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US20080125426A1 - Novel Compounds - Google Patents

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Publication number
US20080125426A1
US20080125426A1 US12/024,375 US2437508A US2008125426A1 US 20080125426 A1 US20080125426 A1 US 20080125426A1 US 2437508 A US2437508 A US 2437508A US 2008125426 A1 US2008125426 A1 US 2008125426A1
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US
United States
Prior art keywords
alkyl
chlorophenyl
carbonitrile
pyrrolo
hydrogen
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US12/024,375
Inventor
Andrew Bailey
Garry Pairaudeau
Anil Patel
Stephen Thom
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AstraZeneca AB
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AstraZeneca AB
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Priority to US12/024,375 priority Critical patent/US20080125426A1/en
Assigned to ASTRAZENECA AB reassignment ASTRAZENECA AB ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BAILEY, ANDREW, PAIRAUDEAU, GARRY, PATEL, ANIL, THOM, STEPHEN
Publication of US20080125426A1 publication Critical patent/US20080125426A1/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D473/00—Heterocyclic compounds containing purine ring systems
    • C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32—Nitrogen atom
    • C07D473/34—Nitrogen atom attached in position 6, e.g. adenine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Definitions

  • the present invention relates to compounds and compositions for treating diseases associated with cysteine protease activity.
  • the compounds are reversible inhibitors of cysteine proteases S, K, F, L and B. Of particular interest are diseases associated with Cathepsin S.
  • this invention also discloses processes for the preparation of such inhibitors.
  • Cathepsin S is a member of the papain superfamily of cysteine proteases which also encompasses Cathepsins B, H, L, O and K. Cathepsin S plays a key role in the processing of invariant chain in MHC class II complexes allowing the complex to associate with antigenic peptides. MHC class II complexes are then transported to the surface of the cell for presentation to effector cells such as T cells. The process of antigen presentation is a fundamental step in initiation of the immune response. In this respect inhibitors of cathepsin S could be useful agents in the treatment of inflammation and immune disorders such as, but not limited to, asthma, rheumatoid arthritis, multiple sclerosis and Crohn's disease. Cathepsin S has also been implicated in a variety of other diseases involving extracellular proteolysis such as the development of emphysema in COPD through degradation of elastin and in Alzheimers disease.
  • Cathepsins notably K and L have been shown to degrade bone collagen and other bone matrix proteins. Inhibitors of these cysteine proteases would be expected to be useful in the treatment of diseases involving bone resorption such as osteoporosis.
  • the present invention therefore provides a compound of formula (I)
  • X is N, NH, :CH or CH 2 ;
  • Y is N, :CH, CO, CH 2 or :CNR 2 R 3 , where R 2 and R 3 are independently hydrogen, C 1-6 alkyl or C 3-6 cycloalkyl; R is aryl or heteroaryl optionally substituted by halogen, amino, hydroxy, cyano, nitro, trifluoromethyl, carboxy, CONR 5 R 6 , SO 2 NR 5 R 6 , SO 2 R 4 , NHSO 2 R 4 , NHCOR 4 , ethylenedioxy, methylenedioxy, C 1-6 alkyl, C 1-6 alkoxy, SR 4 or NR 5 R 6 where R 4 is hydrogen, C 1-6 alkyl or C 3-6 cycloalkyl, R 5 and R 6 are independently hydrogen, C 1-6 alkyl or together with the nitrogen atom to which they are attached form a 5- or 6-membered saturated ring optionally containing a further O, S or NR 4 group; or R is hydrogen, C 1-6 alkyl or C 3-6 cycl
  • an alkyl or alkenyl group or an alkyl or alkenyl moiety in a substituent group may be linear or branched.
  • Aryl groups include phenyl and naphthyl.
  • Heteroaryl groups include 5- or 6-membered, 5,6- or 6,6-fused aromatic rings containing one or more heteroatoms selected from N, S, O. Examples include pyridine, pyrimidine, pyrazine, pyridazine thiazole, oxazole, pyrazole, imidazole, furan and thiophene, quinoline, isoquinoline, benzimidazole, benzofuran, benzothiophene, indole.
  • Certain compounds of formula (I) are capable of existing in stereoisomeric forms. It will be understood that the invention encompasses all geometric and optical isomers of the compounds of formula (I) and mixtures thereof including racemates. Tautomers and mixtures thereof also form an aspect of the present invention.
  • X is N and Y is :CH, X and Y are :CH or X and Y are CH 2
  • R is C 1-4 alkyl, or phenyl substituted by halogen, in particular chloro, SO 2 Me, C 1-6 alkoxy, in particular methoxy, C 1-4 alkyl, in particular methyl or propyl.
  • R 1 is a group Y(CH 2 ) p R 7 where p is 0 and Y is NR 8 where R 8 is hydrogen and R 7 is substituted phenyl.
  • R 7 is phenyl substituted by halogen, especially chloro; or
  • R 1 is NR 9 R 10 where R 9 and R 10 are hydrogen or C 1-3 alkyl or together with the nitrogen atom to which they are attached form a 5 or 6-membered saturated ring optionally containing a O, S or NR 4 .
  • Preferred compounds of the invention include:
  • the present invention further provides a process for the preparation of a compound of formula (I) which comprises
  • L1 and L2 represent a leaving group (e.g. halide, sulphide, sulfoxide or sulphone group), preferably the sulphide is oxidised to a sulphoxide or sulphone group before displacement.
  • An oxidising agent such as a peracid may be used, for example meta-chloroperbenzoic acid in dichloromethane at room temperature.
  • L1 may be displaced by R 1 where R 1 is defined in formula (I) and L2 may be displaced by cyanide, preferably using a salt (e.g. lithium, sodium or potassium cyanide).
  • a salt e.g. lithium, sodium or potassium cyanide.
  • the sequence of displacement of L1, L2 may be varied.
  • Compounds of formula (II) where X ⁇ N and Y ⁇ :CH or :CNR 2 R 3 may be prepared from compounds of formula (III) by ring cyclisations using, for example diethoxymethyl acetate, FMOC-NCS or R 3 R 2 NCSCl.
  • Compounds of formula (II) where X ⁇ NH and Y ⁇ CO can also be prepared from compounds of formula (III) by reaction with phosgene or phosgene equivalent.
  • the sequence of steps may also be varied, for example compounds of formula (III) may first have L1 and/or L2 displaced before the cyclisation step.
  • Compounds of formula (II) may also be prepared from compound of formula (IV) by reaction with a group R-Z, where R is defined in formula (I) and Z is a leaving group (e.g. halide, activated alcohol).
  • R-Z where R is defined in formula (I) and Z is a leaving group (e.g. halide, activated alcohol).
  • a compound of the formula (I), or a pharmaceutically acceptable salt thereof, for use as a therapeutic agent for use as a therapeutic agent.
  • a method for producing inhibition of a cysteine protease in a warm blooded animal, such as man, in need of such treatment which comprises administering to said animal an effective amount of a compound of the present invention, or a pharmaceutically acceptable salt thereof.
  • the invention also provides a compound of the formula (I), or a pharmaceutically acceptable salt thereof, for use as a medicament; and the use of a compound of the formula (I) of the present invention, or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the inhibition of a cysteine protease in a warm blooded animal, such as man.
  • the compounds of the invention are useful in the treatment of inflammation and immune disorders such as, but not limited to, asthma, rheumatoid arthritis, COPD, multiple sclerosis, Crohn's disease, Alzheimers and pain, such as neuropathic pain.
  • the compounds of the invention are used to treat pain, especially neuropathic pain.
  • the invention provides the use of a compound of the formula (I) of the present invention, or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the inhibition of Cathepsin S in a warm blooded animal, such as man.
  • a compound of the formula (I) or a pharmaceutically acceptable salt thereof for the therapeutic treatment of mammals including humans, in particular in the inhibition of a cysteine protease, it is normally formulated in accordance with standard pharmaceutical practice as a pharmaceutical composition.
  • the present invention provides a pharmaceutical composition which comprises a compound of the formula (I) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable diluent or carrier.
  • compositions of this invention may be administered in standard manner for the disease condition that it is desired to treat, for example by oral, rectal or parenteral administration.
  • the compounds of this invention may be formulated by means known in the art into the form of, for example, tablets, capsules, aqueous or oily solutions or suspensions, (lipid) emulsions, dispersible powders, suppositories, ointments, creams, drops and sterile injectable aqueous or oily solutions or suspensions.
  • a suitable pharmaceutical composition of this invention is one suitable for oral administration in unit dosage form, for example a tablet or capsule which contains between 100 mg and 1 g of the compound of this invention.
  • composition of the invention is one suitable for intravenous, subcutaneous or intramuscular injection.
  • Each patient may receive, for example, an intravenous, subcutaneous or intramuscular dose of 1 mgkg ⁇ 1 to 100 mgkg ⁇ 1 of the compound, preferably in the range of 5 mgkg ⁇ 1 to 20 mgkg ⁇ 1 of this invention, the composition being administered 1 to 4 times per day.
  • the intravenous, subcutaneous and intramuscular dose may be given by means of a bolus injection.
  • the intravenous dose may be given by continuous infusion over a period of time.
  • each patient will receive a daily oral dose which is approximately equivalent to the daily parenteral dose, the composition being administered 1 to 4 times per day.
  • Buffers such as polyethylene glycol, polypropylene glycol, glycerol or ethanol or complexing agents such as hydroxy-propyl ⁇ cyclodextrin may be used to aid formulation.
  • the above formulations may be obtained by conventional procedures well known in the pharmaceutical art.
  • the tablets (a)-(c) may be enteric coated by conventional means, for example to provide a coating of cellulose acetate phthalate.
  • Examples 2-12 were prepared according to the general method of example 1 using the appropriate amines.
  • Examples 14-18 were prepared according to the general method of example 13 using the appropriate amines.
  • Triphosgene (0.09 g) was added to a mixture of the product from example 20 step (iii) (0.4 g) and pyridine (0.4 ml) in dichloromethane (30 ml) and the mixture stirred at room temperature. After 1 h more triphosgene (0.02 g) was added, stirred for a further 1 h, water added and the solid filtered. The solid was washed with water, diethylether and dried.
  • step (ii) A solution of the product of step (ii) (2.2 g) in methanol (10 ml) was added to a solution of sodium (0.27 g) in methanol (90 ml). Iodomethane (0.73 ml) was added and the mixture heated at reflux for 1 hour. The solvent was removed under reduced pressure to give a solid.
  • step (iii) and phosphorus oxychloride (30 ml) was heated at 100° C. for 3 h.
  • the excess reagent was removed under reduced pressure, the residue quenched with ice-water, extracted with ethyl acetate, dried(MgSO4) and evaporated to an oil.
  • the oil was purified by chromatography on silica eluting with isohexane:diethylether(4:1) to give a brown oil (0.36 g).
  • step (vi) A mixture of the product from step (vi) (0.1 g) and sodium cyanide (0.022 g) in dimethylsulfoxide (10 ml) was stirred at room temperature for 2 h. The mixture was partitioned between ethyl acetate and water, the organics separated, dried (MgSO 4 ) and evaporated to a yellow solid (0.1 g).
  • Examples 29-32 were prepared according to the method of example 28 steps (vi)-(viii).
  • QFRET Technology Quenched Fluorescent Resonance Energy Transfer
  • Synthetic substrate 20 ⁇ M [final]Z-Val-Val-Arg-AMC in phosphate buffer were added to a 96 well black Optiplate.
  • the assay plates were pre-read for compound auto fluorescence on SpectraMax Gemini at 355 nM excitation and 460 nM emission.
  • 250 pM [final] rHuman Cathepsin S in phosphate buffer was added and incubated for 2 h at room temperature on the SpectraMax Gemini, taking readings every 20 min at 355 nM excitation and 460 nM emission.
  • Activity Based template (5PTB-8) used the auto fluorescent corrected data to calculate the percentage inhibition for each compound concentration using the relevent plate controls. This data was used to construct inhibition curves and pIC 50 estimated by non-linear regression using a 4 parameter logistic model.

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  • Health & Medical Sciences (AREA)
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  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
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  • Thiazole And Isothizaole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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Abstract

The present invention relates to compounds and compositions for treating diseases associated with cysteine protease activity. The compounds are reversible inhibitors of cysteine proteases S, K, F, L and B. Of particular interest are diseases associated with Cathepsin S. In addition this invention also discloses processes for the preparation of such inhibitors.

Description

  • The present invention relates to compounds and compositions for treating diseases associated with cysteine protease activity. The compounds are reversible inhibitors of cysteine proteases S, K, F, L and B. Of particular interest are diseases associated with Cathepsin S. In addition this invention also discloses processes for the preparation of such inhibitors.
    • BACKGROUND OF THE INVENTION
  • Cathepsin S is a member of the papain superfamily of cysteine proteases which also encompasses Cathepsins B, H, L, O and K. Cathepsin S plays a key role in the processing of invariant chain in MHC class II complexes allowing the complex to associate with antigenic peptides. MHC class II complexes are then transported to the surface of the cell for presentation to effector cells such as T cells. The process of antigen presentation is a fundamental step in initiation of the immune response. In this respect inhibitors of cathepsin S could be useful agents in the treatment of inflammation and immune disorders such as, but not limited to, asthma, rheumatoid arthritis, multiple sclerosis and Crohn's disease. Cathepsin S has also been implicated in a variety of other diseases involving extracellular proteolysis such as the development of emphysema in COPD through degradation of elastin and in Alzheimers disease.
  • Other Cathepsins notably K and L have been shown to degrade bone collagen and other bone matrix proteins. Inhibitors of these cysteine proteases would be expected to be useful in the treatment of diseases involving bone resorption such as osteoporosis.
  • The present invention therefore provides a compound of formula (I)
  • Figure US20080125426A1-20080529-C00001
  • in which:
    • X is N, NH, :CH or CH2;
  • Y is N, :CH, CO, CH2 or :CNR2R3, where R2 and R3 are independently hydrogen, C1-6 alkyl or C3-6 cycloalkyl;
    R is aryl or heteroaryl optionally substituted by halogen, amino, hydroxy, cyano, nitro, trifluoromethyl, carboxy, CONR5R6, SO2NR5R6, SO2R4, NHSO2R4, NHCOR4, ethylenedioxy, methylenedioxy, C1-6 alkyl, C1-6 alkoxy, SR4 or NR5R6 where R4 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl, R5 and R6 are independently hydrogen, C1-6 alkyl or together with the nitrogen atom to which they are attached form a 5- or 6-membered saturated ring optionally containing a further O, S or NR4 group;
    or R is hydrogen, C1-6 alkyl or C3-6 cycloalkyl both of which can optionally contain one or more O, S or NR4 groups,
    R1 is a group Y(CH2)pR7 where p is 0, 1 or 2 and Y is O or NR8 where R8 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl;
    and R7 is a 5- or 6-membered saturated ring containing one or more O, S or N atoms, aryl or a heteroaryl group containing one to four heteroatoms selected from O, S or N, the saturated ring, aryl and heteroaryl groups all being optionally substituted by halogen, amino, hydroxy, cyano, nitro, trifluoromethyl, carboxy, CONR5R6, SO2NR5R6, SO2R4, NHSO2R4, NHCOR4, C1-6 alkyl, C1-6 alkoxy, SR4 or NR5R6 where R4 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl, R5 and R6 are independently hydrogen, C1-6 alkyl or together with the nitrogen atom to which they are attached form a 5- or 6-membered saturated ring optionally containing a further O, S or NR4 group;
    or R1 is a group NR9R10 where R9 and R10 are independently hydrogen or C1-6 alkyl optionally containing one or more O, S or NR4 groups, or R9 and R10 together with the nitrogen atom to which they are attached form a 5 or 6-membered saturated ring optionally containing a further O, S or N atom and optionally substituted by NR9R10, CO2C1-6 alkyl, CONR11R12 where R11 and R12 are independently hydrogen or C1-6 alkyl, aryl or heteroaryl group optionally substituted by halogen, amino, hydroxy, cyano, nitro, trifluoromethyl, carboxy, CONR5R6, SO2NR5R6, SO2R4, NHSO2R4, NHCOR4, C1-6 alkyl, C1-6 alkoxy, SR4 or NR5R6 where R4 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl, R5 and R6 are independently hydrogen, C1-6 alkyl or together with the nitrogen atom to which they are attached form a 5- or 6-membered saturated ring optionally containing a further O, S or NR4 group;
    and pharmaceutically acceptable salts or solvates thereof.
  • In the context of the present specification, unless otherwise indicated, an alkyl or alkenyl group or an alkyl or alkenyl moiety in a substituent group may be linear or branched. Aryl groups include phenyl and naphthyl. Heteroaryl groups include 5- or 6-membered, 5,6- or 6,6-fused aromatic rings containing one or more heteroatoms selected from N, S, O. Examples include pyridine, pyrimidine, pyrazine, pyridazine thiazole, oxazole, pyrazole, imidazole, furan and thiophene, quinoline, isoquinoline, benzimidazole, benzofuran, benzothiophene, indole.
  • Certain compounds of formula (I) are capable of existing in stereoisomeric forms. It will be understood that the invention encompasses all geometric and optical isomers of the compounds of formula (I) and mixtures thereof including racemates. Tautomers and mixtures thereof also form an aspect of the present invention.
  • Preferably X is N and Y is :CH, X and Y are :CH or X and Y are CH2
  • Preferably R is C1-4alkyl, or phenyl substituted by halogen, in particular chloro, SO2Me, C1-6alkoxy, in particular methoxy, C1-4alkyl, in particular methyl or propyl.
  • Preferably R1 is a group Y(CH2)pR7 where p is 0 and Y is NR8 where R8 is hydrogen and R7 is substituted phenyl. Preferably R7 is phenyl substituted by halogen, especially chloro; or R1 is NR9R10 where R9 and R10 are hydrogen or C1-3 alkyl or together with the nitrogen atom to which they are attached form a 5 or 6-membered saturated ring optionally containing a O, S or NR4.
  • Preferred compounds of the invention include:
    • 1-[9-(4-Chlorophenyl)-2-cyano-9H-purin-6-yl]-L-prolinamide,
    • 9-(4-Chlorophenyl)-6-(4-pyrrolidin-1-ylpiperidin-1-yl)-9H-purine-2-carbonitrile,
    • 9-(4-Chlorophenyl)-6-[(3-pyrrolidin-1-ylpropyl)amino]-9H-purine-2-carbonitrile,
    • 6-(4-Aminopiperidin-1-yl)-9-(4-chlorophenyl)-9H-purine-2-carbonitrile,
    • 6-[(2-Aminoethyl)amino]-9-(4-chlorophenyl)-9H-purine-2-carbonitrile,
    • 9-(4-Chlorophenyl)-6-(dimethylamino)-9H-purine-2-carbonitrile,
    • 9-(4-Methylphenyl)-6-pyrrolidin-1-yl-9H-purine-2-carbonitrile,
    • 9-(4-Methoxyphenyl)-6-pyrrolidin-1-yl-9H-purine-2-carbonitrile,
    • 9-(4-chlorophenyl)-6-pyrrolidin-1-yl-9H-purine-2-carbonitrile,
    • 9-(4-Chlorophenyl)-6-(ethylamino)-9H-purine-2-carbonitrile,
    • tert-Butyl 4-[9-(4-chlorophenyl)-2-cyano-9H-purin-6-yl]piperazine-1-carboxylate,
    • 9-(4-Chlorophenyl)-6-piperazin-1-yl-9H-purine-2-carbonitrile,
    • 9-(2-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
    • 9-(3,4-Difluorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 9-(4-Isopropylphenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 9-(4-Methoxyphenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 9-(3-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 9-[4-(Methylsulfonyl)phenyl]-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 6-[(4-Chlorophenyl)amino]-9-ethyl-9H-purine-2-carbonitrile,
    • 9-(4-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 8-Amino-6-[(4-chlorophenyl)amino]-9-ethyl-9H-purine-2-carbonitrile,
    • 8-Amino-9-(4-chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 9-(4-Chlorophenyl)-6-morpholin-4-yl-8-oxo-8,9-dihydro-7H-purine-2-carbonitrile,
    • 9-(4-Chlorophenyl)-8-(dimethylamino)-6-morpholin-4-yl-9H-purine-2-carbonitrile,
    • 7-(4-Chlorophenyl)-4-morpholin-4-yl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
    • 7-(4-Chlorophenyl)-4-(ethylamino)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
    • 4-[(4-Chlorophenyl)amino]-7-ethyl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
    • 1-[7-(4-Chlorophenyl)-2-cyano-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-L-prolinamide,
    • 1-[2-Cyano-7-(4-methoxyphenyl)-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-L-prolinamide,
    • 7-(4-Methoxyphenyl)-4-pyrrolidin-1-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
    • 7-(4-Methoxyphenyl)-4-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
    • 1-(4-Methylphenyl)-4-morpholin-4-yl-1H-pyrazolo[3,4-d]pyrimidine-6-carbonitrile,
      and pharmaceutically acceptable salts thereof.
  • The present invention further provides a process for the preparation of a compound of formula (I) which comprises
      • (i) reaction of a compound of general formula (II)
  • Figure US20080125426A1-20080529-C00002
  • wherein L1 and L2 represent a leaving group (e.g. halide, sulphide, sulfoxide or sulphone group), preferably the sulphide is oxidised to a sulphoxide or sulphone group before displacement. An oxidising agent such as a peracid may be used, for example meta-chloroperbenzoic acid in dichloromethane at room temperature.
  • L1 may be displaced by R1 where R1 is defined in formula (I) and L2 may be displaced by cyanide, preferably using a salt (e.g. lithium, sodium or potassium cyanide). The sequence of displacement of L1, L2 may be varied.
  • Compounds of formula (II) where X═N and Y═:CH or :CNR2R3 may be prepared from compounds of formula (III) by ring cyclisations using, for example diethoxymethyl acetate, FMOC-NCS or R3R2NCSCl. Compounds of formula (II) where X═NH and Y═CO can also be prepared from compounds of formula (III) by reaction with phosgene or phosgene equivalent. The sequence of steps may also be varied, for example compounds of formula (III) may first have L1 and/or L2 displaced before the cyclisation step.
  • Figure US20080125426A1-20080529-C00003
  • Compounds of formula (II) may also be prepared from compound of formula (IV) by reaction with a group R-Z, where R is defined in formula (I) and Z is a leaving group (e.g. halide, activated alcohol).
  • Compounds of formula (II) where X and Y═:CH may also be prepared from compounds of formula (V) and compounds of formula (II) where X and Y═CH2 may also be formed from compounds of formula (VI).
  • Figure US20080125426A1-20080529-C00004
  • According to a further feature of the invention there is provided a compound of the formula (I), or a pharmaceutically acceptable salt thereof, for use as a therapeutic agent.
  • According to a further feature of the present invention there is provided a method for producing inhibition of a cysteine protease in a warm blooded animal, such as man, in need of such treatment, which comprises administering to said animal an effective amount of a compound of the present invention, or a pharmaceutically acceptable salt thereof.
  • The invention also provides a compound of the formula (I), or a pharmaceutically acceptable salt thereof, for use as a medicament; and the use of a compound of the formula (I) of the present invention, or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the inhibition of a cysteine protease in a warm blooded animal, such as man. In particular the compounds of the invention are useful in the treatment of inflammation and immune disorders such as, but not limited to, asthma, rheumatoid arthritis, COPD, multiple sclerosis, Crohn's disease, Alzheimers and pain, such as neuropathic pain. Preferably the compounds of the invention are used to treat pain, especially neuropathic pain.
  • In particular the invention provides the use of a compound of the formula (I) of the present invention, or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the inhibition of Cathepsin S in a warm blooded animal, such as man. In order to use a compound of the formula (I) or a pharmaceutically acceptable salt thereof for the therapeutic treatment of mammals including humans, in particular in the inhibition of a cysteine protease, it is normally formulated in accordance with standard pharmaceutical practice as a pharmaceutical composition.
  • Therefore in another aspect the present invention provides a pharmaceutical composition which comprises a compound of the formula (I) or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable diluent or carrier.
  • The pharmaceutical compositions of this invention may be administered in standard manner for the disease condition that it is desired to treat, for example by oral, rectal or parenteral administration. For these purposes the compounds of this invention may be formulated by means known in the art into the form of, for example, tablets, capsules, aqueous or oily solutions or suspensions, (lipid) emulsions, dispersible powders, suppositories, ointments, creams, drops and sterile injectable aqueous or oily solutions or suspensions.
  • A suitable pharmaceutical composition of this invention is one suitable for oral administration in unit dosage form, for example a tablet or capsule which contains between 100 mg and 1 g of the compound of this invention.
  • In another aspect a pharmaceutical composition of the invention is one suitable for intravenous, subcutaneous or intramuscular injection.
  • Each patient may receive, for example, an intravenous, subcutaneous or intramuscular dose of 1 mgkg−1 to 100 mgkg−1 of the compound, preferably in the range of 5 mgkg−1 to 20 mgkg−1 of this invention, the composition being administered 1 to 4 times per day. The intravenous, subcutaneous and intramuscular dose may be given by means of a bolus injection. Alternatively the intravenous dose may be given by continuous infusion over a period of time. Alternatively each patient will receive a daily oral dose which is approximately equivalent to the daily parenteral dose, the composition being administered 1 to 4 times per day.
  • The following illustrate representative pharmaceutical dosage forms containing the compound of formula (I), or a pharmaceutically-acceptable salt thereof (hereafter compound X), for therapeutic or prophylactic use in humans:
  • (a)
    Tablet I mg/tablet
    Compound X. 100
    Lactose Ph.Eur. 179
    Croscarmellose sodium 12.0
    Polyvinylpyrrolidone 6
    Magnesium stearate 3.0
  • (b)
    Tablet II mg/tablet
    Compound X 50
    Lactose Ph.Eur. 229
    Croscarmellose sodium 12.0
    Polyvinylpyrrolidone 6
    Magnesium stearate 3.0
  • (c)
    Tablet III mg/tablet
    Compound X 1.0
    Lactose Ph.Eur. 92
    Croscarmellose sodium 4.0
    Polyvinylpyrrolidone 2.0
    Magnesium stearate 1.0
  • (d)
    Capsule mg/capsule
    Compound X 10
    Lactose Ph.Eur. 389
    Croscarmellose sodium 100
    Magnesium stearate 1.
  • (e)
    Injection I (50 mg/ml)
    Compound X 5.0% w/v
    Isotonic aqueous solution to 100%
  • Buffers, pharmaceutically-acceptable cosolvents such as polyethylene glycol, polypropylene glycol, glycerol or ethanol or complexing agents such as hydroxy-propyl β cyclodextrin may be used to aid formulation.
    • Note
  • The above formulations may be obtained by conventional procedures well known in the pharmaceutical art. The tablets (a)-(c) may be enteric coated by conventional means, for example to provide a coating of cellulose acetate phthalate.
  • The following examples illustrate the invention.
    • EXAMPLE 1 1-[9-(4-Chlorophenyl)-2-cyano-9H-purin-6-yl]-L-prolinamide (i) 6-Chloro-N˜4˜-(4-chlorophenyl)-2-(propylthio)pyrimidine-4,5-diamine
  • A mixture of 4-chloroaniline (5.33 g), N,N-diisopropylethylamine (7.3 ml) and 5-amino-4,6-dichloro-2-propylthiopyrimidine (10 g) was heated at 100° C. for 48 h. The mixture was partitioned between ethyl acetate and water, the organics dried (MgSO4), and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 50% ethyl acetate in isohexane. Yield 4.6 g
  • MS: APCI(+ve) 329 (M+1)
    • (ii) 6-Chloro-9-(4-chlorophenyl)-2-(propylthio)-9H-purine
  • A solution of the product from step (i) (4.6 g) in diethoxymethylacetate (25 ml) was heated at 80° C. for 8 h. The mixture was added dropwise to a vigorously stirred mixture of water and isohexane (400 ml, 1:1), and the solid filtered. The solid was purified by chromatography on silica eluting with 25% ethyl acetate in isohexane. Yield 2.8 g
  • MS: APCI(+ve) 339 (M+1)
    • (iii) 6-Chloro-9-(4-chlorophenyl)-2-(propylsulfonyl)-9H-purine
  • A mixture of the product from step (ii) (2.8 g) and 3-chloroperoxybenzoic acid (3.6 g, Aldrich 77% max.) in dichloroethane (40 ml) was stirred at room temperature for 2 h, washed with aqueous sodium metabisulphite solution, water, aqueous sodium hydrogencarbonate solution, water, dried (MgSO4) and evaporated under reduced pressure.
  • Yield 2.5 g
  • MS: APCI(+ve) 371 (M+1)
    • (iv) 1-[9-(4-Chlorophenyl)-2-cyano-9H-purin-6-yl]-L-prolinamide
  • A solution of the product from step (iii) (0.2 g), L-prolinamide (0.062 g) and N,N-diisopropylethylamine (0.19 ml) in tetrahydrofuran (10 ml) was stirred at room temperature for 24 h. The solvent was removed, the residue dissolved in N,N-dimethylformamide (10 ml) and sodium cyanide (0.05 g) added and heated at 90° C. for 10 h. The mixture was partitioned between ethyl acetate and water, the organics dried (MgSO4) and evaporated under reduced pressure. The residue was purified by RPHPLC. Yield 0.062 g
  • MS: APCI(+ve) 368 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.67 (1H, s), 7.87-7.65 (4H, 2×d), 6.95 (2H, m), 4.08 (2H, m), 2.97 (1H, m), 2.33-1.96 (4H, m).
    • EXAMPLES 2-12
  • Examples 2-12 were prepared according to the general method of example 1 using the appropriate amines.
    • EXAMPLE 2 9-(4-Chlorophenyl)-6-(4-pyrrolidin-1-ylpiperidin-1-yl)-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 408 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.79-8.77 (1H, s), 7.87-7.70 (4H, 2×d), 2.52-2.49 (8H, m), 2.38-2.32 (1H, m), 2.01-1.43 (8H, m)
    • EXAMPLE 3 9-(4-Chlorophenyl)-6-[(3-pyrrolidin-1-ylpropyl)amino]-9H-purine-2-carbonitrile, trifluoroacetate salt
  • MS: APCI(+ve) 382 (M+1)
  • 1H NMR: (DMSO-d6) δ 9.46 (1H, bs), 8.85-8.58 (2H, 2×m), 7.89-7.71 (4H, 2×d), 3.59-3.01 (8H, m), 2.03-1.84 (6H, m)
    • EXAMPLE 4 6-(4-Aminopiperidin-1-yl)-9-(4-chlorophenyl)-9H-purine-2-carbonitrile, trifluoroacetate salt
  • MS: APCI(+ve) 354 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.86-8.84 (1H, s), 7.98-7.71 (6H, 2×d+m), 3.49-3.30 (5H, m), 2.12-1.50 (4H, m)
    • EXAMPLE 5 6-[(2-Aminoethyl)amino]-9-(4-chlorophenyl)-9H-purine-2-carbonitrile, acetate salt
  • MS: APCI(+ve) 314 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.82 (1H, s), 8.59 (1H, m), 7.89-7.70 (4H, 2×d), 3.94 (2H, brm), 3.55-3.51 (2H, t), 2.83-2.80 (2H, t), 1.88 (3H, s)
    • EXAMPLE 6 9-(4-Chlorophenyl)-6-(dimethylamino)-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 299 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.80-8.79 (1H, s), 7.88-7.69 (4H, 2×d), 3.77 (3H, m), 3.12 (3H, m)
    • EXAMPLE 7 9-(4-Methylphenyl)-6-pyrrolidin-1-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 305 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.71 (1H, s), 7.68-7.42 (4H, 2×d), 4.15-4.12 (2H, t), 3.69-3.65 (2H, t), 2.40 (3H, s), 2.08-1.93 (4H, m)
    • EXAMPLE 8 9-(4-Methoxyphenyl)-6-pyrrolidin-1-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 321 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.66 (1H, s), 7.69-7.15 (4H, 2×d), 4.15-4.12 (2H, t), 3.84 (3H, s), 3.68-3.65 (2H, t), 2.06-1.93 (4H, m)
    • EXAMPLE 9 9-(4-chlorophenyl)-6-pyrrolidin-1-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 325 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.08 (1H, s), 7.65 (2H, d), 7.54 (2H, d), 4.21 (2H, t), 3.79 (2H, t), 2.16-2.09 (2H, m), 2.05-1.99 (2H, m)
    • EXAMPLE 10 9-(4-Chlorophenyl)-6-(ethylamino)-9H-purine-2-carbonitrile
  • MS: APCI(−ve) 297 (M−1)
  • 1H NMR: (DMSO-d6) δ 8.80 (1H, s), 8.63 (1H, t), 7.88 (2H, d), 7.72 (2H, d), 3.57-3.50 (2H, m), 1.21 (3H, t)
    • EXAMPLE 11 tert-Butyl 4-[9-(4-chlorophenyl)-2-cyano-9H-purin-6-yl]piperazine-1-carboxylate
  • MS: APCI(+ve) 440 (M+1)
  • 1H NMR: (CDCl3) δ 8.10 (1H, s), 7.63 (2H, d), 7.55 (2H, d), 4.50-4.40 (4H, brs), 3.62-3.59 (4H, m), 1.51 (9H, s)
    • EXAMPLE 12 9-(4-Chlorophenyl)-6-piperazin-1-yl-9H-purine-2-carbonitrile
  • A solution of the product from example 11 (0.27 g) in dichloromethane (10 ml) and trifluoroacetic acid (5 ml) was stirred at room temperature for 0.5 h then evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 0.4% triethylamine/6% methanol in dichloromethane. Yield 0.06 g
  • MS: APCI(+ve) 340 (M+1)
  • 1H NMR: (CDCl3) δ 8.08 (1H, s), 7.63 (2H, d), 7.54 (2H, d), 4.60-4.00 (4H, brs), 3.03 (4H, t)
    • EXAMPLE 13 9-(2-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile (i) 4-[6-Chloro-5-nitro-2-(propylthio)pyrimidin-4-yl]morpholine
  • Morpholine (2.6 g) was added dropwise to a stirred solution of 4,6-dichloro-5-nitro-2-propylthiopyrimidine (8 g) and N,N-diisopropylethylamine (3.85 g) in acetonitrile (70 ml) at 0° C. After 1 h the solvent was evaporated and the residue partitioned between ethyl acetate and water, the organics dried (MgSO4) and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 25% ethyl acetate in isohexane. Yield 7.1 g
  • MS: APCI(+ve) 319 (M+1)
    • (ii) N-(2-Chlorophenyl)-6-morpholin-4-yl-5-nitro-2-(propylthio)pyrimidin-4-amine
  • A mixture of the product from step (i) (1 g), 2-chloroaniline (0.4 g) and N,N-diisopropylethylamine (0.404 g) in isopropylalcohol (12 ml) was heated at 55° C. for 14 h. The mixture was cooled and the isopropylalcohol decanted off. Yield 0.82 g
  • MS: APCI(+ve) 410 (M+1)
    • (iii) N˜4˜-(2-Chlorophenyl)-6-morpholin-4-yl-2-(propylthio)pyrimidine-4,5-diamine
  • A mixture of the product from step (ii) (0.82 g) and iron powder (1.2 g) in glacial acetic acid (40 ml) was stirred at room temperature until the starting material was consumed. The solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and aqueous sodium hydrogen carbonate solution. The organics were dried (MgSO4) and evaporated under reduced pressure. Crude yield 0.82 g
  • MS: APCI(+ve) 380/2 (M+1)
    • (iv) 9-(2-Chlorophenyl)-6-morpholin-4-yl-2-(propylthio)-9H-purine
  • A solution of the product from step (i) (0.82 g) in diethoxymethylacetate (8 ml) was heated at 80° C. for 16 h. The mixture was added dropwise to a vigorously stirred mixture of water and isohexane (300 ml, 1:1), ethyl acetate added, the organic layer dried (MgSO4) and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 25% ethyl acetate in isohexane. Yield 0.42 g
  • MS: APCI(+ve) 390/2 (M+1)
    • (v) 9-(2-Chlorophenyl)-6-morpholin-4-yl-2-(propylsulfonyl)-9H-purine
  • A mixture of the product from step (iv) (2.8 g) and 3-chloroperoxybenzoic acid (0.63 g, Aldrich 77% max.) in dichloromethane (15 ml) was stirred at room temperature for 5 h, washed with aqueous sodium metabisulphite solution, water, aqueous sodium hydrogencarbonate solution, water, dried (MgSO4) and evaporated under reduced pressure. Crude yield 0.74 g
  • MS: APCI(+ve) 422/4 (M+1)
    • (vi) 9-(2-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • Sodium cyanide (0.086 g) was added to a solution of the product from step (v) (0.74 g) in dimethylsulphoxide (10 ml) and heated at 60° C. for 36 h. The mixture was partitioned between ethyl acetate and brine, the organics washed with brine, dried (MgSO4) and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 16% ethyl acetate in toluene. Yield 0.152 g
  • MS: APCI(+ve) 341 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.69 (1H, s), 7.80 (1H, d), 7.73-7.60 (3H, m), 3.78 (4H, t).
    • EXAMPLES 14-18
  • Examples 14-18 were prepared according to the general method of example 13 using the appropriate amines.
    • EXAMPLE 14 9-(3,4-Difluorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 343 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.83 (1H, s), 8.06-8.01 (1H, m), 7.79-7.71 (2H, m), 3.77 (4H, t)
    • EXAMPLE 15 9-(4-Isopropylphenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 349 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.77 (1H, s), 7.68 (2H, d), 7.50 (2H, d), 3.76 (4H, t), 3.04-2.97 (1H, m), 1.26 (6H, d)
    • EXAMPLE 16 9-(4-Methoxyphenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 337 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.73 (1H, s), 7.67 (2H, d), 7.16 (2H, d), 4.20 (4H, broad S), 3.85 (3H, s), 3.76 (4H, t)
    • EXAMPLE 17 9-(3-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 341 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.87 (1H, s), 7.98 (1H, s), 7.85-7.82 (1H, m), 7.68 (1H, t), 7.62-7.59 (1H, m), 4.25 (4H, broad S), 3.77 (4H, t)
    • EXAMPLE 18 9-[4-(Methylsulfonyl)phenyl]-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • MS: APCI(+ve) 385 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.95 (1H, s), 8.20 (2H, d), 8.13 (2H, d), 4.80-3.90 (4H, brs), 3.77 (4H, t)
    • EXAMPLE 19 6-[(4-Chlorophenyl)amino]-9-ethyl-9H-purine-2-carbonitrile (i) 2-Chloro-N-(4-chlorophenyl)-9H-purin-6-amine
  • A mixture of 4-chloroaniline (1.35 g) and 2,6-dichloropurine (1 g) in n-butanol (15 ml) was heated at 100° C. for 3 h. The precipitate was filtered off, partitioned between ethyl acetate and aqueous sodium hydroxide solution, the organics dried (MgSO4), and evaporated under reduced pressure. The residue was triturated with ethyl acetate and filtered. Yield 1.04 g
  • MS: APCI(+ve) 280/2 (M+1)
    • (ii) 2-Chloro-N-(4-chlorophenyl)-9-ethyl-9H-purin-6-amine
  • A mixture of the product from step (i) (1.04 g), potassium carbonate (1.025 g) and ethyl iodide (0.637 g) in N,N-dimethylformamide (15 ml) was stirred vigorously at room temperature for 2 h. The mixture was partitioned between ethyl acetate and water, the organics washed with water, dried (MgSO4) and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 2:1 ethyl acetate in isohexane. Yield 0.63 g
  • MS: APCI(+ve) 308/310 (M+1)
    • (iii) N-(4-Chlorophenyl)-9-ethyl-2-(methylthio)-9H-purin-6-amine
  • A mixture of the product from step (ii) (0.6 g) and sodium thiomethoxide (0.45 g) in dimethylsulphoxide (15 ml) was heated at 110° C. for 4 h. The mixture was partitioned between ethyl acetate and water, the organics washed with water, dried (MgSO4) and evaporated under reduced pressure. Yield 0.45 g
  • MS: APCI(+ve) 320/322 (M+1)
    • (iv) N-(4-Chlorophenyl)-9-ethyl-2-(methylsulfonyl)-9H-purin-6-amine
  • A mixture of the product from step (iii) (0.45 g) and 3-chloroperoxybenzoic acid (1.2 g, Aldrich 77% max.) in ethanol (20 ml) was stirred at room temperature for 4 h, ethyl acetate was added, the mixture washed with aqueous sodium metabisulphite solution, water, aqueous sodium hydrogencarbonate solution, water, dried (MgSO4) and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 4:1 ethyl acetate in isohexane. Yield 0.39 g
  • MS: APCI(+ve) 352/4 (M+1)
    • (v) 6-[(4-Chlorophenyl)amino]-9-ethyl-9H-purine-2-carbonitrile
  • A mixture of the product from step (iv) (0.13 g) and sodium cyanide (0.054 g) in dimethylsulphoxide (3 ml) was stirred at room temperature for 72 h then partitioned between ethyl acetate and water. The organic layer was washed with water, dried (MgSO4), evaporated under reduced pressure and the residue purified by chromatography on silica eluting with 2:1 ethyl acetate in isohexane. Yield 0.035 g
  • MS: APCI(−ve) 297 (M−1)
  • 1H NMR: (DMSO-d6) δ 10.54 (1H, s), 8.62 (1H, s), 7.90 (2H, d), 7.44 (2H, d), 4.28 (2H, q), 1.46 (3H, t)
    • EXAMPLE 20 9-(4-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile (i) N-(4-Chlorophenyl)-6-morpholin-4-yl-5-nitro-2-(propylthio)pyrimidin-4-amine
  • Morpholine (1.31 ml) was added dropwise to a stirred solution of 4,6-dichloro-5-nitro-2-thiopropyl pyrimidine (4 g) and N,N-diisopropylethylamine (7 ml) in dichloromethane (50 ml) at 0° C. After 1 h, 4-chloroaniline (1.9 g) was added, the mixture stirred at room temperature for 24 h, then heated under reflux for 24 h. The mixture was partitioned between dichloromethane and 2M hydrochloric acid, the organics washed with water, dried (MgSO4) and evaporated under reduced pressure. Yield 5 g
  • MS: APCI(+ve) 410/2 (M+1)
    • (ii) 4-[(4-Chlorophenyl)amino]-6-morpholin-4-yl-5-nitropyrimidine-2-carbonitrile
  • A mixture of the product from step (i) (5 g) and 3-chloroperoxybenzoic acid (12 g, Aldrich 77% max.) in dichloromethane (200 ml) was stirred at room temperature for 2 h, washed with aqueous sodium metabisulphite solution, water, aqueous sodium hydrogencarbonate solution, water, dried (MgSO4) and evaporated under reduced pressure. The solid was dissolved in dimethylsulphoxide (30 ml), sodium cyanide (2 g) added and stirred for 1 h at room temperature. Water (500 ml) was added and the solid filtered, washed with water, dried and the residue triturated with ether. Yield 1.7 g
  • MS: APCI(+ve) 361/3 (M+1)
    • (iii) 5-Amino-4-[(4-chlorophenyl)amino]-6-morpholin-4-ylpyrimidine-2-carbonitrile
  • The product from step (ii) (1.7 g) and 10% palladium on charcoal (0.2 g) in ethyl acetate (300 ml) was hydrogenated at 2 Bar for 8 h, filtered through celite and the solvent evaporated under reduced pressure. Yield 1.05 g
  • MS: APCI(+ve) 329/331 (M+1)
    • (iv) 9-(4-Chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • A solution of the product from step (iii) (0.35 g) in diethoxymethylacetate (10 ml) was heated at 80° C. for 12 h, water added and the precipitate filtered. The solid was purified by chromatography on silica eluting with 30-40% ethyl acetate in isohexane. Yield 0.26 g
  • MS: ESI 341 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.84 (1H, s), 7.86 (2H, d), 7.72 (2H, d), 3.78-3.75 (4H, m), 4.3 (4H, brs)
    • EXAMPLE 21 8-Amino-6-[(4-chlorophenyl)amino]-9-ethyl-9H-purine-2-carbonitrile
  • A solution of 5-amino-4-[(4-chlorophenyl)amino]-6-(ethylamino)pyrimidine-2-carbonitrile (0.41 g, prepared using the method of example 20) in acetonitrile (5 ml) was added to a stirred solution of FMOC-NCS (0.44 g) in acetonitrile (10 ml) at 0° C. After 1 h, diisopropylcarbodiimide (0.252 g) was added, the mixture heated under reflux for 4 h, cooled, piperazine (0.1 g) added and stirred at room temperature for 3 h. The solvent was removed under reduced pressure and the residue partitioned between ethyl acetate and brine, the organics dried (MgSO4) and evaporated under reduced pressure. The solid was purified by chromatography on silica eluting with 2-4% methanol in dichloromethane.
  • Yield 0.12 g
  • MS: APCI(+ve) 314 (M+1)
  • 1H NMR: (DMSO-d6) δ 9.62 (1H, s), 7.83 (2H, d), 7.37 (2H, d), 7.14 (2H, s), 4.08 (2H, q), 1.26 (3H, t)
    • EXAMPLE 22 8-Amino-9-(4-chlorophenyl)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • A mixture of the product from example 20 step (iii) (0.6 g) and FMOC-NCS (0.613 g) in dichloromethane was heated at 40° C. for 10 h. The mixture was cooled, 1,4-diisopropylcarbodiimide (0.422 ml) was added, heated for 5 h then piperidine (1 ml) added and stirred at room temperature for 3 h. The solvent was evaporated under reduced pressure, the residue triturated with ether and recrystallised form water and dimethylsulphoxide. Yield 0.344 g
  • MS: APCI(+ve) 356/8 (M+1)
  • 1H NMR: (DMSO-d6) δ 7.68 (2H, d), 7.52 (2H, d), 6.97 (2H, s), 4.15-4.08 (4H, m), 3.73-3.71 (4H, m)
    • EXAMPLE 23 9-(4-Chlorophenyl)-6-morpholin-4-yl-8-oxo-8,9-dihydro-7H-purine-2-carbonitrile
  • Triphosgene (0.09 g) was added to a mixture of the product from example 20 step (iii) (0.4 g) and pyridine (0.4 ml) in dichloromethane (30 ml) and the mixture stirred at room temperature. After 1 h more triphosgene (0.02 g) was added, stirred for a further 1 h, water added and the solid filtered. The solid was washed with water, diethylether and dried.
  • Yield 0.14 g
  • MS: APCI(−ve) 355/7 (M−1)
  • 1H NMR: (DMSO-d6) δ 11.90 (1H, s), 7.66-7.61 (4H, m), 3.73-3.71 (4H, m), 3.62-3.59 (4H, m)
    • EXAMPLE 24 9-(4-Chlorophenyl)-8-(dimethylamino)-6-morpholin-4-yl-9H-purine-2-carbonitrile
  • A mixture of the product from example 20 step (iii) (0.2 g) and dimethylthiocarbamoyl chloride (0.1 g) in acetonitrile (15 ml) was heated at 60° C. for 6 h. The precipitate was filtered, the filtrate evaporated under reduced pressure and the residue purified by chromatography on silica eluting with 40% ethyl acetate in isohexane. Yield 0.034 g
  • MS: APCI(+ve) 384 (M+1)
  • 1H NMR: (DMSO-d6) δ 7.68 (2H, d), 7.58 (2H, d), 4.15 (4H, brs), 3.75-3.72 (4H, m), 2.76 (6H, s)
    • EXAMPLE 25 7-(4-Chlorophenyl)-4-morpholin-4-yl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile (i) 5-Allyl-2,6-dichloro-N-(4-chlorophenyl)pyrimidin-4-amine
  • A mixture of 5-allyl-2,4,6-trichloropyrimidine (7 g), 4-chloroaniline (4 g) and potassium carbonate (4.27 g) in ethanol (100 ml) was stirred at room temperature for 24 h. The mixture was partitioned between ethyl acetate and water, the organics dried (MgSO4), and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with isohexane/diethylether (2:1). Yield 5 g
  • MS: APCI(+ve) 314 (M+1)
    • (ii) {2,4-Dichloro-6-[(4-chlorophenyl)amino]pyrimidin-5-yl}acetaldehyde
  • A solution of the product from step (i) (2 g) in dichloromethane (40 ml) was added to a solution of osmium tetroxide (1 ml, 2.5% wt in isopropylalcohol) and 4-methylmorpholine N-oxide (1.12 g) in dichloromethane (1 ml). After stirring at room temperature for 24 h the mixture was washed with water, aqueous sodium sulphite solution, dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved in methanol (40 ml), cooled to 0° C. and lead tetraacetate (3.85 g) added. After 1 h the mixture was diluted with water, extracted with ethyl acetate, the organics dried (MgSO4) and evaporated under reduced pressure. Yield 2 g
  • MS: APCI(+ve) 316 (M+1)
    • (iii) 2,4-Dichloro-7-(4-chlorophenyl)-7H-pyrrolo[2,3-d]pyrimidine
  • A solution of the product from step (ii) (2 g) and p-toluenesulfonic acid (catalytic) in methanol (30 ml) was stirred at room temperature for 2 h then evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with isohexane/diethylether (2:1). Yield 0.5 g
  • MS: APCI(+ve) 298/300 (M+1)
    • (iv) 7-(4-Chlorophenyl)-2,4-bis(ethylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine
  • Sodium ethanethiolate (0.437 g) was added to a solution of the product from step (iii) (0.5 g) in dimethylsulphoxide (20 ml), stirred at room temperature for 30 min then partitioned between ethyl acetate and water. The organics were dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved in dichloromethane (20 ml), 3-chloroperoxybenzoic acid (1.5 g, Aldrich 77% max.) added, the mixture stirred at room temperature for 2 h, washed with aqueous sodium metabisulphite solution, water, aqueous sodium hydrogencarbonate solution, water, dried (MgSO4) and evaporated under reduced pressure. Crude yield 1 g
  • MS: APCI(+ve) 414 (M+1)
    • (v) 7-(4-Chlorophenyl)-4-morpholin-4-yl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
  • A mixture of the product from step (iv) (0.35 g), morpholine (0.11 ml) and N,N-diisopropylethylamine (0.22 ml) in tetrahydrofuran (10 ml) was stirred at room temperature for 24 h. The mixture was partitioned between ethyl acetate and water, the organics dried (MgSO4) and evaporated under reduced pressure. The residue was dissolved in N,N-dimethylformamide (10 ml), sodium cyanide (0.083 g) added and the mixture heated at 90° C. for 10 h. Water was added, the solid filtered off then purified by RPHPLC 25-95% acetonitrile in aqueous trifluoroacetic acid. Yield 0.075 g
  • MS: APCI(+ve) 340 (M+1)
  • 1H NMR: (DMSO-d6) δ 7.94-7.64 (5H, m), 7.11 (1H, m), 3.94-3.74 (8H, m)
    • EXAMPLE 26 7-(4-Chlorophenyl)-4-(ethylamino)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
  • The above named example was prepared according to the general method of example 25 using the appropriate amine.
  • MS: APCI(+ve) 298 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.26 (1H, t), 7.81-7.63 (5H, m), 6.95-6.94 (1H, m), 3.55-3.49 (2H, q), 1.25-1.21 (3H, t)
    • EXAMPLE 27 4-[(4-Chlorophenyl)amino]-7-ethyl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile (i) 4-Chloro-7-ethyl-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidine
  • Sodium hydride (0.44 g, 60% dispersion in oil) was added portionwise to a stirred solution of 4-chloro-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidine (2 g) in N,N-dimethylformamide (30 ml) at 0° C. After 0.75 h, ethyl iodide (0.88 ml) was added, the mixture stirred for 2 h, quenched with water and partitioned between ethyl acetate and brine. The organics were washed with water, dried (MgSO4), evaporated under reduced pressure and the residue purified by chromatography on silica eluting with 15% ethyl acetate in isohexane. Yield 1.98 g
  • MS: APCI(+ve) 228/230 (M+1)
    • (ii) N-(4-Chlorophenyl)-7-ethyl-2-(methylthio)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
  • A solution of the product from step (i) (0.5 g) and 4-chloroaniline (0.84 g) in ethanol (10 ml) was heated under reflux for 24 h then the solvent evaporated under reduced pressure. The residue was partitioned between ethyl acetate and 2M hydrochloric acid, the organics washed with water, dried (MgSO) and evaporated under reduced pressure. Yield 0.7 g
  • MS: APCI(+ve) 319/321 (M+1)
    • (iii) N-(4-Chlorophenyl)-7-ethyl-2-(methylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
  • A mixture of the product from step (ii) (0.7 g) and 3-chloroperoxybenzoic acid (1.38 g, Aldrich 77% max.) in dichloromethane (30 ml) was stirred at room temperature for 1 h, washed with aqueous sodium metabisulphite solution, water, aqueous sodium hydrogencarbonate solution, water, dried (MgSO4) and evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 50% ethyl acetate in isohexane. Yield 0.37 g
  • MS: APCI(+ve) 351/3 (M+1)
    • (iv) 4-[(4-Chlorophenyl)amino]-7-ethyl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
  • Sodium cyanide (0.103 g) was added to a solution of the product from step (iii) (0.37 g) in dimethylsulphoxide (10 ml) and heated at 90° C. for 48 h. The mixture was partitioned between ethyl acetate and water, the organics dried (MgSO4) and evaporated under reduced pressure. The residue was purified by RPHPLC eluting with 29-95% acetonitrile in aqueous trifluoroacetic acid. Yield 0.14 g
  • MS: APCI(+ve) 298/300 (M+1)
  • 1H NMR: (DMSO-d6) δ 9.94 (1H, s), 7.83 (2H, d), 7.67 (1H, d), 7.46 (2H, d), 6.93 (1H, d), 4.26 (2H, q), 1.38 (3H, t)
  • Mpt 183° C.
    • EXAMPLE 28 1-[7-(4-Chlorophenyl)-2-cyano-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-L-prolinamide (i) Methyl 2-oxotetrahydrofuran-3-carboxylate
  • Cyclopropane-1,1-dicarboxylic acid (10 g) in acetonitrile (200 ml) was treated with triethylamine (43 ml) and iodomethane (19 ml) at room temperature. The solution was stirred for 2 h then heated at 75° C. for 16 h. The solvent was removed under reduced pressure, the residue dissolved in water, extracted with ethyl acetate, dried(MgSO4) and evaporated to a brown oil (6.70 g).
  • 1H NMR: (CDCl3) δ 4.55-4.30 (2H, m), 3.82 (3H, s), 3.59-3.55 (1H, m), 2.73-2.47 (2H, m).
    • (ii) 5-(2-Hydroxyethyl)-2-thioxodihydropyrimidine-4,6 (1H,5H)-dione
  • A solution of the product from step (i) (6.70 g) in absolute ethanol (70 ml) was treated with thiourea (3.53 g) and triethylamine (12.80 ml). The mixture was heated at reflux for 16 h, the solvent was removed under reduced pressure and the solid dissolved in water (100 ml). The solution was acidified with conc. hydrochloric acid to pH2 and extracted with ethyl acetate. Continuous extraction of the aqueous layer with dichloromethane for 80 h gave a brown solid (2.20 g).
  • MS: APCI(+ve) 189 (M+1)
    • (iii) 5-(2-Hydroxyethyl)-2-(methylthio)pyrimidine-4,6 (1H,5H)-dione
  • A solution of the product of step (ii) (2.2 g) in methanol (10 ml) was added to a solution of sodium (0.27 g) in methanol (90 ml). Iodomethane (0.73 ml) was added and the mixture heated at reflux for 1 hour. The solvent was removed under reduced pressure to give a solid.
  • MS: APCI(+ve) 203 (M+1)
    • (iv) 4,6-Dichloro-5-(2-chloroethyl)-2-(methylthio)pyrimidine
  • The product from step (iii) and phosphorus oxychloride (30 ml) was heated at 100° C. for 3 h. The excess reagent was removed under reduced pressure, the residue quenched with ice-water, extracted with ethyl acetate, dried(MgSO4) and evaporated to an oil. The oil was purified by chromatography on silica eluting with isohexane:diethylether(4:1) to give a brown oil (0.36 g).
  • MS: APCI(+ve) 257/259 (M+1)
    • (v) 4-Chloro-7-(4-chlorophenyl)-2-(methylthio)-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine
  • A solution of the product from step (iv) (0.36 g) in acetonitrile (10 ml) was treated with 4-chloroaniline (0.18 g) and N,N-diisopropylethylamine (0.25 ml). The mixture was heated at 150° C., the solvent evaporated to form a melt which solidified after heating for 90 min. The solid was subjected to column chromatography eluting with isohexane:dichloromethane (1:1) to give a yellow solid (0.110 g).
  • MS: APCI(+ve) 312 (M+1)
    • (vi) 4-Chloro-7-(4-chlorophenyl)-2-(methylsulfonyl)-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine
  • A mixture of the product from step (v) (0.11 g) and 3-chloroperoxybenzoic acid (0.15 g) in dichloromethane (20 ml) was stirred at room temperature for 2 h. The mixture was diluted with dichloromethane (100 ml) and washed with sodium metabisulphite solution followed by sodium hydrogencarbonate solution, dried(MgSO4) and evaporated to an orange solid (0.1 g).
  • MS: APCI(+ve) 344 (M+1)
    • (vii) 4-Chloro-7-(4-chlorophenyl)-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
  • A mixture of the product from step (vi) (0.1 g) and sodium cyanide (0.022 g) in dimethylsulfoxide (10 ml) was stirred at room temperature for 2 h. The mixture was partitioned between ethyl acetate and water, the organics separated, dried (MgSO4) and evaporated to a yellow solid (0.1 g).
  • MS: APCI(+ve) 291 (M+1)
    • (viii) 1-[7-(4-Chlorophenyl)-2-cyano-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-L-prolinamide
  • A mixture of the product from step (vii) (0.1 g), L-prolinamide (0.039 g) and N,N-diisopropylethylamine (0.09 ml) in dimethylsulphoxide (10 ml) was heated at 100° C. for 8 h. The mixture was partitioned between ethyl acetate and water, the organics separated, dried (MgSO4) and evaporated under reduced pressure. The residue was purified by reverse phase HPLC using 50 to 95% acetonitrile in 0.1% ammonium acetate buffer to yield a white solid (0.03 g)
  • MS: APCI(+ve) 369 (M+1)
  • 1H NMR: (DMSO-d6) δ 7.72-7.02 (6H, m), 4.52-3.36 (7H, m), 2.14-1.90 (4H, m).
    • EXAMPLES 29-32
  • Examples 29-32 were prepared according to the method of example 28 steps (vi)-(viii).
    • EXAMPLE 29 1-[2-Cyano-7-(4-methoxyphenyl)-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-L-prolinamide
  • MS: APCI(+ve) 365 (M+1)
  • 1H NMR: (DMSO-d6) δ 7.55-6.95 (6H, m), 4.51-3.67 (8H, m), 3.49-3.40 (2H, m), 2.13-1.89 (4H, m).
    • EXAMPLE 30 7-(4-Methoxyphenyl)-4-pyrrolidin-1-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
  • MS: APCI(+ve) 322 (M+1)
  • 1H NMR: (DMSO-d6) δ 7.55-6.94 (4H, m), 3.99-3.38 (11H, m), 1.89-1.85 (4H, m).
    • EXAMPLE 31 7-(4-Methoxyphenyl)-4-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile
  • MS: APCI(+ve) 338 (M+1)
  • 1H NMR: (DMSO-d6) δ 7.55-7.51 (2H, d), 6.99-6.96 (2H, d), 4.04-3.60 (13H, m), 3.33-3.28 (2H, m).
    • EXAMPLE 32 1-(4-Methylphenyl)-4-morpholin-4-yl-1H-pyrazolo[3,4-d]pyrimidine-6-carbonitrile
  • MS: APCI(+ve) 321 (M+1)
  • 1H NMR: (DMSO-d6) δ 8.71 (1H, s), 7.89-7.87 (2H, d), 7.42-7.39 (2H, d), 4.04-3.97 (4H, m), 3.80-3.77 (4H, m), 2.39 (3H, s).
    • Measurement of Cathepsin S Activity.
  • QFRET Technology (Quenched Fluorescent Resonance Energy Transfer) was used to measure the inhibition by test compounds of Cathepsin S-mediated cleavage of the synthetic peptide Z-Val-Val-Arg-AMC. Compounds were screened at five concentrations in duplicate and the pIC50 values reported.
  • Synthetic substrate, 20 μM [final]Z-Val-Val-Arg-AMC in phosphate buffer were added to a 96 well black Optiplate. The assay plates were pre-read for compound auto fluorescence on SpectraMax Gemini at 355 nM excitation and 460 nM emission. 250 pM [final] rHuman Cathepsin S in phosphate buffer was added and incubated for 2 h at room temperature on the SpectraMax Gemini, taking readings every 20 min at 355 nM excitation and 460 nM emission.
  • Activity Based template (5PTB-8) used the auto fluorescent corrected data to calculate the percentage inhibition for each compound concentration using the relevent plate controls. This data was used to construct inhibition curves and pIC50 estimated by non-linear regression using a 4 parameter logistic model.

Claims (9)

1. A compound of formula (I):
Figure US20080125426A1-20080529-C00005
in which:
X is CH or CH2;
Y is CH, CO, CH2 or :CNR2R3, where R2 and R3 are independently hydrogen, C1-6 alkyl or
C3-6 cycloalkyl;
R is aryl or heteroaryl optionally substituted by halogen, amino, hydroxy, cyano, nitro, trifluoromethyl, carboxy, CONR5R6, SO2NR5R6, SO2R4, NHSO2R4, NHCOR4, ethylenedioxy, methylenedioxy, C1-6 alkyl, C1-6 alkoxy, SR4 or NR5R6 where R4 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl, R5 and R6 are independently hydrogen, C1-6 alkyl or together with the nitrogen atom to which they are attached form a 5- or 6-membered saturated ring optionally containing a further O, S or NR4 group;
or R is hydrogen, C1-6 alkyl or C3-6 cycloalkyl,
R1 is a group Y(CH2)pR7 where p is 0, 1 or 2 and Y is O or NR8 where R8 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl;
and R7 is a 5- or 6-membered saturated ring containing one or more O, S or N atoms, aryl or a heteroaryl group containing one to four heteroatoms selected from O, S or N, the saturated ring, aryl and heteroaryl groups all being optionally substituted by halogen, amino, hydroxy, cyano, nitro, trifluoromethyl, carboxy, CONR5R6, SO2NR5R6, SO2R4, NHSO2R4, NHCOR4, C1-6 alkyl, C1-6 alkoxy, SR4 or NR5R6 where R4 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl, R5 and R6 are independently hydrogen, C1-6 alkyl or together with the nitrogen atom to which they are attached form a 5- or 6-membered saturated ring optionally containing a further O, S or NR4 group;
or R1 is a group NR9R10 where R9 and R10 are independently hydrogen or C1-6 alkyl, or R9 and R10 together with the nitrogen atom to which they are attached form a 5 or 6-membered saturated ring optionally containing a further O, S or N atom and optionally substituted by a second NR9R10 where R9 and R10 are independently hydrogen or C1-6 alkyl or R9 and R10 together with the nitrogen atom to which they are attached form a 5 or 6-membered saturated ring optionally containing a further O, S or NR4, CO2C1-6 alkyl, CONR1R2 where R11 and R12 are independently hydrogen or C1-6 alkyl, aryl or heteroaryl group optionally substituted by halogen, amino, hydroxy, cyano, nitro, trifluoromethyl, carboxy, CONR5R6, SO2NR5R6, SO2R4, NHSO2R4, NHCOR4, C1-6 alkyl, C1-6 alkoxy, SR4 or NR5R6 where R4 is hydrogen, C1-6 alkyl or C3-6 cycloalkyl, R5 and R6 are independently hydrogen, C1-6 alkyl or together with the nitrogen atom to which they are attached form a 5- or 6-membered saturated ring optionally containing a further O, S or NR4 group;
and pharmaceutically acceptable salts or solvates thereof.
2. A compound according to claim 1, wherein R1 is C1-4alkyl, or phenyl substituted by halogen, SO2Me, C1-6alkoxy or C1-4alkyl.
3. A compound according to claim 1, wherein R1 is a group Y(CH2)pR7 where p is 0 and Y is NR8 where R8 is hydrogen and R7 is substituted phenyl.
4. A compound according to claim 1, wherein R1 is NR9R10 where R9 and R10 are hydrogen or C1-3 alkyl or together with the nitrogen atom to which they are attached form a 5 or 6-membered saturated ring optionally containing a further O, S or NR4.
5. A compound of formula (I) according to claim 1 selected from:
7-(4-Chlorophenyl)-4-morpholin-4-yl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
7-(4-Chlorophenyl)-4-(ethylamino)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
4-[(4-Chlorophenyl)amino]-7-ethyl-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
1-[7-(4-Chlorophenyl)-2-cyano-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-L-prolinamide,
1-[2-Cyano-7-(4-methoxyphenyl)-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl]-L-prolinamide,
7-(4-Methoxyphenyl)-4-pyrrolidin-1-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
7-(4-Methoxyphenyl)-4-morpholin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine-2-carbonitrile,
and pharmaceutically acceptable salts thereof.
6. A pharmaceutical composition which comprises a compound of the formula (I) as defined in claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable diluent or carrier.
7. A method for producing inhibition of at least one cysteine protease chosen from cathepsins S, K, L, F and B in a mammal comprising administering to said mammal an effective amount of a compound as defined in claim 1, or a pharmaceutically acceptable salt thereof.
8. A method for treating pain in a mammal in need of such treatment comprising administering to said mammal an effective amount of a compound as defined in claim 1, or a pharmaceutically acceptable salt thereof.
9. A method for inhibiting Cathepsin S in a warm blooded animal comprising administering a compound of the formula (I) as defined in claim 1 or a pharmaceutically acceptable salt thereof to a warm blooded animal.
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