude residue was treated with an aqueous saturated solution of NaHCO3. The mixture was extracted with DCM (3 x 5 ml), the organic fractions were dried (Na2SO4) and the solvent was evaporated in vacuo. The crude product was purified by column chromatography (silica gel; diethyl ether as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D17 (0.21 g, 18 %) as a yellow oil.
Description 18
1 '-Cyclopropylmethyl-4-phenyl-3,4,5,6-tetrahydro-2//,i 'H- [ 1 ,4 '] bipyridinyl-2 '-one
Figure imgf000033_0001
4-Phenylpiperidine (0.45 g, 2.78 mmol), palladium(II) acetate (0.016 g, 0.069 mmol), sodium tert-butoxide (0.34 g, 3.5 mmol) and BINAP (0.065 g, 0.104 mmol) were added to a solution of intermediate D3 (0.32 g, 1.39 mmol) in toluene (5 ml). The reaction mixture was heated at 100 0C for 16 hours in a sealed tube, after which it was cooled to room temperature, diluted with water (5 ml) and then extracted with EtOAc (3 x 5 ml).
The combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 0-4% methanol/DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D18 (0.33 g, 78 %).
Description 19 l'-Butyl-4-phenyl-3,4,5,6-tetrahydro-2JΪ,7 Η-[l,4']bipyridinyl-2'-one (D19)
Figure imgf000033_0002
4-Phenylpiperidine (0.45 g, 2.78 mmol), palladium(II) acetate (0.016 g, 0.069 mmol), sodium tert-butoxide (0.34 g, 3.5 mmol) and BINAP (0.065 g, 0.104 mmol) were added to a solution of intermediate D6 (0.32 g, 1.39 mmol) in toluene (5 ml). The reaction mixture was heated at 100 0C for 16 hours in a sealed tube, after which it was cooled to room temperature and then diluted with water (5 ml) and extracted with EtOAc (3 x 5 ml). The combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 0-4% methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D19 (0.38 g, 89 %).
Description 20 l'-Cyclopropylmethyl^'-oxo^-phenyl-S^^jό.l'.Z'-hexahydro-i^-ll^1] bipyridinyl-4-carbonitrile
Figure imgf000034_0001
4-Cyano-4-phenylpiperidine hydrochloride (0.314 g, 1.41 mmol), palladium(II) acetate (0.013 g, 0.059 mmol) sodium tert-butoxide (0.347 g, 3.54 mmol) and BINAP (0.051 g, 0.08 mmol) were added to a stirred solution of intermediate D3 (0.27 g, 1.18 mmol) in toluene (5 ml). The reaction mixture was heated at 100 0C for 16 hours in a sealed tube. After cooling to room temperature the mixture was diluted with water and extracted with EtOAc. The combined organic phase was dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 10 % ammonia in methanol (7M) / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield D20 (0.35 g, 87 %) as a pale yellow oil. Description 21
4-Hydroxy-4-phenylpiperidine-l-carboxilic acid tert-butyl ester (D21)
Figure imgf000035_0001
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 OfNaHCO3 (24 ml). The resulting solution was degassed using a stream of nitrogen and Pd(PPh3)4 (0.747 g, 0.647 mmol) was added to this solution. The reaction was then microwaved in a sealed tube at 140 0C 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 Na2SO4 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 %).
Description 22
4-(2-Fluoro-4-methoxycarbonyl-phenyl)-3,6-dihydro-2//-pyridine-l-carboxylic acid tert-butyl ester (D22)
Figure imgf000035_0002
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 NaHCO3 (18 ml). The resulting solution was degassed using a stream of nitrogen and Pd(P Ph3 )4 (0.561 g, 0.485 mmol) was added to this solution. The reaction was then microwaved in a sealed tube at 150 0C 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 Na2SO4 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 %).
Description 23
4-(2-Fluoro-4-methoxycarbonyl-phenyl)-piperidine-l-carboxylic acid tert-huty\ ester (D23)
Figure imgf000036_0001
A solution of intermediate D22 (2.81 g, 8.379 mmol) in methanol (120 ml) was hydrogenated at room temperature in the presence of palladium 10% on activated carbon (0.588 g) until the reaction was completed. The solids were filtered off and the filtrate was evaporated in vacuo to give D23 (2.73 g, 97 %).
Description 24
4-[2-Fluoro-4-(l-hydroxy-l-methyl-ethyl)-phenyl]-piperidine-l-carboxylic acid tert-butyl ester (D24)
Figure imgf000036_0002
A 1.4 M solution of methylmagnesium bromide in toluene/THF (17.339 ml, 24.274 mmol) was added dropwise to a cooled (0 0C) solution of intermediate D23 (2.73 g, 8.091 mmol) in diethylether (150 ml) under nitrogen atmosphere. The resulting reaction mixture was then stirred at 50 0C for 2 hours. After cooling in an ice bath the mixture was carefully quenched with a saturated aqueous solution of ammonium chloride, and then was extracted with EtOAc. The combined organic phase was dried (Na2SO4) and the solvent evaporated in vacuo to yield D24 (3.16 g, 100 %).
Description 25
2-(3-Fluoro-4-piperidin-4-yl-phenyl)-propan-2-ol (D25)
Figure imgf000037_0001
A mixture of intermediate D24 (3.067 g, 7.852 mmol) and KOH (2.54 g, 45.268 mmol) in isopropyl alcohol (13.5 ml) and water (27 ml) was micro waved in a sealed tube at
180 0C for 60 minutes. The resulting cooled reaction mixture was then diluted with water and brine and extracted with dichloromethane. The combined organic extracts were dried (Na2SO4) and the solvent was evaporated in vacuo. The residue was treated with dichloromethane giving rise to a solid that was filtered off to yield 1.03 g intermediate D25. The filtrate was evaporated in vacuo and the residue thus obtained was then purified by column chromatography (silica gel; DCM/(NH3 7N solution in
MeOH) gradient up to 10 % as eluent). The desired fractions were collected and evaporated in vacuo to yield a second batch of 0.5 g of D25 (total amount = 1.53 g, 82
%). M.P. 151°C.
Description 26
4-(2-Methoxycarbonyl-phenyl)-piperidine-l-carboxylic acid tert-butyl ester (D26)
Figure imgf000037_0002
A solution of intermediate D21 (4.04 g, 12.729 mmol) in methanol (120 ml) was hydrogenated at room temperature in the presence of palladium 10% on activated carbon (0.846 g) until the reaction was completed. The solids were filtered off and the filtrate was evaporated in vacuo to give D26 as white solid (3.67 g, 90 %).
Description 27 4-[2-(l-Hydroxy-l-methyl-ethyl)-phenyl]-piperidine-l-carboxylic acid tert-butyl ester (D27)
Figure imgf000038_0001
A 1.4 M solution of methylmagnesium bromide in toluene/THF (17.443 ml, 24.421 mmol) was added dropwise to a cooled (0 °C) solution of intermediate D26 (2.6 g, 8.14 mmol) in diethyl ether (150 ml) under nitrogen atmosphere. The resulting reaction mixture was stirred at 45 0C for 2 hours. After cooling in an ice bath, the mixture was carefully quenched with a saturated aqueous solution of ammonium chloride, and then extracted with EtOAc. The combined organic phase was dried (Na2SO4) and the solvent evaporated in vacuo to yield D27 (2.77 g, 69 %).
Description 28 2-(2-Piperidin-4-yl-phenyl)-propan-2-ol (D28)
Figure imgf000038_0002
A mixture of intermediate D27 (2.77 g, 5.636 mmol) and KOH (2.43 g, 43.357 mmol) in isopropyl alcohol (13.5 ml) and water (27 ml) was microwaved in a sealed tube at 180 0C for 60 minutes. The resulting cooled reaction mixture was then diluted with water and brine and extracted with dichloromethane. The residue was treated with dichloromethane giving rise to a solid that was filtered off. Yield: 0.737 g of intermediate D28. The filtrate was evaporated in vacuo and the residue was then purified by column chromatography (silica gel; DCM/(NH3 7N solution in MeOH) gradient up to 10 % as eluent). The desired fractions were collected and evaporated in vacuo to yield a second batch of 0.306 g of intermediate D28 (total amount = 1.04 g, 84 %). M.P. 219.50C.
Description 29
4-Hydroxy-4-phenylpiperidine-l-carboxilic acid tert-butyl ester (D29)
Figure imgf000039_0001
Di-tert-butyl dicarbonate (2.95 g, 13.53 mmol) was added to a solution of 4-hydroxy-4- phenylpiperidine (2 g, 11.28 mmol) in DCM (50 ml). The reaction was stirred at room temperature for 5 hours. The solvent was removed in vacuo, affording the desired intermediate D29 (3.12 g, 100 %) as a crude that was used without further purification.
Description 30
4-fluoro-4-phenylpiperidin-l-carboxilic acid tert-butyl ester (D30)
Figure imgf000039_0002
A solution of (diethylamino)sulfur trifiuoride (0.74 ml, 5.67 mmol) in dry DCM (q.s.) was added to a cooled (-78 0C) solution of D29 (1.5 g, 5.4 mmol) in dry DCM (30 ml) under N2 atmosphere. After the addition was complete, the reaction mixture was stirred at -780C for 1 hour and then allowed to reach room temperature and stirred for a further 30 minutes. An aqueous saturated NaHCO3 solution (90 ml) was added and the mixture was stirred for 15 minutes, then the organic layer was separated. After this, 3- chloroperoxybenzoic acid (0.2 g, 1.18 mmol) was added and the reaction stirred at room temperature for 30 minutes. The reaction mixture was washed with aqueous saturated NaHCO3, H2O and brine, dried over Na2SO4, filtered and concentrated in vacuo affording the desired intermediate D30 (1.48 g, 98 %) as a crude that was used without further purification.
Description 31 • 4-fluoro-4-phenylpiperidine hydrochloride (D31)
Figure imgf000040_0001
D30 (1.48 g, 5.29 mmol) was dissolved in 4N HCl in dioxane. The reaction was stirred at room temperature for 2 hours. The solvent was removed. The crude was triturated with diethyl ether and dried in vacuo to afford the desired intermediate D31 (1.10 g, 97 %) as a chlorohydrate that was used without further purification.
Description 32 l'-Butyl-4-fluoro-4-phenyl-3,4,5,6-tetrahydro-2H,2 Η-[l,4']bipyridinyl-2-one
Figure imgf000040_0002
D31 (0.2 g, 0.94 mmol), palladium(II) acetate (0.009 g, 0.04 mmol) sodium tert- butoxide (0.25 g, 2.58 mmol) and BINAP (0.037 g, 0.06 mmol) were added to a stirred solution of intermediate D6 (0.20 g, 0.86 mmol) in toluene (5 ml). The reaction mixture was heated at 100 0C for 16 hours in a sealed tube. After cooling to room temperature the mixture was diluted with water and extracted with EtOAc. The combined organic phase was dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 10 % ammonia in methanol (7N) / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield D32 (0.21 g, 87 %) as a pale yellow oil. Description 33
4-Benzyloxy-3-bromo-l- 2-one (D33)
Figure imgf000041_0001
A solution of intermediate Dl (3.0 g, 11.7 mmol) and N-bromosuccinimide (2.09 g, 11.7 mmol) in DCM (100 ml) was stirred at room temperature for 1 hour. The solvent was evaporated in vacuo and the crude residue was purified by column chromatography (silica gel; DCM as eluent). The desired fractions were collected and evaporated in vacuo yielding D33 (3.56 g, 91%).
Description 34
4-Benzyloxy-3-cyclopro ridin-2-one (D34)
Figure imgf000041_0002
NaHCO3 (1.0 g, excess), cyclopropylboronic acid (0.74 g, 8.93 mmol), potassium carbonate (1.23 g, 8.93 mmol) and [l,l '-bis(diphenylphosphino)ferrocene] dichloropalladium(II) - DCM complex (0.36 g, 0.45 mmol) were added to a solution of intermediate DlO (1.0 g, 2.98 mmol) in 1,4-dioxane (10 ml). The resulting mixture was heated at 175 0C for 20 minutes under microwave irradiation, after which it was filtered through diatomaceous earth and the solvent was evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; 0-3 % methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo yielding D34 (0.6 g, 69 %). Description 35
3-Cyclopropyl-l-cyclopropylm pyridin-2-one (D35)
Figure imgf000042_0001
A mixture of intermediate D34 (1.0 g, 3.38 mmol) and 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.
Description 36
4-Bromo-3-cyclopropyl-l-cyclo ridin-2-one (D36)
Figure imgf000042_0002
Phosphorus oxybromide (2.4 g, 8.28 mmol) was added to a solution of intermediate D35 (0.85 g, 4.14 mmol) in DMF (60 ml), and the mixture was heated at 110 0C for 1 hour. After cooling in an ice bath, the solution was partitioned between water and EtOAc. The mixture was extracted with EtOAc (3 x 200 ml), the combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield intermediate D36 (0.99 g, 89 %).
Description 37
^(l'-Cyclopropylmethyl^'-oxo-S^.S^jl'.Z'-hexahydro-i/T-Il^'lbipyridinyM-yl)- benzoic acid (D37)
Figure imgf000043_0001
4-Piperidin-4-ylbenzoic acid methyl ester (0.40 g, 1.81 mmol), palladium(II) acetate (0.015 g, 0.069 mmol) sodium tert-butoxide (0.34 g, 3.44 mmol) and BINAP (0.06 g, 0.096 mmol) were added to a stirred solution of intermediate D3 (0.31 g, 1.37 mmol) in toluene (10 ml). The reaction mixture was heated at 100 0C for 16 hours in a sealed tube. After cooling to room temperature the mixture was diluted with EtOAc and then filtered through diatomaceous earth, after which the solvent was evaporated in vacuo. The crude residue was treated with a mixture of DCM / methanol and then filtered off. The filtrate was evaporated to dryness in vacuo to yield crude D37 (0.48 g, 100 %) that was used without further purification.
Description 38
4-(l'-Cyclopropylmethyl-2'-oxo-3,4,5,6,r,2'-hexahydro-2Jfir-[l,4']bipyridinyl-4-yl)- benzoic acid methyl es
Figure imgf000043_0002
A mixture of intermediate D37 (0.43 g, 1.23 mmol), DBU (0.18 g, 1.23 mmol), dimethyl carbonate (4.5 ml, excess, 93 mmol), and acetonitrile (5 ml) was heated at 160 0C for 20 minutes under microwave irradiation. The cooled crude mixture was diluted with water and EtOAc was added, after which the organic layer was washed with an aqueous 10% citric acid solution, dried (Na2SO4) and the solvent evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; 0-3% methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield D38 (0.19 g, 38 %).
Description 39 l'-CyclopropylmethyM-^-Cl-hydroxy-l-methyl-ethyO-phenyll-S^.S.β-tetrahydro- 2H,1 Η-[l,4']bipyrid
Figure imgf000044_0001
A 1.4 M solution of methylmagnesium bromide in toluene/THF (1.12 ml, 1.57 mmol) was added dropwise to a cooled (0 °C) solution of intermediate D38 (0.19 g, 0.52 mmol) in THF (20 ml) under nitrogen atmosphere. The resulting reaction mixture was stirred at 45 0C for 2 hours. After cooling in an ice bath the mixture was carefully quenched with a saturated aqueous solution of ammonium chloride, and then was extracted with EtOAc. The combined organic phase was dried (Na2SO4) and the solvent evaporated in vacuo. The residue was purified by column chromatography (silica gel; 0-5% methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield D39 (0.077 g, 40 %) as an oil.
Example 1
S'-Chloro-r-cyclopropylmethyM-phenyl-S^jSjό-tetrahydro-iHj/ 'H- [l,4']bipyridinyl-2'-one (El)
Figure imgf000044_0002
A solution of intermediate D18 (0.2 g, 0.65 mmol) and N-chlorosuccinimide (0.09 g,
0.65 mmol) in DCM (10 ml) was stirred at room temperature for 1 hour. The solvent was evaporated in vacuo and the crude product was purified by column chromatography (silica gel; 0-3 % methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo and the resulting solid was recrystallized from diethyl ether to yield compound El (0.10 g, 47 %) as a white solid. Melting point: 170.8 0C.
1H NMR (400 MHz, CDCl3) δ ppm 0.35 - 0.42 (m, 2 H), 0.57 - 0.64 (m, 2 H), 1.19 - 1.33 (m, 1 H), 1.85 - 2.00 (m, 4 H), 2.64 - 2.76 (m, 1 H), 2.85 - 2.99 (m, 2 H), 3.76 - 3.87 (m, 4 H), 6.05 (d, J=7.6 Hz, 1 H), 7.19 - 7.29 (m, 4 H), 7.29 - 7.38 (m, 2 H).
Example 2 ll-Butyl-3I-chloro-4-phenyl-3,4,5,6-tetrahydro-2H,7'H-[l,4l]bipyridinyl-2'-one
Figure imgf000045_0001
A solution of intermediate D19 (0.43 g, 1.40 mmol) and N-chlorosuccinimide (0.19 g, 1.40 mmol) in DCM (10 ml) was stirred at room temperature for 1 hour. The solvent was evaporated in vacuo and the crude product was purified by column chromatography (silica gel; 0-3 % methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo and the resulting solid was recrystallized from diethyl ether to yield compound E2 (0.39 g, 82 %) as a white solid. Melting point: 149.4 0C.
1H NMR (400 MHz, CDCl3) δ ppm 0.95 (t, J=7.3 Hz, 3 H), 1.31 - 1.42 (m, 2 H), 1.68 - 1.78 (m, 2 H), 1.85 - 1.98 (m, 4 H), 2.64 - 2.73 (m, 1 H), 2.87 - 2.96 (m, 2 H), 3.82 (br d, J=I 2.1 Hz, 2 H), 3.93 (t, J=7.3 Hz, 2 H), 6.03 (d, J=7.6 Hz, 1 H), 7.10 (d, J=7.6 Hz, 1 H), 7.19 - 7.28 (m, 3 H), 7.29 - 7.37 (m, 2 H). Example 3
3'-Bromo-r-cyclopropylmethyl-4-phenyl-3,4,5,6-tetrahydro-2//,77/- [l,4']bipyridinyl-2'-one
Figure imgf000046_0001
iV-Bromosuccinimide (0.145 g, 0.82 mmol) was added to a solution of intermediate D18 (0.25 g, 0.82 mmol) in DCM (10 ml). The reaction mixture was stirred at room temperature for 1 hour. Subsequently, the solvent was evaporated in vacuo and the crude residue was purified by column chromatography (silica gel; 0τ3 % methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield compound E3 (0.20 g, 64 %) as a white solid. Melting point: 15O 0C.
1H NMR (500 MHz, DMSO-^6) δ ppm 0.34 - 0.40 (m, 2 H), 0.44 - 0.50 (m, 2 H), 1.16 - 1.26 (m, 1 H), 1.77 (qd, J=12.38, 3.61 Hz, 2 H), 1.88 (br d, J=12.1 Hz, 2 H), 2.68 - 2.78 (m, 1 H), 2.91 (br t, J=I 1.9 Hz, 2 H) 3.69 (br d, J=12.1 Hz, 2 H), 3.74 (d, MJ.2 Hz, 2 H), 6.21 (d, J=7.5 Hz, 1 H), 7.19 - 7.25 (m, 1 H), 7.27 - 7.36 (m, 4 H), 7.69 (d, J=7.5 Hz, 1 H).
Example 4 l'-CyclopropylmethyM-phenyl-S'-trifluoromethyl-S^jSjό-tetrahydro-i^/'/T- [l,4']bipyridinyl-2'-one (E4)
Figure imgf000046_0002
4-Phenylpiperidine (0.33 g, 2.02 mmol), palladium(II) acetate (0.012 g, 0.05 mmol), sodium tert-butoxide (0.24 g, 2.52 mmol) and BINAP (0.05 g, 0.08 mmol) were added to a solution of intermediate D13 (0.3 g, 1.01 mmol) in toluene (7 ml). The reaction mixture was heated at 100 0C for 16 hours in a sealed tube, after which it was cooled to room temperature and then it was diluted with water (5 ml) and extracted with EtOAc (3 x 5 ml). The combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 0-4% methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield compound E4 (0.11 g, 31 %) as a white solid. Melting point: 177.2 0C.
1H NMR (500 MHz, DMSO-4) δ ppm 0.33 - 0.38 (m, 2 H), 0.45 - 0.50 (m, 2 H), 1.13 - 1.22 (m, 1 H), 1.64 - 1.75 (m, 2 H), 1.84 (br d, J=I 1.0 Hz, 2 H), 2.72 - 2.80 (m, 1 H), 3.14 (br t, J=12.1 Hz, 2 H), 3.59 (br d, J=13.0 Hz, 2 H), 3.65 (d, J=7.2 Hz, 2 H), 6.21 (d, J=7.8 Hz, 1 H), 7.19 - 7.23 m, 1 H), 7.24 - 7.29 (m, 2 H), 7.29 - 7.34 (m, 2 H), 7.73 (d, J=7.8 Hz, 1 H).
Example 5
3'-Chloro-4-phenyl-l'-(4-trifluoromethoxybenzyl)-3,4,5,6-tetrahydro-2H,7'Hr- [M'lbipyridinyl^'-one (E5)
Figure imgf000047_0001
A mixture of intermediate D17 (0.2 g, 0.52 mmol), 4-phenylpiperidine (0.1 g, 0.62 mmol), 2-(2'-Di-tert-butylphosphine)biphenylpalladium(II) acetate (0.01 g, 0.026 mmol) and potassium phosphate (0.23 g, 1.1 mmol) in 1 ,4-dioxane (3 ml) was stirred at 90 0C for 35 hours. The mixture was filtered through diatomaceous earth, and the filtrate was evaporated to dryness after washing with more 1,4-dioxane. The crude product was purified by column chromatography (silica gel; heptane / diethyl ether 1 : 1 as eluent). The desired fractions were collected and evaporated in vacuo to yield compound E5 (0.075 g, 31 %) as a white solid. Melting point: 168.6 0C.
1H NMR (400 MHz, CDCl3) δ ppm 1.83 - 1.98 (m, 4 H), 2.65 - 2.75 (m, 1 H), 2.89 - 2.98 (m, 2 H), 3.84 (br d, J=12.2 Hz, 2 H), 5.12 (s, 2 H), 6.06 (d, J=7.6 Hz, 1 H), 7.14 (d, J=7.6 Hz, 2 H), 7.15 - 7.28 (m, 5 H), 7.29 - 7.40 (m, 4 H). Example 6
S'-Chloro-l'-cyclopropylmethyl-Z'-oxo-^phenyl-S^.Sjόjl'jZ'-hexahydro^H- [l,4']bipyridinyl-4-carbonit
Figure imgf000048_0001
A solution of intermediate D20 (0.35 g, 1.03 mmol) and N-chlorosuccinimide (0.14 g, 1.03 mmol) in DCM (25 ml) was stirred at room temperature for 1 hour. After addition of more DCM, the solution was washed with brine, dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 10 % ammonia in methanol (7N) / DCM as eluent) and further purified by preparative ΗPLC. The desired fractions were collected and evaporated in vacuo to yield compound E6 (0.17 g, 47 %) as a white solid. Melting point: 173.7 0C.
1H NMR (400 MHz, DMSO-J6) δ ppm 0.17 - 0.23 (m, 2 H), 0.26 - 0.33 (m, 2 H), 0.97 - 1.09 (m, 1 H), 1.91 - 2.02 (m, 2 H), 2.11 (br d, J=12.9 Hz, 2 H) 2.98 (br t, J=12.4 Hz, 2 H), 3.54 - 3.63 (m, 4 H), 6.14 (d, J=7.4 Hz, 1 H), 7.20 - 7.26 (m, 1 H), 7.27 - 7.35 (m, 2 H), 7.40 - 7.44 (m, 2 H), 7.52 (d, J=7.4 Hz, 1 H).
Example 7 l'-Butyl-S-chloro^-fluoro-^phenyl-S^.Sjό-tetrahydro-i^i 'ff-Il^'lbipyridinyl-Z- one
Figure imgf000048_0002
A solution of intermediate D32 (0.21 g, 0.66 mmol) and N-chlorosuccinimide (0.08 g, 0.66 mmol) in DCM (30 ml) was stirred at room temperature for 10 minutes. After addition of more DCM the solution was washed with brine, dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 10 % ammonia in methanol (7M) / DCM as eluent) and further purified by preparative HPLC. The desired fractions were collected and evaporated in vacuo to yield compound E7 (0.065 g, 27 %) as a white solid. Melting point: 136.7 0C.
1H NMR (400 MHz, DMSO-J6) δ ppm 0.89 (t, J=7.4 Hz, 3 H), 1.21 - 1.32 (m, 2 H), 1.54 - 1.64 (m, 2 H), 2.03 (t, J=I 1.8 Hz, 2 H), 2.16 (td, J=I 3.9, 4.6 Hz, 1 H), 2.26 (td, J=13.6, 4.6 Hz, 1 H), 3.17 (dd, J=12.3, 11.1 Hz, 2 H), 3.54 - 3.64 (m, 2 H), 3.87 (t, J=7.2 Hz, 2 H), 6.26 (d, J=7.6 Hz, 1 H), 7.32 - 7.38 (m, 1 H), 7.42 (t, J=7.4 Hz, 2 H), 7.45 - 7.51 (m, 2 H), 7.62 (d, J=7.4 Hz, 1 H).
Example 8
3'-Cyclopropyl-l'-cycIopropylmethyl-4-phenyl-3,4,5,6-tetrahydro-2H,7'f-r- [l,4']bipyridinyl-2'-one
Figure imgf000049_0001
4-Phenylpiperidine (0.22 g, 1.34 mmol), palladium(II) acetate (0.008 g, 0.034 mmol), sodium tert-butoxide (0.16 g, 1.68 mmol) and BINAP (0.032 g, 0.05 mmol) were added to a solution of intermediate D36 (0.18 g, 0.67 mmol) in toluene (5 ml). The reaction mixture was heated at 100 0C for 16 hours in a sealed tube, after which it was cooled to room temperature and then diluted with water (5 ml) and extracted with EtOAc (3 x 5 ml). The combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude product was purified by column chromatography (silica gel; 0-4% methanol / DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield compound E8 (0.18 g, 77 %) as a white solid. Melting point: 201.9 0C.
1H NMR (500 MHz, DMSO-^6) δ ppm 0.30 - 0.35 (m, 2 H) 0.41 - 0.47 (m, 2 H) 0.74 - 0.80 (m, 2 H), 0.86 - 0.92 (m, 2 H), 1.11 - 1.21 (m, 1 H), 1.60 - 1.67 (m, 1 H), 1.73 - 1.89 (m, 4 H), 2.63 - 2.72 (m, 1 H), 2.87 (br t, J=I Ll Hz, 2 H), 3.57 - 3.65 (m, 4 H), 6.07 (d, J=7.5 Hz, 1 H), 7.19 - 7.24 (m, 1 H), 7.26 - 7.37 (m, 4 H), 7.46 (d, J=7.5 Hz, 1 H). Example 9 3'-Chloro-l'-cyclopropylmethyl-4-[4-(l-hydroxy-l-methyl-ethyl)-phenyl]-3,4,5,6- tetrahydro-2i/,i 'iy-[l,4']bipyridinyl-2'-one (E9)
Figure imgf000050_0001
A solution of intermediate D39 (0.077 g, 0.21 mmol) and N-chlorosuccinimide (0.03 g, 0.21 mmol) in DCM (8 ml) was stirred at room temperature for 5 minutes. The crude mixture was washed with a saturated NaHCO3 solution, then it was extracted with DCM, the combined organic fractions were dried (Na2SO4) and the solvent evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; 0-5 % methanol / DCM as eluent). A second chromatography was performed (silica gel; DCM / EtOAc 1 :1, and finally 100% EtOAc as eluents). The desired fractions were collected and evaporated in vacuo and the resulting solid was crystallized from diethyl ether to yield compound E9 (0.06 g, 71 %) as a white solid.
1H NMR (400 MHz, CDCl3) δ ppm 0.35 - 0.41 (m, 2 H), 0.56 - 0.64 (m, 2 H), 1.19 - 1.30 (m, 1 H), 1.59 (s, 6 H), 1.73 (s, 1 H), 1.85 - 1.99 (m, 4 H), 2.65 - 2.76 (m, 1 H), 2.87 - 2.97 (m, 2 H), 3.78 - 3.87 (m, 4 H), 6.05 (d, J=7.6 Hz, 1 H), 7.21 - 7.26 (m, 3 H), 7.45 (d, J=8.3 Hz, 2 H).
Example 20
3 '-Chloro- 1 '-cyclopropylmethyl-4-(2-fluoro-ethoxy)-4-phenyl-3,4,5,6-tetrahydro- 2H,1 'i7-[l,4']bipyridinyl-2
Figure imgf000050_0002
A solution of compound E31 (0.164 g, 0.46 mmol) in 1 ,2-dimethoxyethane (3 ml) was added dropwise to a mixture of sodium hydride (0.023 g, 0.58 mmol) in 1 ,2- dimethoxyethane (0.5 ml) at 0 0C. The reaction mixture was stirred at room temperature for 15 minutes and subsequently a solution of 2-fluoroethyl tosylate [CAS: 383-50-6] (0.222 g, 1 mmol) in 1 ,2-dimethoxyethane (1 ml) was added. The reaction mixture was microwaved into a sealed tube at 180 0C for 20 minutes. The mixture was cooled to room temperature and an additional amount of sodium hydride (0.023 g, 0.58 mmol) was added. The mixture was the heated at 180 0C for 20 minutes under microwave irradiation. After cooling to room temperature, an aqueous saturated ammonium chloride solution was added and the mixture was extracted with EtOAc. The organic layer was separated, dried (Na2SO4) and the solvent was evaporated. The crude product was purified first by column chromatography (silica gel; eluent: DCM/EtOAc from 100/0 to 90/10). The desired fractions were collected and evaporated in vacuo to yield compound E20 (0.041 g, 18 %).
1H NMR (400 MHz, CDCl3) δ ppm 0.36 - 0.40 (m, 2 H), 0.58 - 0.62 (m, 2 H), 1.22 - 1.28 (m, 1 H), 2.12 - 2.21 (m, 4 H), 3.27 - 3.36 (m, 4 H), 3.57 (br d, J=12.1 Hz, 2 H), 3.80 (d, J=7.2 Hz, 2 H), 4.51 (dm, J=47.7 Hz, 2 H), 6.08 (d, J=7.5 Hz, 1 H), 7.23 (d, J=7.5 Hz, 1 H), 7.29 - 7.32 (m, 1 H), 7.37 - 7.41 (m, 2 H), 7.44 - 7.46 (m, 2 H).
Example 21
3 '-Chloro- 1 '-cy clopropylmethyl-4-fluoromethyl-4-phenyl-3,4,5,6-tetrahydro- 2H,1 '#-[l,4']bipyridinyl-
Figure imgf000051_0001
(Diethylamino)sulfur trifluoride (0.046 ml, 0.35 mmol) was added to a cooled (- 78 °C) solution of compound E30 (0.119 g, 0.32 mmol) in DCM (1 ml). The reaction mixture was stirred at -78 0C for 3 hours and then additional for 2 hours at 0 0C. Subsequently, additional (diethylamino)sulfur trifluoride (0.046 ml, 0.35 mmol) was added and the mixture was further stirred for 1 hour at room temperature. Na2CO3 (aqueous saturated solution) was added and the mixture was diluted with DCM. The organic layer was separated, dried (Na2SO4) and evaporated till dryness. The crude product was purified by column chromatography (silica gel; eluent: DCM /EtOAc from 100/0 to 80/20). The desired fractions were collected, evaporated in vacuo and finally freeze dried to yield compound E21 (0.019 g, 16 %) as a white foam. 1H NMR (400 MHz, CDCl3) δ ppm 0.33 - 0.40 (m, 2 H), 0.52 - 0.65 (m, 2 H), 1.17 - 1.29 (m, 1 H), 1.74 - 1.96 (m, 4 H), 2.96 (d, J=22.7 Hz, 2 H), 3.06 (dt, J=I 1.6, 3.7 Hz, 2 H), 3.45 - 3.52 (m, 2 H), 3.79 (d, J=7.2 Hz, 2 H), 6.01 (d, J=7.6 Hz, 1 H), 7.20 - 7.36 (m, 6 H).
Example 22 l'-Butyl-3'-chloro-4-hydroxymethyl-4-phenyl-3,4,5,6-tetrahydro-2JH,i 'H- [l,4']bipyridinyl-2'-one
Figure imgf000052_0001
4-Hydroxymethyl-4-phenylpiperidine (0.172 g, 0.9 mmol), palladium(II) acetate (0.007 g, 0.03 mmol), cesium carbonate (0.391 g, 1.2 mmol) and Xantphos (0.035 g, 0.06 mmol) were added to a solution of intermediate D9 (0.2 g, 0.6 mmol) in trifluoromethylbenzene (2 ml). The reaction mixture was heated at 100 0C for 24 hours in a sealed tube, after which it was cooled to room temperature. Subsequently, it was diluted with DCM, H2O (5 ml) and extracted with EtOAc (3 x 5 ml). The mixture was filtered through diatomaceous earth, and the filtrate was evaporated to dryness. The crude product was purified first by column chromatography (silica gel; eluent: DCM/EtOAc from 90/10 to 0/100) and then by reversed phase HPLC. The desired fractions were collected, evaporated in vacuo and finally freeze dried to yield compound E22 (0.041 g, 18 %) as a white foam.
1H NMR (400 MHz, CDCl3) δ ppm 0.93 (t, J=7.3 Hz, 3 H), 1.13 (br t, J=6.7 Hz, 1 H), 1.28 - 1.40 (m, 2 H), 1.64 - 1.75 (m, 2 H), 1.98 - 2.08 (m, 2 H), 2.31 - 2.40 (m, 2 H), 2.98 - 3.10 (m, 2 H), 3.41 - 3.51 (m, 2 H), 3.63 (d, J=6.5 Hz, 2 H), 3.90 (t, J=7.3 Hz, 2 H), 5.92 (d, J=7.5 Hz, 1 H), 7.04 (d, J=7.5 Hz, 1 H), 7.27 - 7.33 (m, 1 H), 7.36 - 7.46 (m, 4 H). Example 28 l'-Butyl-B'-chloro-^IZ-Cl-hydroxy-l-methyl-ethyO-phenyll-S^jSjό-tetrahydro-
Figure imgf000053_0001
A mixture of intermediate D9 (0.254 g, 0.76 mmol), intermediate D28 (0.2 g, 0.912 mmol) and diisopropylethylamine (0.199 ml, 1.114 mmol) in acetonitrile (11 ml) was heated at 180 0C for 5 minutes under microwave irradiation. The cooled crude mixture was evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; DCM/EtOAc/MeOH as eluent). The desired fractions were collected and evaporated in vacuo. The solid residue obtained was treated with diisopropylether. The solid was filtered to yield compound E28 (0.183 g, 61 %). M.P. 182 0C.
1H NMR (400 MHz, CDCl3) δ ppm 0.95 (t, J=I.3 Hz, 3 H), 1.32 - 1.42 (m, 2 H), 1.70 (s, 6 H), 1.71 - 1.77 (m, 2 H), 1.79 (s, 1 H), 1.82 - 1.90 (m, 2 H), 1.91 - 2.05 (m, 2 H), 2.88 - 2.98 (m, 2 H), 3.76 - 3.87 (m, 3 H), 3.93 (t, J=7.3 Hz, 2 H), 6.03 (d, J=7.5 Hz, 1 H), 7.11 (d, J=7.5 Hz, 1 H), 7.16 (td, J=7.8, 1.4 Hz, 1 H), 7.28 (td, J=7.4, 1.4 Hz, 1 H), 7.41 (dd, J=7.7, 1.6 Hz, 1 H), 7.42 (dd, J=7.6, 1.7 Hz, 1 H).
Example 29 l'-Butyl-3'-chloro-4-[2-fluoro-4-(l-hydroxy-l-methyI-ethyl)-phenyl]-3,4,5,6- tetrahydro-2H,i 'H-[l,4']bipyridinyl-2'-one (E29)
Figure imgf000053_0002
A mixture of intermediate D9 (0.261 g, 0.781 mmol), intermediate D25 (0.223 g, 0.938 mmol) and diisopropylethylamine (0.204 ml, 1.172 mmol) in acetonitrile (11 ml) was heated at 180 °C for 5 minutes under microwave irradiation. The cooled crude mixture was evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; DCM/EtOAc/MeOH/NH3 as eluent). The desired fractions were collected and evaporated in vacuo. The solid residue obtained was treated with diisopropylether. The solid was filtered to yield compound E29 (0.239 g, 73 %). M.P. 150.5 0C.
1H NMR (400 MHz, CDCl3) δ ppm 0.95 (t, J=7.3 Hz, 3 H), 1.31 - 1.43 (m, 2 H), 1.57 (s, 6 H), 1.68 - 1.76 (m, 2 H), 1.77 (s, 1 H), 1.87 - 1.96 (m, 4 H), 2.86 - 2.98 (m, 2 H), 2.98 - 3.09 (m, 1 H), 3.81 (br d, J=12.0 Hz, 2 H), 3.93 (t, J=7.3 Hz, 2 H), 6.03 (d, J=7.5 Hz, 1 H), 7.11 (d, J=7.5 Hz, 1 H), 7.16 - 7.25 (m, 3 H).
Example 32 l-butyl^-chloro^-^'HjSH-spiroIZ-benzofuran-l^'-piperidinJ-l'-y^pyridin-
Figure imgf000054_0001
A mixture of intermediate D9 (0.15 g, 0.45 mmol), 3//-spiro[2-benzofuran-l,4'- piperidine] (0.102 g, 0.54 mmol) and diisopropylethylamine (0.097 ml, 0.056 mmol) in acetonitrile (4 ml) was heated at 180 0C for 5 minutes under microwave irradiation. The cooled crude mixture was evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; DCM/EtOAc/MeOH/NH3 as eluent). The desired fractions were collected and evaporated in vacuo. The solid residue obtained was treated with diisopropylether. The solid was filtered to yield compound E32 (0.14 g, 84 %).
1H NMR (400 MHz, CDCl3) δ ppm 0.95 (t, J=7.3 Hz, 3 H), 1.30 - 1.43 (m, 2 H), 1.67 - 1.79 (m, 2 H), 1.85 (dd, J=13.8, 2.20 Hz, 2 H), 2.12 (dt, J=13.0, 4.7 Hz, 2 H), 3.25 (dt, J=I 2.4, 2.31 Hz, 2 H), 3.57 - 3.68 (m, 2 H), 3.94 (t, J=7.3 Hz, 2 H), 6.06 (d, J=7.4 Hz, 1 H), 7.12 (d, J=7.4 Hz, 1 H), 7.16 - 7.34 (m, 7 H). Example 33 l-butyl-3-chloro-4-(7'i7-spiro[l-benzofuran-3,4f-piperidin]-ll-yl)pyridin-2(7JΪ)- one
Figure imgf000055_0001
A mixture of intermediate D9 (0.15 g, 0.45 mmol), spiro[l-benzofuran-3,4'-piperidine] (0.102 g, 0.54 mmol) and diisopropylethylamine (0.097 ml, 0.056 mmol) in acetonitrile (4 ml) was heated at 180 0C for 5 minutes under microwave irradiation. The cooled crude mixture was evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; DCM/EtOAc/MeOH/NH3 as eluent). The desired fractions were collected and evaporated in vacuo. The solid residue obtained was treated with diisopropylether. The solid was filtered to yield compound E33 (0.116 g, 84 %).
1H NMR (500 MHz, CDC13) δ ppm 0.95 (t, J=7.4 Hz, 3 H), 1.30 - 1.43 (m, 2 H), 1.66 - 1.79 (m, 2 H), 1.86 (d, J=I 3.3 Hz, 2 H), 2.05 - 2.19 (m, 2 H), 2.84 - 2.97 (m, 2 H), 3.68 (d, J=12.7 Hz, 2 H), 3.94 (t, J=7.4 Hz, 2 H), 4.44 (s, 2 H), 6.01 (d, J=7.5 Hz, 1 H), 6.83 (d, J=I. S Hz, 1 H), 6.92 (t, J=7.4 Hz, 1 H), 7.07 - 7.24 (m, 3 H).
Compounds ElO, El l, E12, E13, E14, E15, E16, E17, E18, E19, E23, E24, E25 and E26 were prepared according to the reaction procedure described in Example 1. Compound E27 was prepared according to the reaction procedure described in Example 9.
Compound E30 and compound E31 were prepared according to the reaction procedure described in Example 22.
Phvsico-Chemical Data
LCMS - general procedure
The HPLC measurement was performed using a HP 1100 from Agilent
Technologies comprising a pump (quaternary or binary) 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 0C. Data acquisition was performed with MassLynx-Openlynx software.
LCMS Method:_Fρr all_eΛamp]ejLJLx^
E30 and_E31 ,_ the. following jnethod. was_us_e_d_.
In addition to the general procedure: Reversed phase HPLC was carried out on an XDB-C18 cartridge (1.8 μm, 2.1 x 30 mm) from Agilent, with a flow rate of 1 ml/min, at 600C. 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 μl. 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.
LCMS Method :_This_me^hpd_was u_sedJfor ^
In addition to the general procedure: Reversed phase HPLC was carried out on an ACE-C 18 column (3.0 μm, 4.6 x 30 mm) from Advanced Chromatography Technologies, with a flow rate of 1.5 ml/min, at 40 0C. 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 μl. 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.
Figure imgf000057_0001
In addition to the general procedure: Reversed phase HPLC was carried out on a
XDB-Cl 8 cartridge (1.8 μm, 2.1 x 30 mm) from Agilent, with a flow rate of
0.8 ml/min, at 600C. 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
9.0 minutes. Injection volume 2 μl. Low-resolution mass spectra (SQD detector; quadrupole) were acquired only in positive ionization mode by scanning from 100 to
1000 in 0.1 seconds using an inter-channel delay of 0.08 second. The capillary needle voltage was 3 kV and the cone voltage was 20 V.
LCMS Method : JTiisjnethqd was_used for examp_le_E27..
In addition to the general procedure: Reversed phase HPLC was carried out on a Sunfire-C18 column (2.5 μm, 2.1 x 30 mm) from Waters, with a flow rate of 1.0 ml/min, at 600C. 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 μl. 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.
LCMS Method : J[his_methqd was_used for_ exarnp_le^281_E293_ E32_and Ji3_3_.
In addition to the general procedure: Reversed phase HPLC was carried out on a BEH- Cl 8 column (1.7 μm, 2.1 x 50 mm) from Waters, with a flow rate of 0.8 ml/min, at 6O0C 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 μl. Low-resolution mass spectra (SQD detector; quadrupole) were acquired by scanning from 100 to 1000 in 0.1 seconds using an inter-channel delay of 0.08 second. The capillary needle voltage was 3 kV. The cone voltage was 20 V for positive ionization mode and 30 V for negative ionization mode. LCMS Method : JThisjnethod was_used for. exampjes E3_0_ and_E3 L. In addition to the general procedure: Reversed phase HPLC was carried out on an XDB-Cl 8 cartridge (1.8 μm, 2.1 x 30 mm) from Agilent, with a flow rate of 1 ml/min, at 6O0C. 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 μl. 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 0C. The melting point was read from a digital display and were obtained with experimental uncertainties that are commonly associated with this analytical method.
Nuclear Magnetic Resonance (TSfMR)
1H NMR spectra were recorded either on Bruker DPX400 or Bruker AV-500 spectrometers operating at 400 and 500MHz respectively. All reported chemical shifts (S) are expressed in ppm relative to tetramethylsilane.
Table 1 lists compounds of Formula (I) that were prepared according to one of the above Examples.
Table 1:
Figure imgf000059_0001
Figure imgf000060_0001
nd: not determined Table 2:
Figure imgf000061_0001
Figure imgf000061_0002
D. Pharmacological 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. The behaviour of positive allosteric modulators tested at mGluR2 using the [35S]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.
T35SIGTPYS binding assay
The [35S]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, [35S]GTPyS (guanosine 5 '-triphosphate, labelled with gamma-emitting 35S), is measured. The G-protein α subunit catalyzes the exchange of guanosine 5 '-diphosphate (GDP) by guanosine triphosphate (GTP) and on activation of the GPCR by an agonist, [35S]GTPγS, 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 [35S]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 Gαl-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). Here we describe the use of the [35S]GTPyS binding assay using membranes from cells transfected with the human mGluR2 receptor and adapted from Schaffhauser et al ((2003) Molecular Pharmacology 4:798-810) for the detection of the positive allosteric modulation (PAM) properties of the compounds of this invention.
Membrane preparation
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). 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.
[35S]GTPyS binding assay
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 μg/assay well, 30 minutes, 30°C) in assay buffer (50 mM HEPES pH 7.4, 100 mM NaCl, 3 mM MgCl2, 50 μM GDP, 10 μg/ml saponin,) with increasing concentrations of positive allosteric modulator (from 0.3 nϊVl to 50 μM) and either a minimal pre-determined concentration of glutamate (PAM assay), or no added glutamate. For the PAM assay, membranes were pre-incubated with glutamate at EC25 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). After addition of [35S]GTPyS (0.1 nM, f.c.) to achieve a total reaction volume of 200 μl, microplates were shaken briefly and further incubated to allow [35S]GTPyS incorporation on activation (30 minutes, 30 0C). The reaction was stopped by rapid vacuum filtration over glass-fibre filter plates (Unifilter 96-well GF/B filter plates, Perkin-Elmer, Downers Grove, USA) microplate using a 96-well plate cell harvester (Filtermate, Perkin-Elmer, USA), and then by washing three times with 300 μl of ice-cold wash buffer (Na2PO4.2H20 10 mM, NaH2PO4-H2O 10 mM, pH = 7.4). Filters were then air-dried, and 40 μl of liquid scintillation cocktail (Microscint-O) was added to each well, and membrane-bound [35S]GTPyS was measured in a 96-well scintillation plate reader (Top-Count, Perkin-Elmer, USA). Non-specific [35S]GTPyS binding is determined in the presence of cold 10 μM GTP. Each curve was performed at least once using duplicate sample per data point and at 1 1 concentrations.
Data analysis
The concentration-response curves of representative compounds of the present invention in the presence of added EC25 of mGluR2 agonist glutamate to determine positive allosteric modulation (PAM), were generated using the Prism GraphPad software (Graph Pad Inc, San Diego, USA). The curves were fitted to a four-parameter logistic equation (Y=Bottom + (Top-Bottom)/(l+10Λ((LogEC50-X)*Hill Slope) allowing determination of EC5O values. The EC50 is the concentration of a compound that causes a half-maximal potentiation of the glutamate response. This is calculated by subtracting the maximal responses of glutamate in presence of a fully saturating concentration of a positive allosteric modulator from the response of glutamate in absence of a positive allosteric modulator. The concentration producing the half- maximal effect is then calculated as EC50.
Table 3. Pharmacological data for compounds according to the invention.
All compounds were tested in presence of mGluR2 agonist, glutamate at a predetermined EC25 concentration, to determine positive allosteric modulation (GTPyS-PAM). Values shown are averages of duplicate values of 11 -concentration response curves, from at least one experiment. All tested compounds showed a pEC5o (- logEC50) value of more than 5.0, from 6.05 to 7.20. The error of determination of a pEC5o value for a single experiment is estimated to be about 0.3 log-units.
Figure imgf000064_0002
Figure imgf000064_0001
nd = not determined
E. Composition examples
"Active ingredient" as used throughout these examples relates to a final compound of formula (I), the pharmaceutically acceptable salts thereof, the solvates and the stereochemically isomeric forms thereof. Typical examples of recipes for the formulation of the invention are as follows:
1. Tablets
Active ingredient 5 to 50 mg
Di-calcium phosphate 20 mg
Lactose 30 mg
Talcum 10 mg
Magnesium stearate 5 mg
Potato starch ad 200 mg In this Example, 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.
2. Suspension
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.
3. Injectable
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.
4. Ointment
Active ingredient 5 to 1000 mg
Stearyl alcohol 3 g
Lanoline 5 g
White petroleum 15 g
Water ad 100 g
In this Example, 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.
Reasonable variations are not to be regarded as a departure from the scope of the invention. It will be obvious that the thus described invention may be varied in many ways by those skilled in the art.

Claims

1. A compound having the formula (I)
R1
Figure imgf000066_0001
(I) or a stereochemical^ isomeric form thereof, wherein
R1 is Ci-6alkyl; or Ci-3alkyl substituted with C3-7cycloalkyl, phenyl, or phenyl substituted with halo, trifluoromethyl or trifluoromethoxy; R2 is halo, trifluoromethyl, Ci^alkyl or cyclopropyl;
R3 is hydrogen, fluoro, hydroxyl, hydroxyCi-3alkyl, hydroxyCi-3alkyloxy, fluoroCi-3alkyl, fluoroCi-3alkyloxy or cyano; and Ar is unsubstituted phenyl; or phenyl substituted with n radicals R4, wherein n is
1, 2 or 3; R4 is selected from the group consisting of hydrogen, halo, Ci-3alkyl, hydroxyCi^alkyl, polyhaloCi-3alkyl, cyano, hydroxyl, amino, carboxyl,
Ci-3alkyloxyCi-3alkyl, Ci-3alkyloxy, polyhaloCι-3alkyloxy, Ci-3alkylcarbonyl, mono- and di(Ci-3alkyl)amino, and morpholinyl; or two vicinal R4 radicals taken together form a bivalent radical of formula -N=CH-NH- (a),
-CH=CH-NH- (b), or
-0-CH2-CH2-NH- (c); or
R3 and a R4 radical in ortho position taken together form a bivalent radical of formula -CH2-O- (d), or
-0-CH2- (e); or a pharmaceutically acceptable salt or a solvate thereof.
2. The compound according to claim 1 wherein
R1 is 1 -butyl, 2 -methyl- 1 -propyl, 3 -methyl- 1 -butyl, (cyclopropyl)methyl or
2-(cyclopropyl)-l -ethyl; R3 is hydrogen, fluoro or cyano; and Ar is unsubstituted phenyl; or phenyl substituted with halo, trifluoromethyl, morpholinyl or hydroxyCioalkyl; or a pharmaceutically acceptable salt or a solvate thereof
3. The compound according to claim 1 wherein
R1 is 1-butyl, 3-methyl-l -butyl, (cyclopropyl)methyl or 2-(cyclopropyl)-l -ethyl; R2 is chloro;
R3 is hydrogen or fluoro; and
Ar is unsubstituted phenyl; or phenyl substituted with hydroxyCi-3 alkyl; or a pharmaceutically acceptable salt or a solvate thereof.
4. The compound according to claim 1 wherein said compound is selected from: 3'-chloro- 1 '-cyclopropylmethyl-4-phenyl-3,4,5,6-tetrahydro-2//, 1 'H- [ 1 ,4']bipyridinyl-2'-one;
- 1 '-butyl-3'-chloro-4-phenyl-3,4,5,6-tetrahydro-2H, 1 Η-[ 1 ,4I]bipyridinyl-2'- one; or a pharmaceutically acceptable salt or a solvate thereof.
5. A pharmaceutical composition comprising a therapeutically effective amount of a compound according to any one of claims 1 to 4 and a pharmaceutically acceptable carrier or excipient.
6. A compound according to any one of claims 1 to 4 for use as a medicament.
7. Use of a compound according to any one of claims 1 to 4 or a pharmaceutical composition according to claim 5 for the manufacture of a medicament for treating or preventing a condition in a mammal, including a human, the treatment or prevention of which is affected or facilitated by the neuromodulatory effect of mGluR2 positive allosteric modulators.
8. Use of a compound according to any one of claims 1 to 4 or a pharmaceutical composition according to claim 5 for the manufacture of a medicament for treating or preventing 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.
9. Use according to claim 8, wherein 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.
10. Use according to claim 8, wherein 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.
11. Use according to claim 8, wherein the central nervous system disorder is a personality disorder selected from the group of obsessive-compulsive personality disorder and schizoid, schizotypal disorder.
12. Use according to claim 8, wherein 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.
13. Use according to claim 8, wherein the central nervous system disorder is an eating disorder selected from the group of anorexia nervosa and bulimia nervosa.
14. Use according to claim 8, wherein 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.
15. Use according to claim 8, wherein the central nervous system disorder is migraine.
16. Use according to claim 8, wherein 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.
17. Use according to claim 8, wherein the childhood disorder is attention-defϊcit/hyperactivity disorder.
18. Use according to claim 8, wherein 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.
19. Use according to claim 8, wherein the central nervous system disorder is selected from the group of anxiety, schizophrenia, migraine, depression, and epilepsy.
20. Use of a compound according to any one of claims 1 to 4 in combination with an orthosteric agonist of mGluR2 for the manufacture of a medicament for treating or preventing a condition as cited in any one of claims 7 to 19.
21. A compound according to any one of claims 1 to 4 for use in treating or preventing 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.
22. A method of treating or preventing 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 comprising administering to a subject a compound according to any one of claims 1 to 4.
PCT/EP2008/007551 2007-09-14 2008-09-12 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4'] bipyridinyl-2'-ones WO2009033704A1 (en)

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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
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HRP20110278T1 (en) 2011-05-31
CN101801951A (en) 2010-08-11
CA2696948C (en) 2013-04-30
ES2356032T3 (en) 2011-04-04
HK1143820A1 (en) 2011-01-14
AU2008297878A1 (en) 2009-03-19
CY1111219T1 (en) 2015-06-11
NZ584145A (en) 2012-03-30
MY152078A (en) 2014-08-15
US11071729B2 (en) 2021-07-27
AU2008297878B2 (en) 2011-07-07
BRPI0816767B8 (en) 2021-05-25
JP2010539121A (en) 2010-12-16
BRPI0816767B1 (en) 2021-03-09
IL229304A0 (en) 2013-12-31
US9114138B2 (en) 2015-08-25
CN101801951B (en) 2013-11-13
EA201000314A1 (en) 2011-02-28
KR20100080535A (en) 2010-07-08
TW201412313A (en) 2014-04-01
UA100126C2 (en) 2012-11-26
BRPI0816767A2 (en) 2017-05-16
JP5133416B2 (en) 2013-01-30
US20200038391A1 (en) 2020-02-06
IL204032A (en) 2013-11-28
RS51660B (en) 2011-10-31
PT2203439E (en) 2011-02-11
US20130196992A1 (en) 2013-08-01
US9132122B2 (en) 2015-09-15
CA2696948A1 (en) 2009-03-19
KR20140034904A (en) 2014-03-20
US20220000856A1 (en) 2022-01-06
DE602008004794D1 (en) 2011-03-10
CL2008002745A1 (en) 2009-05-22
IL229304A (en) 2015-08-31
CN103342695B (en) 2015-04-22
US20100240688A1 (en) 2010-09-23
CN103342695A (en) 2013-10-09
EA017648B1 (en) 2013-02-28
ATE496906T1 (en) 2011-02-15
US20130197019A1 (en) 2013-08-01
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HK1189885A1 (en) 2014-06-20
KR101520086B1 (en) 2015-05-14

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