Patent Application
20230416233
The present invention relates to compounds inhibiting P2X purinoceptor 3 (hereinafter P2X3 inhibitors); particularly the invention relates to compounds that are (aza)quinoline 4-amines derivatives, methods of preparing such compounds, pharmaceutical compositions containing them and therapeutic use thereof.
The compounds of the invention may be useful in the treatment of many disorders associated with P2X3 receptors mechanisms, such as respiratory diseases including cough, asthma, idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD).
P2X receptors are cell surface ion channels activated by extracellular Adenosine 5-TriPhosphate (ATP). P2X receptor family are trimeric assemblies composed of seven distinct subunit subtypes (P2X1-7) that assemble as homomeric and heteromeric channels. All subunits share a common topology containing intracellular termini, two transmembrane helices forming the ion channels and a large extracellular domain containing the ATP binding site. Homomeric P2X1, P2X2, P2X3, P2X4, P2X5, and P2X7 channels and heteromeric P2X2/3 and P2X1/5 channels have been fully characterized following heterologous expression. P2X receptors are abundantly distributed, and functional responses are seen in neurons, glia, epithelia, endothelia, bone, muscle, and hemopoietic tissues. On smooth muscles, P2X receptors respond to ATP released from sympathetic motor nerves (e.g., in ejaculation). On sensory nerves, they are involved in the initiation of afferent signals in several viscera (e.g., bladder, intestine) and play a key role in sensing tissue-damaging and inflammatory stimuli. Paracrine roles for ATP signaling through P2X receptors are likely in neurohypophysis, ducted glands, airway epithelia, kidney, bone and hemopoietic tissues. (RA. North: Molecular Physiology of P2X Receptors; Physiol Rev, Vol 82, October 2002). All P2X receptors are non-selective cation channels permeable to Na+ and Ca+ ions and are activated by ATP; however, the pharmacology of the receptor subtypes varies with respect to sensitivity to ATP and to small molecules antagonists. (K Kaczmarek-Hajek et al: Molecular and functional properties of P2X receptors—recent progress and persisting challenges; Purinergic Signalling 8:375-417, 2012)
In humans, the P2X3 receptor has been reported in heart and spinal cord at the mRNA level and in DRG, intestine (myenteric plexus neurons), urinary bladder (urothelium and suburothelium), and dental pulp at the protein level (Garcia-Guzman M et al: Molecular characterization and pharmacological properties of the human P2X3 purinoceptor: Brain Res Mol Brain Res. 1997; 47(1-2):59-66).
The neurophysiological role of P2X3 receptors in sensory nerve function in the airways is similar to that mediating somatic nociception (Undem B J and Nassenstein C: Airway nerves and dyspnea associated with inflammatory airway disease, Respir Physiol Nerobiol 167: 36-44, 2009). This similarity has driven hypotheses concerning the involvement of P2X3 receptors in the symptoms of airway dysfunction including cough and bronchial hyper-reactivity (Ford A P: In pursuit of P2X3 antagonists: novel therapeutics for chronic pain and and afferent sensitization, Purinergic signal 8 (suppl 1):3-26, 2012; North R A, Jarvis M F P2X Receptors as Drug Targets; Mol Pharmacol, 83:759-769, 2013). P2X3 subunits are also co-localized in many neurons, particularly within DRG, nodose ganglia, nucleus tractus solitarius, and taste buds (Cheung K K, Burnstock G: Localization of P2X3 receptors and coexpression with P2X2 receptors during rat embryonic neurogenesis. J Comp Neurol 443(4):368-382 2002)
P2X3 antagonists have been proposed for the treatment of diabetic neuropathic pain (Guo J et al: Contributions of purinergic P2X3 receptors within the midbrain periaqueductal gray to diabetes-induced neuropathic pain, J Physiol Sci January; 65(1):99-104 2015).
P2X3 and P2X2/3 channels play an important role in the development of articular hyperalgesia of arthritic joints (Teixeira J M et al: P2X3 and P2X2/3 Receptors Play a Crucial Role in Articular Hyperalgesia Development Through Inflammatory Mechanisms in the Knee Joint Experimental Synovitis, Mol Neurobiol October; 54(8):6174-6186, 2017).
P2X3 are also a potential target for therapeutic treatment of bladder pain. They were also proposed to be analgesic targets to treat ureteral colicky pain and to facilitate ureteral stone passage (Canda A E et al: Physiology and pharmacology of the human ureter: basis for current and future treatments, Urol Int. 78(4):289-98, 2007).
P2X3 over-expression is involved in poor recurrence-free survival in hepatocellular carcinoma patients and identifies the P2X3 as a potential therapeutic target (Maynard J P et al: P2X3 purinergic receptor overexpression is associated with poor recurrence-free survival in hepatocellular carcinoma patients Oncotarget December 1; 6(38):41162-79, 2015).
It has been suggested that P2X3 antagonists may improve recovery of erectile function (Li C L et al: Effects of intracavernous injection of P2X3 and NK1 receptor antagonists on erectile dysfunction induced by spinal cord transection in rats, Andrologia. February; 47(1):25-9, 2015).
ATP enhances citric acid-evoked and histamine-evoked cough in preclinical models, effects that can be attenuated by P2X3 selective antagonists (Kamei J and Takahashi Y: Involvement of ionotropic purinergic receptors in the histamine-induced enhancement of the cough reflex sensitivity in guinea pigs, October 10; 547(1-3):160-4, 2006). In humans, local delivery of ATP initiates cough and bronchospasm (Basoglu O K et al: Effects of aerosolized adenosine 5′-triphosphate vs adenosine 5′-monophosphate on dyspnea and airway caliber in healthy nonsmokers and patients with asthma, Chest. October; 128(4): 1905-9, 2005).
The therapeutic promise of P2X3 antagonists for the treatment of chronic cough was first recognized by Ford and Undem (Ford A P, Undem B J: The therapeutic promise of ATP antagonism at P2X3 receptors in respiratory and urological disorders, Front Cell Neurosci, December 19; 7:267, 2013). P2X3 are expressed by airway afferent nerves and mediate hypersensitivity of the cough reflex, which is dramatically reduced by the oral P2X3 antagonist, AF-219 (Abdulqawi et al: P2X3 receptor antagonist (AF-219) in refractory chronic cough: a randomised, double-blind, placebo-controlled phase 2 study, Lancet 385, 1198-205, 2015).
ATP is a key neurotransmitter in the taste system, acting largely via P2X2/3 heteromultimer receptors. Consequently, disruption of taste function may be an unintentional consequence of therapeutic trials of pain, chronic cough and other conditions using purinergic P2X3 antagonists (Vandenbeuch A et al: Role of the ectonucleotidase NTPDase2 in taste bud function, Proc Natl Acad Sci USA, September 3; 110(36):14789-94, 2013. Bo X et al: Localization of ATP-gated P2X2 and P2X3 receptor immunoreactive nerves in rat taste buds, Neuroreport, 10(5):1107-11, 1999).
Various compounds have been described in the literature as P2X3 and/or P2X2/3 inhibitors.
WO2017058645 (Afferent Pharmaceuticals INC) discloses the use of diaminopyrimidine P2X3/P2X2/3 antagonists for the treatment of disorders including cough, chronic cough and urge to cough, including cough associated with a respiratory disease or disorder, administering an efficacious amount of the compound disclosed. However, (aza)quinoline 4-amines derivatives are not disclosed.
WO2017011729 (Patara Pharma LLC), discloses the use of cromolyn or a pharmaceutically acceptable salt thereof and P2X3 and/or a P2X2/3 receptor antagonist as antitussive agent, for the treatment of lung diseases and conditions.
WO2016091776, (Evotec AG), discloses 1,3-thiazol-2-yl substituted benzamide compounds that inhibit P2X3 receptor and to pharmaceutical compositions containing such compounds, and the use of compounds for the treatment of several disorders, including the respiratory diseases.
WO2016088838 (Shionogi), discloses purine derivatives compounds having a novel P2X3 and/or P2X2/3 receptor antagonizing effect.
WO2016084922, (Shionogi), discloses triazine derivatives compounds having a novel P2X3 and/or P2X2/3 receptor antagonizing effect
WO2008123963 (Renovis) relates to fused heterocyclic compounds of the class tetrahydropyrido[4,3-d]pyrimidines and pharmaceutical compositions comprising such compounds. Also provided are methods for preventing and/or treating several disorders, such as neurodegenerative disorders, pain, asthma, autoimmune disorders administering the disclosed compounds.
WO2008130481 (Renovis) discloses 2-cyanophenyl fused heterocyclic compounds of the class tetrahydropyrido[4,3-d]pyrimidines and pharmaceutical compositions comprising such compounds.
WO2010033168 (Renovis) discloses a series of benzamides substituted with phenyl or pyridyl which are stated to be useful for treatment of diseases associated with P2X purinergic receptors, and more particularly to P2X3 receptor and/or P2X2/3 receptor antagonists. However, (aza)quinoline 4-amines derivatives are not disclosed.
WO2009110985 (Renovis) relates to phenyl- and pyridyl-substituted benzamide compounds and pharmaceutical compositions comprising such compounds, but not thiazole-substituted benzamides, rendering said compounds different from the compounds of the present invention.
WO2008000645 (Roche) discloses tetrazole substituted arylamides compounds antagonists of P2X3 and/or P2X2/3 receptors, useful for the treatment of genitourinary, pain, gastrointestinal and respiratory diseases, conditions and disorders.
Despite the above cited prior art, there is still the need of novel compounds for treatment of diseases associated with P2X3 receptors in many therapeutic areas such as in particular the respiratory diseases, preferably having a selective action versus the P2X3 receptor to avoid the side effect on taste.
Of note, the state of the art does not describe or suggest (aza)quinoline 4-amines derivatives compounds of general formula (I) of the present invention which represent a solution to the aforementioned need.
The present invention refers to compounds of formula (I)
wherein
X is CH or N;
Z is selected from the group consisting of (5-6 membered)-heteroaryl, aryl, wherein any of such heteroaryl and aryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl- and halo;
R1 is H or (C1-C4)alkyl;
R2 is heteroaryl wherein any of such heteroaryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl, (C1-C6)haloalkyl- and halo;
R3 is H or (C1-C4)alkyl;
Y is H or —O(C1-C4)alkyl.
In a second aspect, the invention refers to a pharmaceutical composition comprising a compound of formula (I) or pharmaceutically acceptable salt thereof, either alone or in combination with another one or more active ingredient, in admixture with one or more pharmaceutically acceptable carrier or excipient.
In a third aspect, the invention provides a compound of formula (I) for the use as a medicament.
In a further aspect, the invention provides the use of a compound of formula (I) for use in treatment of any disease wherein the P2X3 receptors are involved.
In a further aspect, the invention refers to a compound of formula (I) for use in the prevention and/or treatment of respiratory diseases including cough, sub-acute or chronic cough, treatment-resistant cough, idiopathic chronic cough, post-viral cough, iatrogenic cough, asthma, idiopathic pulmonary fibrosis (IPF), chronic obstructive pulmonary disease (COPD) and cough associated with respiratory diseases such as COPD, asthma and bronchospasm.
Unless otherwise provided, the term compound of formula (I) comprises in its meaning stereoisomer, tautomer or pharmaceutically acceptable salt or solvate.
The term “pharmaceutically acceptable salts”, as used herein, refers to derivatives of compounds of formula (I) wherein the parent compound is suitably modified by converting any of the free acid or basic group, if present, into the corresponding addition salt with any base or acid conventionally intended as being pharmaceutically acceptable.
Suitable examples of said salts may thus include mineral or organic acid addition salts of basic residues such as amino groups, as well as mineral or organic basic addition salts of acid residues such as carboxylic groups.
Cations of inorganic bases which can be suitably used to prepare salts comprise ions of alkali or alkaline earth metals such as potassium, sodium, calcium or magnesium.
Those obtained by reacting the main compound, functioning as a base, with an inorganic or organic acid to form a salt comprise, for example, salts of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, methane sulfonic acid, camphor sulfonic acid, acetic acid, oxalic acid, maleic acid, fumaric acid, succinic acid and citric acid.
The term “halogen” or “halogen atoms” as used herein includes fluorine, chlorine, bromine, and iodine atom, preferably chlorine or fluorine.
The term “(Cx-Cy) alkyl” wherein x and y are integers, refers to a straight or branched chain alkyl radical having from x to y carbon atoms. Thus, when x is 1 and y is 6, for example, the term includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, t-butyl, n-pentyl and n-hexyl.
The expressions “(Cx-Cy) haloalkyl” wherein x and y are integers, refer to the above defined “Cx-Cyalkyl” groups wherein one or more hydrogen atoms are replaced by one or more halogen atoms, which can be the same or different.
Examples of said “(Cx-Cy) haloalkyl” groups may thus include halogenated, poly-halogenated and fully halogenated alkyl groups wherein all of the hydrogen atoms are replaced by halogen atoms, e.g. trifluoromethyl or difluoro methyl, trifluoroethyl groups.
By way of analogy, the terms “(C1-C6) hydroxyalkyl” or “(C1-C6) aminoalkyl” refer to the above defined “(C1-C6) alkyl” groups wherein one or more hydrogen atoms are replaced by one or more hydroxy (OH) or amino group respectively. Examples include respectively hydroxymethyl, aminomethyl, dimethylaminopropyl and the like.
In the present description, unless otherwise provided, the aminoalkyl encompasses alkyl groups (i.e. “(C1C6) alkyl” groups) substituted by one or more amino group (—NRARB). Thus, an example of aminoalkyl is a mono-aminoalkyl group such as RARBN-(C1C6) alkyl.
The term “(Cx-Cy) cycloalkyl” wherein x and y are integers, refers to saturated cyclic hydrocarbon groups containing the indicated number of ring carbon atoms. Examples include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl.
The term “aryl” refers to mono cyclic carbon ring systems which have 6 ring atoms wherein the ring is aromatic. Examples of suitable aryl monocyclic ring systems include, for instance, phenyl.
The term “heteroaryl” refers to a mono- or bi-cyclic aromatic radical containing one or more heteroatoms selected from S, N and O, and includes radicals having two such monocyclic rings, or one such monocyclic ring and one monocyclic aryl ring, which are fused through a common bond. Examples of suitable 5,6-membered heteroaryl are: are thienyl, furyl, pyrrolyl, imidazolyl, thiazolyl, isothiazolyl, pyrazolyl, oxazolyl, isoxazolyl, isothiazolyl, triazolyl, thiadiazolyl, oxadiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, tetrazolyl and triazinyl.
The term “heterocyclyl” or “heterocyclic” relate to a saturated mono-, bi- or tri-cyclic non-aromatic radical containing one or more heteroatoms selected from S, N and O. In the case of bicyclic heterocyclic systems, included within the scope of the term are fused, spiro and bridged bicyclic systems.
The term “(Cx-Cy) heterocycloalkyl” wherein x and y are integers, refers to saturated or partially unsaturated monocyclic (Cx-Cy) cycloalkyl groups in which at least one ring carbon atom is replaced by at least one heteroatom (e.g. N, S or O) or may bear an -oxo (═O) substituent group. Said heterocycloalkyl (i.e. heterocyclic radical or group) may be further optionally substituted on the available positions in the ring, namely on a carbon atom, or on an heteroatom available for substitution. Substitution on a carbon atom includes spiro disubstitution as well as substitution on two adjacent carbon atoms, in both cases thus form additional condensed 5 to 6 membered heterocyclic ring. Examples of (Cx-Cy) heterocycloalkyl are represented by: pyrrolidinyl, imidazolidinyl, thiazolidinyl, piperazinyl, piperidinyl, morpholinyl, thiomorpholinyl, dihydro- or tetrahydro-pyridinyl, tetrahydrothiophenyl, azetidinyl, oxetanyl, tetrahydropyranyl, pyranyl, 2H- or 4H-pyranyl, dihydro- or tetrahydrofuranyl, dihydroisoxazolyl, pyrrolidin-2-one-yl, dihydropyrrolyl radicals and the like.
Specific examples of said heterocycle radicals are tetrahydrothiophene 1,1-dioxide, 3,3-difluoropyrrolidinyl, 1-pyrrolidinyl, 1-methyl-2-pyrrolidinyl, 1-piperidinyl, 1-piperazinyl, 4-morpholinyl.
The term (Cz-Ck)heterocycloalkyl-(Cx-Cy)alkyl wherein z and k are integers, refers to an heterocyclic ring linked to a straight-chained or branched alkyl groups having from x to y carbon atoms.
Likewise, the term “heteroaryl (Cx-Cy)alkyl” or “aryl (Cx-Cy)alkyl” refers to an heteroaryl or aryl ring linked to a straight-chained or branched alkyl groups having from x to y carbon atoms.
The expression “ring system” refers to mono- or bicyclic or polycyclic ring systems which may be saturated, partially unsaturated or unsaturated, such as aryl, (C3-C10) cycloalkyl, (C3-C6) heterocycloalkyl or heteroaryl.
The terms “group”, “radical” or “fragment” or “substituent” are synonymous and are intended to indicate functional groups or fragments of molecules attachable to a bond or other fragments or molecules. Thus, as an example, a “heterocyclic radical” herein refers to a mono- or bi-cyclic saturated or partially saturated heterocyclic moiety (group, radical), preferably a 4 to 11 membered monocyclic radical, at least one further ring carbon atom in the said heterocyclic radical is optionally replaced by at least one further heteroatom independently selected from N, S or O and/or may bear an -oxo (═O) substituent group, said heterocyclic radical is further optionally including spiro disubstitution as well as substitution on two adjacent or vicinal atoms forming an additional 5 to 6 membered cyclic or heterocyclic, saturated, partially saturated or aromatic ring. Examples of said heterocycle radicals are 1-pyrrolidinyl, 1-piperidinyl, 1-piperazinyl, 4-morpholinyl and the like.
A dash (“-”) that is not between two letters or symbols is meant to represent the point of attachment for a substituent. When graphically represented the point of attachment in a cyclic functional group is indicated with a dot (“⋅”) localized in one of the available ring atom where the functional group is attachable to a bond or other fragment of molecules.
An oxo moiety is represented by (O) as an alternative to the other common representation, e.g. (═O). Thus, in terms of general formula, the carbonyl group is herein represented as —C(O)—, in general, the bracketed group is a lateral group, not included into the chain, and brackets are used, when deemed useful, to help disambiguating linear chemical formulas; e.g. the sulfonyl group —SO2— might be also represented as —S(O)2— to disambiguate e.g. with respect to the sulfinic group —S(O)O—.
Whenever basic amino or quaternary ammonium groups are present in the compounds of formula I, physiologically acceptable anions may be present, selected among chloride, bromide, iodide, trifluoroacetate, formate, sulfate, phosphate, methanesulfonate, nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate, succinate, benzoate, p-toluenesulfonate, pamoate and naphthalene disulfonate. Likewise, in the presence of acidic groups such as COOH groups, corresponding physiological cation salts may be present as well, for instance including alkaline or alkaline earth metal ions.
It will be apparent that compounds of formula (I) when contain one or more stereogenic center, may exist as optical stereoisomers.
Where the compounds according to the invention have at least one stereogenic center, they may accordingly exist as enantiomers. Where the compounds according to the invention possess two or more stereogenic centers, they may additionally exist as diastereoisomers. All such single enantiomers, diastereoisomers and mixtures thereof in any proportion are encompassed within the scope of the present invention. The absolute configuration (R) or (S) for carbon bearing a stereogenic center is assigned on the basis of Cahn-Ingold-Prelog nomenclature rules based on groups' priorities.
The invention further concerns the corresponding deuterated derivatives of compounds of formula (I).
All preferred groups or embodiments described above and herebelow for compounds of formula I may be combined among each other and apply as well mutatis mutandis.
As above indicated, the present invention refers to a series of compounds represented by the general formula (I) as herein below described in details, which are endowed with an antagonist property versus receptor P2X3.
Differently from similar compounds of the prior art, the compounds of formula (I) of the present invention are able to act as antagonist P2X3 in a substantive and effective way, particularly appreciated by the skilled person when looking at a suitable and efficacious compounds useful for the treatment of respiratory disease, in particular chronic cough.
As indicated in the experimental part, the compounds of formula (I) have an activity as shown in Table 2, wherein for each compound is reported the potency expressed as half maximal inhibitory concentration (pIC50) on receptors.
As further advantage, the compound of formula (I) have surprisingly been found to effectively and selectively inhibit mainly the P2X3 receptor and said compounds are useful for the treatment of respiratory disease avoiding adverse effect, such as loss of taste response. In fact, as it can be appreciated in Table 3, the compounds of formula (I) show a greater activity versus the receptor P2X3 in comparison to the receptor P2X2/3.
Thus, in one aspect the present invention relates to a compound of general formula (I) as P2X3 antagonist
wherein
X is CH or N;
Z is selected from the group consisting of (5-6 membered)-heteroaryl and aryl, wherein any of such heteroaryl and aryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl- and halo;
R1 is H or (C1-C4)alkyl;
R2 is heteroaryl wherein any of such heteroaryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl, (C1-C6)haloalkyl and halo;
R3 is H or (C1-C4)alkyl;
Y is H or —O(C1-C4)alkyl.
In a preferred embodiment Z is aryl or (5-6 membered)-heteroaryl selected form the group consisting of thiazole, pyridine and pyrimidine.
In a further preferred embodiment R2 is heteroaryl selected from pyrimidine and pyridazine.
In a preferred embodiment, the invention refers to at least one of the compounds listed in the Table 1 below and pharmaceutical acceptable salts thereof.
In one preferred embodiment, the invention refers to a compound of formula (I), wherein X is N, represented by the formula Ia
wherein
Z is selected from the group consisting of (5-6 membered)-heteroaryl and aryl, wherein any of such heteroaryl and aryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl- and halo;
R1 is H;
R2 is heteroaryl wherein any of such heteroaryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl and (C1-C6)haloalkyl;
R3 is H or (C1-C4)alkyl;
Y is H or —O(C1-C4)alkyl.
In one preferred embodiment, the invention refers to a compound of formula (I), wherein X is CH, represented by the formula Ib
wherein
Z is selected from the group consisting of (5-6 membered) heteroaryl and aryl, wherein any of such heteroaryl and aryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl- and halo;
R1 is H;
R2 is heteroaryl wherein any of such heteroaryl may be optionally substituted by one or more groups selected from (C1-C3)alkyl and (C1-C6)haloalkyl;
R3 is H or (C1-C4)alkyl;
Y is H.
The compounds of formula (I) including all the compounds or at least one of the here above listed can be generally prepared according to the procedure outlined in detail in the Schemes shown below using generally known methods.
In one embodiment of the present invention, compound (Ia) wherein Y is H may be prepared according to SCHEME 1 from compound (II).
Compound (III) may be prepared from Compound (II) by a deoxyahalogenation reaction mediated by reagents like, for example, Phosphorous oxychloride.
Compound (IV) may be prepared from Compound (III) by a reaction with a suitable amine (Reag. 1) in the presence of a base like, for example TEA or DIPEA.
Compound (Ia) may be prepared from Compound (IV) by a metal-catalyzed cross coupling reactions like Stille or Suzuki or similars as described in “Transition Metals for Organic Synthesis”, 2nd Ed, 1, 2004 with a suitable reagent like (Reag. 2).
Alternatively Compound (V) may be prepared from Compound (II) by a metal-catalyzed cross coupling reactions like Stille or Suzuki or similars as described in “Transition Metals for Organic Synthesis”, 2nd Ed, 1, 2004 with a suitable reagent like (Reag. 2).
Compound (VI) may be prepared from Compound (V) by a deoxyahalogenation reaction mediated by reagents like, for example, Phosphorous oxychloride.
Compound (Ia) may be prepared from Compound (VI) by a reaction with a suitable amine (Reag. 1) in the presence of a base like, for example TEA or DIPEA
Some compounds (Ia) may contain a protected hydroxyl or amino group which were then removed under well known procedures.
In one embodiment of the present invention, compound (Ia) wherein Y is —OCH3 may be prepared according to SCHEME 2 from compound (VII).
Compound (VIII) may be prepared from Compound (VII) by Halogenation with suitable reagents like Bromine, NBS, NIS, Iodine, iodonium salts or similar.
Compound (IX) may be prepared from Compound (VIII) by a ring closing reaction mediated by Sodium Nitrite.
Compound (X) may be prepared from Compound (IX) by a metal-catalyzed cross coupling reactions like Stille or Suzuki or similars as described in “Transition Metals for Organic Synthesis”, 2nd Ed, 1, 2004 with a suitable reagent like (Reag. 2).
Compound (XI) may be prepared from Compound (X) by a deoxyahalogenation reaction mediated by reagents like, for example, Phosphorous oxychloride.
Compound (Ia) may be prepared from Compound (XI) by a reaction with a suitable amine (Reag. 1) in the presence of a base like, for example TEA or DIPEA
Some compounds (Ia) may contain a protected hydroxyl or amino group which were then removed under well known procedures.
In one embodiment of the present invention, compound (Ib) may be prepared according to SCHEME 3 from compound (XIII).
Compound (XIV) may be prepared from Compound (XIII) by metal-catalyzed Miyaura borylation reaction.
Compound (XV) may be prepared from Compound (XIV) by a metal-catalyzed cross coupling reactions like Stille or Suzuki or similars as described in “Transition Metals for Organic Synthesis”, 2nd Ed, 1, 2004 with a suitable reagent like (Reag. 3).
Compound (Ib) may be prepared from Compound (XV) by a reaction with a suitable amine (Reag. 1) in the presence of a base like, for example TEA or DIPEA.
Alternatively Compound (XVII) may be prepared from Compound (XIII) by a reaction with a suitable amine (Reag. 1) in the presence of a base like, for example TEA or DIPEA
Compound (Ib) may be prepared from Compound (XVII) by a metal-catalyzed cross coupling reactions like Stille or Suzuki or similars as described in “Transition Metals for Organic Synthesis”, 2nd Ed, 1, 2004 with a suitable reagent like (Reag. 2).
Alternatively Compound (XVIII) may be prepared from Compound (XIII) by a metal-catalyzed cross coupling reactions like Stille or Suzuki or similars as described in “Transition Metals for Organic Synthesis”, 2nd Ed, 1, 2004 with a suitable reagent like (Reag. 2).
Compound (Ib) may be prepared from Compound (XVIII) by a reaction with a suitable amine (Reag. 1) in the presence of a base like, for example TEA or DIPEA.
Some compounds (Ib) may contain a protected hydroxyl or amino group which were then removed under well known procedures.
The compounds of the present invention have surprisingly been found to effectively inhibit P2X3 receptor and said compounds are useful for the treatment of respiratory disease.
In one embodiment, representative compounds of formula (I) of the present invention have surprisingly been found to effectively and selectively inhibit P2X3 receptor and said compounds are useful for the treatment of respiratory disease avoiding adverse effect, such as loss of taste response.
In a preferred embodiment, the compound of formula (I) are selective P2X3 antagonist wherein the selective P2X3 antagonist is at least 10-fold selective for P2X3 homomeric receptor antagonism versus P2X2/3 heteromeric receptor antagonism.
In a further preferred embodiment, the selective P2X3 antagonist is at least 30-fold selective for P2X3 homomeric receptor antagonism versus P2X2/3 heteromeric receptor antagonism.
In a further preferred embodiment, the selective P2X3 antagonist is at least 50-fold selective for P2X3 homomeric receptor antagonism versus P2X2/3 heteromeric receptor antagonism.
The present invention also provides a pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof in admixture with one or more pharmaceutically acceptable carrier or excipient, either alone or in combination with one or more further active ingredient.
In one aspect, the invention refers to a compound of formula (I) according to the invention for use as a medicament.
In a further aspect, the invention refers to the use of a compound of formula (I) of the invention, or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment of disorders associated with P2X3 receptors mechanism, preferably for the treatment of respiratory diseases.
Preferably, the invention refers to a compound of formula (I) for use in the prevention and/or treatment of respiratory diseases, preferably cough, sub-acute or chronic cough, treatment-resistant cough, idiopathic chronic cough, post-viral cough, iatrogenic cough, asthma, idiopathic pulmonary fibrosis (IPF), chronic obstructive pulmonary disease (COPD) and cough associated with respiratory diseases such as COPD, asthma and bronchospasm.
More preferably, the invention refers to a compounds of formula (I) for use in the prevention and/or treatment of chronic cough and cough associated with respiratory diseases such as COPD, asthma and bronchospasm.
The invention also provides a method for the prevention and/or treatment of disorders associated with P2X3 receptors mechanisms, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound of the invention.
In particular the invention refers to a method for the prevention and/or treatment wherein the disorder is cough, sub-acute or chronic cough, treatment-resistant cough, idiopathic chronic cough, post-viral cough, iatrogenic cough, asthma, idiopathic pulmonary fibrosis (IPF), chronic obstructive pulmonary disease (COPD) and cough associated with respiratory diseases such as COPD, asthma and bronchospasm, wherein said method comprises the administration of a proper amount of a compound of formula (I) to a patient in the need thereof.
In a further preferred embodiment, the disorder is chronic cough.
The methods of treatment of the invention comprise administering a safe and effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof to a patient in need thereof. As used herein, “safe and effective amount” in reference to a compound of formula (I) or a pharmaceutically acceptable salt thereof or other pharmaceutically-active agent means an amount of the compound sufficient to treat the patient's condition but low enough to avoid serious side effects and it can nevertheless be routinely determined by the skilled artisan. The compounds of formula (I) or pharmaceutically acceptable salts thereof may be administered once or according to a dosing regimen wherein a number of doses are administered at varying intervals of time for a given period of time. Typical daily dosages may vary depending upon the particular route of administration chosen.
The invention also provides pharmaceutical compositions of compounds of formula (I) in admixture with one or more pharmaceutically acceptable carrier or excipient, for example those described in Remington's Pharmaceutical Sciences Handbook, XVII Ed., Mack Pub., N.Y., U.S.A.
Administration of the compounds of the invention and their pharmaceutical compositions may be accomplished according to patient needs, for example, orally, nasally, parenterally (subcutaneously, intravenously, intramuscularly, intrasternally and by infusion) and by inhalation.
Preferably the compounds of the present invention may be administered orally or by inhalation. More preferably the compounds of the present invention are administered orally.
Various solid oral dosage forms can be used for administering compounds of the invention including such solid forms as tablets, gelcaps, capsules, caplets, granules, lozenges and bulk powders. The compounds of the invention can be administered alone or combined with various pharmaceutically acceptable carriers, diluents (such as sucrose, mannitol, lactose, starches) and known excipients, including suspending agents, solubilizers, buffering agents, binders, disintegrants, preservatives, colorants, flavorants, lubricants and the like. Time release capsules, tablets and gels are also advantageous in administering the compounds of the invention.
Preferably the compounds of the invention are administered in forms of tablets.
Various liquid oral dosage forms can also be used for administering compounds of the invention, including aqueous and non-aqueous solutions, emulsions, suspensions, syrups, and elixirs. Such dosage forms can also contain suitable known inert diluents such as water and suitable known excipients such as preservatives, wetting agents, sweeteners, flavorants, as well as agents for emulsifying and/or suspending the compounds of the invention. The compounds of the invention may be injected, for example, intravenously, in the form of an isotonic sterile solution.
For the treatment of the diseases of the respiratory tract, the compounds according to the invention are preferably administered by inhalation.
Inhalable preparations include inhalable powders, propellant-containing metering aerosols or propellant-free inhalable formulations.
For administration as a dry powder, single- or multi-dose inhalers known from the prior art may be utilized. In that case the powder may be filled in gelatine, plastic or other capsules, cartridges or blister packs or in a reservoir.
A diluent or carrier chemically inert to the compounds of the invention, e.g. lactose or any other additive suitable for improving the respirable fraction may be added to the powdered compounds of the invention.
Inhalation aerosols containing propellant gas such as hydrofluoroalkanes may contain the compounds of the invention either in solution or in dispersed form. The propellant-driven formulations may also contain other ingredients such as co-solvents, stabilizers and optionally other excipients.
The propellant-free inhalable formulations comprising the compounds of the invention may be in form of solutions or suspensions in an aqueous, alcoholic or hydroalcoholic medium and they may be delivered by jet or ultrasonic nebulizers known from the prior art or by soft-mist nebulizers.
Preferably, the compound of the present invention are administered orally.
The compounds of the invention can be administered as the sole active agent or in combination with other pharmaceutical active ingredients.
Preferably, the compound of the present invention can be combined with therapeutic agents or active ingredients useful for the treatment of disease which are related to or mediated by P2X3 receptor.
The dosages of the compounds of the invention depend upon a variety of factors including among others the particular disease to be treated, the severity of the symptoms, the route of administration, and the like.
The invention is also directed to a device comprising a pharmaceutical composition comprising a compound of formula (I) according to the invention, in form of a single- or multi-dose dry powder inhaler or a metered dose inhaler.
The various aspects of the invention described in this application are illustrated buy the following examples which are not meant to limit the invention in any way. following examples illustrate the invention.
The example testing experiments described herein serve to illustrate the present invention and the invention is not limited to the examples given.
Chemical names were generated using the Dotmatics software. In some cases generally accepted names of commercially available reagents were used in place of Dotmatics software generated names.
All reagents, for which the synthesis is not described in the experimental part, are either commercially available, or are known compounds or may be formed from known compounds by known methods by a person skilled in the art.
(R)-1-(2-(trifluoromethyl)pyrimidin-5-yl)ethanamine hydrochloride and (R)-1-(6-methylpyridazin-3-yl)ethan-1-amine hydrochloride were prepared accordingly to the procedure described in WO2016/091776.
Et2O: diethyl ether;
Et3N: triethyl amine;
TEA: triethyl amine;
DCC: N,N′-Dicyclohexylcarbodiimide;
PyBOP: (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate;
DMF: dimethylformamide;
EtOAc: Ethyl acetate;
RT: room temperature;
THF: tetrahydrofuran;
DCM: dichloromethane;
MeOH: methyl alcohol;
EtOH: ethylic alcohol;
TFA: Trifluoroacetic acid;
LC-MS: Liquid Chromatography/Mass Spectrometry;
HPLC: high pressure liquid chromatography;
MPLC: medium pressure liquid chromatography;
SFC: Supercritical Fluid Chromatography;
dppf: 1,1′-Bis(diphenylphosphino) ferrocene;
MgSO4: Magnesium sulfate
DIEA or DIPEA: N,N-Diisopropylethylamine;
MeCN: Acetonitrile;
MTBE: tert-Butyl methyl ether;
TBDMSCl: tert-Butyl(chloro)dimethylsilane;
DMSO: Dimethylsulfoxide;
Boc2O: di-tert-butyl dicarbonate;
UPLC: Ultra Performance Liquid Chromatography.
UPLC-MS was performed on a Waters Acquity I-Class with Waters Diode Array Detector coupled to a Waters SQD2 single quadrapole mass spectrometer using an Waters BEH Shield RP18 column (1.7 μm, 100×2.1 mm) being initially held at 5% MeCN/water (with 10 mM ammonium bicarbonate in each mobile phase) for 1.2 minutes, followed by a linear gradient of 5-100% within 3.5 minutes and then held at 100% for 1.5 minutes (F=0.5 mL/min).
UPLC-MS was performed on a Waters DAD+Waters SQD2, single quadrapole UPLC-MS spectrometer using an Acquity UPLC BEH Shield RP18 1.7 um 100×2.1 mm (Plus guard cartridge), maintained at temp column being initially held at 5% MeCN/water (with 10 mM ammonium bicarbonate in each mobile phase) for 0.4 minutes, followed by a linear gradient of 5-95% within 6.4 minutes and then held at 95% for 1.2 minutes (F=0.4 mL/min).
UPLC-MS was performed on a Waters DAD+Waters SQD2, single quadrapole UPLC-MS spectrometer using an Acquity UPLC BEH Shield RP18 1.7 um 100×2.1 mm (Plus guard cartridge), maintained at temp column being initially held at 5% MeCN (Far UV grade) with 0.1% (V/V) formic acid/Water (High purity via PureLab Option unit) with 0.1% formic acid for 0.4 minutes, followed by a linear gradient of 5-95% within 6.4 minutes and then held at 95% for 1.2 minutes (F=0.4 mL/min).
1H Nuclear magnetic resonance (NMR) spectroscopy was carried out using a Bruker or Varian instruments operating at 400 MHz using the stated solvent at around RT unless otherwise stated. In all cases, NMR data were consistent with the proposed structures. Characteristic chemical shifts (δ) are given in parts-per-million using conventional abbreviations for designation of major peaks: e.g. s, singlet; d, doublet; t, triplet; q, quartet; dd, doublet of doublets; dt, doublet of triplets; m, multiplet; br, broad.
Preparative HPLC purification was performed by reverse phase HPLC using a Waters Fractionlynx preparative HPLC system (2525 pump, 2996/2998 UV/VIS detector, 2767 liquid handler) or an equivalent HPLC system such as a Gilson Trilution UV directed system. The Waters 2767 liquid handler acted as both auto-sampler and fraction collector. The columns used for the preparative purification of the compounds were a Waters Sunfire OBD Phenomenex Luna Phenyl Hexyl or Waters Xbridge Phenyl at 10 μm 19×150 mm or Waters CSH Phenyl Hexyl, 19×150, 5 μm column. Appropriate focused gradients were selected based on MeCN and MeOH solvent systems under either acidic or basic conditions. The modifiers used under acidic/basic conditions were formic acid or trifluoroacetic acid (0.1% V/V) and ammonium bicarbonate (10 mM) respectively. The purification was controlled by Waters Fractionlynx software through monitoring at 210-400 nm and triggered a threshold collection value at 260 nm and, when using the Fractionlynx, the presence of target molecular ion as observed under API conditions. Collected fractions were analysed by LCMS (Waters Acquity systems with Waters SQD).
The diastereomeric separation of compounds was achieved by Supercritical Fluid Chromatography (SFC) using a Waters Thar Prep100 preparative SFC system (P200 CO2 pump, 2545 modifier pump, 2998 UV/VIS detector, 2767 liquid handler with Stacked Injection Module). The Waters 2767 liquid handler acted as both auto-sampler and fraction collector. Appropriate isocratic methods were selected based on MeOH, ethanol or isopropanol solvent systems under un-modified or basic conditions. The standard SFC method used was modifier, CO2, 100 mL/min, 120 Bar backpressure, 40° C. column temperature. The modifier used under basic conditions was diethylamine (0.1% V/V). The modifier used under acidic conditions was either formic acid (0.1% V/V) or trifluoroacetic acid (0.1% V/V). The SFC purification was controlled by Waters Fractionlynx software through monitoring at 210-400 nm and triggered at a threshold collection value, typically 260 nm. Collected fractions were analysed by SFC (Waters/Thar SFC systems with Waters SQD). The fractions that contained the desired product were concentrated by vacuum centrifugation.
SFC-MS was performed on a Waters/Thar SFC systems with Waters SQD using a YMC Cellulose-SC column with a 35% MeOH/CO2 (with 0.1% diethylamine) isocratic run at 5 mL/min, 120 Bar backpressure, 40° C. column temperature.
SFC-MS was performed on a Waters/Thar SFC systems with Waters SQD using a YMC Amylose-C column with a 55% MeOH/CO2 (with 0.1% diethylamine) isocratic run at 5 mL/min, 120 Bar backpressure, 40° C. column temperature.
6-Bromo-4-chlorocinnoline (200 mg, 0.821 mmol) and (6-methylpyridazin-3-yl)methanamine hydrochloride salt (144 mg, 0.904 mmol) were dissolved in DMF (2 mL) and subsequently N,N-diisopropylamine (0.57 ml, 3.29 mmol) was added. The reaction mixture was stirred at 90° C. for 4 hours. Then, the reaction was allowed to cool to RT and the solvent was removed in vacuo. The residue was purified by chromatography on silica gel eluting with 0-20% MeOH in DCM to give the desired product as an off-white solid (60 mg, 22%).
LCMS (Method 2): [MH+]=330.0 at 2.95 min.
The following compound reported in the table below was prepared according to the procedure described for the preparation of 6-bromo-N-((6-methylpyridazin-3-yl)methyl)cinnolin-4-amine
1H NMR
A mixture of 4-chloro-6-bromo-quinoline (250 mg, 1.03 mmol), (6-methylpyridazin-3-yl)methanamine dihydrochloride (222 mg, 1.13 mmol) and N,N-diisopropylamine (0.9 mL, 5.15 mmol), dioxane (2 mL), DMF (1 mL) was heated at reflux for 16 hours. Solvent removed in vacuo. The residue was purified by chromatography on silica gel eluting with 0-20% MeOH in DCM to give the title compound as a brown oil (124 mg, 37%).
1H NMR (400 MHz, DMSO): δ 9.47-9.43 (m, 1 H), 8.86 (d, J=1.5 Hz, 1 H), 8.54 (d, J=6.6 Hz, 1 H), 8.05 (dd, J=1.4, 9.0 Hz, 1 H), 7.91 (d, J=8.8 Hz, 1 H), 7.70 (d, J=8.6 Hz, 1 H), 7.61 (d, J=8.6 Hz, 1 H), 6.79 (d, J=6.3 Hz, 1 H), 5.01 (d, J=5.8 Hz, 2 H), 2.65 (s, 3 H). LCMS (Method 2): [MH+]=329 at 3.57 min.
To a mixture of 6-bromo-4-chloroquinoline (500 mg, 2.06 mmol), 4-fluorophenylboronic acid (317 mg, 2.27 mmol), potassium carbonate (427 mg, 3.09 mmol) and tetrakis(triphenylphosphine)palladium(0) (238 mg, 0.21 mmol) in 1,4-dioxane (20 mL), was added water (2 mL). The mixture was heated at 90° C. for 12 hours under an atmosphere of nitrogen. After return to RT, the reaction mixture was diluted with EtOAc (20 mL) and washed with saturated aqueous solution of sodium hydrogen carbonate (2×10 mL). The organic phases were combined and the solvent was removed in vacuo. The residue was purified by chromatography on silica gel eluting with 0-10% MeOH in DCM to give the title compound as an off-white solid (410 mg, 82%).
LCMS (Method 1): [MH+]=258 at 5.51 min.
6-bromo-4-chloroquinoline (500 mg, 2.06 mmol), bis(pinacolato)diboron (576 mg, 2.27 mmol), pd(dppf)Cl2 (75 mg, 0.10 mmol) and potassium acetate (607 mg, 6.19 mmol) were combined in a round bottom flask, evacuated and back filled with nitrogen. 1,4-Dioxane (30.0 mL) was added and the mixture was heated at 90° C. for 16 hours. The reaction was cooled to RT, filtered through Celite® and the solvent was removed in vacuo. The residue was purified by chromatography on silica gel eluting with 0-10% MeOH in DCM to give the title compound as a brown solid (547 mg, 91%).
LCMS (Method 2): [MH+]=290 at 5.45 min.
To a mixture of 2-bromo-5-methylpyridine (54 mg, 0.31 mmol), tetrakis(triphenylphosphine)palladium(0) (36 mg, 0.03 mmol) and potassium carbonate (372 mg, 3.79 mmol), 4-chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinolone (100 mg, 0.35 mmol) in 1,4-dioxane (4.0 mL) was added water (0.5 mL) and the mixture was heated at 95° C. for 16 hours. The reaction was cooled to RT, diluted with EtOAc (20 mL) and washed with saturated aqueous solution of sodium bicarbonate (2×10 mL). The combined organic phases were filtered through a hydrophobic frit and the solvent was removed in vacuo. The residue was purified by chromatography on silica gel eluting with 0-10% MeOH in DCM to give the title compound as a brown solid (50 mg, 62%).
LCMS (Method 2): [MH+]=255 at 4.82 min.
To a solution of 1-(3-methoxy-2-nitrophenyl)ethan-1-one (4.0 g, 20.5 mmol) and ammonium chloride (2.2 g, 41.0 mmol, 2 eq.) in MeOH (30 mL), THF (30 mL) and water (3 mL) was added iron powder (5.7 g, 102.5 mmol). The resulting mixture was heated to 80° C. for 2 hours. The reaction mixture was cooled to RT and diluted with EtOAc (20 mL). The resulting suspension was passed through a pad of Celite®, and the pad was washed with EtOAc (3×40 mL). The organic phases were combined, washed with water (80 mL), brine (80 mL), passed through a hydrophobic frit and concentrated in vacuo to give the title compound as a yellow solid (3.3 g, 98%).
1H NMR (400 MHz, CDCl3) δ 7.34 (d, J=7.9 Hz, 1 H), 6.84 (d, J=7.9 Hz, 1 H), 6.60 (br s, 2 H), 6.58 (t, J=7.9 Hz, 1 H), 3.87 (s, 3 H), 2.57 (s, 3 H).
Nitrogen was bubbled for 5 minutes through a solution of 1-(2-amino-3-methoxyphenyl)ethan-1-one (3.3 g, 20.2 mmol) in DMF (30 mL) and the mixture subsequently cooled to 0° C. To the resulting mixture was added N-bromosuccinimide (4.3 g, 24.2 mmol, 1.2 eq.) and the resulting mixture was stirred at 0° C. for 2 hours. The reaction mixture was quenched at 0° C. with aqueous saturated sodium sulfite (5 mL). The reaction was diluted with water (100 mL) and extracted with EtOAc (3×40 mL). The organic phases were combined, washed with brine (80 mL), passed through a hydrophobic frit and concentrated in vacuo. The resulting residue was purified by column chromatography on silica gel eluting with 0-30% EtOAc in cyclohexane to give the title compound as a yellow solid (3.92 g, 85%).
1H NMR (400 MHz, CDCl3): δ 7.44 (d, J=2.1 Hz, 1 H), 6.90 (d, J=1.9 Hz, 1 H), 6.62-6.62 (m, 2 H), 3.87 (s, 3 H), 2.55 (s, 3 H).
Nitrogen was bubbled for 5 minutes through a suspension of 1-(2-amino-5-bromo-3-methoxyphenyl)ethan-1-one (990 mg, 4.06 mmol) in concentrated hydrochloric acid (3 mL) and water (3 mL) and the mixture was subsequently cooled to 0° C. To the resulting solution was added a solution of sodium nitrite (336 mg, 4.87 mmol) in water (0.8 mL) dropwise. The mixture then was stirred at 0° C. for 1.5 hours, followed by 0.5 hour at RT and finally at reflux for 2.5 hours. The reaction mixture was cooled to 0° C. and the resulting solid was filtered, washed with water (4×5 mL) and air dried to give the title compound as a yellow solid (973 mg, 82%).
1H NMR (400 MHz, DMSO): δ 13.51 (s, 1 H), 7.83 (s, 1 H), 7.68 (d, J=1.8 Hz, 1 H), 7.50 (d, J=1.8 Hz, 1 H), 4.05 (s, 3 H). LCMS (Method 3): [MH+]=256 at 3.10 min.
Nitrogen was bubbled for 10 minutes through a suspension of 6-bromo-8-methoxycinnolin-4-ol hydrochloride (990 mg, 3.4 mmol), 4-fluorophenyl boronic acid (713 mg, 5.09 mmol), pd(dppf)Cl2 (139 mg, 0.17 mmol) in 1,4-dioxane (20 mL). A solution of cesium carbonate (2213 mg, 6.80 mmol) in water (3 mL) was added and the mixture was stirred at 100° C. for 1.5 hours. The reaction mixture was cooled to RT, water (10 mL) was added and the resulting solids filtered. The filter cake was washed with 9:1 Et2O/MeOH (3×10 mL) and air dried to give the title compound as a brown solid (615 mg, 71%).
1H NMR (400 MHz, DMSO) 13.49-13.49 (m, 1 H), 7.92-7.86 (m, 3 H), 7.83 (d, J=1.8 Hz, 1 H), 7.52 (d, J=1.5 Hz, 1 H), 7.37 (t, J=8.8 Hz, 2 H), 4.13 (s, 3 H). LCMS (Method 2): [MH+]=271 at 3.74 min.
Phosphorus(V) oxychloride (4110 mg, 26.8 mmol) was added to a solution of 6-(4-fluorophenyl)-8-methoxycinnolin-4-ol hydrochloride (580 mg, 2.15 mmol) in 1,2-dichloroethane (2.5 mL). The resulting mixture was heated to 90° C. for 2 hours. The reaction mixture was cooled to RT and excess phosphorus(V) oxychloride was removed in vacuo, azeotroping with toluene (3×10 mL). The resulting residue was partitioned with a saturated aqueous solution of sodium bicarbonate (15 mL) and extracted with DCM (3×15 mL). The combined organic phases were passed through a hydrophobic frit and concentrated in vacuo. The resulting residue was purified by column chromatography on silica gel eluting with 0-80% EtOAc in cyclohexane to give the title compound as a pale yellow solid (280 mg, 45%).
1H NMR (400 MHz, CDCl3): δ 9.37 (s, 1 H), 7.81 (d, J=1.5 Hz, 1 H), 7.75-7.70 (m, 2 H), 7.34 (d, J=1.5 Hz, 1 H), 4.25 (s, 3 H). LCMS (Method 2): [MH+]=289 at 4.69 min.
Nitrogen was bubbled for 10 minutes through a suspension of 2-bromo-5-methylpyrimidine (300 mg, 1.73 mmol), hexamethylditin (682 mg, 2.08 mmol), tetrakis(triphenylphosphine)palladium(0) (100 mg, 0.09 mmol) in 1,4-dioxane (12 mL). The mixture was then stirred at 110° C. for 16 hours. The reaction mixture was cooled to RT, 1 M aqueous solution of cesium fluoride (15 mL) was added and the resulting biphasic mixture was stirred for a further 30 minutes. The resulting solution was partitioned with EtOAc (20 mL) and extracted. The combined organic phases were passed through a hydrophobic frit and concentrated in vacuo to give the title compound as a pale brown oil (482 mg, 108%).
1H NMR (400 MHz, CDCl3) 8.55 (s, 2 H), 3.70 (s, 3 H), 0.38 (s, 9 H); Residual triphenylphosphine oxide was observed.
Nitrogen was bubbled for 10 minutes through a suspension of 6-bromo-8-methoxycinnolin-4-ol hydrochloride (303 mg, 1.04 mmol), 5-methyl-2-(trimethylstannyl)pyrimidine (400 mg, 1.56 mmol), tetrakis(triphenylphosphine)palladium(0) (60 mg, 0.05 mmol) in 1,4-dioxane (6 mL). The mixture was then stirred at 100° C. for 48 hours. The reaction mixture was cooled to RT and the resulting solid was filtered. The filter cake was washed with EtOAc (4×5 mL) and air dried to give the title compound as an orange solid (160 mg, 57%).
1H NMR (400 MHz, DMSO): δ 13.50 (s, 1 H), 8.81 (s, 2 H), 8.67 (s, 1 H), 8.20 (s, 1 H), 7.83 (s, 1 H), 4.12 (s, 3 H), 2.36 (s, 3 H). LCMS (Method 2): [MH+]=269 at 2.96 min.
Phosphorus(V) oxychloride (2 mL) was added to 8-methoxy-6-(5-methylpyrimidin-2-yl)cinnolin-4-ol (160 mg, 0.60 mmol) and the resulting mixture was heated to 120° C. for 2 hours. The reaction mixture was cooled to RT and excess phosphorus(V) oxychloride was removed in vacuo, azeotroping with toluene (3×5 mL). The resulting residue was partitioned with saturated aqueous solution of sodium bicarbonate (15 mL) and extracted with DCM (3×15 mL). The combined organic phases were passed through a hydrophobic frit and concentrated in vacuo. The resulting residue was purified by column chromatography on silica gel eluting with 0-80% EtOAc in DCM to give the title compound as a pale yellow solid (60 mg, 35%).
1H NMR (400 MHz, CDCl3): δ 9.40 (s, 1 H), 8.83 (s, 1 H), 8.74 (s, 2 H), 8.31 (s, 1 H), 4.31 (s, 3 H), 2.43 (s, 3 H). LCMS (Method 3): [MH+]=287 at 4.1 min.
A mixture of 6-bromo-N-((6-methylpyridazin-3-yl)methyl)cinnolin-4-amine (intermediate 1) (60 mg, 0.182 mmol), potassium carbonate (75 mg, 0.545 mmol), 4-fluorophenylboronic acid (28 mg, 0.200 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (13 mg, 0.0182 mmol), 1,4-dioxane (2 mL) and water (0.5 mL) were placed in a microwave vial. Nitrogen was bubbled through the mixture was 10 minutes. The reaction mixture was heated at 110° C. for 20 minutes in a microwave reactor. Water (2 mL) was added and the mixture was extracted with EtOAc (2×15 mL). The organics were dried over MgSO4 and the solvent was removed in vacuo. The residue was purified by purified by flash chromatography on silica gel eluting with 0 to 20% MeOH in DCM to give the desired product as a yellow solid (1 mg, 1.5%).
1H NMR (400 MHz, CDCl3): δ 8.77 (s, 1 H), 8.41 (d, J=8.8 Hz, 1 H), 8.07 (s, 1 H), 7.97 (d, J=8.8 Hz, 1 H), 7.70 (dd, J=5.2, 8.5 Hz, 2 H), 7.50 (d, J=8.6 Hz, 1 H), 7.43 (d, J=8.3 Hz, 1 H), 7.21 (dd, J=8.6, 8.6 Hz, 3 H), 4.87 (s, 2 H), 2.78 (s, 3 H). LCMS (Method 2): [MH+]=346.2 at 3.52 min.
6-Bromo-N-((1R)-1-(2-(trifluoromethyl)pyrimidin-5-yl)ethyl)cinnolin-4-amine (intermediate 2) (100 mg, 0.25 mmol), 4-fluorophenylboronic acid (176 mg, 1.26 mmol), tetrakis(triphenylphosphine)palladium(0) (44 mg, 0.038 mmol) and potassium carbonate (139 mg, 1.00 mmol) were dissolved in water (1 mL) and 1,4-dioxane (2 mL). The reaction mixture was heated to 100° C. for 1 hour. After return to RT, the reaction mixture was filtered through Celite®. DCM (20 mL) was added and the resulting solution was washed with brine (2×20 mL). The organic phase was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 0 to 20% MeOH in DCM to give the title compound as a brown solid (35 mg, 34%).
1H NMR (400 MHz, DMSO): δ 9.22 (s, 2 H), 8.71 (s, 1 H), 8.63 (s, 1 H), 8.23 (d, J=8.9 Hz, 1 H), 8.15 (dd, J=8.9, 2.0 Hz, 1 H), 7.99-7.95 (m, 2 H), 7.42 (t, J=8.8 Hz, 2 H), 5.36 (q, J=7.0 Hz, 1 H), 1.76 (d, J=7.0 Hz, 3 H). LCMS (Method 3): [MH+]=414 at 3.57 min. Chiral analysis (Method 4) at 3.65 min.
Nitrogen gas was bubbled for 10 minutes through a mixture of 6-bromo-N-((1R)-1-(2-(trifluoromethyl)pyrimidin-5-yl)ethyl)cinnolin-4-amine (intermediate 2) (145 mg, 0.365 mmol) and tetrakis(triphenylphosphine)palladium(0) (63 mg, 0.0548 mmol) in DMF (2 mL). 5-methyl-2-(tributylstannyl)thiazole (0.26 mL, 0.73 mmol) was added and the reaction mixture was heated to 85° C. for 12 hours. After return to RT, the reaction mixture was then filtered through Celite®. The solvent was removed in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 0 to 20% MeOH in DCM to give the title compound as a brown solid (38 mg, 25%).
1H NMR (400 MHz, DMSO): δ 9.25 (s, 2 H), 9.98 (d, J=1.5 Hz, 1 H), 8.69 (s, 1 H), 8.28 (dd, J=8.9, 1.7, 1 H), 8.21 (d, J=8.9, 1 H), 8.17 (d, J=7.5 Hz, 1 H), 7.76 (d, J=1.2 Hz, 1 H), 5.38-5.36 (m, 1 H), 2.58 (d, J=1.0 Hz, 3 H), 1.78 (d, J=7.0 Hz, 3 H). LCMS (Method 3): [MH+]=417 at 4.15 min. Chiral analysis (Method 5) at 3.34 min.
The following compounds were synthesised following the procedure used for the synthesis of 6-(5-methylthiazol-2-yl)-N-((1R)-1-(2-(trifluoromethyl)pyrimidin-5-yl)ethyl)cinnolin-4-amine
1H NMR
1H NMR (400 MHz, DMSO): δ 9.26 (s, 2 H), 9.10 (d, J = 1.8 Hz, 1 H), 8.68 (s, 1 H), 8.64 (m, 1 H), 8.55 (dd, J = 9.0, 1.8 Hz, 1 H), 8.23 (d, J = 9 Hz, 1 H), 8.18 (d, J = 8.1 Hz, 1 H), 8.05 (d, J = 7.5 Hz, 1 H), 7.87-7.84 (m, 1 H), 5.38 (quint, J = 7.0 Hz, 1 H), 2.41 (s, 3 H), 1.79 (d, J = 7.0, 3 H). LCMS (Method 3): [MH+] = 411 at 3.26 min.
Nitrogen gas was bubbled for 5 min through a mixture of 6-bromo-4-chlorocinnoline (120 mg, 0.493 mmol), tetrakis(triphenylphosphine)palladium(0) (85 mg, 0.073 mmol) and 5-methyl-2-(tributylstannyl)pyridine (0.34 mL, 0.986 mmol) in DMF (2 mL). The reaction mixture was heated at 85° C. overnight. Crude 4-chloro-6-(5-methylpyridin-2-yl)cinnoline was used for the next reaction assuming 100% conversion. After return to RT, the crude was split in two and (6-methylpyridazin-3-yl)methanamine hydrochloride salt (34 mg, 0.215 mmol) and DIPEA (0.14 mL, 0.782 mmol) were added to the reaction mixture, which was heated at 70° C. for 5 hours. The residue was dissolved in MeOH (3 mL) and loaded onto an SCX-2 cartridge. The cartridge was washed with MeOH and then the free base was eluted with 7 M ammonia in MeOH. The solvent was removed in vacuo. The crude material was purified by reverse phase preparative HPLC affording the title compound as an off-white solid (5.9 mg, 9%).
1H NMR (400 MHz, CDCl3): δ 8.76 (s, 1 H), 8.64 (s, 1 H), 8.61-8.58 (m, 1 H), 8.44-8.36 (m, 2 H), 7.84 (d, J=7.8 Hz, 1 H), 7.66 (d, J=8.3 Hz, 1 H), 7.52-7.46 (m, 1 H), 7.40 (d, J=8.3 Hz, 1 H), 4.91 (s, 2 H), 2.78 (s, 3 H), 2.43 (s, 3H), (NH not observed). LCMS (Method 2): [MH+]=343 at 3.11 min.
Nitrogen was bubbled for 10 minutes through a suspension of 4-chloro-6-(4-fluorophenyl)-8-methoxycinnoline (intermediate 6) (65 mg, 0.23 mmol), (R)-1-(6-methylpyridazin-3-yl)ethan-1-amine hydrochloride (71 mg, 0.34 mmol), tris(dibenzylideneacetone)dipalladium(0) (11 mg, 0.012 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (22 mg, 0.037 mmol) and cesium carbonate (220 mg, 0.68 mmol) in 1,4-dioxane (2 mL). The mixture was then stirred at 90° C. for 16 hours. The resulting solution was cooled to RT and the solvent was removed in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 0-20% MeOH then by preparative HPLC to give the title compound as a yellow solid (24.5 mg, 28%).
1H NMR (400 MHz, DMSO): δ 8.52 (s, 1 H), 8.27 (d, J=1.6 Hz, 1 H), 8.04-7.99 (m, 2 H), 7.84 (s, 1 H), 7.68 (d, J=8.7 Hz, 1 H), 7.55 (d, J=8.7 Hz, 1 H), 7.47-7.40 (m, 3 H), 5.29-5.29 (m, 1 H), 4.10 (s, 3 H), 2.60 (s, 3 H), 1.75 (d, J=6.9 Hz, 3 H). LCMS (Method 2): [MH+]=390. at 4.01 min.
The following compounds reported in the table below were prepared according to the procedure described for the preparation of (R)-6-(4-fluorophenyl)-8-methoxy-N-(1-(6-methylpyridazin-3-yl)ethyl)cinnolin-4-amine:
1H NMR
1H NMR (400 MHz, DMSO): δ 9.23 (s, 2 H), 8.67 (s, 1 H), 8.21 (d, J = 1.4 Hz, 1 H), 8.02-7.98 (m, 2 H), 7.48-7.40 (m, 3 H), 5.35 (d, J = 4.1 Hz, 1 H), 4.11 (s, 3 H), 1.76 (d, J = 6.9 Hz, 3 H). LCMS (Method 2): [MH+] = 444 at 4.45 min.
Nitrogen was bubbled for 10 minutes through a suspension of 4-chloro-8-methoxy-6-(5-methylpyrimidin-2-yl)cinnoline (intermediate 7) (65 mg, 0.192 mmol), (R)-1-(6-methylpyridazin-3-yl)ethan-1-amine hydrochloride (60 mg, 0.29 mmol), tris(dibenzylideneacetone)dipalladium(0) (9 mg, 0.010 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (19 mg, 0.02 mmol) and cesium carbonate (188 mg, 0.58 mmol) in 1,4-dioxane (2 mL). The mixture was then stirred at 90° C. for 16 hours. The resulting solution was cooled to RT and the solvent was removed in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 0-30% MeOH in DCM, followed by preparative HPLC to give the title compound as an off-white solid (24.1 mg, 32%).
1H NMR (400 MHz, DMSO): δ 9.04 (d, J=1.3 Hz, 1 H), 8.89 (s, 2 H), 8.58 (s, 1 H), 8.22 (s, 1 H), 8.13 (d, J=1.3 Hz, 1 H), 7.73 (d, J=8.7 Hz, 1 H), 7.55 (d, J=8.7 Hz, 1 H), 5.29 (d, J=6.4 Hz, 1 H), 4.09 (s, 3 H), 2.61 (s, 3 H), 2.40 (s, 3 H), 1.77 (d, J=6.9 Hz, 3 H). LCMS (Method 2): [MH+]=388 at 3.37 min.
To a mixture of 4-chloro-6-(5-methylpyridin-2-yl)quinoline (intermediate 5) (50 mg, 0.20 mmol) and (R)-1-(2-(trifluoromethyl)pyrimidin-5-yl)ethan-1-amine dihydrochloride (57 mg, 0.22 mmol), in dioxane (1.5 mL) was added N,N-diisopropylamine (0.1 mL, 0.59 mmol) and the mixture was heated at reflux for 60 hours. After return to RT, the solvent was removed in vacuo. Dimethylsulfoxide (1.5 mL) and water (30 mL) were added to the residue. The mixture was extracted with EtOAc (2×30 mL). Saturated sodium bicarbonate aqueous solution (15 mL) was added to the aqueous phase and the mixture was extracted with EtOAc (30 mL). The organic extracts were combined and filtered through a hydrophobic frit. The solvent was removed in vacuo and purified by preparative HPLC to give the title compound as an off-white solid (29 mg, 32%).
1H NMR (400 MHz, DMSO): δ 9.22 (s, 2 H), 9.03 (d, J=1.6 Hz, 1 H), 8.60 (d, J=1.9 Hz, 1 H), 8.40 (dd, J=1.9, 8.8 Hz, 1 H), 8.36 (d, J=5.4 Hz, 1 H), 8.16 (s, 1 H), 7.89 (d, J=8.8 Hz, 1 H), 7.83-7.77 (m, 2 H), 6.46 (d, J=5.5 Hz, 1 H), 5.21-5.16 (m, 1 H), 2.40 (s, 3 H), 1.78 (d, J=6.9 Hz, 3 H). LCMS (Method 3): [MH+]=410 at 3.3 min.
The following compound reported in the table below was prepared according to the procedure described for the preparation of (R)-6-(5-methylpyridin-2-yl)-N-(1-(2-(trifluoromethyl)pyrimidin-5-yl)ethyl) quinolin-4-amine:
1H NMR
1H NMR (400 MHz, DMSO): δ 8.96 (d, J = 1.8 Hz, 1 H), 8.58 (d, J = 1.8 Hz, 1 H), 8.40 (dd, J = 1.8, 8.8 Hz, 1 H), 8.34 (d, J = 5.3 Hz, 1 H), 8.26 (dd, J = 6.0, 6.0 Hz, 1 H), 8.12 (d, J = 8.2 Hz, 1 H), 7.87 (d, J = 8.9 Hz, 1 H), 7.80 (dd, J = 1.9, 8.2 Hz, 1 H), 7.59 (d, J = 8.5 Hz, 1 H), 7.52 (d, J = 8.5 Hz, 1 H), 6.42 (d, J = 5.4 Hz, 1 H), 4.85 (d, J = 6.0 Hz, 2 H), 2.61 (s, 3 H), 2.39 (s, 3 H). LCMS (Method 3): [MH+] = 342 at 2.40 min.
To a mixture of 6-bromo-N-((6-methylpyridazin-3-yl)methyl)quinolin-4-amine (intermediate 3) (124 mg, 0.38 mmol), 4-fluorophenylboronic acid, pinacol ester (92 mg, 0.41 mmol), tetrakis(triphenylphosphine)palladium(0) (44 mg, 0.04 mmol) and potassium carbonate (78 mg, 0.57 mmol) was added 1,4-dioxane (4.0 mL) and water (0.5 mL). The mixture was heated at 95° C. for 60 hours. The reaction was cooled and filtered through Celite® plug. Celite® was washed with EtOAc (20 mL). The organic phases were combined, filtered through hydrophobic frit and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give the title compound as an off white solid (53 mg, 40%).
1H NMR (400 MHz, DMSO) d 8.60 (d, J=1.9 Hz, 1H), 8.34 (d, J=5.4 Hz, 1H), 8.27 (dd, J=5.9, 5.9 Hz, 1H), 8.17 (s, 1H), 7.99 (dd, J=2.0, 8.8 Hz, 1H), 7.96-7.91 (m, 2H), 7.88 (d, J=8.8 Hz, 1H), 7.59 (d, J=8.7 Hz, 1H), 7.52 (d, J=8.7 Hz, 1H), 7.39 (dd, J=8.9, 8.9 Hz, 2H), 6.44 (d, J=5.5 Hz, 1H), 4.85 (d, J=5.9 Hz, 2H), 2.61 (s, 3H). LCMS (Method 3): [MH+]=345 at 2.92 min.
To a solution of 4-chloro-6-(4-fluorophenyl)quinolone (intermediate 4) (50 mg, 0.20 mmol) in 1,4-dioxane (1.5 mL), was added (S)-1-(2-(trifluoromethyl)pyrimidin-5-yl)ethan-1-amine dihydrochloride (57 mg, 0.22 mmol) and N,N-diisopropylethylamine (0.1 mL, 0.59 mmol) in a microwave vial. The resulting mixture was heated at 150° C. for 0.5 hour followed by 160° C. for 0.5 hour in a microwave reactor. The reaction mixture was then heated to reflux for 16 hours. The solvent was removed in vacuo and the residue was purified by preparative HPLC to give the title compound as an off-white solid (7 mg, 8%).
1H NMR (400 MHz, DMSO): δ 9.20 (s, 2 H), 8.66 (d, J=1.8 Hz, 1 H), 8.35 (d, J=5.3 Hz, 1 H), 7.99-7.92 (m, 3 H), 7.88 (d, J=8.8 Hz, 1 H), 7.66 (d, J=7.2 Hz, 1 H), 7.40 (dd, J=8.9, 8.9 Hz, 2 H), 6.44 (d, J=5.5 Hz, 1 H), 5.20-5.14 (m, 1 H), 1.76 (d, J=6.9 Hz, 3 H). LCMS (Method 3): [MH+]=413 at 3.69 min.
Nitrogen was bubbled for 10 minutes through a suspension of 6-bromo-cinnolin-4-ol (500 mg, 2.22 mmol), 4-fluorophenyl boronic acid (466 mg, 3.33 mmol), pd(dppf)Cl2 (91 mg, 0.11 mmol) in 1,4-dioxane (10 mL). A solution of cesium carbonate (1448 mg, 4.44 mmol) in water (3 mL) was added and the mixture was stirred at 120° C. for 18 hours. The reaction mixture was cooled to RT, water (10 mL) was added and the resulting solid was collected by filtration, washed with 9:1 Et2O/MeOH (3×10 mL) and air dried to give the title compound as a brown solid (514 mg, 96%).
1H NMR (400 MHz, DMSO): δ 8.22 (d, J=2.0 Hz, 1 H), 7.91-7.89 (m, 2 H), 7.81-7.73 (m, 3 H), 7.32 (dd, J=8.8, 8.8 Hz, 2 H). OH not observed.
Phosphorus(V) oxychloride (7403 mg, 48.28 mmol) was added to a solution of 6-(4-fluorophenyl)-cinnolin-4-ol (534 mg, 2.22 mmol) in 1,2-dichloroethane (10.0 mL). The resulting mixture was heated to 90° C. for 18 hours. Then further Phosphorus(V) oxychloride (822 mg, 5.36 mmol) was added and the heating was maintained at 90° C. for 2 hours. The reaction mixture was cooled to RT and excess phosphorus(V) oxychloride was removed in vacuo, azeotroping with toluene (3×10 mL). The resulting residue was partitioned with a saturated aqueous solution of sodium bicarbonate (15 mL) and extracted with DCM (3×15 mL). The combined organic phases were passed through a hydrophobic frit and concentrated in vacuo. The resulting residue was purified by column chromatography on silica gel eluting with 0-80% EtOAc in cyclohexane to give the title compound as an off-white solid (300 mg, 52%).
1H NMR (400 MHz, CDCl3): δ 9.36 (s, 1 H), 8.62 (d, J=8.9 Hz, 1 H), 8.28 (d, J=1.8 Hz, 1 H), 8.13 (dd, J=1.9, 8.8 Hz, 1 H), 7.77-7.73 (m, 2 H), 7.29-7.23 (m, 2 H).
Nitrogen was bubbled for 10 minutes through a suspension of 4-chloro-6-(4-fluorophenyl)-cinnoline (129 mg, 0.50 mmol), (R)-1-(6-methylpyridazin-3-yl)ethan-1-amine hydrochloride (198 mg, 0.75 mmol), tris(dibenzylideneacetone)dipalladium(0) (24 mg, 0.026 mmol), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (48 mg, 0.083 mmol) and cesium carbonate (489 mg, 1.50 mmol) in 1,4-dioxane (4 mL). The mixture was then stirred at 90° C. for 18 hours. After return to room temperature, the reaction was filtered through a pad of celite which was rinsed with ethyl acetate. The solvent was removed in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 0-100% EtOAc in cyclohexane then with 3% MeOH in EtOAc. The obtained solid was further triturated in chloroform to give the title compound as an off-white solid (193 mg, 33%).
1H NMR (400 MHz, DMSO): δ 8.78 (d, J=1.6 Hz, 1 H), 8.51 (d, J=1.6 Hz, 1 H), 8.18-8.16 (m, 1 H), 8.14-8.12 (m, 1 H), 8.02-7.98 (m, 3 H), 7.71 (d, J=8.8 Hz, 1 H), 7.54 (d, J=8.8 Hz, 1 H), 7.46-7.41 (m, 2 H), 5.33-5.30 (m, 1 H), 2.58 (s, 3 H), 1.75 (d, J=6.8 Hz, 3 H). LCMS (Method 3): [MH+]=360 at 2.94 min.
Cells expressing P2X3 receptors were grown according to standard practice and maintained at 37° C. in a 5% humidified CO2 atmosphere. The cells were seeded into T175 flask 2 days prior to the day of the assay and dissociated from the flasks using TrypLE when grown to confluence of 80-90%. The dissociated cells were resuspended in serum free media at a cell density of 3×106 cells/ml and loaded onto the Sophion Qube automated patch-clamp system. The extracellular assay buffer contained 145 mM NaCl, 4 mM KCl, 2 mM CaCl2, 1 mM MgCl2, 10 mM HEPES, and 10 mM glucose at pH 7.4. The intracellular assay solution contained 140 mM CsF, 10 mM NaCl, 10 mM EGTA, 10 mM HEPES at pH 7.2. Agonist stock solutions were prepared in H2O and diluted in bath solution prior to use. All antagonists were prepared as 10 mM stock solutions in DMSO and diluted in bath solution prior to use. All experiments were performed under the whole-cell patch clamp configuration at room temperature with 384 individual cells being voltage clamped at −60 mV simultaneously on the Sophion Qube instrument. Two baseline responses were established with the application of α,β-MeATP (800 nM), with the subsequent agonist applications being washed out using extracellular assay buffer containing 0.5 U/ml apyrase. Following the second agonist application, antagonist was incubated in the absence of α,β-MeATP for 10 minutes. After antagonist preincubation, 800 nM α,β-MeATP and antagonist were co-administered to determine the inhibitory effect of the antagonist. One concentration of an antagonist was assessed against a single cell, with different concentrations of the antagonist applied to other cells on the 384 recording substrate. The control P2X3 current amplitude was taken from the peak current amplitude from the second agonist response prior to preincubation with antagonist. The peak P2X3 current amplitude in the presence of antagonist was used to calculate the inhibitory effect at each concentration of the antagonist according to the following equation:
Percentage inhibition of P2X3=(P2X3 control peak amplitude−P2X3 antagonist peak amplitude)/P2X3 control peak amplitude)*100
Concentration-response curves were constructed from ten different concentrations with each concentration of antagonist tested on at least two individual cells. The concentration of the antagonist to inhibit P2X3 current by 50% (IC50) was determined by fitting the data with the following equation:
Y=a+[(b−a)/(1+10{circumflex over ( )}((log c−x)d)]
Where ‘a’ is minimum response, ‘b’ is maximum response, ‘c’ is IC50 and ‘d’ is Hill slope.
The results for individual compounds are provided below in Table 2 and are expressed as range of activity.
Representative compound of the present invention have been also tested for P2X2/3 receptor.
The same assay protocol was used for the P2X2/3 assay as the P2X3 assay with two modifications: 1) 10 μM ATP was used as the agonist; and 2) the mean current amplitude was measured seven seconds after the application of agonist.
The results of Table 3 indicate that representative compounds of the present invention are selective P2X3 antagonist.
The activity of comparative Example A as has been tested in the in vitro assay for the determination of activity on P2X3 receptor as described above.
Differently from the compounds of formula (I) of the present invention, the comparative Example A do not show a proper inhibitory activity on P2X3, in fact the activity on receptor P2X3 expressed as pIC50 is <5.5.
The above results demonstrate that a proper position of the nitrogen atoms in the scaffold unexpectedly lead to a series of compounds that is active against the receptor P2X3.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20210195.2 | Nov 2020 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/083143 | 11/26/2021 | WO |
