WO2014060384A1 - Ethynyl derivatives as modulators of mglur5 receptor activity - Google Patents
Ethynyl derivatives as modulators of mglur5 receptor activity Download PDFInfo
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- WO2014060384A1 WO2014060384A1 PCT/EP2013/071476 EP2013071476W WO2014060384A1 WO 2014060384 A1 WO2014060384 A1 WO 2014060384A1 EP 2013071476 W EP2013071476 W EP 2013071476W WO 2014060384 A1 WO2014060384 A1 WO 2014060384A1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
Definitions
- the present invention relates to ethynyl derivatives of formula I
- R 1 is fluoro or chloro
- Compounds of formula I are distinguished by having valuable therapeutic properties. They can be used in the treatment or prevention of mGluR5 receptor mediated disorders.
- the transmission of stimuli takes place by the interaction of a neurotransmitter, which is sent out by a neuron, with a neuroreceptor.
- Glutamate is the major excitatory neurotransmitter in the brain and plays a unique role in a variety of central nervous system (CNS) functions.
- the glutamate-dependent stimulus receptors are divided into two main groups.
- the first main group namely the ionotropic receptors, forms ligand-controlled ion channels.
- the metabotropic glutamate receptors (mGluR) belong to the second main group and, furthermore, belong to the family of G-protein coupled receptors.
- these eight receptors can be sub-divided into three sub-groups:
- Negative allosteric modulators of metabotropic glutamate receptors can be used for the treatment or prevention of acute and/or chronic neurological disorders such as Parkinson's disease, Fragile-X syndrome, autistic disorders, cognitive disorders and memory deficits, as well as chronic and acute pain and gastroesophageal reflux disease (GERD).
- acute and/or chronic neurological disorders such as Parkinson's disease, Fragile-X syndrome, autistic disorders, cognitive disorders and memory deficits, as well as chronic and acute pain and gastroesophageal reflux disease (GERD).
- treatable indications in this connection are restricted brain function caused by bypass operations or transplants, poor blood supply to the brain, spinal cord injuries, head injuries, hypoxia caused by pregnancy, cardiac arrest and hypoglycaemia.
- Further treatable indications are ischemia, Huntington's chorea, amyotrophic lateral sclerosis (ALS), dementia caused by AIDS, eye injuries, retinopathy, idiopathic parkinsonism or parkinsonism caused by ALS
- medicaments as well as conditions which lead to glutamate-deficiency functions, such as e.g. muscle spasms, convulsions, migraine, urinary incontinence, nicotine addiction, opiate addiction, anxiety, vomiting, dyskinesia and depressions.
- glutamate-deficiency functions such as e.g. muscle spasms, convulsions, migraine, urinary incontinence, nicotine addiction, opiate addiction, anxiety, vomiting, dyskinesia and depressions.
- Disorders mediated full or in part by mGluR5 are for example acute, traumatic and chronic degenerative processes of the nervous system, such as Alzheimer's disease, senile dementia, Parkinson's disease, Huntington's chorea, amyotrophic lateral sclerosis and multiple sclerosis, psychiatric diseases such as schizophrenia and anxiety, depression, pain and drug dependency (Expert Opin. Then Patents (2002), 12, (12)).
- Selective mGluR5 antagonists are especially useful for the treatment of disorders where reduction of mGluR5 receptor activation is desired, such as anxiety and pain, depression, Fragile-X syndrom, autism spectrum disorders, Parkinson's disease, and gastroesophageal reflux disease (GERD).
- disorders where reduction of mGluR5 receptor activation is desired such as anxiety and pain, depression, Fragile-X syndrom, autism spectrum disorders, Parkinson's disease, and gastroesophageal reflux disease (GERD).
- Objects of the present invention are compounds of formula I and their pharmaceutically acceptable salts, the above-mentioned compounds as pharmaceutically active substances and their production.
- Further objects of the invention are medicaments based on a compound in accordance with the invention and their manufacture as well as the use of the compounds in the control or prevention of mGluR5 receptor (NAM) mediated disorders, which are anxiety and pain, depression, Fragile-X syndrom, autism spectrum disorders, Parkinson's disease, and gastroesophageal reflux disease (GERD, and, respectively, for the production of corresponding medicaments.
- NAM mGluR5 receptor
- One embodiment of the present invention are compounds of formula I wherein Y is N.
- One further embodiment of the present invention are compounds of formula I wherein Y is CH.
- a mGluR5 positive allosteric modulator leads to increased receptor activity (Ca 2+ mobilisation) in presence of a fixed concentration of glutamate, whereas an allosteric antagonist (negative allosteric modulator, NAM) leads to a reduction of receptor activation.
- PAM mGluR5 positive allosteric modulator
- NAM negative allosteric modulator
- Figure 1 shows the general behavior of a NAM and a PAM under the same conditions.
- mGluR5-NAMs are beneficial for indications where a reduction of excessive receptor activity is desired, such as anxiety and pain, depression, Fragile-X syndrom, autism spectrum disorders, Parkinson's disease, and gastroesophageal reflux disease (GERD).
- mGluR5 PAMs on the other hand are useful in indications where a normalization of decreased receptor activity is desired, such as in psychosis, epilepsy, schizophrenia, Alzheimer's disease and associated cognitive disorders, as well as tuberous sclerosis. This difference can be practically shown for example in an anxiety animal model, such as in the "rat Vogel conflict drinking test", where the compounds of the invention show anxiolytic activity, whereas mGluR-PAMs do not show activity in this animal model.
- PAMs a cell line with low receptor expression levels and low constitutive receptor activity was selected to allow the differentiation of agonistic versus PAM activity.
- Cells were cultured according to standard protocols (Freshney, 2000) in Dulbecco's Modified Eagle Medium with high glucose supplemented with 1 mM glutamine, 10% (vol/vol) heat- inactivated bovine calf serum, Penicillin/Streptomycin, 50 g/ml hygromycin and 15 g/ml blasticidin (all cell culture reagents and antibiotics from Invitrogen, Basel, Switzerland).
- 5xl0 4 cells/well were seeded in poly-D-lysine coated, black/clear-bottomed 96-well plates.
- the cells were loaded with 2.5 ⁇ Fluo-4AM in loading buffer (lxHBSS, 20 mM HEPES) for 1 hr at 37°C and washed five times with loading buffer.
- the cells were transferred into a Functional Drug Screening System 7000 (Hamamatsu, Paris, France), and 11 half logarithmic serial dilutions of test compound at 37°C were added and the cells were incubated for 10-30 min. with on-line recording of fluorescence.
- the agonist L-glutamate was added to the cells at a concentration corresponding to EC 2 o (typically around 80 ⁇ ) with on-line recording of fluorescence; in order to account for day-to-day variations in the responsiveness of cells, the EC 2 o of glutamate was determined immediately ahead of each experiment by recording of a full dose-response curve of glutamate. Responses were measured as peak increase in fluorescence minus basal (i.e. fluorescence without addition of L-glutamate), normalized to the maximal stimulatory effect obtained with saturating concentrations of L-glutamate.
- Graphs were plotted with the % maximal stimulatory using XLfit, a curve fitting program that iteratively plots the data using Levenburg Marquardt algorithm.
- cDNA encoding human mGlu 5a receptor was transiently transfected into EBNA cells using a procedure described by Schlaeger and Christensen
- membranes were filtered onto unifilter (96-well white microplate with bonded GF/C filter preincubated 1 h in 0.1% PEI in wash buffer, Packard Bioscience,
- NAM compounds of the invention
- the compounds of formula I can be manufactured by the methods given below, by the methods given in the examples or by analogous methods. Appropriate reaction conditions for the individual reaction steps are known to a person skilled in the art.
- the reaction sequence is not limited to the one displayed in the schemes, however, depending on the starting materials and their respective reactivity the sequence of reaction steps can be freely altered. Starting materials are either commercially available or can be prepared by methods analogous to the methods given below, by methods described in references cited in the description or in the examples, or by methods known in the art.
- An ethynyl-pyridine or ethynyl-pyrimidine compound of formula I can be obtained for example by Sonogashira coupling of 5-bromo-pyridine-2-carboxylic acid methyl ester or 5- bromo-pyrimidine-2-carboxylic acid methyl ester 1 with an appropriately substituted arylacetylene 2 followed by saponification with a base such as LiOH to yield the corresponding acid 3 or by Sonogashira coupling of 5-bromo-pyridine-2-carboxylic acid or 5-bromo- pyrimidine-2-carboxylic acid 1 with an appropriately substituted arylacetylene 2 to yield directly the corresponding acid 3.
- Pharmaceutically acceptable salts of compounds of formula I can be manufactured readily according to methods known per se and taking into consideration the nature of the compound to be converted into a salt.
- Inorganic or organic acids such as, for example, hydrochloric acid, hydrobromic acid, sulphuric acid, nitric acid, phosphoric acid or citric acid, formic acid, fumaric acid, maleic acid, acetic acid, succinic acid, tartaric acid, methanesulphonic acid, p-toluenesulphonic acid and the like are suitable for the formation of pharmaceutically acceptable salts of basic compounds of formula I.
- Compounds which contain the alkali metals or alkaline earth metals, for example sodium, potassium, calcium, magnesium or the like, basic amines or basic amino acids are suitable for the formation of pharmaceutically acceptable salts of acidic compounds.
- the invention relates also to medicaments containing one or more compounds of the present invention and pharmaceutically acceptable excipients for the treatment and prevention of mGluR5 receptor mediated disorders (NAM), such as anxiety and pain, depression, Fragile -X syndrom, autism spectrum disorders, Parkinson's disease, and gastroesophageal reflux disease (GERD).
- NAM mGluR5 receptor mediated disorders
- the invention also relates to the use of a compound in accordance with the present invention as well as its pharmaceutically acceptable salt for the manufacture of medicaments for the treatment and prevention of mGluR5 receptor mediated disorders (NAM) as outlined above.
- cDNA encoding rat mGlu 5a receptor was transiently transfected into EBNA cells using a procedure described by E.-J. Schlaeger and K. Christensen (Cytotechnology 1998, 15, 1-13).
- [Ca 2+ ]i measurements were performed on mGlu 5a transfected EBNA cells after incubation of -l ithe cells with Fluo 3-AM (obtainable by FLUKA, 0.5 ⁇ final concentration) for 1 hour at 37°C followed by 4 washes with assay buffer (DMEM supplemented with Hank's salt and 20 mM HEPES.
- [Ca 2+ ]i measurements were done using a fluorometric imaging plate reader (FLIPR, Molecular Devices Corporation, La Jolla, CA, USA). When compounds were evaluated as antagonists they were tested against 10 ⁇ glutamate as agonist.
- the inhibition (antagonists) curves were fitted with a four parameter logistic equation giving IC 50 , and Hill coefficient using the iterative non linear curve fitting software Origin (Microcal Software Inc., Northampton, MA, USA).
- the Ki values of the compounds tested are given.
- the Ki value is defined by the following formula:
- the IC50 values are those concentrations of the compounds tested in ⁇ by which 50 % of the effect of compounds are antagonised.
- [L] is the concentration and the EC50 value is the concentration of the compounds in ⁇ which brings about 50 % stimulation.
- the compounds of the present invention are mGluR5a receptor antagonists.
- the activities of compounds of formula I as measured in the assay described above are in the range of Ki ⁇ 100 ⁇ .
- the compounds of formula I and pharmaceutically acceptable salts thereof can be used as medicaments, e.g. in the form of pharmaceutical preparations.
- the pharmaceutical preparations can be administered orally, e.g. in the form of tablets, coated tablets, dragees, hard and soft gelatine capsules, solutions, emulsions or suspensions.
- the administration can also be effected rectally, e.g. in the form of suppositories, or parenterally, e.g. in the form of injection solutions.
- the compounds of formula I and pharmaceutically acceptable salts thereof can be processed with pharmaceutically inert, inorganic or organic carriers for the production of pharmaceutical preparations.
- Lactose, corn starch or derivatives thereof, talc, stearic acid or its salts and the like can be used, for example, as such carriers for tablets, coated tablets, dragees and hard gelatine capsules.
- Suitable carriers for soft gelatine capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like; depending on the nature of the active substance no carriers are, however, usually required in the case of soft gelatine capsules.
- Suitable carriers for the production of solutions and syrups are, for example, water, polyols, sucrose, invert sugar, glucose and the like.
- Adjuvants such as alcohols, polyols, glycerol, vegetable oils and the like, can be used for aqueous injection solutions of water-soluble salts of compounds of formula I, but as a rule are not necessary.
- Suitable carriers for suppositories are, for example, natural or hardened oils, waxes, fats, semi-liquid or liquid polyols and the like.
- the pharmaceutical preparations can contain preservatives, solubilizers, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They can also contain still other therapeutically valuable substances.
- pharmaceutically acceptable salts thereof and a therapeutically inert excipient are also an object of the present invention, as is a process for the production of such medicaments which comprises bringing one or more compounds of formula I or pharmaceutically acceptable salts thereof and, if desired, one or more other therapeutically valuable substances into a galenical dosage form together with one or more therapeutically inert carriers.
- the dosage can vary within wide limits and will, of course, be fitted to the individual requirements in each particular case.
- the effective dosage for oral or parenteral administration is between 0.01-20 mg/kg/day, with a dosage of 0.1-10 mg/ kg/day being preferred for all of the indications described.
- Step 1 5-(3-Fluoro-phenylethynyl)-pyridine-2-carboxylic acid methyl ester
- Bis-(triphenylphosphine)-palladium(II)dichloride (406 mg, 580 ⁇ , 0.05 equiv.) was dissolved in 25 ml DMF. (2.5 g, 11.6 mmol) 5-Bromo-pyridine-2-carboxylic acid methyl ester and 3- fluorophenylacetylene (2.22 g, 18.5 mmol, 1.6 equiv.) were added at room temperature.
- Triethylamine (3.5 g, 4.84 ml, 34.7 mmol, 3 equiv.), triphenylphosphine (91 mg, 347 ⁇ , 0.03 equiv.) and copper(I)iodide (66 mg, 347 ⁇ , 0.03 equiv.) were added and the mixture was stirred for 20 hours at 80°C.
- the reaction mixture was cooled and evaporated to dryness with Isolute® sorbent.
- the crude product was purified by flash chromatography on silica gel (70 g) eluting with an ethyl acetate:heptane gradient 0: 100 to 80:20.
- the crude product was purified by flash chromatography by directly loading the dichloromethane layers onto a silica gel column and eluting with an ethyl acetate:heptane gradient 0: 100 to 0: 100.
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JP2015537217A JP6263542B2 (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives as modulators of MGLUR5 receptor activity |
SG11201500729SA SG11201500729SA (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives as modulators of mglur5 receptor activity |
EA201590676A EA026941B1 (en) | 2012-10-18 | 2013-10-15 | ETHYNYL DERIVATIVES AS MODULATORS OF mGluR5 RECEPTOR ACTIVITY |
CN201380046124.7A CN104603110B (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives serving as the regulator of mGluR5 receptor active |
UAA201504679A UA114008C2 (en) | 2012-10-18 | 2013-10-15 | ETHINYL DERIVATIVES AS MGLUR5 RECEPTOR ACTIVITY MODULATORS |
AU2013331782A AU2013331782B2 (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives as modulators of mGluR5 receptor activity |
ES13776507.9T ES2599507T3 (en) | 2012-10-18 | 2013-10-15 | Ethinyl derivatives as modulators of mGluR5 receptor activity |
BR112015002320A BR112015002320A2 (en) | 2012-10-18 | 2013-10-15 | ethinyl derivatives as modulators of mglur5 receptor activity |
EP13776507.9A EP2909178B1 (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives as modulators of mglur5 receptor activity |
CA2879489A CA2879489A1 (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives as modulators of mglur5 receptor activity |
MX2015002823A MX2015002823A (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives as modulators of mglur5 receptor activity. |
KR1020157006701A KR20150070102A (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives as modulators of mglur5 receptor activity |
NZ703537A NZ703537A (en) | 2012-10-18 | 2013-10-15 | Ethynyl derivatives |
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PH12015500346A PH12015500346A1 (en) | 2012-10-18 | 2015-02-17 | Ethynyl derivatives as modulators of mglur5 receptor activity |
CR20150158A CR20150158A (en) | 2012-10-18 | 2015-03-20 | ETHYLLY DERIVATIVES AS MGLUR5 ACTIVITY RECEIVER MODULATORS |
MA38010A MA38010B1 (en) | 2012-10-18 | 2015-04-17 | Ethynyl derivatives used as modulators of mglur5 receptor activity |
US14/689,387 US9359301B2 (en) | 2012-10-18 | 2015-04-17 | Ethynyl derivatives |
HK15107144.3A HK1206715A1 (en) | 2012-10-18 | 2015-07-27 | Ethynyl derivatives as modulators of mglur5 receptor activity mglur5 |
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PH (1) | PH12015500346A1 (en) |
SG (1) | SG11201500729SA (en) |
TW (1) | TWI504593B (en) |
UA (1) | UA114008C2 (en) |
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WO2016193234A1 (en) * | 2015-06-03 | 2016-12-08 | F. Hoffmann-La Roche Ag | Ethynyl derivatives |
US11034699B2 (en) | 2015-07-15 | 2021-06-15 | Hoffmann-La Roche Inc. | Ethynyl derivatives |
US11033545B2 (en) | 2016-03-30 | 2021-06-15 | Sinntaxis AB | Negative allosteric modulators of MGLUR5 for use in the treatment of mature brain damages |
US11242349B2 (en) | 2016-07-18 | 2022-02-08 | Hoffmann-La Roche Inc. | Ethynyl derivatives |
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