澳大利亚专利AU2004255855A1 Specific glucocorticosteroid compound having anti- inflammatory activity

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公开号:AU2004255855A1
申请号:U2004255855
申请日:2004-07-09
公开日:2005-01-20
发明作者:Keith Biggadike；Deborah Needham
申请人:Glaxo Group Ltd；
IPC主号:C07J3-00

专利说明:
WO 2005/005452 PCTIEP2004/007820 SPECIFIC GLUCOCORTICOSTEROID COMPOUND HAVING ANTI-INFLAMMATORY ACTIVITY The present invention relates to a compound which is a glucocorticoid receptor agonist of the androstane series. The present invention also relates to 5 pharmaceutical formulations containing the compound and to therapeutic uses thereof, particularly for the treatment of inflammatory and allergic conditions. Glucocorticosteroids which have anti-inflammatory properties are known and are widely used for the treatment of inflammatory disorders or diseases such as asthma 10 and rhinitis. However, we have identified a novel glucocorticosteroid. Thus, according to one aspect of the invention, there is provided a compound of formula (1) liN 0 0 HO H FH 0() 15 F or a physiologically acceptable solvate thereof. 20 Examples of solvates include hydrates. References hereinafter to the compound according to the invention includes both compound of formula (1) and solvates thereof. 25 It will be appreciated that the invention includes within its scope all stereoisomers of the compound of formula (1) and mixtures thereof. Preferably, the absolute stereochemistry will be as shown in the representation of compound of formula (1). 30 The compound of formula (1) is named: 1 WO 2005/005452 PCT/EP2004/007820 2 6a,9a-Difluoro-1 1p -hydroxy-16a-methyl-3-oxo-1 7a-(2, 2
,
3
,
3 tetramethycyclopropylcarbonyl)oxy-androsta-1,4-diene-17p-carboxylic acid cyanomethyl ester. 5 The compound of formula (1) has potentially beneficial anti-inflammatory or anti allergic effects, particularly upon topical administration, demonstrated by, for example, its ability to bind to the glucocorticoid receptor and to illicit a response via that receptor. Hence, the compound of formula (1) is potentially useful in the treatment of inflammatory and/or allergic disorders. 10 Examples of disease states in which the compound of the invention may have utility include skin diseases such as eczema, psoriasis, allergic dermatitis neurodermatitis, pruritis and hypersensitivity reactions; inflammatory conditions of the nose, throat or lungs such as asthma (including allergen-induced asthmatic reactions), rhinitis 15 (including hayfever), nasal polyps, chronic obstructive pulmonary disease, interstitial lung disease, and fibrosis; inflammatory bowel conditions such as ulcerative colitis and Crohn's disease; and auto-immune diseases such as rheumatoid arthritis. The compound of the invention may also have use in the treatment of conjunctiva 20 and conjunctivitis. It will be appreciated by those skilled in the art that reference herein to treatment extends to prophylaxis as well as the treatment of established conditions. 25 As mentioned above, the compound of formula (1) may be useful in human or veterinary medicine, in particular as an anti-inflammatory and anti-allergic agent. There is thus provided as a further aspect of the invention a compound of formula (1) or a physiologically acceptable solvate thereof for use in human or veterinary 30 medicine, particularly in the treatment of patients with inflammatory and/or allergic conditions. According to another aspect of the invention, there is provided the use of a compound of formula (1) or a physiologically acceptable solvate thereof for the 35 manufacture of a medicament for the treatment of patients with inflammatory and/or allergic conditions.
WO 2005/005452 PCTIEP2004/007820 3 In a further or alternative aspect, there is provided a method for the treatment of a human or animal subject with an inflammatory and/or allergic condition, which method comprises administering to said human or animal subject an effective 5 amount of a compound of formula (I) or physiologically acceptable solvate thereof. The compound according to the invention may be formulated for administration in any convenient way, and the invention therefore also includes within its scope pharmaceutical compositions comprising a compound of formula (1) or 10 physiologically acceptable solvate thereof together, if desirable, in admixture with one or more physiologically acceptable diluents or carriers. Further, there is provided a process for the preparation of such pharmaceutical compositions which comprises mixing the ingredients. 15 The compound according to the invention may, for example, be formulated for oral, buccal, sublingual, parenteral, local or rectal administration, especially local administration. 20 Local administration as used herein, includes administration by insufflation and inhalation. Examples of various types of preparation for local administration include ointments, lotions, creams, gels, foams, preparations for delivery by transdermal patches, powders, sprays, aerosols, capsules or cartridges for use in an inhaler or insufflator or drops (e.g. eye or nose drops), solutions/suspensions for nebulisation, 25 suppositories, pessaries, retention enemas and chewable or suckable tablets or pellets (e.g. for the treatment of aphthous ulcers) or liposome or microencapsulation preparations. Ointments, creams and gels, may, for example, be formulated with an aqueous or 30 oily base with the addition of suitable thickening and/or gelling agent and/or solvents. Such bases may thus, for example, include water and/or an oil such as liquid paraffin or a vegetable oil such as arachis oil or castor oil, or a solvent such as polyethylene glycol. Thickening agents and gelling agents which may be used according to the nature of the base include soft paraffin, aluminium stearate, cetostearyl alcohol, 35 polyethylene glycols, woolfat, beeswax, carboxypolymethylene and cellulose derivatives, and/or glyceryl monostearate and/or non-ionic emulsifying agents.
WO 2005/005452 PCTIEP2004/007820 4 Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilising agents, dispersing agents, suspending agents or thickening agents. 5 Powders for external application may be formed with the aid of any suitable powder base, for example, talc, lactose or starch. Drops may be formulated with an aqueous or non-aqueous base also comprising one or more dispersing agents, solubilising agents, suspending agents or preservatives. 10 Spray compositions may for example be formulated as aqueous solutions or suspensions or as aerosols delivered from pressurised packs, such as a metered dose inhaler, with the use of a suitable liquefied propellant. Aerosol compositions suitable for inhalation can be either a suspension or a solution and generally contain 15 a compound of formula (1) and a suitable propellant such as a fluorocarbon or hydrogen-containing chlorofluorocarbon or mixtures thereof, particularly hydrofluoroalkanes, especially 1,1,1,2-tetrafluoroethane, 1,1,1,2,3,3,3-heptafluoro-n propane or a mixture thereof. The aerosol composition may optionally contain additional formulation excipients well known in the art such as surfactants e.g. oleic 20 acid or lecithin and cosolvents e.g. ethanol. Advantageously, the formulations of the invention may be buffered by the addition of suitable buffering agents. 25 Capsules and cartridges for use in an inhaler or insufflator, of for example gelatine, may be formulated containing a powder mix for inhalation of a compound of the invention and a suitable powder base such as lactose or starch. Each capsule or cartridge may generally contain between 20pg-10mg of the compound of formula (1). Alternatively, the compound of the invention may be presented without excipients 30 such as lactose. The proportion of the active compound of formula (1) in the local compositions according to the invention depends on the precise type of formulation to be prepared but will generally be within the range of from 0.001 to 10% by weight. Generally, 35 however for most types of preparations advantageously the proportion used will be within the range of from 0.005 to 1% and preferably 0.01 to 0.5%. However, in WO 2005/005452 PCTIEP2004/007820 5 powders for inhalation or insufflation the proportion used will be within the range of from 0.1 to 5%. Aerosol formulations are preferably arranged so that each metered dose or "puff" of 5 aerosol contains 20ptg-2000ltg, preferably about 20pLg-5 00 Ig 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 100 g-10mg preferably, 200lig-2000 g. The overall daily dose and the metered dose delivered by capsules and cartridges in an 10 inhaler or insufflator will generally be double those with aerosol formulations. Topical preparations may be administered by one or more applications per day to the affected area; over skin areas occlusive dressings may advantageously be used. Continuous or prolonged delivery may be achieved by an adhesive reservoir system. 15 For internal administration the compounds according to the invention may, for example, be formulated in conventional manner for oral, parenteral or rectal administration. Formulations for oral administration include syrups, elixirs, powders, granules, tablets and capsules which typically contain conventional excipients such 20 as binding agents, fillers, lubricants, disintegrants, wetting agents, suspending agents, emulsifying agents, preservatives, buffer salts, flavouring, colouring and/or sweetening agents as appropriate. Dosage unit forms are, however, preferred as described below. 25 Preferred forms of preparation for internal administration are dosage unit forms i.e. tablets and capsules. Such dosage unit forms contain from 0.1mg to 20mg preferably from 2.5 to 10mg of the compounds of the invention. The compound according to the invention may in general may be given by internal 30 administration in cases where systemic adreno-cortical therapy is indicated. In general terms preparations, for internal administration may contain from 0.05 to 10% of the active ingredient dependent upon the type of preparation involved. The daily dose may vary from 0.1mg to 60mg, e.g. 5-30mg, dependent on the condition 35 being treated, and the duration of treatment desired.
WO 2005/005452 PCTIEP2004/007820 6 Slow release or enteric coated formulations may be advantageous, particularly for the treatment of inflammatory bowel disorders. The compound and pharmaceutical formulations according to the invention may be 5 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
3 receptor antagonist), P 2 -adrenoreceptor agonists, antiinfective agents (e.g. antibiotics, antivirals), or antihistamines. The invention thus provides, in a further aspect, a combination comprising a compound of formula (1) or a 10 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 another corticosteroid or an NSAID), an anticholinergic agent, a P 2 -adrenoreceptor agonist, an antiinfective agent (e.g. an antibiotic or an antiviral), or an antihistamine. Preferred are combinations 15 comprising a compound of formula (1) or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof together with a p 2 -adrenoreceptor agonist, and/or an anticholinergic, and/or a PDE-4 inhibitor. Preferred combinations are those comprising one or two other therapeutic agents. 20 It will be clear to a person skilled in the art that, where appropriate, 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 andlor stability and/or physical characteristics (e.g. solubility) of the therapeutic ingredient. It will be clear 25 also that where appropriate, the therapeutic ingredients may be used in optically pure form. A combination comprising of compound of the invention together with a p 2 -adrenoreceptor agonist is particularly preferred. 30 Examples of P 2 adrenoreceptor agonists include salmeterol (e.g. as racemate or a single enantiomer such as the R-enantiomer), salbutamol, formoterol, salmefamol, fenoterol or terbutaline and salts thereof, for example the xinafoate salt of salmeterol, the sulphate salt or free base of salbutamol or the fumarate salt of 35 formoterol. Long-acting p 2 -adrenoreceptor agonists are preferred, especially those having a therapeutic effect over a 24 hour period such as salmeterol or formoterol.
WO 2005/005452 PCTIEP2004/007820 7 Preferred long acting P 2 adrenoreceptor agonists include those described in WO 02/066422, WO 02/070490, WO 02/076933, WO 03/024439, WO 03/072539, WO 03/091204, WO 04/016578, WO 04/022547, WO 04/037807, 5 WO 04/037773, WO 04/037768, WO 04/039762, WO 04/039766, WO 01/42193 and WO 03/042160. Especially preferred long-acting P 2 adrenoreceptor agonists include compounds of formula (XX): 10 HOCH2 R Rp HO / CHCH 2
NHCR
24
R
25 (CH)-O-(CHXX) OH
R
23 or a salt or solvate thereof, wherein: m is an integer of from 2 to 8; n is an integer of from 3 to 11, 15 with the proviso that m + n is 5 to 19, R2 is -XS0 2
NR
26
R
27 wherein X is -(CH 2 )p- or C2- alkenylene;
R
2 6 and R 27 are independently selected from hydrogen, C 16 alkyl, C 3 7 cycloalkyl, C(O)NR "R , phenyl, and phenyl (C 1
.
4 alkyl)-, or R and R , together with the nitrogen to which they are bonded, form a 5-, 6-, or 20 7- membered nitrogen containing ring, and R 2 6 and R 27 are each optionally substituted by one or two groups selected from halo, C 1 .salkyl, C 16 haloalkyl,
C
1 salkoxy, hydroxy-substituted Cl-.alkoxy, -CO2R2, -S0 2 NR 2
R
2 9 , -CO N R 2 R 29 ,
-NR
28 C(O)R2 9 , or a 5-, 6- or 7-membered heterocylic ring;
R
28 and R 2 9 are independently selected from hydrogen, Cj 1 alkyl, 25 C 3 _rcycloalkyl, phenyl, and phenyl (Cl4alkyl)-; and p is an integer of from 0 to 6, preferably from 0 to 4;
R
22 and R 23 are independently selected from hydrogen, C 1
.
6 alkyl, C 16 alkoxy, halo, phenyl, and C 1 .shaloalkyl; and
R
24 and R 25 are independently selected from hydrogen and C 14 alkyl with the proviso 30 that the total number of carbon atoms in R 24 and R 25 is not more than 4. Especially preferred long-acting P 2 -adrenoreceptor agonists are: 3-(4-{[6-({(2R)-2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethyl}amino) WO 2005/005452 PCTIEP2004/007820 8 hexyl]oxy}butyl)benzenesulfonamide; 3-(3-{[7-({(2R)-2-hydroxy-2-[4-hydroxy-3-hydroxymethyl)phenyl]ethyl} amino)heptylloxy}propyl)benzenesulfonamide; 4-1R)-2-[(6-{2-[(2,6-dichorobenzyl)oxy]ethoxyhexyl)amino]-1 -hydroxyethyl}-2 5 (hydroxymethyl)phenol; 4-{(1 R)-2-[(6-4-[3-(cyclopentylsulfonyl)phenyl]butoxy hexyl)amino]-1-hydroxyethyl} 2-(hydroxymethyl)phenol; N-[2-hydroxyl-5-[(1 R)-1 -hydroxy-2-[[2-4-[[(2R)-2-hydroxy-2 phenylethyl]amino]phenyl]ethy]amino]ethyl]phenyl]foramide, and 10 N-2{2-[4-(3-phenyl-4-methoxyphenyl)aminophenyl]ethyl}-2-hydroxy-2-(8-hydroxy 2(1 H)-quinolinon-5-yl)ethylamine. Suitable anti-inflammatory agents include corticosteroids. Suitable corticosteroids which may be used in combination with the compounds of the invention are those 15 oral and inhaled corticosteroids and their pro-drugs which have anti-inflammatory activity. Examples include methyl prednisolone, prednisolone, dexamethasone, fluticasone propionate, 6a,9a-difluoro-1 1 p-hydroxy-1 6a-methyl-1 7a-[(4-methyl-1,3 thiazole-5-carbonyl)oxy]-3-oxo-androsta-1,4-diene-1 7p-carbothioic acid S fluoromethyl ester, 6a,9ax-difluoro-1 7a-[(2-furanylcarbonyl)oxy]-1 I p-hydroxy-1 6a 20 methyl-3-oxo-androsta-1,4-diene-1 7p-carbothioic acid S-fluoromethyl ester, 6C,9a difluoro-1 Ip-hydroxy-1 6a-methyl-3-oxo-1 7a-propionyloxy- androsta-1,4-diene-1 7p carbothioic acid S-(2-oxo-tetrahydro-furan-3S-yl) ester, beclomethasone esters (eg. the 17-propionate ester or the 17,21 -dipropionate ester), budesonide, flunisolide, mometasone esters (eg. the furoate ester), triamcinolone acetonide, rofleponide, 25 ciclesonide (16a,17-[[(R)-cyclohexymethylenebis(oxy)]-IIp,21-dihydroxy-pregna 1,4-diene-3,20-dione), butixocort propionate, RPR-i 06541, and ST-I 26. Preferred corticosteroids include fluticasone propionate, 6a,9a-difluoro-11 p-hydroxy-1 6a methyl-17a-[(4-methyl-1,3-thiazole-5-carbonyl)oxy]-3-oxo-androsta-1,4-diene-17p carbothioic acid S-fluoromethyl ester and 6c,9a-difluoro-17a-[(2 30 furanylcarbonyl)oxy]-1p-hydroxy-16ax-methyl-3-oxo-androsta-1,4-diene-I7p carbothioic acid S-fluoromethyl ester, more preferably 6a,9a-difluoro-17a-[(2 furanylcarbonyl)oxy]-11p-hydroxy-16-methyl-3-oxo-androsta-1,4-diene-17p carbothioic acid S-fluoromethyl ester. 35 Non-steroidal compounds having glucocorticoid agonism that may posess selectivity for transrepression over transactivation and that may be useful in combination WO 2005/005452 PCTIEP2004/007820 9 therapy include those covered in the following patents: W003/082827, W001/10143, WO98/54159, WO04/005229, WO04/009016, W004/009017, W004/018429, WO03/104195, WO031082787, WO03/082280, WO03/059899, WO03/101932, W002/02565, WOO1/16128, WOOO/66590, W003/086294, W004/026248, 5 W003/061651, WO03/08277. Suitable anti-inflammatory agents include non-steroidal anti-inflammatory drugs (NSAID's). 10 Suitable NSAID's include sodium cromoglycate, nedocromil sodium, phosphodiesterase (PDE) inhibitors (e.g. theophylline, PDE4 inhibitors or mixed PDE3/PDE4 inhibitors), leukotriene antagonists, inhibitors of leukotriene synthesis (eg. montelukast), iNOS inhibitors, tryptase and elastase inhibitors, beta-2 integrin antagonists and adenosine receptor agonists or antagonists (e.g. adenosine 2a 15 agonists), cytokine antagonists (e.g. chemokine antagonists, such as a CCR3 antagonist) or inhibitors of cytokine synthesis, or 5-lipoxygenase inhibitors. Suitable other p 2 -adrenoreceptor agonists include salmeterol (e.g. as the xinafoate), salbutamol (e.g. as the sulphate or the free base), formoterol (e.g. as the fumarate), fenoterol or terbutaline and salts thereof. An iNOS (inducible nitric oxide synthase 20 inhibitor) is preferably for oral administration. Suitable iNOS inhibitors include those disclosed in W093/13055, WO98/30537, W002/50021, W095/34534 and W099/62875. Suitable CCR3 inhibitors include those disclosed in WO02/26722. Of particular interest is use of the compound of formula (1) in combination with a 25 phosphodiesterase 4 (PDE4) inhibitor, especially in the case of a formulation adapted for inhalation. The PDE4-specific inhibitor useful in this aspect of the invention may be 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 30 PDE5, as well as PDE4. Compounds of interest include cis-4-cyano-4-(3-cyclopentyloxy-4 methoxyphenyl)cyclohexan-1 -carboxylic acid, 2-carbomethoxy-4-cyano-4-(3 cyclopropymethoxy-4-difluoromethoxyphenyl)cyclohexan-1-one and cis-[4-cyano-4 35 (3-cyclopropylmethoxy-4-difluoromethoxyphenyl)cyclohexan-1-oIl. Also, cis-4-cyano 4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexane-I -carboxylic acid (also known as WO 2005/005452 PCTIEP2004/007820 10 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. 5 AWD-12-281 from Elbion (Hofgen, N. et al. 15th EFMC Int Symp Med Chem (Sept 6 10, Edinburgh) 1998, Abst P.98; CAS reference No. 247584020-9); a 9 benzyladenine derivative nominated NCS-613 (INSERM); D-4418 from Chiroscience and Schering-Plough; a benzodiazepine PDE4 inhibitor identified as Cl-1 018 (PD 168787) and attributed to Pfizer; a benzodioxole derivative disclosed by Kyowa 10 Hakko in W099/16766; K-34 from Kyowa Hakko; V-11294A from Napp (Landells, L.J. et al. Eur Resp J [Annu Cong Eur Resp Soc (Sept 19-23, Geneva) 1998] 1998, 12 (Suppl. 28): Abst P2393); roflumilast (CAS reference No 162401-32-3) and a pthalazinone (W099/47505, the disclosure of which is hereby incorporated by reference) from Byk-Gulden; Pumafentrine, (-)-p-[(4aR*,10bS*)-9-ethoxy 15 1,2,3,4,4a, I0b-hexahydro-8-methoxy-2-methylbenzo[c][1,6]naphthyridin-6-yl]-N,N diisopropylbenzamide which is a mixed PDE3/PDE4 inhibitor which has been prepared and published on by Byk-Gulden, now Altana; arofylline under development by Almirall-Prodesfarma; VM554/UM565 from Vernalis; or T-440 (Tanabe Seiyaku; Fuji, K. et al. J Pharmacol Exp Ther,1998, 284(1): 162), and T2585. 20 Further compounds of interest are disclosed in the published international patent application W004/024728 (Glaxo Group Ltd), PCT/EP2003/014867 (Glaxo Group Ltd) and PCT/EP2004/005494 (Glaxo Group Ltd). 25 Suitable 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 M 1 /M3 or M 2
/M
3 , receptors or pan antagonists of the M 1
/M
2
/M
3 receptors. Exemplary compounds for administration via inhalation include ipratropiurn (e.g. as the bromide, CAS 22254-24-6, sold under the 30 name Atrovent), oxitropium (e.g. as the bromide, CAS 30286-75-0) and tiotropium (e.g. as the bromide, CAS 136310-93-5, sold under the name Spiriva). Also of interest are revatropate (e.g. as the hydrobromide, CAS 262586-79-8) and LAS 34273 which is disclosed in WO01/04118. Exemplary compounds for oral administration include pirenzepine (CAS 28797-61-7), darifenacin (CAS 133099-04 35 4, or CAS 133099-07-7 for the hydrobromide sold under the name Enablex), oxybutynin (CAS 5633-20-5, sold under the name Ditropan), terodiline (CAS 15793- WO 2005/005452 PCTIEP2004/007820 11 40-5), tolterodine (CAS 124937-51-5, or CAS 124937-52-6 for the tartrate, sold under the name Detrol), otilonium (e.g. as the bromide, CAS 26095-59-0, sold under the name Spasmomen), trospium chloride (CAS 10405-02-4) and solifenacin (CAS 242478-37-1, or CAS 242478-38-2 for the succinate also known as YM-905 and sold 5 under the name Vesicare). Other suitable anticholinergic agents include compounds of formula (XXI), which are disclosed in US patent application 60/487981: N+ X N H (XXI) SR3 10 in which the preferred orientation of the alkyl chain attached to the tropane ring is endo;
R
31 and R 32 are, independently, selected from the group consisting of straight or branched chain lower alkyl groups having preferably from I to 6 carbon atoms, 15 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 20 but is not limited to chloride, bromide, iodide, sulfate, benzene sulfonate, and toluene sulfonate, including, for ample: (3-endo)-3-(2,2-di-2-thienylethenyl)-8,8-dimethyl-8-azoniabicyclo[3.2.1 ]octane bromide; 25 (3-endo)-3-(2,2-diphenylethenyl)-8,8-dimethyl-8-azoniabicyclo[3.2.1]octane bromide; (3-endo)-3-(2,2-diphenylethenyl)-8,8-dimethyi-8-azoniabicyclo[ 3 .2.1 ]octane 4 methylbenzenesulfonate; (3-endo)-8,8-dimethyl-3-[2-phenyl-2-(2-thienyl)ethenyl]-8-azoniabicyclo[3.2.1 ]octane bromide; and/or 30 (3-endo)-8,8-dimethyl-3-[2-phenyl-2-(2-pyridinyl)ethenyl]-8 azoniabicyclo[3.2.i]octane bromide.
WO 2005/005452 PCTIEP2004/007820 12 Further suitable anticholinergic agents include compounds of formula (XXII) or (XXIII), which are disclosed in US patent application 60/511009:
SR
4 1 N H (XXII) H (XXIII)
R
43 R4 R44 R42 R44 R42 5 wherein: the H atom indicated is in the exo position;
R
4 ' represents an anion associated with the positive charge of the N atom. R 4 ' may be but is not limited to chloride, bromide, iodide, sulfate, benzene sulfonate and 10 toluene sulfonate;
R
42 and R 4 3 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 0 as the 15 heteroatom, heterocycloalkyl-alkyl (having 6 to0 carbon atoms) and N or 0 as the heteroatom, aryl, optionally substituted aryl, heteroaryl, and optionally substituted heteroaryl; R4 is slected from the group consisting of (C-C 6 )alkyl, (C 3
-C
12 )cycloalkyl, (C 3 C 7 )heterocycloalkyl,
(C-C
6 )alkyl(C 3
-C
12 )cycloalkyl, (C-C 6 )alkyl(C3 20 C 7 )heterocycloalkyl, aryl, heteroaryl, (C-C 6 )al.kyl-aryl, (C-CB)alkyl-heteroaryl, -OR
-CH
2 0R 45 , -CH 2 OH, -CN, -CF 3 , -CH 2 O(CO)R4, -CO 2 R4, -CH 2
NH
2 , CH 2 N(R4 7
)SO
2
R
45 , -80 2
N(R
4 7)(R4), -CON(R 4 7)(R 4 1), -CH 2
N(R
4
)CO(R
4 1),
-CH
2
N(R
4
)SO
2
(R
4 6 ), -CH 2
N(R
4
)CO
2
(R
4 5 ), -CH 2
N(R
4 )CONH(R 47);
R
4 is selected from the group consisting of (C 1
C
6 )alkyl, (C-C 6 )alkyl(C 3 25 C 12 )cycloalkyl, (Cr-C 6 )alkyl(C 3 -C)heterocycloalkyl,
(C-C
6 )alkyl-aryl, (C-C 6 )alkyl heteroaryl;
R
4 is selected from the group consisting of (C-C 6 )alkyl, (C 3
-C
12 )cycloalkyl,
(C
3 -C)heterocycloalkyl,
(C-C
6 )alkyl(C 3 -Cl 2 )cycloalkyl, (C-C 6 )alkyl(C 3 C 7 )heterocycloalkyl, aryl, heteroaryl, (C-C 6 )alkyl-aryl, (C-C 6 )alkyl-heteroaryl; 30 R 47 and R 48 are, independently, selected from the group consisting of H, (Cj-C 6 )alkyl,
(C
3
-C
12 )cycloalkyl, (C 3
-C
7 )heterocycloalkyl, (Cr-C 6 )alkyl(C 3
-C
12 )cyclOalkyl, WO 2005/005452 PCTIEP2004/007820 13 (Cr C 6 )alkyl(C-C 7 )heterocycloalkyl,
(C-C
6 )alkyl-aryl, and (C-C 6 )alkyl-heteroaryl, including, for example: (Endo)-3-(2-methoxy-2,2-di-thiophen-2-yl-ethyl)-8,8-dimethyl-8-azonia bicyclo[3.2.1]octane iodide; 5 3-((Endo)-8-methyl-8-aza-bicyclo[3.
2 .1]oct-3-yl)-2,2-diphenyI-propionitrile; (Endo)-8-methyl-3-(2,2,2-triphenyl-ethyl)-8-aza-bicyclo[3.2.1 ]octane; 3-((Endo)-8-methyl-8-aza-bicyclo[3.2. 1 oct-3-yl)-2,2-diphenyl-propionamide; 3-((Endo)-8-methyl-8-aza-bicyclo[ 3 .2.1]oct-3-yl)-2,2-diphenyl-propionic acid; (Endo)-3-(2-cyano-2,2-diphenyl-ethyl)-8,8-dimethyl-8-azonia-bicyclo[3.2.1 ]octane 10 iodide; (Endo)-3-(2-cyano-2,2-diphenyl-ethyl)-8,8-dimethyl-8-azonia-bicyclo[3.2.1 ]octane bromide; 3-((Endo)-8-methyl-8-aza-bicyclo[3.
2 .1]oct-3-yl)-2,2-diphenyl-propan-1-ol; N-Benzyl-3-((endo)-8-methyl-8-aza-bicyclo[ 3 .2.1loct-3-yl)-2,2-diphenyl 15 propionamide; (Endo)-3-(2-carbamoyl-2,2-diphenyl-ethyl)-8,8-dimethyl-8-azonia bicyclo[3.2.1]octane iodide; 1 -Benzyl-3-[3-((endo)-8-methyl-8-aza-bicyclo[3.2.1 ]oct-3-yl)-2,2-diphenyl-propyl] urea; 20 1 -Ethy-3-[3-((endo)-8-methyl-8-aza-bicyclo[3.2.1 ]oct-3-yl)-2,2-diphenyl-propyl]-urea; N-[3-((Endo)-8-methyl-8-aza-bicyclo[ 3
.
2 .1 ]oct-3-yl)-2,2-diphenyl-propyl]-acetamide; N-[3-((Endo)-8-methyl-8-aza-bicyclo[ 3
.
2 .1]oct-3-yl)-2,2-diphenyl-propyl]-benzamide; 3-((Endo)-8-methyl--aza-bicyclo[3.
2 .1 ]oct-3-yI)-2,2-di-thiophen-2-yI-propionitrile; (Endo)-3-(2-cyano-2,2-di-thiophen-2-yl-ethyl)- 8 ,8-dimethyl-8-azonia 25 bicyclo[3.2.1 ]octane iodide; N-[3-((Endo)-8-methyl-8-aza-bicyclo[ 3
.
2 .1]oct-3-yl)-2,2-diphenyl-propyl] benzenesulfonamide; [3-((Endo)-8-methyl-8-az-biyclo[3.
2 .I ]oct-3-yI)-2,2-diphenyl-propyl]-urea; iV-[3-((Endo)-8-methyl-8-aza-bicyclo[3.2. 1 ]oct-3-yl)-2,2-diphenyl-propyl] 30 methanesulfonamide; and/or (Endo)-3-{2,2-diphenyl-3-[(1 -phenyl-methanoyl)-amino]-propyl}-8,8-dimethyl-8 azonia-bicyclo[3.2.1]octane bromide. More preferred compounds useful in the present invention include: (Endo)-3-(2-methoxy-2,2-di-thiophen-2-yI-ethyl)-8,8-dimethyl-8-azonia 35 bicyclo[3.2.1]octane iodide; WO 2005/005452 PCTIEP2004/007820 14 (Endo)-3-(2-cyano-2,2-dipheny-ethyl)-8,8-dimethyl-8-azonia-bicyclo[3.
2 .1 ]octane iodide; (Endo)-3-(2-cyano-2,2-diphenyl-ethyl)-8,8-dimethyl-8-azonia-bicyclo[3.2. 1]octane bromide; 5 (Endo)-3-(2-carbamoyl-2,2-diphenyl-ethyl)-8,8-dimethyl-8-azonia bicyclo[3.2.1]octane iodide; (Endo)-3-(2-cyano-2,2-di-thiophen-2-yl-ethyl)- 8 ,8-dimethyl-8-azonia bicyclo[3.2.1]octane iodide; and/or (Endo)-3-{2,2-diphenyl-3-[(I-phenyl-methanoyl)-amino]-propyl}- 8
,
8 -dimethyl-8 10 azonia-bicyclo[3.2.1]octane bromide. Suitable antihistamines (also referred to as HI-receptor antagonists) include any one or more of the numerous antagonists known which inhibit H1-receptors, and are safe for human use. First generation antagonists, include derivatives of ethanolamines, 15 ethylenediamines, and alkylamines, e.g diphenylhydramine, pyrilamine, clemastine, chloropheniramine. Second generation antagonists, which are non-sedating, include loratidine, desloratidine,terfenadine,astemizole,acrivastine, azelastine, levocetirizine fexofenadine and cetirizine. 20 Examples of preferred anti-histamines include loratidine, desloratidine, fexofenadine and cetirizine. The invention thus provides, in a further aspect, a combination comprising a compound of formula (1) a pharmaceutically acceptable solvate or physiologically 25 functional derivative thereof together with a PDE4 inhibitor. The invention thus provides, in a further aspect, a combination comprising a compound of formula (1) a pharmaceutically acceptable solvate or physiologically functional derivative thereof together with a p 2 -adrenorecptor agonist. 30 The invention thus provides, in a further aspect, a combination comprising a compound of formula (1) a pharmaceutically acceptable solvate or physiologically functional derivative thereof together with an anticholinergic.
WO 2005/005452 PCTIEP2004/007820 15 The invention thus provides, in a further aspect, a combination comprising a compound of formula (1) a pharmaceutically acceptable solvate or physiologically functional derivative thereof together with an antihistamine. 5 The invention thus provides, in a further aspect, a combination comprising a compound of formula (1) a pharmaceutically acceptable solvate or physiologically functional derivative thereof together with a PDE4 inhibitor and a 2 -adrenoreceptor agonist. 10 The invention thus provides, in a further aspect, a combination comprising a compound of formula (1) a pharmaceutically acceptable solvate or physiologically functional derivative thereof together with an anticholinergic and a PDE-4 inhibitor. The combinations referred to above may conveniently be presented for use in the 15 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 20 sequentially or simultaneously in separate or combined pharmaceutical formulations. Preferably the individual compounds of such combinations may be administered simultaneously in a combined pharmaceutical combination. Appropriate doses of known therapeutic agents will be readily appreciated by those skilled in the art. 25 Solvates of the compound of formula (1) which are not physiologically acceptable may be useful as intermediates in the preparation of compounds of formula (1) or physiologically acceptable solvates thereof. The compound of formula (1) or solvates thereof demonstrates agonism at the 30 glucocorticoid receptor. The compound of formula (1) or solvates thereof may demonstrate good anti inflammatory properties, with predictable pharmacokinetic and pharmacodynamic behaviour. It may have an attractive side-effect profile, demonstrated, for example, 35 by increased selectivity for the glucocorticoid receptor over the progesterone receptor and increased selectivity for glucocorticoid receptor mediated WO 2005/005452 PCTIEP2004/007820 16 transrepression over transactivation and is likely to be compatible with a convenient regime of treatment in human patients. The following non-limiting Examples illustrate the invention: 5 EXAMPLES General Chromatographic purification was performed using pre-packed Bond Elut silica gel cartridges available commercially from Varian or by flash chromatography on pre 10 packed Biotage silica columns. These cartridges were pre-conditioned with dichloromethane prior to use. LCMS was conducted on a Supelcosil LCABZ+PLUS column (3.3 cm x 4.6 mm ID) eluting with 0.1% HCO 2 H and 0.01 M ammonium acetate in water (solvent A), and 0.05% HCO 2 H 5% water in acetonitrile (solvent B), using the following elution gradient 0-0.7 min 0%B, 0.7-4.2 min 100%B, 4.2-5.3 min 15 0%B, 5.3-5.5 min O%B at a flow rate of 3 ml/min. The mass spectra were recorded on a Fisons VG Platform spectrometer using electrospray positive and negative mode (ES+ve and ES-ve). 1H NMR spectra were obtained in CDC 3 on a Bruker DPX 400 spectrometer working at 400.13 MHz and 9.4 Tesla using as internal standard the signal from the residual protonated solvent at 7.25 ppm. 20 Intermediates 25 Intermediate 1: 2,3-dimethyl-1-(2,2,3,3-tetramethylcyclopropyl)carbonyll-1H imidazol-3-ium chloride Oxalyl chloride (360mi, 4.1mol) was added over 65min to a stirred solution of 2,2,3,3-tetramethylcyclopropane carboxylic acid (600g, 4.2mol) in dichloromethane (3.6L) at 34*C. The solution was then heated to reflux for 30 min and then cooled to 30 5*C. A solution of 1,2-dimethylimidazole (490g, 5.1mol) in dichloromethane (1.2L) was added over 45min maintaining the internal temperature around 5*C. The resulting suspension was then warmed to 180C and acetone (4.8L) was added over 45 minutes maintaining the internal temperature around 18*C. The slurry was cooled to 5oC over 30 minutes, stirred at 5C for 30 minutes and then filtered. The 35 product was collected by filtration, washed with acetone:dichloromethane (3:1, 3x1.2L), sucked dry and then dried in a vacuum oven at 25-30*C for 10 hours to give WO 2005/005452 PCTIEP2004/007820 17 Intermediate 1 as a white solid (890g) 1 H nmr: SH (CDC1 3 , 400MHz) 8.45 (d, J 2.4Hz, IH), 8.11 (d, J 2.4Hz, 1H), 4.21 (s, 3H), 2.96 (s, 3H), 2.21 (s, 1H), 1.43 (s, 6H), 1.33 (s, 6H). 5 Examples Example 1: 6a,9cc-Difluoro-1 1p-hydroxy-1 6cc-methyl-3-oxo-1 7a-(2,2,3,3 tetramethycyclopropylcarbonyl)oxy-androsta-1,4-diene-1 70-carboxylic acid 10 cyanomethyl ester Method A Bromoacetonitrile (0.229m], 3.29mmol) was added to a stirred and cooled (ice) solution of 6a,9ca-Difluoro-1 1p -hydroxy-1 6a-methyl-3-oxo-1 7a-(2,2,3,3 15 tetramethycyclopropylcarbonyl)oxy-androsta-1,4-diene-17p-carboxylic acid (prepared as described in WO 2003/3072592)_(634mg, 1.22mmol) and sodium carbonate (1.29g, 12.2mmol) in DMF (15ml) under nitrogen and the mixture stiirred at room temperature for 2h. More sodium carbonate (258mg) was added and the mixture stirred for a further 18h. 2M HCI (20ml) was added dropwise followed by water 20 (25ml) and the mixture was extracted with ethyl acetate (2x50ml). The combined organic extracts were washed successively with aqueous sodium hydrogen carbonate (50ml) and brine (50mI) and dried through a hydrophobic frit and evaporated to dryness. Purification on a Bond Elut cartridge using initially cyclohexane and finally cyclohexane:ethyl acetate 3:1 gave the title compound as a 25 white solid (485mg): LCMS retention time 3.79 min, m/z 560 MH* Method B 6,cc9-Difluoro- 11p,17a-dihydroxy-16oc-methyl-3-oxo-androsta-1,4-diene-17p 30 carboxylic acid (G. H. Phillipps et aj., (1994) Journal of Medicinal Chemistry, 37, 3717-3729) (490g, 1.2mol) and Intermediate 1 (790g, 3.1mol) were suspended in 3-pentanone (7.3L). To the stirred suspension was added over 10 min a solution of 1,2-dimethylimidazole (120g, 1.2mol) in water (730ml) maintaining the internal temperature around 19*C. After 35 min, 1-methylpiperazine (230ml, 2.1mol) was 35 added over 10 min keeping the internal temperature around 190C. The mixture was stirred for 30 min and then washed sequentially with 2M HCI (290ml) and water (290ml). Diisopropylethylamine (430ml, 2.5mol) and bromoacetonitrile (120ml, WO 2005/005452 PCTIEP2004/007820 18 1.7mol) were added sequentially to the solution and the mixture was heated to 53*C for 13 hours. The solution was cooled to 340C and 1-methylpiperazine (105ml) was added. The mixture was stirred around 340C for a further hour, cooled to 25*C and washed sequentially with 2M HCI (290ml), water (290ml), 2% potassium carbonate 5 solution (290ml) and water (290ml). The organic solution was concentrated to 3.9L by atmospheric distillation, cooled to 750C and seeded with crystals of Example I . 2,2,4-Trimethylpentane (6.83L) was added over 3 hours at 75*C and the slurry was then cooled to 10C over 2 hours, stirred for a further 30min and then filtered. The product was washed with 3-pentanone:2,2,4-trimethylpentane (1:3, 3x1L), sucked 10 dry and finaly dried in a vacuum oven at 500C for 12 hours to give Example 1 as a white solid (640g) identical to material obtained using Method A. Pharmacological Activity Pharmacological activity may be assessed in functional in vitro assays of glucocorticoid agonist activity. 15 The functional assay based on that described by K.P.Ray et al., Biochem J. (1997), 328, 707-715 provides a measure of transrepressive activity of a glucocorticoid agonist. A549 cells stably transfected with a reporter gene containing the NF-cB responsive elements from the ELAM gene promoter coupled to sPAP (secreted 20 alkaline phosphatase) are treated with test compounds at appropriate doses for I hour at 37"C. The cells are then stimulated with tumour necrosis factor (TNF, 1Ong/ml) for 16 hours, at which time the amount of alkaline phosphatase produced is measured by a standard colourimetric assay. Dose response curves are constructed from which EC0o values may be estimated. 25 An EC 5 o value of < 0.InM was observed for Example I The functional assay based on that described by R.J.H. Austin et al., Eur Resp J. (2002), 20,1386-1392 measures the ability of compounds to directly transactivate 30 gene expression. A549 cells stably transfected with a reporter gene containing the glucocorticoid responsive region of the mouse mammary tumour virus long terminal repeat (MMTV-LTR) coupled to renilla luciferase were treated with test compounds at appropriate doses for 6 hour at 370C. The amount of luciferase activity present within the cells is then determined by measuring the light emitted following incubation 35 with a suitable substrate. Dose response curves were constructed from which EC 50 WO 2005/005452 PCTIEP2004/007820 19 values were estimated and from which maximal responses are calculated relative to Dexamethasone (100%). Compound of Example 1 showed a maximal response of <5% in this assay. 5 Assay for Progesterone receptor activity The human breast cancer cell line T47D has been reported to upregulate an endogenous alkaline phosphatase in response to progestins (Di Lorenzo et al., Cancer Research (1991) 51, 4470-4475. T47D cells were seeded into 96 well plates 10 at a density of 1x10 5 cells per well and grown overnight at 37 0 C. Steroids were dissolved in DMSO, added to the cells (final DMSO concentration 0.7%), and incubated for 24 hours at 37 0 C. The cells were then washed with PBS and lysed with RIPA buffer (1% IGEPAL, 0.5% Na deoxycholate, 0.1% SDS in phosphate buffered saline). Alkaline phosphatase activity was measured spectrophotometrically (405nm) 15 using p-nitrophenylphosphate (1.5mg/ml) as a substrate dissolved in 1M diethanolamine, 0.28M NaCl, 0.5mM MgCl 2 . Dose response curves were constructed from which EC 5 o values were estimated. The EC 5 o value for compound of Example I in this assay was >1 OOnM. 20 Throughout the specification and the claims which follow, unless the context requires otherwise, the word 'comprise', and variations such as 'comprises' and 'comprising', will be understood to imply the inclusion of a stated integer or step or group of integers but not to the exclusion of any other integer or step or group of integers or 25 steps. The application of which this description and claims forms part may be used as a basis for priority in respect of any subsequent application. The claims of such subsequent application may be directed to any feature or combination of features 30 described herein. They may take the form of product, composition, process, or use claims and may include, by way of example and without limitation, the following claims. The patents and patent applications described in this application are herein incorporated by reference.

权利要求:
Claims (8)
[1] 1. A compound of formula (1): 0 0 0 HO 0 H o F H F 5 or a physiologically acceptable solvate thereof.
[2] 2. A compound of formula (1) as defined in claim 1 or a physiologically 10 acceptable solvate thereof for use in veterinary or human medicine.
[3] 3. Use of a compound of formula (1) as defined in claim 1 or a physiologically acceptable solvate thereof for the manufacture of a medicament for the treatment of inflammatory and/or allergic conditions. 15
[4] 4. A pharmaceutical composition comprising a compound of formula (1) as defined in claim 1 or a physiologically acceptable solvate thereof together, if desirable, in admixture with one or more physiologically acceptable diluents or carriers. 20
[5] 5. A pharmaceutical aerosol formulation comprising a compound of formula (1) as defined in claim I or a physiologically acceptable solvate thereof, and a fluorocarbon or hydrogen-containing chlorofluoro carbon as propellant, optionally in combination with a surfactant and/or a cosolvent. 25
[6] 6. A pharmaceutical composition according to claim 5 which further comprises another therapeutically active agent.
[7] 7. A pharmaceutical composition according to claim 6 in which said another 30 therapeutically active agent is a 32-adrenoreceptor agonist. WO 2005/005452 PCTIEP2004/007820 21
[8] 8. A method for the treatment of a human or animal subject with an anti inflammatory and/or allergic condition, which method comprises administering to said human or animal subject an effective amount of a compound of formula (1) as 5 defined in claim 1 or a physiologically acceptable solvate thereof.

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法律状态:
2009-11-26| FGA| Letters patent sealed or granted (standard patent)|

优先权:

申请号 | 申请日 | 专利标题

GBGB0316290.6A|GB0316290D0|2003-07-11|2003-07-11|Novel compounds|

GB0316290.6||2003-07-11||

PCT/EP2004/007820|WO2005005452A1|2003-07-11|2004-07-09|Specific glucocorticosteroid compound having anti- inflammatory activity|

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