Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
  • C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
  • C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
  • C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
  • C07H19/16—Purine radicals
• • A—HUMAN NECESSITIES
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  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
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  • A61P17/00—Drugs for dermatological disorders
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• • A—HUMAN NECESSITIES
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  • A61P19/00—Drugs for skeletal disorders
  • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
• • A—HUMAN NECESSITIES
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  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
• • 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
  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P3/00—Drugs for disorders of the metabolism
  • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
  • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/04—Antineoplastic agents specific for metastasis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
  • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/08—Antiallergic agents
• • A—HUMAN NECESSITIES
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  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/08—Vasodilators for multiple indications
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

• This invention relates to new chemical compounds, processes for their preparation, pharmaceutical formulations containing them and to their use in therapy.
• Inflammation is a primary response to tissue injury or microbial invasion and is characterised by leukocyte adhesion to the endothelium, diapedesis and activation within the tissue.
• Leukocyte activation can result in the generation of toxic oxygen species (such as superoxide anion), and the release of granule products (such as peroxidases and proteases).
• Circulating leukocytes include neutrophils, eosinophils, basophils, monocytes and lymphocytes.
• Different forms of inflammation involve different types of infiltrating leukocytes, the particular profile being regulated by the profile of adhesion molecule, cytokine and chemotactic factor expression within the tissue.
• leukocytes The primary function of leukocytes is to defend the host from invading organisms such as bacteria and parasites. Once a tissue is injured or infected a series of events occurs which causes the local recruitment of leukocytes from the circulation into the affected tissue. Leukocyte recruitment is controlled to allow for the orderly destruction and phagocytosis of foreign or dead cells, followed by tissue repair and resolution of the inflammatory infiltrate. However, in chronic inflammatory states, recruitment is often inappropriate, resolution is not adequately controlled and the inflammatory reaction causes tissue destruction.
• Adenosine agonists may also down-regulate other classes of leucocytes (Elliot KRF, Leonard EJ, (1989), FEBS Letters 254, pp 94-98; Peachell PT, Lichtenstein LM, Schleimer RP, (1989), Biochem. Pharmacol. 38, pp 1717-1725).
• the selective A2A agonist, CGS-21680 has shown anti-inflammatory activity in rats in pulmonary inflammation induced by allergen challenge and is blocked by pre- treament with selective A2A receptor antagonist ZM241385 (Fozard, John R.; Ellis, Karen M.; ViIIeIa Dantas, Maria F.; Tigani, Bruno; Mazzoni, Lazzaro, European Journal of Pharmacology (2002), 438(3), 183-188).
• Adenosine itself, and compounds that raise circulating levels of adenosine also show anti-inflammatory effects in vivo (Green PG, Basbaum Al, Helms C, Levine JD, (1991 ), Proc. Natl. Acad Sci.
• a 2A adenosine 2 A receptor
• the compounds are therefore of potential therapeutic benefit in providing protection from leukocyte-induced tissue damage in diseases where leukocytes are implicated at the site of inflammation.
• the compounds of the invention may also represent a safer alternative to corticosteroids in the treatment of inflammatory diseases, whose uses may be limited by their side-effect profiles.
• the compounds of the invention may show an improved profile over known A 2A - selective agonists in that they may possess one or more of the following properties:
• V less pronounced cardiovascular effects, in particular reduced tachycardia.
• a 3 receptors are also found on leucocytes (e.g. eosinophils) and other inflammatory cells (e.g. mast cells) and activation of these receptors may have pro-inflammatory effects (Kohno Y, Xiao-duo J, Mawhorter SD, Koshiba M, Jacobson KA, (1996), Blood 88 pp 3569-3574; 1996; Van Schaick EA, Jacobson KA, Kim HO, Ijzerman AP, Danhof M, (1996), Eur. J. Pharmacol. 308 pp 311- 314).
• adenosine A 3 receptor Kohno Y, Xiao-duo J, Mawhorter SD, Koshiba M, Jacobson KA, (1996), Blood 88 pp 3569-3574.
• a 2B receptors are also found on mast cells and may thus be implicated in mast cell activation.
• a 1 receptors have a wide tissue distribution and can be found on inter alia heart, adipocytes, respiratory smooth muscle, neutrophils, kidney, hippocampus and cortex.
• a 1 receptor activation may thus cause decreased lipolysis, diuresis and CNS activation (Fozard JR, McCarthy C, (2002), Current Opinion in Investigational Drugs 3 pp 69-77).
• a compound that exhibits greater than approximately 90% binding to human serum albumin may be expected to have a reduced free fraction in whole blood.
• R 1 represents methyl or ethyl
• R 2 represents a group selected from the list consisting of: (i) ( ⁇ ) (iii)
• R 3 represents a group selected from the list consisting of:
• R 4 represents a group selected from the list consisting of:
• R 5 represents hydrogen, C 1-4 alkyl, C ⁇ alkylaryl, C ⁇ alkylheteroaryl or C 1-4 hydroxyalkyl;
• R 6 and R 7 independently represent hydrogen, methyl or phenyl
• C 1-4 alkyl as used herein is meant an alkyl function having between one to four carbon atoms in total, which may optionally be branched.
• Exemplary C 1-4 alkyl groups include methyl, ethyl, propyl (n-propyl and iso-propyl) and butyl (n-butyl, sec-butyl and tert-butyl).
• d ⁇ alkylaryl is meant a C ⁇ alkyl function as described above, which is substituted by an aryl group.
• aryl is meant a phenyl or naphthyl group which may optionally be substituted.
• An exemplary aryl group is phenyl.
• Exemplary C 1-4 alkylaryl groups include benzyl.
• C 1-4 alkylheteroaryl a C 1-4 alkyl function as described above, which is substituted by a heteroaryl group.
• heteroaryl is meant a 5 or 6 membered aromatic group containing heteroatoms e.g. 1-4 heteroatoms selected from nitrogen, oxygen and sulphur.
• exemplary heteroaryl groups include 5 membered rings (e.g. pyrrole, furan, thiophene) and 6 membered rings (e.g. pyridine, pyrimidine and pyrazine).
• C 1-4 hydroxyalkyl a C 1-4 alkyl function as described above which is substituted with one or more (eg 1 ) hydroxyl groups.
• Alkyl groups may optionally be substituted by one or more (e.g. one) fluorine atoms.
• exemplary fluorine substituted alkyl groups include fluoromethyl and trifluoromethyl.
• Aryl and heteroaryl groups may optionally be substituted, for example by one or more groups selected from amino, cyano, halo (e.g. fluorine or chlorine), nitro, thio and methoxy (optionally substituted by halo, e.g. trifluoromethoxy).
• halo e.g. fluorine or chlorine
• nitro e.g. thio and methoxy
• halo e.g. trifluoromethoxy
• R 1 may for example represent ethyl.
• R 2 may for example represent group (i), (ii), (iii) or (iv), e.g. group (iv). In one embodiment of the invention R 2 represents group (ii) or (iv). In another embodiment of the invention R 2 represents group (ii). In a further embodiment of the invention R 2 represents group (iv).
• R 3 represents group (a). In a second embodiment of the invention R 3 represents group (b).
• R 4 may for example represent group (i), (ii), (iii), (iv) or (v) e.g. group (i), (ii), (iii) or (iv) , e.g. group (iv). In one embodiment of the invention R 4 represents group (ii) or (iv). In another embodiment of the invention R 4 represents group (ii). In a further embodiment of the invention R 4 represents group (iv).
• R 5 may, for example, represent hydrogen.
• R 6 may, for example, represent phenyl.
• R 7 may, for example, represent hydrogen.
• R 2 and R 4 are the same. In a second embodiment of the invention R 2 and R 4 are not the same.
• the compound of formula (I) is:
• stereochemistry about the cyclohexyl ring in the conserved core and the substituent groups where R 2 represents (v) or R 4 represents (v) are defined in relative terms.
• the invention encompasses all stereoisomers of the compounds of formula (I) (e.g. enantiomers or diastereoisomers) whether as individual stereoisomers isolated such as to be substantially free of the other stereoisomer (i.e. pure) or as mixtures thereof.
• An individual stereoisomer isolated such as to be substantially free of the other stereoisomer (i.e. pure) will be isolated such that less than about 10%, for example less than about 1 % or less than about 0.1 % of the other stereoisomer is present.
• Salts of the compounds of the present invention are also encompassed within the scope of the invention. Because of their potential use in medicine, the salts of the compounds of formula (I) are preferably pharmaceutically acceptable salts. Suitable pharmaceutically acceptable salts can include acid addition salts.
• a pharmaceutically acceptable acid addition salt can be formed by reaction of a compound of formula (I) with a suitable inorganic or organic acid (such as hydrobromic, hydrochloric, formic, sulfuric, nitric, phosphoric, succinic, maleic, acetic, fumaric, citric, tartaric, benzoic, xinafoate, p- toluenesulfonic, methanesulfonic or naphthalenesulfonic acid), optionally in a suitable solvent such as an organic solvent, to give the salt which may be isolated for example by crystallisation and filtration.
• a suitable inorganic or organic acid such as hydrobromic, hydrochloric, formic, sulfuric, nitric,
• a pharmaceutically acceptable acid addition salt of a compound of formula (I) can be for example a hydrobromide, hydrochloride, formate, sulfate, nitrate, phosphate, succinate, maleate, acetate, fumarate, citrate, tartrate, benzoate, p-toluenesulfonate, methanesulfonate or naphthalenesulfonate salt.
• Other non- pharmaceutically acceptable salts e.g. oxalates or trifluoroacetates, may be used, for example in the isolation of compounds of the invention, and are included within the scope of this invention.
• the invention includes within its scope all possible stoichiometric and non-stoichiometric forms of the salts of the compounds of formula (I).
• solvates for example hydrates, and complexes of compounds and salts of the invention.
• R 4 is as defined above for compounds of formula (I).
• L suitably represents halogen, for example bromine or chlorine, in particular chlorine.
• the reaction will generally involve heating the reagents to an elevated temperature of 5O 0 C to 15O 0 C, such as 100 0 C to 13O 0 C, particularly about 12O 0 C to 13O 0 C, in the presence of an inert solvent such as DMSO and a base, such as an amine base (e.g. diisopropylethylamine).
• an inert solvent such as DMSO
• a base such as an amine base (e.g. diisopropylethylamine).
• the nitrogen to which it is attached may suitably be protected, for example as the tetrahydropyran-2-yl derivative.
• the nitrogen may then be deprotected. Suitable conditions for deprotection will depend upon the chosen protecting group, for example, where the protecting group is tetrahydropyran-2-yl suitable deprotection conditions include treatment with formic acid in methanol/water.
• R 5 is as defined above for compounds of formula (I) and L represents a leaving group.
• L suitably represents halogen, for example bromine or chlorine, in particular chlorine.
• the reaction will generally be performed in the presence of a base, such as an amine base (e.g. diisopropylethylamine), in a suitable solvent, such as an alcohol (e.g. isopropanol), at an elevated temperature (e.g. 5O 0 C to 7O 0 C).
• a base such as an amine base (e.g. diisopropylethylamine)
• a suitable solvent such as an alcohol (e.g. isopropanol)
• R 5 represents hydrogen
• the nitrogen to which it is attached i.e. the 9 position of the purine ring
• the nitrogen may suitably be protected, for example as the tetrahydropyran-2-yl derivative.
• the nitrogen may then be deprotected. Suitable conditions for deprotection will depend upon the chosen protecting group, for example, where the protecting group is tetrahydropyran-2-yl suitable deprotection conditions include treatment with formic acid in methanol/water.
• R 1 is as defined above for compounds of formula (I) and L represents a leaving group
• R 2 is as defined above for compounds of formula (I).
• L suitably represents halogen, for example bromine or chlorine, in particular chlorine.
• the reaction will generally involve heating the reagents to an elevated temperature of 5O 0 C to 15O 0 C, such as 100 0 C to 13O 0 C, particularly about 12O 0 C to 13O 0 C, in the presence of an inert solvent such as DMSO and a base, such as an amine base (e.g. diisopropylethylamine).
• an inert solvent such as DMSO
• a base such as an amine base (e.g. diisopropylethylamine).
• the primary amine group attached to the cyclohexyl ring in compounds of formula (Vl) is protected, for example as the dimethylethyloxycarbonyl (Boc) derivative.
• the amine protecting group may be removed, for example, where the protecting group represents dimethylethyloxycarbonyl this may be removed, for example, by treatment with trifluoroacetic acid in dichloromethane.
• R 2 represents a group of formula (v)
• the amine function of R 2 may suitably be protected by a different protecting group employed to that employed to protect the amine function of the compound of formula (Vl).
• the former may be protected using CbZ (which may subsequently be removed by catalytic hydrogenation) and the latter may be protected using Boc.
• Compounds of formula (Vl), or protected derivatives thereof may be prepared by the reaction of a compound of formula (VIII), or a protected derivative thereof:
• R 1 is as defined above for compounds of formula (I) and L represents a leaving group
• L suitably represents halogen, for example bromine or chlorine, in particular chlorine.
• the reaction will typically be performed in the presence of a base, such as an amine base (e.g. diisopropylethylamine), in a suitable solvent, such as an alcohol (e.g. isopropanol), at an elevated temperature (e.g. 5O 0 C to 7O 0 C).
• a base such as an amine base (e.g. diisopropylethylamine)
• a suitable solvent such as an alcohol (e.g. isopropanol)
• R 1 is as defined above for compounds of formula (I);
• a compound such as 2,6-dichloropurine in a suitable solvent (e.g. acetonitrile), under inert conditions and in the presence of a Lewis acid (such as trimethylsilyl triflate) and optionally with a catalyst (e.g. 1 ,8-diazabicyclo[5.4.0]undec-7-ene).
• a suitable solvent e.g. acetonitrile
• a Lewis acid such as trimethylsilyl triflate
• a catalyst e.g. 1 ,8-diazabicyclo[5.4.0]undec-7-ene.
• compounds of formula (I), or a protected derivative thereof may be prepared by reacting a compound of formula (IV) as described above, or a protected derivative thereof:
• L suitably represents halogen, for example bromine or chlorine, in particular chlorine.
• Said reaction will generally involve heating the reagents to a temperature of 5O 0 C to 15O 0 C, in the presence of an inert solvent such as ethanol, propan-2-ol or DMSO and a base, such as an amine base (e.g. diisopropylethylamine).
• an inert solvent such as ethanol, propan-2-ol or DMSO
• a base such as an amine base (e.g. diisopropylethylamine).
• R 5 represents H
• the nitrogen to which it is attached i.e. the 9-position of the purine ring
• THP tetrahydropyran-2- yl
• the THP group may subsequently be removed following the reaction with a compound of formula (IV).
• Suitable deprotection conditions include treatment with formic acid in methanol/water.
• R 4 is as defined above for compounds of formula (I);
• R 4 is as defined above for compounds of formula (I).
• the reaction is typically performed in diglyme at a temperature of approximately 170 0 C.
• R 4 is as defined above for compounds of formula (I);
• Compounds of formula (XIB) wherein R 5 does not represent H may be prepared by the alkylation of compounds of formula (XIB) wherein R 5 represents H.
• Alkylation may be performed using an alkylating agent such as R 5 -l, in the presence of a base (e.g. potassium carbonate) and a suitable solvent (e.g. DMF), for example see Langli, G et al. (1996) Tetrahedron, 52 pp5625-5638.
• alkylation may be performed using an alcohol R 5 -OH in the presence of diethylazodicarboxylate and triphenylphosphine in THF (see Maruyama, T et al. (2000) Nucleosides, Nucleotides and Nucleic Acids, 19 pp1193-1203).
• compounds of formula (I) wherein R 2 and R 4 are the same, or a protected derivative thereof may be prepared by reacting a compound of formula (XIVA) or (XIVB), or a protected derivative thereof:
• R 1 and R 5 are as defined above for compounds of formula (I) and L represents a leaving group
• R 2 is as defined above for compounds of formula (I).
• L suitably represents halogen, for example bromine or chlorine, in particular chlorine.
• Said reaction will generally involve heating the reagents to a temperature of 50 0 C to 15O 0 C, such as 100 0 C to 13O 0 C, particularly about 12O 0 C to 13O 0 C, in the presence of an inert solvent such as DMSO and a base, such as an amine base (e.g. diisopropylethylamine).
• an inert solvent such as DMSO
• a base such as an amine base (e.g. diisopropylethylamine).
• the nitrogen to which it is attached may suitably be protected, for example as the tetrahydropyran-2-yl derivative.
• the nitrogen may then be deprotected. Suitable conditions for deprotection will depend upon the chosen protecting group, for example, where the protecting group is tetrahydropyran-2-yl suitable deprotection conditions include treatment with formic acid in methanol/water.
• R 1 is as defined above for compounds of formula (I) and L represents a leaving group
• R 5 is as defined above for compounds of formula (I) and L represents a leaving group.
• L suitably represents halogen, for example bromine or chlorine, especially chlorine.
• the compound of formula (VA) may, for example, be 2,4-dichloropyrimidine.
• the compound of formula (VB) may, for example, be 2,6-dichloro-9-(tetrahydropyran-2-yl)purine.
• the reaction will generally be performed in the presence of a base, such as an amine base (e.g. diisopropylethylamine), in a suitable solvent, such as an alcohol (e.g. isopropanol), at an elevated temperature (e.g. 5O 0 C to 7O 0 C).
• the purine nitrogen may be then deprotected.
• Suitable conditions for deprotection will depend upon the chosen protecting group, for example, where the protecting group is tetrahydropyran-2-yl suitable deprotection conditions include the use of formic acid in methanol/water.
• Compounds of formula (MA), (HB), (IV), (Vl), (VIII), (X), (XIVA) and (XIVB) may be used in a form in which the hydroxyl groups are protected with suitable protecting groups, e.g. with acetonide or acetyl groups, in particular acetyl groups.
• Suitable hydroxyl protecting groups include alkyl (e.g. methyl), acetal (e.g. acetonide) and acyl (e.g. acetyl or benzoyl) which may be removed by hydrolysis, and arylalkyl (e.g. benzyl) which may be removed by catalytic hydrogenolysis.
• Suitable amine protecting groups include sulphonyl (e.g. tosyl), acyl (e.g. benzyloxycarbonyl or t-butoxycarbonyl) and arylalkyl (e.g. benzyl) which may be removed by hydrolysis or hydrogenolysis as appropriate.
• compounds of formula (I) to inhibit leukocyte function may be demonstrated, for example, by their ability to inhibit superoxide (O 2 " ) generation from neutrophils stimulated with chemoattractants such as N-formylmethionyl-leucyl- phenylalanine (fMLP). Accordingly, compounds of formula (I) are of potential therapeutic benefit in providing protection from leukocyte-induced tissue damage in diseases where leukocytes are implicated at the site of inflammation.
• Examples of disease states in which the compounds of the invention have potentially beneficial anti-inflammatory effects include diseases of the respiratory tract such as adult respiratory distress syndrome (ARDS), bronchitis (including chronic bronchitis), cystic fibrosis, asthma (including allergen-induced asthmatic reactions), emphysema, rhinitis and septic shock.
• Other relevant disease states include diseases of the gastrointestinal tract such as intestinal inflammatory diseases including inflammatory bowel disease (e.g. Crohn's disease or ulcerative colitis), Helicobacter pylori induced gastritis and intestinal inflammatory diseases secondary to radiation exposure or allergen exposure, and nonsteroidal anti-inflammatory drug-induced gastropathy.
• compounds of the invention may be used to treat skin diseases such as psoriasis, allergic dermatitis and hypersensitivity reactions and diseases of the central nervous system which have an inflammatory component e.g. Alzheimer's disease and multiple sclerosis.
• cardiac conditions such as peripheral vascular disease, post- ischaemic reperfusion injury and idiopathic hypereosinophilic syndrome.
• Compounds of the invention which inhibit lymphocyte function may be useful as immunosuppressive agents and so have use in the treatment of auto-immune diseases such as rheumatoid arthritis and diabetes.
• Compounds of the invention may also be useful in inhibiting metastasis.
• the treatment and/or prophylaxis is of asthma or COPD including chronic bronchitis and emphysemia in a mammal (e.g. human).
• compounds of formula (I) are useful in human or veterinary medicine, in particular as anti-inflammatory agents.
• a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof for use in human or veterinary medicine, particularly in the treatment of patients with an inflammatory condition and/or allergic condition who are susceptible to leukocyte-induced tissue damage.
• a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof for the manufacture of a medicament for the treatment of patients with an inflammatory condition and/or allergic condition who are susceptible to leukocyte-induced tissue damage.
• a method for the treatment of a human or animal subject with an inflammatory condition and/or allergic condition who is susceptible to leukocyte-induced tissue damage comprises administering to said human or animal subject an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof.
• the compounds of the present invention are usually administered as a pharmaceutical composition.
• the present invention therefore provides in a further aspect a pharmaceutical composition
• a pharmaceutical composition comprising a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof optionally with one or more pharmaceutically acceptable carriers and/or excipients.
• the pharmaceutical composition may be for use in the treatment and/or prophylaxis of any of the conditions described herein.
• Compounds of formula (I) and salts and solvates thereof and/or the pharmaceutical composition containing them may be administered, for example, by parenteral (eg. intravenous, subcutaneous, or intramuscular), inhaled, nasal, transdermal or rectal administration, or as topical treatments (eg. ointments or gels).
• parenteral eg. intravenous, subcutaneous, or intramuscular
• inhaled nasal, transdermal or rectal administration
• topical treatments eg. ointments or gels.
• Routes of administration of particular interest include inhaled and intra-nasal.
• Inhaled administration involves topical administration to the lung, eg. by aerosol or dry powder composition.
• the compound of formula (I) and salts and solvates thereof and/or the pharmaceutical composition may be administered by a controlled or sustained release formulation as described in WO 00/50011.
• a parenteral composition may comprise a solution or suspension of the compound or pharmaceutically acceptable salt in a sterile aqueous carrier or parenterally acceptable oil.
• the solution may be lyophilised; the lyophilised parenteral pharmaceutical composition may be reconstituted with a suitable solvent just prior to administration.
• compositions for nasal or inhaled administration may conveniently be formulated as aerosols, solutions, suspensions, drops, gels or dry powders, with aqueous or nonaqueous vehicles optionally with the addition of agents such as thickening agents, buffer salts or acid or alkali to adjust the pH, isotonicity adjusting agents, antioxidants and/or preservatives.
• agents such as thickening agents, buffer salts or acid or alkali to adjust the pH, isotonicity adjusting agents, antioxidants and/or preservatives.
• Capsules and cartridges of for example gelatine, or blisters of for example laminated aluminium foil, for use in an inhaler or insufflator may be formulated containing a powder mix of a compound of the invention and a suitable powder base such as lactose or starch.
• the compound or salt or solvate of formula (I) is typically in a particle-size-reduced form, and particularly the size-reduced form is obtained or obtainable by micronisation.
• the particle size of the size-reduced (e.g. micronised) compound or salt can be defined by a D50 value of about 0.5 to about 10 microns (for example as measured using laser diffraction).
• Aerosol formulations can comprise a solution or fine suspension of the active substance in a pharmaceutically acceptable aqueous or nonaqueous solvent. Aerosol formulations can be presented in single or multidose quantities in sterile form in a sealed container, which can take the form of a cartridge or refill for use with an atomising device or inhaler. Alternatively the sealed container may be a unitary dispensing device such as a single dose nasal inhaler or an aerosol dispenser fitted with a metering valve (metered dose inhaler) which is intended for disposal once the contents of the container have been exhausted.
• a metering valve metered dose inhaler
• the dosage form comprises an aerosol dispenser
• it preferably contains a suitable propellant under pressure such as compressed air, carbon dioxide or an organic propellant such as a chlorofluorocarbon (CFC) or hydrofluorocarbon (HFC).
• CFC chlorofluorocarbon
• HFC hydrofluorocarbon
• Suitable CFC propellants include dichlorodifluoromethane, trichlorofluoromethane and dichlorotetrafluoroethane.
• Suitable HFC propellants include 1 ,1 ,1 ,2,3,3,3- heptafluoropropane and 1 ,1 ,1 ,2-tetrafluoroethane.
• the aerosol dosage forms can also take the form of a pump-atomiser.
• a pharmaceutical composition for inhaled administration can be incorporated into a plurality of sealed dose containers ⁇ e.g. containing the dry powder composition) mounted longitudinally in a strip or ribbon inside a suitable inhalation device.
• the container is rupturable or peel-openable on demand and the dose of e.g. the dry powder composition can be administered by inhalation via the device such as the DISKUSTM device, marketed by GlaxoSmithKline.
• the DISKUS TM inhalation device is for example described in GB 2242134 A 1 and in such a device at least one container for the pharmaceutical composition in powder form (the container or containers preferably being a plurality of sealed dose containers mounted longitudinally in a strip or ribbon) is defined between two members peelably secured to one another; the device comprises: a means of defining an opening station for the said container or containers; a means for peeling the members apart at the opening station to open the container; and an outlet, communicating with the opened container, through which a user can inhale the pharmaceutical composition in powder form from the opened container.
• the formulation may be presented if desired together with one or more other therapeutic agents in an inhalation device wherein the individual therapeutic agents are administrable simultaneously but are stored separately (or wholly or partly stored separately for triple combinations), e.g. in separate pharmaceutical compositions, for example as described in WO 03/061743.
• the proportion of the active compound of formula (I) or salt or solvate thereof in the topical compositions according to the invention depends on the precise type of formulation to be prepared but may generally be within the range of from 0.001 to 20% by weight, for example 0.001 to 10% by weight. Generally, however for most types of preparations the proportion used may be within the range of from 0.005 to 1% such as 0.01 to 0.5%. However, in powders for inhalation or insufflation the proportion used may be within the range of from 0.1 to 5%.
• Aerosol formulations are preferably arranged so that each metered dose or "puff" of aerosol contains 10 ⁇ g-2000 ⁇ g, for example 20 ⁇ g-2000 ⁇ g, preferably about 20 ⁇ g-500 ⁇ g of a compound of formula (I).
• Administration may be once daily or several times daily, for example 2, 3, 4 or 8 times, giving for example 1 , 2 or 3 doses each time.
• the overall daily dose with an aerosol will be within the range 20 ⁇ g-10mg, for example 100 ⁇ g-10mg, preferably 200 ⁇ g-2000 ⁇ g.
• the overall daily dose and the metered dose delivered by capsules and cartridges in an inhaler or insufflator will generally be double those with aerosol formulations.
• the compound (or salts and solvates thereof) and pharmaceutical formulations according to the invention may be used in combination with or include one or more other therapeutic agents, for example selected from anti-inflammatory agents, anticholinergic agents (particularly an M 1 , M 2 , M 1 ZM 2 or M 3 receptor antagonist), ⁇ 2 -adrenoreceptor agonists, antiinfective agents (e.g. antibiotics, antivirals), or antihistamines.
• anti-inflammatory agents particularly an M 1 , M 2 , M 1 ZM 2 or M 3 receptor antagonist
• antiinfective agents e.g. antibiotics, antivirals
• antihistamines e.g. antibiotics, antivirals
• the invention thus provides, in a further aspect, a combination comprising a compound of formula (I) or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with one or more other therapeutically active agents, for example selected from an anti-inflammatory agent (for example a corticosteroid or an NSAID), an anticholinergic agent, a ⁇ 2 -adrenoreceptor agonist, an antiinfective agent (e.g. an antibiotic or an antiviral), or an antihistamine.
• an anti-inflammatory agent for example a corticosteroid or an NSAID
• an anticholinergic agent for example a corticosteroid or an NSAID
• an anticholinergic agent for example a corticosteroid or an NSAID
• an anticholinergic agent for example a corticosteroid or an NSAID
• an anticholinergic agent for example a corticosteroid or an NSAID
• a ⁇ 2 -adrenoreceptor agonist
• Particular combinations of the invention include a compound of formula (I) or a physiologically acceptable salt or solvate thereof together with a steroid, a ⁇ 2 -adrenoreceptor agonist, an anticholinergic, and/or a PDE-4 inhibitor.
• Preferred combinations are those comprising one or two other therapeutic agents.
• the other therapeutic ingredient(s) may be used in the form of salts, (e.g. as alkali metal or amine salts or as acid addition salts), or prodrugs, or as esters (e.g. lower alkyl esters), or as solvates (e.g. hydrates) to optimise the activity and/or stability and/or physical characteristics (e.g. solubility) of the therapeutic ingredient.
• the therapeutic ingredients may be used in optically pure form.
• the invention thus provides, in a further aspect, a combination comprising a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof with one or more other therapeutically active agents, for example, a ⁇ 2 -adrenoreceptor agonist, an anti-histamine, an anti-allergic agent, an anti-inflammatory agent (including a steroid or a PDE-4 inhibitor), an anticholinergic agent or an antiinfective agent (eg. antibiotics or antivirals).
• a ⁇ 2 -adrenoreceptor agonist for example, a ⁇ 2 -adrenoreceptor agonist, an anti-histamine, an anti-allergic agent, an anti-inflammatory agent (including a steroid or a PDE-4 inhibitor), an anticholinergic agent or an antiinfective agent (eg. antibiotics or antivirals).
• a ⁇ 2 -adrenoreceptor agonist for example, a ⁇ 2 -adrenorecept
• ⁇ 2 -adrenoreceptor agonists examples include salmeterol (e.g. as the racemate or a single enantiomer, such as the R-enantiomer), salbutamol (e.g. as the racemate or a single enantiomer such as the R-enantiomer), formoterol (e.g.
• salmeterol which may be a racemate or a single enantiomer, such as the R-enantiomer
• salbutamol formoterol
• salmefamol formoterol
• fenoterol formoterol
• terbutaline and salts thereof, for example the xinafoate salt of salmeterol, the sulphate salt or free base of salbutamol or the fumarate salt of formoterol.
• Long-acting ⁇ 2 - adrenoreceptor agonists for example those which provide bronchodilation for 12 hours or longer, may be preferred. Examples include salmeterol and formoterol.
• ⁇ 2 -adrenoreceptor agonists include those described in WO02/66422A,
• ⁇ 2 -adrenoreceptor agonists are:
• the ⁇ 2 -adrenoreceptor agonist may be in the form of a salt formed with a pharmaceutically acceptable acid selected from sulphuric, hydrochloric, fumaric, hydroxynaphthoic (for example 1- or 3-hydroxy-2-naphthoic), cinnamic, substituted cinnamic, triphenylacetic, sulphamic, sulphanilic, naphthaleneacrylic, benzoic, 4-methoxybenzoic, 2- or 4-hydroxybenzoic, 4-chlorobenzoic and 4-phenylbenzoic acid.
• a pharmaceutically acceptable acid selected from sulphuric, hydrochloric, fumaric, hydroxynaphthoic (for example 1- or 3-hydroxy-2-naphthoic), cinnamic, substituted cinnamic, triphenylacetic, sulphamic, sulphanilic, naphthaleneacrylic, benzoic, 4-
• Anti-inflammatory agents that may be incorporated in a combination include corticosteroids particularly inhaled corticosteroids and their pro-drugs which have anti- inflammatory activity.
• corticosteroids include methyl prednisolone, prednisolone, dexamethasone, fluticasone propionate, 6 ⁇ ,9 ⁇ -difluoro-17 ⁇ -[(2- furanylcarbonyl)oxy]-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo-androsta-1 ,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester, 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo-17 ⁇ - propionyloxy-androsta-1 ,4-diene-17 ⁇ -carbothioic acid S-(2-oxo-tetrahydro-furan-3S-yl) ester, 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-17 ⁇ -(1-methylc
• Preferred corticosteroids include fluticasone propionate, 6 ⁇ ,9 ⁇ -difluoro-11 ⁇ -hydroxy-16 ⁇ -methyl-17 ⁇ -[(4-methyl- 1 ,3-thiazole-5-carbonyl)oxy]-3-oxo-androsta-1 ,4-diene-17 ⁇ -carbothioic acid S- fluoromethyl ester and 6 ⁇ ,9 ⁇ -difluoro-17 ⁇ -[(2-furanylcarbonyl)oxy]-11 ⁇ -hydroxy-16 ⁇ - methyl-3-oxo-androsta-1 ,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester, more preferably 6 ⁇ ,9 ⁇ -difluoro-17 ⁇ -[(2-furanylcarbonyl)oxy]-11 ⁇ -hydroxy-16 ⁇ -methyl-3-oxo- androsta-1 ,4-diene-17 ⁇ -carbothioic acid S-fluoromethyl ester.
• Non-steroidal compounds that may have glucocorticoid activity include those covered in the following patent applications WO03/082827, WO01/10143, WO98/54159, WO04/005229, WO04/009016, WO04/009017, WO04/018429, WO03/104195, WO03/082787, WO03/082280, WO03/059899, WO03/101932, WO02/02565, WO01/16128, WO00/66590, WO03/086294, WO04/026248, WO03/061651 , WO03/08277.
• Anti-inflammatory agents include non-steroidal anti-inflammatory drugs (NSAID's).
• Possible NSAID's that may be used in a combination include sodium cromoglycate, nedocromil sodium, phosphodiesterase (PDE) inhibitors (for example, theophylline, PDE4 inhibitors or mixed PDE3/PDE4 inhibitors), leukotriene antagonists, inhibitors of leukotriene synthesis (for example, montelukast), iNOS inhibitors, tryptase and elastase inhibitors, beta-2 integrin antagonists and adenosine receptor agonists or antagonists (for example, adenosine 2a agonists), cytokine antagonists (for example, chemokine antagonists, such as a CCR3 antagonist) or inhibitors of cytokine synthesis, or 5- lipoxygenase inhibitors.
• PDE phosphodiesterase
• An iNOS inducible nitric oxide synthase inhibitor
• Other iNOS inhibitors include those disclosed in WO93/13055, WO98/30537, WO02/50021 , WO95/34534 and WO99/62875.
• Suitable CCR3 inhibitors include those disclosed in WO02/26722.
• Phosphodiesterase 4 (PDE4) inhibitors that may be used in a combination include any compound that is known to inhibit the PDE4 enzyme or which is discovered to act as a PDE4 inhibitor, and which are only PDE4 inhibitors, not compounds which inhibit other members of the PDE family, such as PDE3 and PDE5, as well as PDE4.
• Compounds include c/s-4-cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohexan-1 - carboxylic acid, 2-carbomethoxy-4-cyano-4-(3-cyclopropylmethoxy-4- difluoromethoxyphenyl)cyclohexan-1 -one and c/s-[4-cyano-4-(3-cyclopropylmethoxy-4- difluoromethoxyphenyl)cyclohexan-1-ol].
• Another compound of interest is c/s-4-cyano-4- [3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexane-1 -carboxylic acid (also known as cilomilast) and its salts, esters, pro-drugs or physical forms, which is described in U.S. patent 5,552,438 issued 03 September, 1996; this patent and the compounds it discloses are incorporated herein in full by reference.
• PDE4 inhibitors include AWD-12-281 from Elbion (Hofgen, N. et_al. 15th EFMC lnt Symp Med Chem (Sept 6-10, Edinburgh) 1998, Abst P.98; CAS reference No.
• Anticholinergic agents are those compounds that act as antagonists at the muscarinic receptors, in particular those compounds which are antagonists of the M 1 or M 3 receptors, dual antagonists of the MiZM 3 or M 2 /M 3 , receptors or pan-antagonists of the M 1 ZM 2 ZM 3 receptors.
• Exemplary compounds for administration via inhalation include ipratropium (for example, as the bromide, CAS 22254-24-6, sold under the name Atrovent), oxitropium (for example, as the bromide, CAS 30286-75-0) and tiotropium (for example, as the bromide, CAS 136310-93-5, sold under the name Spiriva). Also of interest are revatropate (for example, as the hydrobromide, CAS 262586-79-8) and LAS-34273 which is disclosed in WO01Z04118.
• Exemplary compounds for oral administration include pirenzepine (for example, CAS 28797-61-7), darifenacin (for example, CAS 133099-04-4, or CAS 133099-07-7 for the hydrobromide sold under the name Enablex), oxybutynin (for example, CAS 5633-20-5, sold under the name Ditropan), terodiline (for example, CAS 15793-40-5), tolterodine (for example, CAS 124937-51-5, or CAS 124937-52-6 for the tartrate, sold under the name Detrol), otilonium (for example, as the bromide, CAS 26095- 59-0, sold under the name Spasmomen), trospium chloride (for example, CAS 10405-02- 4) and solifenacin (for example, CAS 242478-37-1 , or CAS 242478-38-2, or the succinate also known as YM-905 and sold under the name Vesicare
• anticholinergic agents include compounds of formula (XXI), which are disclosed in US patent application 60Z487981 :
• R 31 and R 32 are, independently, selected from the group consisting of straight or branched chain lower alkyl groups having preferably from 1 to 6 carbon atoms, cycloalkyl groups having from 5 to 6 carbon atoms, cycloalkyl-alkyl having 6 to 10 carbon atoms, 2-thienyl, 2-pyridyl, phenyl, phenyl substituted with an alkyl group having not in excess of 4 carbon atoms and phenyl substituted with an alkoxy group having not in excess of 4 carbon atoms;
• X " represents an anion associated with the positive charge of the N atom.
• X " may be but is not limited to chloride, bromide, iodide, sulfate, benzene sulfonate, and toluene sulfonate, including, for example:
• anticholinergic agents include compounds of formula (XXII) or (XXIII), which are disclosed in US patent application 60/511009:
• R 41 represents an anion associated with the positive charge of the N atom.
• R1 ' may be but is not limited to chloride, bromide, iodide, sulfate, benzene sulfonate and toluene sulfonate;
• R 42 and R 43 are independently selected from the group consisting of straight or branched chain lower alkyl groups (having preferably from 1 to 6 carbon atoms), cycloalkyl groups (having from 5 to 6 carbon atoms), cycloalkyl-alkyl (having 6 to 10 carbon atoms), heterocycloalkyl (having 5 to 6 carbon atoms) and N or O as the heteroatom, heterocycloalkyl-alkyl (having 6 to10 carbon atoms) and N or O as the heteroatom, aryl, optionally substituted aryl, heteroaryl, and optionally substituted heteroaryl;
• R 44 is sleeted from the group consisting of (d-C 6 )alkyl, (C 3 -C 12 )cycloalkyl, (C 3 - C 7 )heterocycloalkyl, (C r C 6 )alkyl(C 3 -Ci 2 )cycloalkyl, (d-CeJalkyKCs-CzJheterocycloalkyl, aryl, heteroaryl, (d-QOalkyl-aryl, (d-QOalkyl-heteroaryl, -OR 45 , -CH 2 OR 45 , -CH 2 OH, -CN, -CF 3 , -CH 2 O(CO)R 46 , -CO 2 R 47 , -CH 2 NH 2 , -CH 2 N(R 47 )SO 2 R 45 , -SO 2 N(R 47 )(R 48 ), -
• R 45 is selected from the group consisting of (C ⁇ C 6 )alkyl, (C r C6)alkyl(C3-C 12 )cycloalkyl, (CrCeJalkyKCa-CrJheterocycloalkyl, (C r C 6 )alkyl-aryl, (C r C 6 )alkyl-heteroaryl;
• R 46 is selected from the group consisting of (C r C 6 )alkyl, (C 3 -Ci 2 )cycloalkyl, (C 3 -
• C 7 heterocycloalkyl, (Ci-C 6 )alkyl(C 3 -C 12 )cycloalkyl, (CrC 6 )alkyl(C 3 -C 7 )heterocycloalkyl, aryl, heteroaryl, (CrCeJalkyl-aryl, (C r C 6 )alkyl-heteroaryl;
• R 47 and R 48 are, independently, selected from the group consisting of H, (C ⁇ CeJalkyl, (C 3 - Ci 2 )cycloalkyl, (C 3 -C 7 )heterocycloalkyl, (C r C 6 )alkyl(C 3 -Ci 2 )cycloalkyl, (d-C 6 )alkyl(C 3 -
• C 7 heterocycloalkyl, (Ci-C 6 )alkyl-aryl, and (CrC ⁇ Jalkyl-heteroaryl, including, for example:
• Antihistamines include any one or more of the numerous antagonists known which inhibit H 1 -receptors, and are safe for human use.
• First generation antagonists include derivatives of ethanolamines, ethylenediamines, and alkylamines, such as diphenylhydramine, pyrilamine, clemastine, chlorpheniramine.
• Second generation antagonists which are non-sedating, include loratidine, desloratidine, terfenadine, astemizole, acrivastine, azelastine, levocetirizine fexofenadine, cetirizine and efletirizine.
• the invention thus provides, in a further aspect, a combination comprising a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof together with a PDE4 inhibitor.
• the invention thus provides, in a further aspect, a combination comprising a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof together with a ⁇ 2 - adrenoreceptor agonist.
• the invention thus provides, in a further aspect, a combination comprising a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof together with an anticholinergic.
• the invention thus provides, in a further aspect, a combination comprising a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof together with an antihistamine.
• the combinations referred to above may conveniently be presented for use in the form of a pharmaceutical formulation and thus pharmaceutical formulations comprising a combination as defined above together with a pharmaceutically acceptable diluent or carrier represent a further aspect of the invention.
• the individual compounds of such combinations may be administered either sequentially or simultaneously in separate or combined pharmaceutical formulations.
• the individual compounds will be administered simultaneously in a combined pharmaceutical formulation.
• Appropriate doses of known therapeutic agents will be readily appreciated by those skilled in the art.
• compositions comprising a combination as defined above optionally together with one or more pharmaceutically acceptable carriers and/or excipients represent a further aspect of the invention.
• the individual compounds of such combinations may be administered either sequentially or simultaneously in separate or in combined pharmaceutical compositions.
• compositions comprising a combination as defined above together with a pharmaceutically acceptable diluent or carrier represent a further aspect of the invention.
• the compounds of the invention may be more efficacious, show greater selectivity, have fewer side effects, have a longer duration of action, show less systemic activity when administered by inhalation or have other more desirable properties than similar known compounds.
• the compounds of the invention may be highly potent at the A 2A receptor, show greater selectivity for the adenosine 2 A receptor subtype over other adenosine receptor subtypes (especially the A 1 and A 3 receptor subtypes), be capable of being highly bound to human serum albumin (greater than about 90%) and/or may exhibit less pronounced cardiac effects than hitherto known compounds.
• 'flash silica 1 refers to silica gel for chromatography, 0.035 to 0.070mm (220 to 440mesh) (e.g. Fluka silica gel 60), where column elution was accelerated by an applied pressure of nitrogen at up to 10 p.s.i.
• thin layer chromatography TLC
• Biotage refers to prepacked silica gel cartridges containing KP-SiI run on a flash 12i chromatography module.
• Solid Phase Extraction (SPE) columns are pre-packed cartridges used in parallel purifications, normally under vacuum. These are commercially available from Varian. SCX cartridges are Ion Exchange SPE columns where the stationary phase is polymeric benzene sulfonic acid. These are used to isolate amines.
• the Companion XL is an automated single user flash chromatography system which utilises disposable cartridges (120gm to 1500gm). It provides binary on-line solvent mixing to enable gradient methods to be run. Samples are logged in using the multi functional open access software which manages flow rates, gradient profile and collection conditions.
• the system is equipped with a variable wavelength uv detector and two Foxy 200 fraction collectors enabling automated peak cutting, collection and tracking.
• Flash silica gel refers to Merck ART No. 9385; silica gel refers to Merck ART No. 7734
• the amine in Examples 1 and 6 is commercially available from, for example, Sigma.
• the amine in Examples 2 and 7 was used as the free base.
• the free base may be derived from the dihydrochloride salt which is commercially available from, for example. Sigma. Preparation of the free base is described in, for example, Intermediate 5 below.
• the amine in Examples 3 and 8 may be prepared by, for example, the method describe in J. Het. Chem., (1981 ), 18(4), 831 to 832.
• the amine in Examples 4 and 9 is commercially available from, for example, Apin.
• the amine in Examples 5 and 10 is commercially available from, for example, Aldrich.
• the reaction mixture was allowed to cool to room temperature and evaporated down in vacuo.
• the residue was partitioned between ethyl acetate and water.
• the organic phase was separated and the aqueous extracted twice with ethyl acetate.
• the organic phases were combined, dried (MgSO 4 ), and evaporated down in vacuo.
• the residue was purified on a silica SPE cartridge (100g), eluting with 0 to 100% ethyl acetate - dichloromethane gradient over 60 min. The appropriate fractions were combined and evaporated down in vacuo to give the title compound, 1.53g.
• Example 2 the amine was used as the free base which may be derived from the commercially available dihydrochloride salt.
• Example 7 the amine was used as the free base which may be derived from the commercially available dihydrochloride salt.
• the mixture was allowed to cool to room temperature and washed with diethyl ether (2 x 100ml). The mixture was poured onto water (200ml), stirred for 25min and the precipitated solid was filtered, washed with water, and dried under vacuum. The solid was dissolved in methanol (30ml) and 2N HCI added (30ml). The mixture was heated a 6O 0 C for 1-2h. The solvent was removed in vacuo and the residue partitioned between dichloromethane and 2N aq. sodium bicarbonate solution. The product went into the aqueous layer. The aqueous layer was evaporated down in vacuo and the residue trituated with methanol.
• Biological activity of compounds may be assessed using the following assays or similar assays:
• the agonist potency and selectivity of compounds against human adenosine receptors is determined using Chinese hamster ovary (CHO) cells transfected with the gene for the relevant receptor. These cells are used to measure the production of cAMP in response to compound stimulation.
• the DiscoveRx assay is an enzyme complementation assay based on CHO cells that involves two fragments of ⁇ -galactosidase, enzyme acceptor (EA) and enzyme donor (ED). Following the production of cAMP EA binds to ED, active enzyme is produced and a luminescent product is formed following the addition of substrate.
• EA enzyme acceptor
• ED enzyme donor
• test compounds In all of the in vitro assays the activity of test compounds is expressed as a ratio to that of the non-selective adenosine receptor agonist, N-ethyl carboxamide adenosine (NECA).
• NECA N-ethyl carboxamide adenosine
• compounds demonstrating activity at the A2 A receptor of at least two times that of NECA may be preferred. On testing, the compounds of Examples 1 - 9 were found to meet this criteria.
• compounds demonstrating greater than 100-fold selectivity for the A2 A receptor over the A1 receptor may be preferred. On testing, the compounds of Examples 1 - 9 were found to meet this criteria.
• compounds demonstrating greater than 100-fold selectivity for the A2 A receptor over the A2 B receptor may be preferred. On testing, the compounds of Examples 4 and 6 - 9 were found to meet this criteria.
• DiscoveRx the agonist potency and selectivity of compounds against human adenosine receptors is determined using Chinese hamster ovary (CHO) cells transfected with the gene for the relevant receptor. These cells are used to measure the production of cAMP in response to compound stimulation.
• a cAMP tracer is formed by the interaction between Biotin-cAMP and Streptavidin labelled with Europium-W8044 Chelate. This tracer then competes with cellular cAMP for binding to cAMP specific antibodies labelled with the dye Alexa Fluor 647.
• Gs-coupled receptors such as the Adenosine A2a and A2b receptors
• agonist stimulation results in an increase in cAMP levels and hence a decrease in fluorescence at 665nm.
• Antagonist addition will have the reverse effect.
• -coupled receptors such as the Adenosine A1 receptor
• agonist addition inhibits forskolin induced cAMP production and hence leads to an increase in fluorescence at 665nm.
• Antagonism blocks the effect of the agonist and hence increases cellular cAMP and decreases the fluorescent signal.
• compounds demonstrating activity at the A2 A receptor of at least two times that of NECA may be preferred. On testing, the compounds of Examples 2, 4 and 7 were found to meet this criteria.
• compounds demonstrating greater than 100-fold selectivity for the A2 A receptor over the A1 receptor may be preferred.
• the compounds of Examples 2, 4 and 7 were found to meet this criteria.
• compounds demonstrating greater than 100-fold selectivity for the A2 A receptor over the A2 B receptor may be preferred. On testing, the compounds of Examples 2, 4 and 7 were found to meet this criteria.
• HSA Human Serum Albumin
• the mobile phase A was 50 mM pH 7.4 ammonium acetate solution, while mobile phase B was 2-Propanol (HPLC grade, Runcorn, UK).
• the mobile phase flow rate was 1.8 ml/min.
• the column temperature was kept at 30 0 C.
• the gradient profile and run time were the same with each column, the linear gradient from 0 to 30% 2- propanol was applied from 0 to 3 minutes. From 3 to 5 minutes, the mobile phase composition was constant 30% 2-propanol and 70% 50-mM ammonium acetate. From 5 min to 5.2 min the mobile phase composition was change to 100% ammonium acetate buffer only and remained the same until the end of the run. Each separation was stopped after 6 minutes.
• the column temperature was kept at 30 0 C.
• Chromatograms were recorded at 230 and 254 nm by a diode array UV absorption detector at room temperature.
• compounds demonstrating HSA binding greater than 90% may be preferred.
• the compounds of Examples 1 - 10 were found to meet this criteria on testing.
• Rats are lightly anaesthetized (isofluorane in oxygen) and vehicle or test substance administered intratracheally using a cannula placed trans-orally (200 ⁇ l). Following intratracheal administration, rats are returned to their cages and allowed free access to both food and water. Thirty min later, rats are placed in a perspex box and exposed to aerosolized lipopolysaccharide (LPS) (0.15 mg/ml, serotype 0127:B8) for 15 min (Devilbiss nebuliser) at a flow rate of 15 ml/min. Animals are killed 4 h later with pentobarbital (250 mg/kg i.p.).
• LPS lipopolysaccharide
• the lungs are lavaged using 3 aliquots (5 ml) of phosphate-buffered saline (Sigma catalogue no. P3813, pH 7.4) containing heparin (10 units/ml); recovered cells are pooled (pooled volume of recovered fluid will be recorded) and centrifuged (1300 rpm for 7 min). The supernatant is removed by aspiration and the cell pellet resuspended in 1 ml phosphate-buffered saline. Total cells are counted (Sysmex Microcell Counter F-500, TOA Medical Electronics Ltd., Japan).
• Smears are made by diluting recovered fluid (to approximately 10 6 cells/ml) and spinning an aliquot (100 ⁇ l) in a centrifuge (Cytospin, Shandon, UK). Smears are air dried, fixed using a solution of methanol for 10 s and stained with buffered eosin (10 s) and methylene blue/Azur 1 (5 s) (Speedy-Diff, ClinTech Ltd, Essex, UK) in order to differentiate eosinophils, neutrophils, macrophages and lymphocytes. A total of 300 cells per smear are counted by light microscopy under oil immersion (x1000).
• compounds demonstrating inhibition of neutrophilia of may be preferred. On testing at a concentration of 100 ug/kg, the compounds of Examples 1 , 2, 3, 4, 6 and 7 were found to meet this criteria. The compounds of Examples 5, 8, 9 and 10 were not tested.
• Example 2 was retested at 30ug/kg using a method similar to that described above. Of these 3 compounds only Example 4 gave > 50% inhibition.
• the adenosine A 3 agonist potency of compounds are determined using Chinese Hamster ovary cells stably expressing the human adenosine A 3 receptor and the cAMP response element SPAP (secreted placental alkaline phosphatase). Increasing the level of cAMP in theses cell causes an increase in the transcription of the SPAP reporter gene, which can be quantified by addition of a colour substrate to measure a coloured product.
• the adenosine A 3 receptor is Gi linked so levels cAMP have to be enhanced by forskolin in these cells. Activation of the adenosine A 3 receptor is determined by the reduction of forskolin enhanced cAMP, which is measured as a decrease in the coloured product.
• the Adenosine A 3 activity of the test compounds is expressed as a ratio to that of the non- selective adenosine receptor agonist, N-ethyl carboxamide adenosine (NECA).
• Examples 2, 8, 9, and 10 were functionally inactive over the concentration range of the assay.
• Examples 1 , 3, 6 and 7 were greater than 100-fold selective over A 2A -
• Examples 4 and 5 were greater than 10-fold selective over A 2A -

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• 2005
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