WO2005080397A2 - Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders - Google Patents
Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders Download PDFInfo
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- WO2005080397A2 WO2005080397A2 PCT/US2005/005218 US2005005218W WO2005080397A2 WO 2005080397 A2 WO2005080397 A2 WO 2005080397A2 US 2005005218 W US2005005218 W US 2005005218W WO 2005080397 A2 WO2005080397 A2 WO 2005080397A2
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- alkyl
- alkylnr
- oxadiazol
- triazolo
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- 0 **C1=NNCN1I Chemical compound **C1=NNCN1I 0.000 description 8
- FICAQKBMCKEFDI-UHFFFAOYSA-N Cc1n[o]c(C)c1 Chemical compound Cc1n[o]c(C)c1 FICAQKBMCKEFDI-UHFFFAOYSA-N 0.000 description 2
- HNJOAIYFUCQZAA-UHFFFAOYSA-N Cc1n[o]c(C)n1 Chemical compound Cc1n[o]c(C)n1 HNJOAIYFUCQZAA-UHFFFAOYSA-N 0.000 description 2
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Definitions
- the present invention relates to a new heterocyclic compounds, to pharmaceutical 5 compositions containing the compounds and to the use of the compounds in therapies related to metabotropic glutamate receptor-mediated conditions.
- the present invention further relates to processes for the preparation of the compounds and to new intermediates used in the preparation thereof.
- Glutamate is the major excitatory neurotransmitter in the mammalian central nervous 10 system (CNS). Glutamate produces its effects on central neurons by binding to and thereby activating cell surface receptors. These receptors have been divided into two major classes, the ionotropic and metabotropic glutamate receptors, based on the structural features of the receptor proteins, the means by which the receptors transduce signals into the cell, and pharmacological profiles.
- mGluRs metabotropic glutamate receptors
- Activation of mGluRs in intact mammalian neurons elicits one or more of the following responses: activation of phospholipase C; increases in phosphoinositide (PI) hydrolysis; intracellular calcium release; activation of phospholipase D; 20 activation or inhibition of adenyl cyclase; increases or decreases in the formation of cyclic adenosine monophosphate (cAMP); activation of guanylyl cyclase; increases in the formation of cyclic guanosine monophosphate (cGMP); activation of phospholipase A 2 ; increases in arachidonic acid release; and increases or decreases in the activity of voltage- and ligand-gated ion channels.
- PI phosphoinositide
- Metabotropic glutamate receptor subtypes may be subdivided into three groups, Group I, Group II, and Group III mGluRs, based on amino acid sequence homology, 5 the second messenger systems utilized by the receptors, and by their pharmacological characteristics.
- Group I mGluR comprises mGluRl, mGluR5 and their alternatively spliced variants. The binding of agonists to these receptors results in the activation of phospholipase C and the subsequent mobilization of intracellular calcium.
- Group I mGluRs 10 Neurological, psychiatric and pain disorders. Attempts at elucidating the physiological roles of Group I mGluRs suggest that activation of these receptors elicits neuronal excitation. Various studies have demonstrated that Group I mGluRs agonists can produce postsynaptic excitation upon application to neurons in the hippocampus, cerebral cortex, cerebellum, and thalamus, 15 as well as other CNS regions. Evidence indicates that this excitation is due to direct activation of postsynaptic mGluRs, but it also has been suggested that activation of presynaptic mGluRs occurs, resulting in increased neurotransmitter release. Baskys, Trends Pharmacol Sci. 15:92 (1992), Schoepp, Neurochem. Int.
- mGluR activation has been suggested to play a modulatory role in a variety of other normal processes including synaptic transmission, neuronal development, 30 apoptotic neuronal death, synaptic plasticity, spatial learning, olfactory memory, central control of cardiac activity, waking, motor control and control of the vestibulo-
- Group I mGluRs appear to increase glutamate- mediated neuronal excitation via postsynaptic mechanisms and enhanced presynaptic 15 glutamate release, their activation probably contributes to the pathology. Accordingly, selective antagonists of Group I mGluR receptors could be therapeutically beneficial in all conditions underlain by excessive glutamate-induced excitation of CNS neurons, specifically as neuroprotective agents, analgesics or anticonvulsants. Recent advances in the elucidation of the neurophysiological roles of metabotropic 20 glutamate receptors generally and Group I in particular, have established these receptors as promising drug targets in the therapy of acute and chronic neurological and psychiatric disorders and chronic and acute pain disorders.
- Gastro intestinal disorders 25 The lower esophageal sphincter (LES) is prone to relaxing intermittently. As a consequence, fluid from the stomach can pass into the esophagus since the mechanical barrier is temporarily lost at such times, an event hereinafter referred to as "reflux”.
- Gastro-esophageal reflux disease (GERD) is the most prevalent upper gastrointestinal 30 tract disease. Current pharmacotherapy aims at reducing gastric acid secretion, or at neutralizing acid in the esophagus. The major mechanism behind reflux has been
- TLESRs transient lower esophageal sphincter relaxations
- TLESR transient lower esophageal sphincter relaxations
- Mittal R.K., Holloway, R.H., Penagini, R., Blackshaw, L.A., Dent, J., 1995
- Transient lower esophageal sphincter relaxation Gastroenterology 109, pp. 601-610.
- the term “reflux” is herein defined as fluid from the stomach being able to pass into 15 the esophagus, since the mechanical barrier is temporarily lost at such times.
- GSD gastro-esophageal reflux disease
- M.A. SmoutA.J.P.M.
- Diagnosis of reflux disease Bailliere 's Clin. Gastroenterol. 14, pp. 759-774.
- X 1 , X 2 , X 3 , X 4 , and X 5 are independently selected from the group 5 consisting of C, CR 5 , N, O, and S, wherein at least one of X 1 , X 2 , X 3 , X 4 , and X 5 is not N;
- X 6 is selected from the group consisting of a bond and CR 5 R 6 ;
- X 7 is CR 5 or N;
- X 8 is selected from the group consisting of a bond, CR 5 R 6 , NR 5 , O, S, SO, and SO 2 ;
- X 9 is CR 5 or N; and
- X 10 is selected from the group consisting of a bond, CR 5 R 6 , (CR 5 R 6 ) 2 , O, S, andNR 5 .
- R 1 is selected from the group consisting of hydroxy, halo, nitro, C h alky-halo, OC]. 6 alkylhalo, d- ⁇ alkyl, Od- ⁇ alkyl, C . 6 alkenyl, OC 2 . 6 alkenyl, C 2 . 6 alkynyl, OC 2 . 6 alkynyl, Co- 6 alkylC 3 . 6 cycloalkyl, OC 0 . 6 alkylC . 6 cycloalkyl, C 0 . 6 alkylaryl, OC 0 .
- 6 alkylaryl CHO, (CO)R 5 , O(CO)R 5 , O(CO)OR 5 , O(CN)OR 5 , C-ealkylOR 5 , OC 2 . 6 alkylOR 5 , C ⁇ . 6 alkyl(CO)R 5 , OC 1 . 6 alkyl(CO)R 5 , C 0 . 6 alkylCO 2 R 5 , OC ⁇ . 6 alkylCO 2 R 5 , 15 Co- 6 alkylcyano, OC 2 . 6 alkylcyano, C 0 . 6 alkylNR 5 R 6 , OC 2 . 6 alkylNR 5 R 6 , Ci.
- R 2 is selected from the group consisting of hydrogen, hydroxy, halo, nitro, Ci. 6 alkylhalo, OC ⁇ alkylhalo, C h alky!, OC ⁇ an y!, C 2 . 6 alkenyl, OC 2 . 6 alkenyl, C 2 _
- R 4 is selected from the group consisting of hydroxy, halo, nitro, Ci- ⁇ alkylhalo, OC ⁇ . 6 alkylhalo, C ⁇ . 6 alkyl, OC ⁇ . 6 alkyl, C 2 . 6 alkenyl, OC 2 . 6 alkenyl, C .ealkynyl, OC 2 . 6 alkynyl, C 0 - 6 alkylC 3 . 6 cycloalkyl, OC 0 . 6 alkylC 3 . 6 cycloalkyl, C 0 . 6 alkylaryl, OC 0 .
- R and R are independently selected from the group consisting of hydrogen, Ci. 6 alkyl, C 3 . cycloalkyl and aryl.
- A is selected from the group consisting of hydrogen, hydroxy, halo, nitro, Ci. 6 alkylhalo, OC ⁇ . - 6 alkylhalo, C 2 . 6 alkenyl, OC 2 _ 6 alkenyl, C 2 . 5 6 alkynyl, OC 2 _ 6 alkynyl, Co- 6 alkylC 3 . 6 cycloalkyl, OC 0 . 6 alkylC 3 . 6 cycloalkyl, C 0 .
- compositions comprising a therapeutically effective amount of a compound of formula I and a 20 pharmaceutically acceptable diluent, excipient and/or inert carrier.
- a pharmaceutical composition comprising a compound of formula I for use in the treatment of mGluR5 receptor mediated disorders, and for use in the treatment of neurological disorders, psychiatric disorders, gastrointestinal disorders and pain disorders.
- the compound of formula I for use in therapy, especially for the treatment of mGluR5 receptor mediated disorders, and for the treatment of neurological disorders, psychiatric disorders, gastrointestinal disorders and pain disorders.
- a further aspect of the invention is the use of a compound according to formula I for 30 the manufacture of a medicament for the treatment or prevention of obesity and obesity related conditions, as well as treating eating disorders by inhibition of
- the object of the present invention is to provide compounds exhibiting an activity at metabotropic glutamate receptors (mGluRs), especially at the mGluR5 receptors.
- mGluRs metabotropic glutamate receptors
- 10 Listed below are definitions of various terms used in the specification and claims to describe the present mvention.
- a group is qualified by 'hereinbefore defined', 'defined hereinbefore' or 'defined above' said group encompasses the first occurring and broadest definition as well as 15 each and all of the other definitions for that group.
- 'Ci- ⁇ ' means a carbon group having 1, 2, 3, 4, 5 or 6 carbon atoms.
- alkyl includes both straight and branched chain alkyl groups and may be, but are not limited to methyl, ethyl, n- propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, n-pentyl, i-pentyl, t-pentyl, neo- pentyl, n-hexyl or i-hexyl, t-hexyl.
- Ci. 3 alkyl has 1 to 3 carbon atoms and 25 may be methyl, ethyl, n-propyl or i-propyl.
- cycloalkyl refers to an optionally substituted, saturated cyclic hydrocarbon ring system.
- C 3 . cycloalkyl may be cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyi or cycloheptyl.
- alkoxy includes both straight or branched alkoxy groups. C ⁇ - 3 alkoxy may be, but is not limited to methoxy, ethoxy, n-propoxy or i-propoxy.
- bond may be a saturated or 5 unsaturated bond.
- alkylhalo means an alkyl group as defined above, which is substituted with halo as described above.
- C ⁇ - 6 alkylhalo may include, but is not limited to fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl or bromopropyl.
- OCi. 6 alkylhalo may include, but is not limited to fluoromethoxy, difluoromethoxy, trifluoromethoxy, fluoroethoxy or difluoroethoxy.
- alkenyl includes both straight 15 and branched chain alkenyl groups.
- C 2 - 6 alkenyl refers to an alkenyl group having 2 to 6 carbon atoms and one or two double bonds, and may be, but is not limited to vinyl, allyl, propenyl, i-propenyl, butenyl, i-butenyl, crotyl, pentenyl, i- pentenyl and hexenyl.
- alkynyl includes both straight 20 and branched chain alkynyl groups.
- C 2 - 6 alkynyl having 2 to 6 carbon atoms and one or two triple bonds may be, but is not limited to ethynyl, propargyl, butynyl, i-butynyl, pentynyl, i-pentynyl and hexynyl.
- aryl refers to an optionally substituted monocyclic or bicyclic hydrocarbon ring system containing at least one 25 unsaturated aromatic ring. Examples and suitable values of the term “aryl” are phenyl, naphthyl, 1,2,3,4-tetrahydronaphthyl, indyl and indenyl.
- heteroaryl refers to an optionally substituted monocyclic or bicyclic unsaturated, ring system containing at least one heteroatom selected independently from N, O or S.
- heteroaryl may be, but are not limited to fhiophene, thienyl, pyridyl, thiazolyl, furyl, pyrrolyl, triazolyl, imidazolyl, oxadiazolyl, oxazolyl, isoxazolyl, pyrazolyl,
- alkylaryl refers to a substituent that is attached via the alkyl group to an aryl, heteroaryl and cycloalkyl group.
- heterocycloalkyl refers to an 10 optionally substituted, saturated cyclic hydrocarbon ring system wherein one or more of the carbon atoms are replaced with heteroatom.
- heterocycloalkyl includes but is not limited to pyrrolidine, tetrahydrofuran, tetrahydrothiophene, piperidine, piperazine, morpholine, thiomorpholine, tetrahydropyran, tetrahydrothiopyran. 15
- the term “5- or 6-membered ring containing atoms independently selected from C, N, O or S” includes aromatic and heteroaromatic rings as well as carbocyclic and heterocyclic rings, which may be saturated, partially saturated or unsaturated.
- Such rings may be, but are not limited to furyl, isoxazolyl, isothiazolyl, oxazolyl, pyrazinyl, pyrazolyl, 20 pyridazinyl, pyridyl, pyrimidyl, pyrrolyl, thiazolyl, thienyl, imidazolyl, imidazolidinyl, imidazolinyl, triazolyl, morpholinyl, piperazinyl, piperidyl, piperidonyl, pyrazolidinyl, pyrazolinyl, pyrrolidinyl, pyrrolinyl, tetrahydropyranyl, thiomorpholinyl, phenyl, cyclohexyi, cyclopentyl and cyclohexenyl.
- a subscript is the integer 0 (zero) the group to which the subscript refers, indicates that the group is absent, i.e. there is a direct bond between the 30 groups.
- fused rings refers to two rings which share 2 common atoms.
- bridge means a molecular fragment, containing one or more atoms, or a bond, which connects two remote atoms in a ring, thus forming either bi- or tricyclic systems.
- bridge means a molecular fragment, containing one or more atoms, or a bond, which connects two remote atoms in a ring, thus forming either bi- or tricyclic systems.
- X 1 , X 2 , X 3 , X 4 , and X 5 are independently selected from the group consisting of C, CR 5 , N, O, and S, wherein at least one of X 1 , X 2 , X 3 , X 4 , and X 5 is not N;
- X 6 is selected from the group consisting of a bond and CR 5 R 6 ;
- X 7 is CR 5 or N, 10 preferably N;
- X 8 is selected from the group consisting of a bond, CR 5 R 6 , NR 5 , O, S, SO, and SO 2 .
- X 8 is a bond, CR 5 R 6 , NR 5 , O, or S.
- X 9 is CR 5 or N and X 10 is selected from the group consisting of a bond, CR 5 R 6 , (CR 5 R 6 ) 2 , O, S, and NR 5 , preferably a bond, CR 5 R 6 , (CR 5 R 6 ) 2 , O, or S.
- R 1 is selected from the group consisting of hydroxy, halo, nitro, d-ealkylhalo, OCi. 15 6 alkylhalo, C ⁇ - 6 alkyl, Od- 6 alkyl, C 2 . 6 alkenyl, OC 2 . 6 alkenyl, C 2 . 6 alkynyl, OC 2 . 6 alkynyl, C 0 .
- R 1 is halo, C ⁇ _ 6 alkylhalo, d- 6 alkyl, Od- ⁇ alkyl, or C 0 - 6 alkylcyano.
- R 2 is selected from the group consisting of hydrogen, hydroxy, halo, nitro, d. 5 6 alkylhalo, Od-ealkylhalo, C ⁇ - 6 alkyl, Od. 6 alkyl, C 2 - 6 alkenyl, OC 2 - 6 alkenyl, C 2 - 6 alkynyl, OC 2 .
- R 3 is a 5- or 6-membered ring containing atoms independently selected from the 20 group consisting of C, N, O and S, wherein said ring may be substituted by one or more A.
- R is a 6-membered ring.
- R 4 is selected from the group consisting of hydroxy, halo, nitro, d- 6 alkylhalo, OCi. 6 alkylhalo, C ⁇ _ 6 alkyl, Od-ealkyl, d-ealkenyl, OC 2 . 6 alkenyl, C 2 . 6 alkynyl, OC . 6 alkynyl, C 0 .
- R 4 when not hydrogen, preferably is d- 6 alkylhalo or d- 6 alkyl.
- R 5 and R 6 are independently selected from the group consisting of hydrogen, C ⁇ . 6 alkyl, C 3 . cycloalkyl and aryl.
- R 5 and R 6 are selected from hydrogen and Ci- ⁇ alkyl.
- 10 A is selected from the group consisting of hydrogen, hydroxy, halo, nitro, Ci. 6 alkylhalo, Od ⁇ alkylhalo, d. 6 alkyl, OC ⁇ _ 6 alkyl, C2- 6 alkenyl, OC 2 .
- X 3 is C 15 orN.
- the ring containing X 1 , X 2 , X 3 , X 4 , and X 5 is selected from the group consisting of:
- the ring is either: 7 R 5
- X preferably is N, while X is preferably a bond.
- X 9 is CR 5
- X 10 is NR 5 , O, CR 5 R 6 , or (CR 5 R 6 ) 2 .
- X 8 is preferably S.
- X 9 preferably is CR 5
- X 10 is a bond.
- X 9 is N.
- the fused ring containing X 7 , X 8 , X 9 , and 10 X 10 is selected from the group consisting of:
- Certain other embodiments of the invention are represented by the following exemplary compounds: 15 7-[5-(5-Chloro-2-fluorophenyl)-l,2,4-oxadiazol-3-yl]-3-(2-thienyl)-6,7-dihydro- 5H-[1 ,2,4]triazolo[3,4-b] [1 ,3]thiazine, 9- ⁇ [5-(3-chloro ⁇ henyl)-l,2,4-oxadiazol-3-yl]methyl ⁇ -3-pyridin-4-yl-6,7,8,9- tetrahydro-5H-[l,2,4]triazolo[4,3-a][l,3]diazepine, 9- ⁇ l-[5-(3-chlorophenyl)-l,2,4-oxadiazol-3-yl]ethyl ⁇ -3- ⁇ yridin-4-yl-6,7,8,9- 20 tetrahydro-5H-[
- Embodiments of the invention include salt forms of the compounds of Formula I.
- Salts for use in pharmaceutical compositions will be pharmaceutically acceptable salts, but other salts may be useful in the production of the compounds of Formula I.
- a suitable pharmaceutically acceptable salt of the compounds of the invention is, for example, an acid-addition salt, for example an inorganic or organic acid.
- a 25 suitable pharmaceutically acceptable salt of the compounds of the invention is an alkali metal salt, an alkaline earth metal salt or a salt with an organic base.
- Other pharmaceutically acceptable salts and methods of preparing these salts may be found in, for example, Remington's Pharmaceutical Sciences (18 th Edition, Mack Publishing Co.) 1990.
- Some compounds of formula I may have chiral centres and/or geometric isomeric centres (E- and Z- isomers), and it is to be understood that the invention encompasses all such optical, diastereoisomeric and geometric isomers.
- the invention also relates to any and all tautomeric forms of the compounds of 5 Formula I.
- the invention further relates to hydrate and solvate forms of the compounds of Formula I.
- composition 10 comprising as active ingredient a therapeutically effective amount of the compound of Formula I, or salts, solvates or solvated salts thereof, in association with one or more pharmaceutically acceptable diluent, excipients and/or inert carrier.
- the composition may be in a form suitable for oral administration, for example as a 15 tablet, pill, syrup, powder, granule or capsule, for parenteral injection (including intravenous, subcutaneous, intramuscular, intravascular or infusion) as a sterile solution, suspension or emulsion, for topical administration e.g. as an ointment, patch or cream or for rectal administration e.g. as a suppository.
- compositions may be prepared in a conventional manner using 20 one or more conventional excipients, pharmaceutical acceptable diluents and/or inert carriers.
- Suitable daily doses of the compounds of formula I in the treatment of a mammal, including man are approximately 0.01 to 250 mg/kg bodyweight at peroral administration and about 0.001 to 250 mg/kg bodyweight at parenteral administration.
- the typical daily dose of the active ingredients varies within a wide range and will depend on various factors such as the relevant indication, severity of the illness being treated, the route of administration, the age, weight and sex of the patient and the particular compound being used, and may be determined by a physician.
- the compounds according to the present invention exhibit a high degree of potency and selectivity for individual metabotropic glutamate receptor (mGluR) subtypes. Accordingly, the compounds of the present invention are expected to be useful in the treatment of conditions associated with excitatory activation of 5 mGluR5 and for inhibiting neuronal damage caused by excitatory activation of mGluR5.
- the compounds may be used to produce an inhibitory effect of mGluR5 in mammals, including man.
- the mGluR Group I receptor including mGluR5 are highly expressed in the central and peripheral nervous system and in other tissues.
- the 10 compounds of the invention are well suited for the treatment of mGluR5-mediated disorders such as acute and chronic neurological and psychiatric disorders, gastrointestinal disorders, and chronic and acute pain disorders.
- the invention relates to compounds of Formula I, as defined hereinbefore, for use in therapy.
- the invention relates to compounds of Formula I, as defined hereinbefore, for use in treatment of mGluR5-mediated disorders.
- the invention relates to compounds of Formula I, as defined hereinbefore, for use in treatment of Alzheimer's disease senile dementia, AIDS-induced dementia, Parkinson's disease, amylotropic lateral sclerosis, Huntington's Chorea, migraine, 20 epilepsy, schizophrenia, depression, anxiety, acute anxiety, ophthalmological disorders such as retinopathies, diabetic retinopathies, glaucoma, auditory neuropathic disorders such as tinnitus, chemotherapy induced neuropathies, post-herpetic neuralgia and trigeminal neuralgia, tolerance, dependency, Fragile X, autism, mental retardation, schizophrenia and Down's Syndrome.
- the invention relates to compounds of Formula I, as defined hereinbefore, for use in treatment of pain related to migraine, inflammatory pain, neuropathic pain disorders such as diabetic neuropathies, arthritis and rheumatoid diseases, low back pain, postoperative pain and pain associated with various conditions including angina, renal or biliary colic, menstruation, migraine and gout.
- the invention relates to compounds of Formula I as defined hereinbefore, for use in treatment of stroke, head trauma, anoxic and ischemic injuries, hypoglycemia, cardiovascular diseases and epilepsy.
- a further aspect of the invention is the use of a compound according to formula I for 5 the manufacture of a medicament for the treatment or prevention of obesity and obesity related conditions, as well as treating eating disorders by inhibition of excessive food intake and the resulting obesity and complications associated therewith.
- the present invention relates also to the use of a compound of Formula I as defined 10 hereinbefore, in the manufacture of a medicament for the treatment of mGluR Group I receptor-mediated disorders and any disorder listed above.
- One embodiment of the invention relates to the use of a compound according to Formula I in the treatment of gastrointestinal disorders.
- Another embodiment of the invention relates to the use of a compound according to 15 Formula I, for the manufacture of a medicament for the inhibition of transient lower esophageal sphincter relaxations, for the treatment of GERD, for the prevention of G.I. reflux, for the treatment regurgitation, treatment of asthma, treatment of laryngitis, treatment of lung disease and for the management of failure to thrive.
- a further embodiment of the invention relates to the use of a compound according to 20 Formula I for the manufacture of a medicament for the treatment or prevention of functional gastrointestinal disorders, such as functional dyspepsia (FD).
- FD functional dyspepsia
- Yet another aspect of the invention is the use of a compound according to Formula I for the manufacture of a medicament for the treatment or prevention of irritable bowel syndrome (IBS), such as constipation predominant IBS, diarrhea predominant IBS or 25 alternating bowel movement predominant IB S .
- IBS irritable bowel syndrome
- the invention also provides a method of treatment of mGluR5 -mediated disorders and any disorder listed above, in a patient suffering from, or at risk of, said condition, which comprises administering to the patient an effective amount of a compound of 30 Formula I, as hereinbefore defined.
- the dose required for the therapeutic or preventive treatment of a particular disorder will necessarily be varied depending on the host treated, the route of administration and the severity of the illness being treated.
- the term “therapy” and “treatment” includes 5 prevention or prophylaxis, unless there are specific indications to the contrary.
- the terms “therapeutic” and “therapeutically” should be construed accordingly.
- the term “antagonist” and “inhibitor” shall mean a compound that by any means, partly or completely, blocks the transduction pathway leading to the production of a response by the ligand. 10
- disorder unless stated otherwise, means any condition and disease associated with metabotropic glutamate receptor activity.
- Non- Medical use In addition to their use in therapeutic medicine, the compounds of Formula I, salts or 15 hydrates thereof, are also useful as pharmacological tools in the development and standardization of in vitro and in vivo test systems for the evaluation of the effects of inhibitors of mGluR related activity in laboratory animals such as cats, dogs, rabbits, monkeys, rats and mice, as part of the search for new therapeutics agents.
- Another aspect of the present mvention provides processes for preparing compounds of Formula I, or salts or hydrates thereof. Processes for the preparation of the compounds in the present invention are described herein. Throughout the following description of such processes it is to be understood that, 25 where appropriate, suitable protecting groups will be added to, and subsequently removed from, the various reactants and intermediates in a manner that will be readily understood by one skilled in the art of organic synthesis. Conventional procedures for using such protecting groups as well as examples of suitable protecting groups are described, for example, in "Protective Groups in Organic Synthesis", T. W. Green, 30 P.G.M. Wuts, Wiley-Interscience, New York, (1999). It is also to be understood that a transformation of a group or substituent into another group or substituent by
- OAc acetate OMs mesylate or methane sulfonate ester 20 OTs tosylate, toluene sulfonate or 4-methylbenzene sulfonate ester PPTS pyridinium ⁇ -toluenesulfonate pTsOH / toluenesulfonic acid RT, rt, r.t. room temperature sat.
- alkylsulphonyl[l,2,4]triazoles can be prepared from the corresponding [l,2,4]triazolethiones by initial alkylation of the sulphur atom with primary alkyl halides such as Mel and Etl (alkyl is Me and Et respectively) in MeOH, 15 EtOH, THF, acetone or the like at -30 to 100 °C, followed by oxidation of the sulphur atom using for example KMnO in mixtures of water and acetic acid, or mCPBA in DCM, at -20 to 120 °C, or by using any other suitable oxidant.
- primary alkyl halides such as Mel and Etl (alkyl is Me and Et respectively) in MeOH, 15 EtOH, THF, acetone or the like at -30 to 100 °C
- oxidation of the sulphur atom using for example KMnO in mixtures of water and acetic acid, or mCPBA in DCM, at -20 to 120
- [l,2,4]triazolethiones wherein R' is a suitable side chain which may or may not be protected as appropriate, are for example prepared by N- acylation of a thiosemicarbazide, using any suitable acylating agent such as acid 5 chlorides, bromides or fluorides (LG is CI, Br or F) in for example pyridine, or acids (LG is OH), that are activated by the treatment with standard activating reagents as described herein below, in DMF, THF, DCM or the like at -20 to 120 °C, followed by ring closure of the initially formed acyclic intermediate either spontaneously under the conditions of the acylation, or by heating at 50 to 150 °C in pyridine or in aqueous 10 solvents in the presence of a base, such as NaHCO 3 or Na 2 CO 3 , with or without co- solvents such as dioxane, THF, MeOH, EtOH or
- [l,2,4]oxadiazoles with a carbon alpha to the 20 heterocycle wherein G 1 , G 2 and G 3 are defined as described in scheme 2, are formed by cyclization of G - and G -substituted-acyloxyimidamides in solvents such as pyridine, DMF, or water containing mixtures thereof, at 40 to 140 °C, alternatively in aqueous alcoholic solvents in the presence of sodium acetate at temperatures from 40 to 140 °C, with the later method being preferred if one of the groups G or G contains 25 a chiral stereocenter.
- solvents such as pyridine, DMF, or water containing mixtures thereof
- acylating agent carrying a leaving group LG with a G 1 -substituted hydroxamidine.
- the leaving group LG may be chloro or any other suitable leaving group as for example generated by in situ treatment of the corresponding acid (LG is OH) with standard activating reagents as described herein below.
- G 1 -substituted 5 hydroxamidines are formed by reaction of the corresponding nitrile with the free base of hydroxylamine, or hydroxylamine hydrochloride in the presence of a base such as triethylamine, pyridine or sodium carbonate, in solvents such as ethanol, water or pyridine at temperatures from -20 to 120 °C
- suitable solvent such as THF, pyridine or DMF
- Cyclic carbono-2-one hydrazones may be generated from 25 isothioureas, in which the S-alkyl (for example S-Me or S-Et) moiety acts as a leaving group upon treatment with hydrazine in solvents such as pyridine, methanol, ethanol, 2-propanol, THF or the like at -20 to 180 °C.
- the open intermediate can also be
- Cyclic isothioureas are obtained by S-alkylation of the corresponding thioureas, which are commercially available or prepared according to standard procedures as known to the one skilled in the art, with for example Mel or Etl in acetone, EtOH, THF, DCM or the like at -100 to 100 °C.
- carbocylic [l,2,4]triazoles are obtained by treating cyclic lactam hydrazones with a proper acylating agent to lead to an open chain intermediate 15 which forms the triazole ring spontaneously or by heating as described herein above.
- Such cyclic lactam hydrazones are generated from the cyclic enol ether, in which the O-alkyl (alkyl is Me) moiety acts as a leaving group upon treatment with hydrazine as described herein above.
- Such open chain intermediates may also be formed directly by treatment of lactam enol ethers by treatment with acyl hydrazides as described 20 herein above. Lactam enol ethers are prepared from their corresponding lactams by treatment with Me 3 OBF 4 or dimethylsulfate [Org.Prep.Proced.Int;24, 1992, pp. 147- 158 or Tetrahedron Lett. 42, 2001, pp. 173-1776].
- R-substituted lactams are either commercially available or may be prepared by alkylation in the alpha position by treatment with 2 equivalents of a strong base such as n-BuLi followed by addition of 25 1 equivalent of alkylating agent, such as alkyl halide, mesylate or ttiflate, in an aprotic solvents such as THF [J.Org. Chem. 64, 1999, pp. 6041-6048] or, alternatively, via a
- N-protected lactam e.g. trimefhylsilyl valerolactam or the likes, where only one equivalent of base is needed to generate the anion for alkylation [J.Org. Chem. 65, 2000, pp. 2684-2695].
- the alkylation results in the formation of racemic product which may be separated into its enantiopure forms here, or at a later stage of the synthetic pathway by e.g. chiral chromatography.
- Aryl glucosettiazoles may be obtained by 15 cyclization of the intermediate aryl glucosazone in the presence of copper (II) sulfate in aqueous mixtures of for example dioxane or THF at-20 to 120 °C.
- the aryl glucosazone in turn is made by coupling of arylhydrazines with fructose in acetic acid and water at -20 to 120 °C.
- isoxazoles are formed by reaction and in-situ cyclization of dioxo butyric ester derivatives with hydroxylamine hydrochloride in solvents such as ethanol, 2-propanol or DMF at temperatures from 40 to 140 °C.
- Dioxo butyric esters are formed through the reaction of acetophenones with dialkyl oxolates (alkyl is for example Me or Et) in the presence of a sttong base such as sodium hydride in solvents such as DMF or toluene at temperatures from -20 to 120 °C.
- R is H or alkyl (Me, Et)
- coupling with an aliphatic acid chloride derivative in THF, DMF, toluene or the like, optionally in the presence of a base such as triethylamine or a carbonate, 15 leads to the formation of an acyl benzohydrazide derivative, which is cyclized at elevated temperatures in the presence of a dehydrating agent such as phosphorous pentoxide in solvents such as toluene or DMF or mixtures thereof to yield the [l,3,4]oxadiazole product.
- [l,3,4]oxadiazoles may be made directly from the acid hydrazide using trialkyl ortho esters either neat or in solvents such as 20 toluene or xylenes at elevated temperatures.
- oxygen linked triazoles may be prepared by bond formation through nucleophilic replacement of a leaving group (LG) in which an alcohol acts as O- nucleophile under basic conditions.
- a base is used, for example, NaH or Cs 2 CO 3 , at temperatures from 0 to 80 °C in polar aprotic solvents such as DMF or acetonitrile.
- suitable leaving groups are alkylsulfonyls, such as methanesulfonyl and ethanesulfonyl, and halogens, such as chloro.
- arylsulfonylhydrazones are prepared through condensation between aldehydes, for example cinnamaldehyde or glyoxalic acid, with arylsulphonylhydrazines, such as 4-toluensulfonylhydrazine, in a suitable solvent, for example
- 02.1338789.2 example methanol, ethanol, DMF or dialkylethers, at a temperature between 0 to 100 °C, alternatively without solvent under microwave irradiation.
- arylhydrazones may be formed from the reaction of arylhydrazines, with aldehydes.
- tetrazoles wherein G is an electron withdrawing group, such as an olefm, carbonyl or aryl group, may be prepared by 1,3-dipolar cycloaddition of a diazonium salt onto an aryl sulfonyl hydrazone followed by elimination of the arylsulfmic acid to generate the tetrazole ring, in protic solvents 15 such as water and alcohol or mixtures thereof, in basic aprotic solvents such as pyridine, or mixtures of these solvents with protic solvents used to generate the diazonium salt.
- protic solvents 15 such as water and alcohol or mixtures thereof
- basic aprotic solvents such as pyridine
- Diazonium salts in turn are available from a suitably substituted aryl or heteroaryl amine using well known methods, via diazotization using a nitrite source such as sodium nitrite or isoamyl 20 nitrite in the presence of a suitable acid source such as hydrochloric acid or tetrafluoroboric acid in a solvent such as water at a temperature between -10 to 0 °C.
- a suitable acid source such as hydrochloric acid or tetrafluoroboric acid
- a solvent such as water at a temperature between -10 to 0 °C.
- a less soluble counterion X " such as tetrafluoroborate
- Soluble diazonium salts formed 25 using other acid sources may be precipitated by the addition of a suitable reagent such as tetrafluoroboric acid or sodium tetrafluoroborate.
- tetrazoles may also be prepared from the reaction of an arylhydrazone, wherein G is defined as in scheme 9 and 10, with an aryl azide in a suitable solvent such as ethanol or pyridine.
- a suitable solvent such as ethanol or pyridine.
- Aryl azides may be formed for example by using sodium azide with an aryl diazonium salt, which may in turn be prepared as described above from an aryl amine, for example 10 aniline or 2,4,6-tribromoaniline.
- the aryl azide may be considered as a nitrogen transfer reagent since cycloaddition onto the hydrazone is followed by elimination to regenerate the aryl amine precursor to the diazonium salt.
- G is a group which may be employed as a precursor to the X 6 moiety in compounds of formula I, such as an 20 olefm or carboxylic acid or acid derivative.
- G is an aryl olefm, derived for example from cinnamaldehyde where R is H
- the olef ⁇ n group can be cleaved to provide an aldehyde directly in a one-pot process using a reagent such as ozone or via the diol using a dihydroxylation reagent such as osmium
- aliphatic alcohols may for example be converted by standard methods to the corresponding halides by the use of for example triphenylphosphine in combination with either iodine, N-bromosuccinimide or N- chlorosuccinimide, or alternatively by treatment with ttibromophosphine or thionyl chloride.
- Alcohols may be transformed to other leaving groups such as mesylates or 15 tosylates by employing the appropriate sulfonyl halide or sulfonyl anhydride in the presence of a non-nucleophilic base together with the alcohol to obtain the corresponding sulphonates.
- Chlorides or sulphonates may be converted to the corresponding bromides or iodides by treatment with bromide salts, for example LiBr, or iodide salts, such as Lil.
- bromide salts for example LiBr
- iodide salts such as Lil.
- Further standard methods to obtain alcohols include the 20 reduction of the corresponding carbonyl containing groups such as methyl or ethyl esters, aldehydes or ketones, by employing common reducing agents such as boranes, lithium borohydride, lithium aluminium hydride, or hydrogen in the presence of a transition metal catalyst such as complexes of for example ruthenium or iridium, or alternatively palladium on charcoal.
- Ketones and secondary alcohols may be obtained 25 by treatment of carboxylic acid esters and aldehydes respectively, with the appropriate carbon nucleophile, such as alkyl-Grignard reagents or alkyl-lithium reagents according to standard protocols.
- Heteroaromatic aldehydes may be prepared from the
- compounds of formula I can for example 20 be prepared by bond formation through nucleophilic displacement of a leaving group (LG) in which the nucleophilic atom might be the amino-nitrogen atom of a heterocyclic amine, the alpha-carbon of an alkyl substituted heteroaromatic ring.
- LG leaving group
- Amino-nitrogen atoms of heterocyclic amines, and the alpha-carbons of alkyl substituted heteroaromatics, are generally not reactive in the neutral protonated form 25 and are therefore preferably fully or partly converted to more nucleophilic anionic forms by treatment with bases in suitable solvents such as LDA, HMDS-alkali, or n-
- the nitrogen atoms of secondary aliphatic amines are generally 5 nucleophilic enough to displace a leaving group in the corresponding neutral forms, but preferably a base such as K 2 CO 3 , Cs 2 CO 3 , TEA, DEA or the like is added to facilitate the reaction in solvents such as acetonitrile, DMF or DCM at 0 to 150 °C.
- the leaving group is preferably bromo
- suitable leaving groups LG include chloro, bromo, OMs and 10 OTs.
- catalytic or stoichiometric amounts of an alkali metal iodide, such as Lil can be present in the reaction to facilitate the same through in situ displacement of the leaving group to iodo.
- compounds of formula I can for example be prepared by intramolecular bond 20 formation through nucleophilic displacement of a leaving group (LG) in which the nucleophilic atom might be the alpha-cavbon of an alkyl substituted heteroaromate under conditions as described herein above for intermolecular displacements where preferred bases are for example LDA, HMDS-alkali, or NaH as described herein above. 25 Preparation of fused Piper azine-triazoles
- the triazolopiperazines can be prepared from the piperazinone derivative by initial N-protection to give intermediate II.
- the intermediate can then be hydrolyzed to the acid III.
- the corresponding 1,2,4- oxadiazole IN can then be generated as described above.
- the triazolopiperazine intermediate NI can then be obtained by first converting IN to the cyclic imidoate, with a reagent such as Me 3 O + BF 4 " or dimethyl sulfate (ref: a) Sheu, Jennline; Smith, 10 Michael B.; Oeschger, Thomas R.; Satchell, Jacqueline; Org.Prep.Proced.Int.; 24; 2; 1992; 147 - 158; b) Hutchinson, Ian S.; Matlin, Stephen A.; Mete, Antonio, Tetrahedron Lett.; 42; 9; 2001; 1773 - 1776).
- the alkoxy group can then be
- acyl hydrazide or hydrazine with an acylating agent as described in Scheme 4
- a ring closing condensation to form the triazole heterocycle.
- This can be done in ethanol, toluene, DMF or pyridine under thermal conditions with regular heating or microwave irradiation (ref: Lawson, Edward C; Hoekstta, William 5 J.; Addo, Michael F.; Andrade-Gordon, Patricia; Damiano, Bruce P.; Kauffman, Jack A.; Mitchell, John A.; Maryanoff, Bruce E.; Bioorg.Med.Chem.Lett.; EN; 11; 19; 2001; 2619 - 2622).
- Isoxazole compounds of the invention may be prepared as shown in Scheme 16, below.
- One of groups A and B represents the substituted phenyl group, and the other represents the bicyclic ring system, of compounds of Formula I; alternatively, A and B represent precursors of those groups:
- compounds of formula 16e may be prepared by a 1,3-dipolar cycloaddition between compounds of formula 16a and 16b under basic conditions, 10 using a suitable base such as sodium bicarbonate or ttiethylamine at suitable temperatures (0°C - 100°C) in solvents such as toluene.
- a suitable base such as sodium bicarbonate or ttiethylamine at suitable temperatures (0°C - 100°C) in solvents such as toluene.
- 1,3-Dipolar cycloaddition with acetylenes of type 16b can also be effected using substituted nittomethanes of type 15 16c via activation with an electrophilic reagent such as PhNCO in the presence of a base such as ttiethylamine at elevated temperatures (50-100 °C). Li, C-S.; Lacasse, E.; Tetrahedron Lett. (2002) 43; 3565 - 3568.
- Several compounds of type 16c are commercially available, or may be synthesized by standard methods known by one skilled in the art. 20 Alternatively, compounds of formula 16d, which are available via a Claisen condensation of a methyl ketone and an ester using basic conditions using such bases as sodium hydride or potassium tert-butoxide, may yield compounds of formula 16e
- 002.1338789.2 was applied a linear gradient from 5 % to 100% acetonitrile inlO mM ammonium acetate (aq.), or in 0.1% TFA (aq.).
- Preparative reversed phase chromatography was run on a Gilson autopreparative HPLC with a diode array detector using an XTerra MS C8, 19x300mm, 7mm as 5 column. Purification by a chromatotron was performed on rotating silica gel / gypsum (Merck, 60 PF-254 with calcium sulphate) coated glass sheets, with coating layer of 1, 2, or 4 mm using a TC Research 7924T chromatotron.
- Example 1 20 [3-(2-Thienyl)-5-thioxo-l,5-dihydro-4H-l,2,4-triazol-4-yl]acetic acid Methyl ⁇ -(thioxomethylene)glycinate (2.06 g) and thiophene-2-carbohydrazide (2.57 g) in isopropanol (50 ml) was heated at 70 °C while stirring for 16 h. The mixture was allowed to come to r.t. and the formed precipitate collected and heated at reflux inl.O M aqueous NaHCO 3 solution for 2 h. After cooling to r.t. and acidification with cone. 25 HCl (aq.) the product was extracted into EA, which was washed with brine and then dried over MgSO before concentration to dryness to yield crude title compound which was used directly in the next step.
- Example 4 2-[3-( ⁇ [5-(5-Chloro-2-fluorophenyl)-l,2,4-oxadiazol-3-yl]methyl ⁇ thio)-5-(2- thienyl)-4H-l,2,4-triazol-4-yl]ethyl methanesulfonate
- 2-[3-( ⁇ [5-(5-chloro-2-fluorophenyl)-l,2,4-oxadiazol-3- yl]methyl ⁇ thio)-5-(2-thienyl)-4H-l,2,4-triazol-4-yl]ethanol in a mixture of DMF (1 ml) and pyridine (0.5 ml) was added methanesulfonyl chloride (20 uL).
- the mixture 30 was stirred at r.t. for 24 h before poured onto water (10 ml).
- the crude product was filtered off and purified by chromatography on silica gel using 0-5% MeO ⁇ in
- Example 5 5 a) 3-pyridin-4-yl-6,7,8,9-tetrahydro-5H-[l,2,4]triazolo[4,3- ⁇ ] [l,3]diazepine
- a mixture of l,3-diazepan-2-one hydrazone hydroiodide(1.00 g, 3.9 mmol) and isonicotinoyl chloride hydrochloride(695 mg, 3.9 mmol) was heated in a microwave reactor at 160 °C for 10 min. The reaction mixture was poured into Na a CO 3 solution, sat., and extracted with DCM. The organic phase was dried and concentrated.
- Example 8 10 2-(methylthio)-4,5,6,7-tetrahydro-lH-l,3-diazepine Methyl iodide (0.55 ml, 1.15 mmol) was added to a solution of l,3-diazepane-2- thione (1.00 g, 7.68 mmol) in acetone (8 ml). The reaction mixture was refluxed for 15 min. EtO ⁇ was added to the hot solution to dissolve the solids. After cooling to r.t. hex. was added and the precipitate was collected by filtration, washed with hex. and 15 dried to give 1.79 g (86%) crude title compound which was used directly in the next step.
- Step A The acyclic intermediate was obtained from 3-chlorobenzoic acid (2.82 g, 18 mmol), EDC1 (3.46 g, 18 mmol), HOBt (2.76 g, 18 mmol) and 2-chloro-N-hydroxy- acetamidine (1.75 g, 16.2 mmol) [Chem. Ber. 1907, 40, 1639] in DMF (40 mL).
- Step B The cyclic compound was obtained from heating in DMF (40 mL) and purified by 5 SPE chromatography on silica gel using 2% acetone in hex.s yielded the title compound (1.46 g, 39% yield over 2 steps).
- 1HNMR 8.17 (m, IH), 8.07 (dd, IH), 7.60 (m, IH), 7.55 (t, IH), 4.69 (s, 2H).
- Example 11 10 3-(Bromomethyl)-5-(3-chlorophenyl)-l,2,4-oxadiazole 3-(chloromethyl)-5-(3-chlorophenyl)-l,2,4-oxadiazole (1.38 g, 6.0 mmol) and LiBr (0.90 g, 10.3 mmol) in THF (50 ml) was heated to reflux under a nitrogen atmosphere o.n. After cooling to r.t. EA was added and the organic phase was washed with H 2 O and brine, dried and evaporated to give the title compound (1.40 g, 85%). MS (M + +l) 15 275
- Example 12 20 3-(l-chloroethyl)-5-(3-chlorophenyl)-l,2,4-oxadiazole 5 drops of DMF was added to l-[5-(3-chlorophenyl)-l,2,4-oxadiazol-3-yl]ethanol (12.3 g, 54.9 mmol) in SOCl 2 (150 mL) and the reaction was heated at 70 °C for 5 h. The excess SOCl 2 was evaporated and the residue was purified by column chromatography (Hep to Hep-EA 5:1) to give 12.4 g (93 %) of the title compound.
- Example 13 l-[5-(3-chlorophenyl)-l,2,4-oxadiazol-3-yl]ethyl methanesulfonate Methane sulfonyl chloride (40 ⁇ l, 0.49 mmol) was added to a mixture of TEA (95 ⁇ l, 30 0.67 mmol) and l-[5-(3-chlorophenyl)-l,2,4-oxadiazol-3-yl]ethanol (100 mg, 0.45 mmol) in DCM (5 ml). After stirring for 15 min the mixture was washed with water
- Example 16 25 N',2-dihydroxypropanimidamide 44.2 g (0.64 mol) of hydroxylamine hydrochloride and 25.5 g (0.64 mol) sodium hydroxide were dissolved in ethanol (500 mL) at r.t. and stirred for 3 h. After filtration, 8.11 g (0.11 mol) 2-hydroxypropanenitrile were added to the filtrate, followed by stirring for 4 h. After concentration to dryness the title compound was 30 obtained which was directly used in the next step.
- Example 18 15 2-Carboxymethyl-3-oxo-piperazine-l-carboxylic acid tert-butyl ester IN Sodium hydroxide (11.4 mL, 11.4 mmol) was added to 2-ethoxycarbonylmethyl- 3-oxo-piperazine-l -carboxylic acid tert-butyl ester (2.5 g, 8.73 mmol) in methanol (20 mL) at room temperature and then stirred for 2.5 hours. The reaction mixture was concentrated, acidified with 2N HCl to pH ⁇ 2 and extracted with dichloromethane (3 20 times).
- Example 21 8-[3-(3-Chloro-phenyl)-[l,2,4]oxadiazol-5-yl]-3-(4-methoxy-phenyl)-5,6-dihydro- 25 8H-[l,2,4]triazolo[4,3-a]pyrazine-7-carboxylic acid tert-butyl ester 6-[3-(3-Chloro-phenyl)-[l,2,4]oxadiazol-5-yl]-5-methoxy-3,6-dihydro-2H-pyrazine- 1 -carboxylic acid tert-butyl ester (284.6 mg, 0.70 mmol) and 4-methoxy-benzoic acid hydrazide (116.2 mg, 0.70 mmol) under argon in methanol (10 mL) were heated at reflux for 3 days.
- Example 24 5-(5-Chloro-2-fluoro-phenyI)-3-chloromethyl- [1 ,2,4] oxadiazole
- the acyclic intermediate was prepared from 2-fluoro-5-chlorobenzoic acid (550 mg, 20 3.15 mmol), EDCI (665 mg, 3.47 mmol), HOBT (469 mg, 3.47 mmol) and 2-chloro- N-hydroxy-acetamidine (377 mg, 3.47 mmol) in DMF (10 mL).
- DMF 15 mL was added to the intermediate residue and the mixture was heated for 1 hour.
- Example 26 a) 9- ⁇ [5-(3-chlorophenyl)-l,2,4-oxadiazol-3-yl]methyl ⁇ -3-pyridin-4-yl-6,7,8,9- tetrahydro-5H-[l,2,4]triazolo[4,3-a][l,3]diazepine 15 NaH (65 mg, 0.28 mmol) was added to a solution of 3-pyridin-4-yl-6,7,8,9- tetrahydro-5H-[l,2,4]triazolo[4,3- ⁇ ][l,3]diazepine (54 mg, 0.25 mmol) in DMF (5 ml).
- Example 28 7- ⁇ [5-(3-chlorophenyl)-l,2,4-oxadiazol-3-yl]methyl ⁇ -3-pyridin-4-yl-6,7-dihydro- 10 5 ⁇ -pyrrolo[2,l-c][l,2,4]triazole nBuLi (2.5 M, hex., 600 ⁇ l) was added to a solution of 3-pyridin-4-yl-6,7-dihydro- 5H-pyrrolo[2,l-c][l,2,4]ttiazole (250 mg, 1.33 mmol) in T ⁇ F (13 ml) at 0 °C.
- Example 29 9- ⁇ [5-(3-chlorophenyl)-l,2,4-oxadiazol-3-yl]methyl ⁇ -3-(trifluoromethyl)-6,7,8,9- 25 tetrahydro-5H-[l,2,4]triazolo[4,3-a] [l,3]diazepine
- the title compound was prepared analogous to 9- ⁇ [5-(3-chlorophenyl)-l,2,4- oxadiazol-3-yl]methyl ⁇ -3-pyridin-4-yl-6 5 7,8,9-tetrahydro-5H-[l,2,4]triazolo[4,3- a][l,3]diazepine from 3-(chloromethyl)-5-(3-chlorophenyl)-l,2,4-oxadiazole (89 mg, 0.39 mmol), 3-(trifluoromethyl)-6,7,8,9-tetrahydro-5H-[l ,2,4]
- Example 30 5 8-[3-(3-Chloro-phenyl)-[l,2,4]oxadiazol-5-yl]-3-(4-methoxy-phenyl)-5,6,7,8- tetrahy dro- [1 ,2,4] triazolo [4,3-a] py razine Trifluoroacetic acid (0.5mL) was added to a solution of 8-[3-(3-chloro-phenyl)- [l,2,4]oxadiazol-5-yl]-3-(4-methoxy-phenyl)-5,6-dihydro-8H-[l,2,4]ttiazolo[4,3- a]pyrazine-7-carboxylic acid tert-butyl ester (72.5 mg, 0.14 mmol) in 10 dichloromethane (1 mL) at 0°C.
- reaction mixture was then diluted with dichloromethane, After 15 minutes, the reaction was warmed to room temperature and stirred for an additional hour, washed with saturated sodium bicarbonate, dried over anhydrous sodium sulfate, filtered and concentrated. Purification was performed by flash column chromatography on silica gel using 85 - 90% ethyl acetate in hexanes to 15 2% ammonia in methanol in dichloromethane followed by trituration with diethyl ether to afford the titled compound (40.6 mg, 69%).
- the pharmacological properties of the compounds of the invention can be analyzed using standard assays for functional activity.
- glutamate receptor assays are well known in the art as described in for example Aramori et al, Neuron 8:757 10 (1992), Tanabe et al, Neuron 8:169 (1992), Miller et al, J. Neuroscience 15: 6103 (1995), Balazs, et al, J. Neurochemistry 69:151 (1997).
- the methodology described in these publications is incorporated herein by reference.
- the compounds of the invention can be studied by means of an assay that measures the mobilization of intracellular calcium, [Ca 2+ ]i in cells expressing mGluR5.
- FLIPR analysis cells expressing human mGluR5d as described in WO97/05252 were seeded on collagen coated clear bottom 96-well plates with black sides and 94- analysis of [Ca ]; mobilization was done 24 h after seeding.
- FLIPR experiments were done using a laser setting of 0.800 W and a 0.4 second CCD camera shutter speed. Each FLIPR experiment was initiated with 160 ⁇ l of buffer 20 present in each well of the cell plate. After each addition of the compound, the fluorescence signal was sampled 50 times at 1 second intervals followed by 3 samples at 5 second intervals. Responses were measured as the peak height of the response within the sample period.
- EC 5 0 and IC 50 determinations were made from data obtained from 8-point 25 concentration response curves (CRC) performed in duplicate. Agonist CRC were generated by scaling all responses to the maximal response observed for the plate. Antagonist block of the agonist challenge was normalized to the average response of the agonist challenge in 14 control wells on the same plate.
- IP 3 Inositol Phosphate
- 002.1338789.2 stably expressing the human mGluR5d receptors were incubated with [3H] myo- inositol overnight, washed three times in HEPES buffered saline and pre-incubated for 10 min with 10 mM LiCl. Compounds (agonists) were added and incubated for 30 min at 37°C. Antagonist activity was determined by pre-incubating test compounds 5 for 15 min, then incubating in the presence of glutamate (80 ⁇ M) or DHPG (30 ⁇ M) for 30 min. Reactions were terminated by the addition of perchloric acid (5%). Samples were collected and neutralized, and inositol phosphates were separated using Gravity-Fed Ion-Exchange Columns.
- Antagonist block of the agonist challenge was normalized to the average response of the agonist challenge in 14 control wells on the same plate.
- HEPES buffered saline 146 mM NaCl, 4.2 mM KCl, 10 0.5 mM MgCl 2 , 0.1% glucose, 20 mM HEPES, pH 7.4
- HEPES buffered saline 146 mM NaCl, 4.2 mM KCl, 10 0.5 mM MgCl 2 , 0.1% glucose, 20 mM HEPES, pH 7.4
- Cells were washed once in HEPES buffered saline and pre-incubated for 10 min in HEPES buffered saline containing 10 mM LiCl.
- Compounds (agonists) were added and incubated at 37°C for 30 min.
- Antagonist activity was determined by pre-incubating test compounds for 15 15 min, then incubating in the presence of glutamate (80 ⁇ M) or DHPG (30 ⁇ M) for 30 min. The reaction was terminated by the addition of 0.5 ml perchloric acid (5%>) on ice, with incubation at 4°C for at least 30 min. Samples were collected in 15 ml Falcon tubes and inositol phosphates were separated using Dowex columns, as described below. 20 Assay For Inositol Phosphates Using Gravity-Fed Ion-Exchange Columns
- Ion-exchange resin (Dowex AG1-X8 formate form, 200-400 mesh, BIORAD) was 25 washed three times with distilled water and stored at 4°C. 1.6 ml resin was added to each column, and washed with 3 ml 2.5 mM HEPES, 0.5 mM EDTA, pH 7.4. a) Sample Treatment Samples were collected in 15 ml Falcon tubes and neutralized with 0.375 M HEPES, 30 0.75 M KOH. 4 ml of HEPES / EDTA (2.5 / 0.5 mM, pH 7.4) were added to
- One aspect of the invention relates to a method for inhibiting activation of mGluR 5, comprising treating a cell containing said receptor with an effective amount of the compound of formula I.
- Motility measurement 20 In brief, after fasting for approximately 17 h with free supply of water, a multilumen sleeve/sidehole assembly (Dentsleeve, Sydney, South Australia) is introduced through the esophagostomy to measure gastric, lower esophageal sphincter (LES) and esophageal pressures. The assembly is perfused with water using a low-compliance manomettic perfusion pump (Dentsleeve, Sydney, South Australia). An air-perfused 25 tube is passed in the oral direction to measure swallows, and an antimony electrode monitored pH, 3 cm above the LES. All signals are amplified and acquired on a personal computer at 10 Hz.
- nutrient meal (10% peptone, 5% D-glucose, 5%> Intralipid, pH 3.0) is infused into the stomach through the central lumen of the assembly at 100 ml/min to a final volume of 30 ml/kg.
- the infusion of the nutrient meal is followed by air infusion at a rate of 500 ml/min until an inttagastric pressure of 10+1 mmHg is obtained.
- the pressure is then 5 maintained at this level throughout the experiment using the infusion pump for further air infusion or for venting air from the stomach.
- the experimental time from start of nuttient infusion to end of air insufflation is 45 min. The procedure has been validated as a reliable means of triggering TLESRs.
- TLESRs is defined as a decrease in lower esophageal sphincter pressure (with reference to inttagastric pressure) at a rate of >1 mmHg/s.
- the relaxation should not be preceded by a pharyngeal signal ⁇ 2s before its onset in which case the relaxation is classified as swallow-induced.
- the pressure difference between the LES and the stomach should be less than 15 2 mmHg, and the duration of the complete relaxation longer than 1 s.
- Typical IC 50 values as measured in the assays described above are 10 ⁇ M or less. In one aspect of the invention the IC 50 is below 2 ⁇ M. In another aspect of the invention the IC 50 is below 0.2 ⁇ M. In a further aspect of the invention the IC 50 is below 0.05 30 ⁇ M.
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DK05713794T DK1716152T3 (en) | 2004-02-18 | 2005-02-17 | Condensed heterocyclic compounds and their use as metabotropic receptor antagonists in the treatment of gastrointestinal disorders |
JP2006554237A JP2007523183A (en) | 2004-02-18 | 2005-02-17 | Fused heterocyclic compounds and their use as metabotropic glutamate receptor antagonists |
UAA200608820A UA82435C2 (en) | 2004-02-18 | 2005-02-17 | Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders, pharmaceutical composition based thereon |
CA002556320A CA2556320A1 (en) | 2004-02-18 | 2005-02-17 | Fused heterocyclic compounds and their use as metabotropic glutamate receptor antagonists for the treatment of gastrointestinal disorders |
BRPI0507495-9A BRPI0507495A (en) | 2004-02-18 | 2005-02-17 | compound, pharmaceutical composition, use of the compound method for the treatment of mglur5-mediated disorders, and method for inhibiting activation of mglur5 receptors |
EP05713794A EP1716152B1 (en) | 2004-02-18 | 2005-02-17 | Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders |
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SI200530394T SI1716152T1 (en) | 2004-02-18 | 2005-02-17 | Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders |
RU2006129324/04A RU2006129324A (en) | 2004-02-18 | 2005-02-17 | CONDENSED HETEROCYCLIC COMPOUNDS AND THEIR APPLICATION AS ANTAGONISTS OF METABOTROPIC GLUTAMATE RECEPTORS |
AU2005214380A AU2005214380A1 (en) | 2004-02-18 | 2005-02-17 | Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders |
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US10/588,699 US20070185095A1 (en) | 2004-02-18 | 2005-02-17 | Fused heterocyclic compounds and their use as metabotropic glutamate receptor antagonists |
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NO20063562A NO20063562L (en) | 2004-02-19 | 2006-08-07 | Fused heterocyclic compounds and their use as metabotrophic glutamate receptor antagonists |
HK07104630A HK1098460A1 (en) | 2004-02-18 | 2007-04-30 | Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders |
HR20080480T HRP20080480T3 (en) | 2004-02-18 | 2008-09-26 | Fused hetrocyclic compounds and their use as metabotropic receptor antagonists for the treatment of gastrointestinal disorders |
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Cited By (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007130824A2 (en) * | 2006-05-05 | 2007-11-15 | Astrazeneca Ab | Fused heterocylic compounds and their use as mglur5 modulators |
WO2007130825A2 (en) * | 2006-05-05 | 2007-11-15 | Astrazeneca Ab | Fused heterocyclic compounds and their use as mglur5 modulators |
WO2008078725A1 (en) * | 2006-12-26 | 2008-07-03 | Daiichi Sankyo Company, Limited | Thiazepine derivative |
US7456200B2 (en) | 2002-08-09 | 2008-11-25 | Astrazeneca Ab | Compounds |
WO2008150232A1 (en) * | 2007-06-07 | 2008-12-11 | Astrazeneca Ab | Metabotropic glutamate receptor oxadiazole ligands and their use as potentiators - 841 |
WO2008150233A1 (en) * | 2007-06-07 | 2008-12-11 | Astrazeneca Ab | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators - 842 |
US7476684B2 (en) | 2005-09-29 | 2009-01-13 | Astrazeneca Ab | Compounds for the treatment of neurological, psychiatric or pain disorders |
WO2009054793A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | Thiophene 1,2,4-triazole derivatives as modulators of mglur5 |
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WO2009054792A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | Aminopyridine derivatives as modulators of mglur5 |
WO2009054786A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | 1,2,4-triazole aryl n-oxides derivatives as modulators of mglur5 |
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US7678796B2 (en) | 2006-05-05 | 2010-03-16 | Astrazeneca Ab | MGluR5 modulators I |
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US8148372B2 (en) | 2008-06-06 | 2012-04-03 | Astrazeneca Ab | Metabotropic glutamate receptor isoxazole ligands and their use as potentiators—286 |
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US10065960B2 (en) | 2010-04-02 | 2018-09-04 | Ogeda Sa | NK-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in NK-3 receptors mediated disorders |
US10183948B2 (en) | 2013-03-29 | 2019-01-22 | Ogeda Sa | N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
US10787458B2 (en) | 2014-09-25 | 2020-09-29 | Ogeda Sa | Chiral synthesis of N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-A]pyrazines |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001012627A1 (en) * | 1999-08-19 | 2001-02-22 | Nps Pharmaceuticals, Inc. | Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
WO2004014902A2 (en) * | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Compounds having an activity at metabotropic glutamate receptors |
-
2005
- 2005-02-17 ES ES05713794T patent/ES2309718T3/en active Active
- 2005-02-17 MY MYPI20050602 patent/MY152888A/en unknown
- 2005-02-17 JP JP2006554237A patent/JP2007523183A/en not_active Withdrawn
- 2005-02-17 KR KR1020067015826A patent/KR20070026380A/en not_active Application Discontinuation
- 2005-02-17 PT PT05713794T patent/PT1716152E/en unknown
- 2005-02-17 SI SI200530394T patent/SI1716152T1/en unknown
- 2005-02-17 EP EP05713794A patent/EP1716152B1/en active Active
- 2005-02-17 DK DK05713794T patent/DK1716152T3/en active
- 2005-02-17 RU RU2006129324/04A patent/RU2006129324A/en not_active Application Discontinuation
- 2005-02-17 BR BRPI0507495-9A patent/BRPI0507495A/en not_active IP Right Cessation
- 2005-02-17 DE DE602005008558T patent/DE602005008558D1/en not_active Expired - Fee Related
- 2005-02-17 CA CA002556320A patent/CA2556320A1/en not_active Abandoned
- 2005-02-17 US US10/588,699 patent/US20070185095A1/en not_active Abandoned
- 2005-02-17 AT AT05713794T patent/ATE402935T1/en not_active IP Right Cessation
- 2005-02-17 WO PCT/US2005/005218 patent/WO2005080397A2/en active Application Filing
- 2005-02-17 PL PL05713794T patent/PL1716152T3/en unknown
-
2006
- 2006-08-03 IL IL177291A patent/IL177291A0/en unknown
-
2007
- 2007-04-30 HK HK07104630A patent/HK1098460A1/en not_active IP Right Cessation
-
2008
- 2008-09-26 HR HR20080480T patent/HRP20080480T3/en unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001012627A1 (en) * | 1999-08-19 | 2001-02-22 | Nps Pharmaceuticals, Inc. | Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
EP1210344A1 (en) * | 1999-08-19 | 2002-06-05 | Nps Pharmaceuticals, Inc. | Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
WO2004014902A2 (en) * | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Compounds having an activity at metabotropic glutamate receptors |
Cited By (70)
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---|---|---|---|---|
US7456200B2 (en) | 2002-08-09 | 2008-11-25 | Astrazeneca Ab | Compounds |
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US7476684B2 (en) | 2005-09-29 | 2009-01-13 | Astrazeneca Ab | Compounds for the treatment of neurological, psychiatric or pain disorders |
US7678796B2 (en) | 2006-05-05 | 2010-03-16 | Astrazeneca Ab | MGluR5 modulators I |
WO2007130825A2 (en) * | 2006-05-05 | 2007-11-15 | Astrazeneca Ab | Fused heterocyclic compounds and their use as mglur5 modulators |
WO2007130825A3 (en) * | 2006-05-05 | 2008-05-15 | Astrazeneca Ab | Fused heterocyclic compounds and their use as mglur5 modulators |
WO2007130824A3 (en) * | 2006-05-05 | 2008-05-22 | Astrazeneca Ab | Fused heterocylic compounds and their use as mglur5 modulators |
WO2007130824A2 (en) * | 2006-05-05 | 2007-11-15 | Astrazeneca Ab | Fused heterocylic compounds and their use as mglur5 modulators |
WO2008078725A1 (en) * | 2006-12-26 | 2008-07-03 | Daiichi Sankyo Company, Limited | Thiazepine derivative |
US7799792B2 (en) | 2007-06-07 | 2010-09-21 | Astrazeneca Ab | Metabotropic glutamate receptor oxadiazole ligands and their use as potentiators 841 |
US8377940B2 (en) | 2007-06-07 | 2013-02-19 | Astrazeneca Ab | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators—842 |
RU2470931C2 (en) * | 2007-06-07 | 2012-12-27 | Астразенека Аб | Oxadiazole derivatives and use thereof as metabotropic glutamate receptor potentiators 842 |
EP2444399A1 (en) * | 2007-06-07 | 2012-04-25 | AstraZeneca AB | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators - 842 |
WO2008150233A1 (en) * | 2007-06-07 | 2008-12-11 | Astrazeneca Ab | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators - 842 |
CN101679403B (en) * | 2007-06-07 | 2013-01-02 | 阿斯利康(瑞典)有限公司 | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators 842 |
CN102977086B (en) * | 2007-06-07 | 2015-04-01 | 阿斯利康(瑞典)有限公司 | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators - 842 |
WO2008150232A1 (en) * | 2007-06-07 | 2008-12-11 | Astrazeneca Ab | Metabotropic glutamate receptor oxadiazole ligands and their use as potentiators - 841 |
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US8377939B2 (en) | 2007-06-07 | 2013-02-19 | Astrazeneca Ab | Oxadiazole derivatives and their use as metabotropic glutamate receptor potentiators 842 |
WO2009054791A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | Fused pyrrolidine 1,2,4-triazole derivatives as modulators of mglur5 |
WO2009054793A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | Thiophene 1,2,4-triazole derivatives as modulators of mglur5 |
WO2009054789A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | 1,2,3-triazole pyrrolidine derivatives as modulators of mglur5 |
WO2009054786A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | 1,2,4-triazole aryl n-oxides derivatives as modulators of mglur5 |
WO2009054792A1 (en) * | 2007-10-26 | 2009-04-30 | Astrazeneca Ab | Aminopyridine derivatives as modulators of mglur5 |
US8148372B2 (en) | 2008-06-06 | 2012-04-03 | Astrazeneca Ab | Metabotropic glutamate receptor isoxazole ligands and their use as potentiators—286 |
WO2010084050A2 (en) | 2009-01-13 | 2010-07-29 | Novartis Ag | Quinazolinone derivatives useful as vanilloid antagonists |
US8575160B2 (en) | 2009-11-30 | 2013-11-05 | Novartis Ag | Imidazole derivatives as aldosterone synthase inhibitors |
WO2011082010A1 (en) | 2009-12-29 | 2011-07-07 | Eli Lilly And Company | Tetrahydrotriazolopyridine compounds as selective mglu5 receptor potentiators useful for the treatment of schizophrenia |
US8592590B2 (en) | 2009-12-29 | 2013-11-26 | Eli Lilly And Company | Tetrahydrotriazolopyridine compounds as selective MGLU5 receptor potentiators useful for the treatment of schizophrenia |
WO2011092293A2 (en) | 2010-02-01 | 2011-08-04 | Novartis Ag | Cyclohexyl amide derivatives as crf receptor antagonists |
WO2011092290A1 (en) | 2010-02-01 | 2011-08-04 | Novartis Ag | Pyrazolo[5,1b]oxazole derivatives as crf-1 receptor antagonists |
WO2011095450A1 (en) | 2010-02-02 | 2011-08-11 | Novartis Ag | Cyclohexyl amide derivatives as crf receptor antagonists |
US8871761B2 (en) | 2010-04-02 | 2014-10-28 | Euroscreen S.A. | NK-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in NK-3 receptors mediated disorders |
US9926325B2 (en) | 2010-04-02 | 2018-03-27 | Ogeda Sa | NK-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in NK-3 receptors mediated disorders |
US10544150B2 (en) | 2010-04-02 | 2020-01-28 | Ogeda Sa | NK-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in NK-3 receptors mediated disorders |
US10065960B2 (en) | 2010-04-02 | 2018-09-04 | Ogeda Sa | NK-3 receptor selective antagonist compounds, pharmaceutical composition and methods for use in NK-3 receptors mediated disorders |
CN102858766A (en) * | 2010-04-30 | 2013-01-02 | 阿斯利康(瑞典)有限公司 | Polymorphs of a metabotropic glutamate receptor positive allosteric modulator |
CN105175421B (en) * | 2011-10-03 | 2018-07-13 | 欧歌达有限公司 | Midbody compound and application thereof for synthesis of selective NK-3 receptor antagonists |
CN105175421A (en) * | 2011-10-03 | 2015-12-23 | 欧洲筛选有限公司 | Novel chiral n-acyl-5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective nk-3 receptor antagonists, pharmaceutical composition, methods for use in nk-3 receptor mediated disorders and chiral synthesis thereof |
EP3029042A1 (en) * | 2011-10-03 | 2016-06-08 | Euroscreen S.A. | Novel chiral n-acyl-5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective nk-3 receptor antagonists, pharmaceutical composition, methods for use in nk-3 receptor mediated disorders and chiral synthesis thereof |
US10941151B2 (en) | 2011-10-03 | 2021-03-09 | Ogeda Sa | Chiral N-acyl-5,6,7(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor mediated disorders and chiral synthesis thereof |
US9475814B2 (en) | 2011-10-03 | 2016-10-25 | Euroscreen S.A. | Chiral N-acyl-5,6,7(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor mediated disorders and chiral synthesis thereof |
US10683295B2 (en) | 2011-10-03 | 2020-06-16 | Ogeda Sa | Chiral N-acyl-5,6,7(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-A]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor mediated disorders and chiral synthesis thereof |
AU2012320568B2 (en) * | 2011-10-03 | 2017-07-06 | Ogeda S.A. | Novel chiral N-acyl-5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor mediated disorders and chiral synthesis thereof |
US10065961B2 (en) | 2011-10-03 | 2018-09-04 | Ogeda Sa. | Chiral N-acyl-5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor mediated disorders and chiral synthesis thereof |
AU2012320568C1 (en) * | 2011-10-03 | 2018-07-19 | Ogeda S.A. | Novel chiral N-acyl-5,6,7,(8-substituted)-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor mediated disorders and chiral synthesis thereof |
EA029340B1 (en) * | 2011-10-03 | 2018-03-30 | Огеда Са | CHIRAL N-ACYL-5,6,7-(8-SUBSTITUTED)TETRAHYDRO[1,2,4]TRIAZOLO[4,3-a]PYRAZINES AS SELECTIVE NK-3 RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITION, METHODS FOR USE IN NK-3 RECEPTOR MEDIATED DISORDERS AND CHIRAL SYNTHESIS THEREOF |
WO2013050424A1 (en) * | 2011-10-03 | 2013-04-11 | Euroscreen S.A. | NOVEL CHIRAL N-ACYL-5,6,7,(8-SUBSTITUTED)-TETRAHYDRO-[1,2,4]TRIAZOLO[4,3-a]PYRAZINES AS SELECTIVE NK-3 RECEPTOR ANTAGONISTS, PHARMACEUTICAL COMPOSITION, METHODS FOR USE IN NK-3 RECEPTOR MEDIATED DISORDERS AND CHIRAL SYNTHESIS THEREOF |
US9969745B2 (en) | 2013-03-29 | 2018-05-15 | Ogeda Sa | N-acyl-(3-substituted)-(8-methyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor-mediated disorders |
US9969738B2 (en) | 2013-03-29 | 2018-05-15 | Ogeda Sa | N-acyl-(3-substituted)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor-mediated disorders |
US9987274B2 (en) | 2013-03-29 | 2018-06-05 | Ogeda Sa | N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
US11731974B2 (en) | 2013-03-29 | 2023-08-22 | Ogeda Sa | N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
US9422299B2 (en) | 2013-03-29 | 2016-08-23 | Euroscreen Sa | Substituted [1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
US10030025B2 (en) | 2013-03-29 | 2018-07-24 | Ogeda Sa | Substituted [1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
US10836768B2 (en) | 2013-03-29 | 2020-11-17 | Ogeda Sa | N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
US9840508B2 (en) | 2013-03-29 | 2017-12-12 | Oged Sa | N-acyl-(3-substituted)-(8-methyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a] pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor-mediated disorders |
US10183948B2 (en) | 2013-03-29 | 2019-01-22 | Ogeda Sa | N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists |
US10214533B2 (en) | 2013-03-29 | 2019-02-26 | Ogeda Sa | N-acyl-(3-substituted)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazines as selective NK-3 receptor antagonists, pharmaceutical composition, methods for use in NK-3 receptor-mediated disorders |
US10246432B2 (en) | 2013-07-17 | 2019-04-02 | Heptares Therapeutics Limited | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
AU2018241104B2 (en) * | 2013-07-17 | 2019-07-11 | Nxera Pharma Uk Limited | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
WO2015008073A1 (en) * | 2013-07-17 | 2015-01-22 | Heptares Therapeutics Limited | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mglu5 modulators |
US10584111B2 (en) | 2013-07-17 | 2020-03-10 | Heptares Therapeutics Limited | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
US9676745B2 (en) | 2013-07-17 | 2017-06-13 | Heptares Therapeutics Limited | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
GB2532641A (en) * | 2013-07-17 | 2016-05-25 | Heptares Therapeutics Ltd | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mglu5 modulators |
CN105377832A (en) * | 2013-07-17 | 2016-03-02 | 赫普泰雅治疗有限公司 | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
US10981889B2 (en) | 2013-07-17 | 2021-04-20 | Heptares Therapeutics Limited | 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
US11584732B2 (en) | 2013-07-17 | 2023-02-21 | Heptares Therapeutics Limited | Methods of treatment using 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
US11680053B2 (en) | 2013-07-17 | 2023-06-20 | Heptares Therapeutics Limited | Methods of treatment using 4-(3-cyanophenyl)-6-pyridinylpyrimidine mGlu5 modulators |
CN105377832B (en) * | 2013-07-17 | 2018-05-04 | 赫普泰雅治疗有限公司 | 4- (3- cyano-phenyls) -6- pyridyl-pyrimidine MGLU5 conditioning agents |
US10787458B2 (en) | 2014-09-25 | 2020-09-29 | Ogeda Sa | Chiral synthesis of N-acyl-(3-substituted)-(8-substituted)-5,6-dihydro-[1,2,4]triazolo[4,3-A]pyrazines |
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ATE402935T1 (en) | 2008-08-15 |
DK1716152T3 (en) | 2008-11-03 |
WO2005080397A8 (en) | 2006-06-22 |
DE602005008558D1 (en) | 2008-09-11 |
HK1098460A1 (en) | 2007-07-20 |
EP1716152A2 (en) | 2006-11-02 |
RU2006129324A (en) | 2008-04-10 |
HRP20080480T3 (en) | 2008-11-30 |
PL1716152T3 (en) | 2009-01-30 |
IL177291A0 (en) | 2006-12-10 |
KR20070026380A (en) | 2007-03-08 |
CA2556320A1 (en) | 2005-09-01 |
EP1716152B1 (en) | 2008-07-30 |
PT1716152E (en) | 2008-10-02 |
MY152888A (en) | 2014-11-28 |
SI1716152T1 (en) | 2008-12-31 |
BRPI0507495A (en) | 2007-07-10 |
WO2005080397A3 (en) | 2005-12-22 |
ES2309718T3 (en) | 2008-12-16 |
US20070185095A1 (en) | 2007-08-09 |
JP2007523183A (en) | 2007-08-16 |
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