WO2015161924A1 - 3-oxo-tetrahydro-furo[3,2-b]pyrrol-4(5h)-yl) derivatives ii - Google Patents
3-oxo-tetrahydro-furo[3,2-b]pyrrol-4(5h)-yl) derivatives ii Download PDFInfo
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- WO2015161924A1 WO2015161924A1 PCT/EP2015/000839 EP2015000839W WO2015161924A1 WO 2015161924 A1 WO2015161924 A1 WO 2015161924A1 EP 2015000839 W EP2015000839 W EP 2015000839W WO 2015161924 A1 WO2015161924 A1 WO 2015161924A1
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- alkyl
- pyrrol
- furo
- chloro
- cyclopentyl
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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- 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
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- 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]
Definitions
- the present invention relates to compounds that are dual inhibitors of the cysteine proteinases cathepsin S (CatS) and cathepsin K (CatK), pharmaceutical com positions containing said compounds, and their use in medical therapy. Such compounds are particularly useful for the therapeutic treatment of diseases which are at least partially modulated by CatS and CatK.
- Cysteine proteases represent a specific class of peptidases which bear a cysteine residue in the catalytic site of the enzyme. Many pathological disorders or diseases are the results of abnormal activity of cysteine proteases such as over expression or enhanced activation.
- the cysteine cathepsins are a class of lysosomal protease enzymes which are implicated in a multitude of house-keeping roles, but also in various disease processes and disorders including inflammation, autoimmune diseases, e.g. rheumatoid arthritis, psoriasis, asthma, osteoarthritis, osteoporosis, tumors, coronary disease, atherosclerosis, and infectious diseases.
- autoimmune diseases e.g. rheumatoid arthritis, psoriasis, asthma, osteoarthritis, osteoporosis, tumors, coronary disease, atherosclerosis, and infectious diseases.
- cathepsin S In contrast to the ubiquitously expressed housekeeping enzymes cathepsins B, 0 and L, cathepsin S (CatS) is highly expressed in antigen presenting cells of lymphatic tissues, primarily in dendritic cells, B cells and macrophages (Wiener et al., Curr. Top. Med. Chem. , 2010, 10, 717). In the antigen presenting cells, CatS plays a major role in antigen presentation by degradation of invariant chain that is associated with the major histocompatibility class II complex.
- Destruction of the ECM takes place through proteolysis of its elastin, collagen and proteoglycan constituents, which provide structure, elasticity and tensile strength to materials such as cartilage, bone, lung and vascular tissue.
- US 2007/01 17785 discloses inhibitors of CatS, supporting the use of CatS inhibitors for the treatment of certain allergic conditions, such as rheumatoid arthritis or psoriasis.
- CatS has also been demonstrated to mediate a pro-nociceptive effect, thereby indicating that endogenous CatS released by peripheral macrophages may contribute to the maintenance of neuropathic hyperalgesia following nerve injury (Barclay et al., Pain, 2007, 130, 225).
- CatK is predominantly expressed in osteoclasts (Yasuda et al., Adv. Drug Deliv. Rev. , 2005, 57, 973).
- CatK is involved in extracellular matrix metabolism necessary for normal bone growth and remodelling (Bossard et al., J. Biol. Chem. 1996, 271 , 12517).
- inhibition of CatK should result in a reduction of osteoclast mediated bone resorption.
- Odanacatib has been validated in humans for the treatment of osteoporosis (Zerbini and McClung, Ther. Adv.
- the proteolytic enzymes cathepsin S and cathepsin K are up-regulated under inflammatory conditions and have been implicated in the degradation of ECM components.
- CatK and CatS are found over-expressed in rheumatoid and osteoarthritic synovium. They have been shown to degrade collagen type-l and type-ll, as well as aggrecan (a multidomain proteoglycan component of articular cartilage) respectively (Yasuda et al., Adv. Drug Deliv. Rev., 2005, 57, 973).
- CatS and CatK Besides destruction of articular cartilage, CatS and CatK demonstrate potent elastinolytic activity and are involved in a broad spectrum of pathological conditions associated with elastin degradation, such as COPD and cardiovascular disease. Both enzymes are readily secreted by macrophages and smooth muscle cells and have been shown to degrade elastins from bovine aorta and lung tissue. CatS and CatK are also responsible for the vascular tissue damage associated with chronic cardiovascular disease and vascular injury.
- CatS and CatK have been found to play a crucial role in in atherosclerotic lesion destabilization and eventually induction of atherosclerotic plaque rupture (Sukhova et al., J. Clin. Invest., 1998, 102, 576). CatS and CatK have also been associated with vascular remodeling and causing ECM damage during the development of atherosclerosis and vascular injury-induced neointimal formation (Cheng et al. , Am. J. Pathol., 2004, 164, 243).
- WO 2009/1 12839 A1 describes particular 6-( iS)-chlorotetrahydrofuro[3,2-fo]pyrrol-3-ones according to general formula (I * ), exhibiting potent dual inhibition versus both human CatS and CatK:
- CatL cathepsin L
- CatL knock-out mice Petermann et al., FASEB J. 2006, 20, 1266; Stypmann et al., PNAS, 2002, 99, 6234.
- disruption of the cathepsin L gene leads to major abnormalities in skin and hair development and differentiation and alterations in trabecular bone deposition (Potts et al, Int. J. Exp. Path. 2004, 85, 85).
- the cathepsins K, L and S possess a high sequence homology (Lee-Dutra et al., Expert Opin. Ther. Patents 201 1 , 21 , 31 1 ; Turk et al., Biochim. Biophys. Acta, 2012. 1824, 68). Therefore, a sufficient selectivity over ubiquitously expressed CatL to avoid the undesired effects associated with inhibition of CatL is regarded to be one of the prerequisites for therapeutic suitability of CatS inhibitors (Wiener et al., Curr. Top. Med. Chem. 2010, 10, 717), but will equally refer to dual CatS/CatK inhibitors.
- the compounds should be suitable in particular as pharmacological active ingredients in pharmaceutical compositions, preferably in pharmaceutical compositions for the treatment and/or prophylaxis of disorders or diseases which are at least partially mediated by both human CatS and human CatK.
- the compounds according to the invention have surprisingly been found not to possess an equipotent dual inhibition versus both human CatS and CatK. Instead, they exhibit a more pronounced inhibition of human CatK, while still retaining high inhibition versus human CatS. As CatK is predominantly expressed in osteoclasts, compounds with an unbalanced dual inhibition mode on human CatS and CatK may be particularly suitable for the treatment of inflammatory bone diseases, such as rheumatoid arthritis or osteoarthritis.
- the present invention therefore relates to a compound of general formula (I),
- R 1 represents H or F
- X represents S or O
- Y 1 and Y 2 independently represents CH or N;
- Z 1 , Z 2 , Z 3 , Z 4 and Z 5 independently represents CH or N, with the proviso that 1 , 2 or 3 of Z 1 , Z 2 , Z 3 , Z 4 and
- n 0, 1 or 2;
- n denotes 0, 1 , 2 or 3;
- substituents Ci. 4 -alkyl and cyclopropyl may in each case be unsubstituted or substituted one or more times by identical or different substituents, and the above-mentioned substituent C ⁇ -alkyl may in each case be branched or unbranched; in the form of an individual stereoisomer or a mixture thereof; in the form of a tautomer; of a free compound; of an N-oxide; or in the form of a solvate and/or of a physiologically acceptable salt.
- physiologically acceptable salt preferably comprises in the sense of this invention a salt of at least one compound according to the present invention and at least one physiologically acceptable acid or base.
- physiologically acceptable solvate preferably comprises in the sense of this invention an adduct of one compound according to the present invention and/or a physiologically acceptable salt of at least one compound according to the present invention with distinct molecular equivalents of one solvent or more solvents.
- C _ 4 -alkyl comprise in the sense of this invention acyclic saturated aliphatic hydrocarbon residues, which can be respectively branched or unbranched and can be unsubstituted or can be mono- or polysubstituted, e.g. mono-, di- or trisubstituted, and which contain 1 to 6 carbon atoms, i.e. 1 , 2, 3 or 4 carbon atoms.
- Preferred C 1-4 -alkyl groups are selected from the group consisting of methyl, ethyl, n-pro- pyl, 2-propyl, n-butyl, isobutyl, sec-butyl and tert-butyl.
- the term "monosubstituted” or “polysubstituted” such as di- or tri-sub- stituted refers in the sense of this invention, with respect to the corresponding groups, to the single substitution or multiple substitution, e.g. disubstitution or trisubstitution, of one or more hydrogen atoms each independently of one another by at least one substituent.
- polysubstituted such as di- or tri- substituted with respect to polysubstituted groups such as di- or tri-substituted groups includes the poly- substitution of these groups either on different or on the same atoms, for example trisubstituted on the same carbon atom, as in the case of CF 3 or CH 2 CF 3 or at various points, as in the case of CH(OH)CHCI 2 .
- the multiple substitution can be carried out using the same or using different substituents.
- C 1-4 -alkyl and "cyclopropyl”
- the term “mono- or polysubstituted” refers in the sense of this invention, with respect to the corresponding residues or groups, to the single substitution or multiple substitution, e.g.
- C 3 . 10 -cycloalkyl mean for the purposes of this invention cyclic aliphatic hydrocarbons containing 3, 4, 5, 6, 7, 8, 9 or 10 carbon atoms, respectively, wherein the hydrocarbons in each case can be saturated or unsaturated (but not aromatic), unsubstituted or mono- or polysubstituted.
- the cycloalkyi group can be bound to the respective superordinate general structure via any desired and possible ring member of the cycloalkyi group.
- the cycloalkyi group can also be condensed with further saturated, (partially) unsaturated, (hetero)cyclic, aromatic or heteroaromatic ring systems, i.e.
- C 3 . 10 -cycloalkyls can furthermore be singly or multiply bridged such as, for example, in the case of adamantyl, bicyclo[2.2.1]heptyl or bicyclo[2.2.2]octyl.
- Preferred C 3 - 0 -cycloalkyl groups are selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, adamantly, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl,
- C 3 _6-cycloalkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentenyl and cyclohexenyl, in particular cyclopropyl.
- the cycloalkyi groups can also be condensed with further saturated or (partially) unsaturated cycloalkyi or heterocyclyl, aromatic or heteroaromatic ring systems, which in each case can in turn be unsubstituted or mono- or polysubstituted.
- the heterocyclyl group can be bound to the superordinate general structure via any desired and possible ring member of the heterocycloaliphatic residue if not indicated otherwise.
- aryl means for the purpose of this invention aromatic hydrocarbons having 6 to 14, i.e. 6, 7, 8, 9, 10, 11 , 12, 13 or 14 ring members, preferably having 6 to 10, i.e. 6, 7, 8, 9 or 10 ring members, including phenyls and naphthyls.
- Each aryl residue can be unsubstituted or mono- or polysubstituted.
- the aryl can be bound to the superordinate general structure via any desired and possible ring member of the aryl residue.
- aryl residues can also be condensed with further saturated or (partially) unsaturated cycloalkyi or heterocyclyl, aromatic or heteroaromatic ring systems, which can in turn be unsubstituted or mono- or polysubstituted.
- condensed aryl residues are benzodioxolanyl and benzodioxanyl.
- aryl is selected from the group consisting of phenyl, 1 -naphthyl, 2-naphthyl, fluorenyl and anthracenyl, each of which can be respectively unsubstituted or mono- or polysubstituted.
- a particularly preferred aryl is phenyl, unsubstituted or mono- or polysubstituted.
- heteroaryl for the purpose of this invention represents a 5-, 6-, 8-, 9- or 10-membered cyclic aromatic residue containing at least 1 , if appropriate also 2, 3, 4 or 5 heteroatoms, wherein the hetero- atoms are each selected independently of one another from the group S, N and 0 and the heteroaryl residue can be unsubstituted or mono- or polysubstituted; in the case of substitution on the heteroaryl, the substituents can be the same or different and be in any desired and possible position of the heteroaryl.
- the binding to the superordinate general structure can be carried out via any desired and possible ring member of the heteroaryl residue if not indicated otherwise.
- the heteroaryl can also be part of a bi- or polycyclic system having up to 10 ring members, wherein the ring system can be formed with further saturated or (partially) unsaturated cycloalkyl or heterocyclyl, aromatic or heteroaromatic ring systems, which can in turn be unsubstituted or mono- or polysubstituted.
- heteroaryl residue is selected from the group consisting of benzofuranyl, benzoimidazolyl, benzothienyl, benzothiadi- azolyl, benzothiazolyl, benzotriazolyl, benzooxazolyl, benzooxadiazolyl, quinazolinyl, quinoxalinyl, carb- azolyl, quinolinyl, dibenzofuranyl, dibenzothienyl, furyl (furanyl), imidazolyl, imidazothiazolyl, indazolyl, indolizinyl, indolyl, isoquinolinyl, isoxazoyl, isothiazolyl, indolyl, naphthyridinyl, oxazolyl, oxadiazolyl, phenazinyl, phenothiazinyl, phthalazinyl, pyrazolyl, pyridyl (2-
- the symbols ? or— used in the formulae denotes a link of a corresponding residue to the respective superordinate general structure.
- the compound according to general formula (I) is characterized in that R 1 is H.
- the compound according to general formula (I) is characterized in that Y 1 represents CH or N and Y 2 represents CH; or Y 1 represents CH and Y 2 represents CH or N.
- the compound according to general formula (I) is characterized in that X represents S.
- R 1 is H and X represents S, as given in formula (1-1 ):
- the compound according to general formula (I) is characterized in that X represents S, Y represents CH and Y 2 represents CH. resents CH, as given in formula (I-2):
- the compound according to general formula (I) is characterized in that X represents S, Y 1 represents CH and Y 2 represents N. resents N, as given in formula (I-3):
- Yet another embodiment of the first aspect of the invention is characterized in that the compound according to general formula (I) is a compound according to general formula (la),
- n denotes 0 or 1 ;
- Y 2 represents N or CH
- R 2 is selected from the group consisting of F; CI; Br; CN; CF 3 ; CF 2 H; CFH 2 ; CF 2 CI; CFCI 2 ; d_ 4 -alkyl;
- n denotes 0, 1 or 2 and
- R 3 is independently selected from the group consisting of F; CI; Br; CN; CF 3 ; CF 2 H; CFH 2 ; CF 2 CI; CFCI 2 ;
- n denotes 0, 1 or 2 and
- the compound according to general formula (la) is characterized in that m denotes 0; Y 2 represents N or CH; n denotes 0, 1 or 2 and
- n denotes 0, 1 or 2 and
- m denotes 0; Y 2 represents N; n denotes 0, 1 or 2 and
- the compound according to general formula (la) is characterized in that m denotes 0; Y 2 represents N or CH;
- n denotes 0 or 1
- the compound according to general formula (la) is characterized in that m de
- n denotes 0 or 1
- Z 3 , Z 4 and Z 5 each represent CH and Z 1 represents N or
- Z 1 , Z 4 and Z 5 each represent CH and Z 3 represents N or
- Z Z 3 and Z 5 each represent CH and Z 4 represents N or
- Z 1 , Z 3 and Z 4 each represent CH and Z 5 represents N;
- n denotes 0 or 1
- R 3 is selected from the group consisting of F; CI; CN; CF 3 ; CF 2 H; CFH 2 ; CH 3 ; CH 2 CH 3 ; OCH 3 cyclopropyl and OCF 3 .
- Y 2 represents CH or N
- Z 1 , Z 2 , Z 4 and Z 5 each represent CH or
- Z 2 , Z 4 and Z 5 each represent CH and Z 1 represents N or
- z Z 4 and Z 5 each represent CH and Z 2 represents N;
- n denotes 0 or 1 or 2 and R 3 is selected from the group consisting of F; CI; CN; CF 3 ; CF 2 H; CFH 2 ; CH 3 ; CH 2 CH 3 ; OCH 3 ; cyclopropyl and OCF 3 .
- the compound according to general formula (lb) or (Ic) is characterized in that Y 2 represents CH. Yet preferably, the compound according to general formula (lb) or (Ic) is characterized in that Y 2 represents N.
- the compound according to general formula (lb) is characterized in that Y 2 represents CH;
- Z 3 , Z 4 and Z 5 each represent CH and Z 1 represents N or
- Z 1 , Z 4 and Z 5 each represent CH and Z 3 represents N and n denotes 0.
- Particularly preferred compounds according to the invention are selected from the group consisting of N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2-
- the compound of general formula (I) is useful for the in vivo treatment or prevention of diseases participation of a cysteine protease is implicated.
- the compound of general formula (I) is a dual inhibitor of CatS and CatK (CatS/K inhibitors). More preferably, the compound of general formula (I) is a dual inhibitor of Cats and CatK with a pronounced effect on CatK (CatS/K inhibitors with preference for CatK).
- the term "dual for Cats and CatK” is to be understood that the inhibitor is a potent inhibitor of both CatS and CatK.
- a 50% inhibition at a concentration of 3 ⁇ in a functional enzyme assay for both CatS as well as CatK preferably less than 1000 nM for both CatS and CatK, particularly preferably less than 500 nM for both CatS and CatK, more preferably less than 400 nM for both CatS and CatK, even more preferably less than 300 nM for both CatS and CatK, even more preferably less than 200 nM for both CatS and CatK, even more preferably less than 150 nM for both CatS and CatK, even more preferably less than 100 nM for both CatS and CatK, and most preferably less than 50 nM for both CatS and CatK.
- the compounds according to present invention possess a high activity in both CatS enzyme assay and CatK enzyme assay, but exhibit a preference for the CatK enzyme assay.
- the Ki value of CatK enzyme assay is significantly lower than the Ki value of CatS enzyme assay, while still retaining high inhibition in both CatS and CatK enzyme assays.
- the preference in activity for CatK over Cat S is at least 20 fold (relating to Ki(CatS)/Ki(CatK) > 20), preferably at least 50 fold (relating to Ki(CatS)/Ki(CatK) > 50), more preferably at least 100 fold (relating to Ki(CatS)/Ki(CatK) > 100), even more preferably at least 150 fold (relating to Ki(CatS)/Ki(CatK) > 150), and most preferably at least 200 fold (relating to Ki(CatS)/Ki(CatK) > 200), while in each case the compound still causes at least a 50% inhibition at a concentration of 1000 nM in a functional enzyme assay for CatS, preferably less than 500 nM for CatS, more preferably less than 400 nM for CatS, even more preferably less than 300 nM for CatS, even more preferably less than 200 nM for CatS, even more preferably less than 150 nM for CatS, even more preferably less than 100 nM for CatS, and most
- the compounds possess a selectivity to CatS and to CatK over CatL of at least 100 (Ki(CatL)/Ki(CatK) > 00 and Ki(CatL)/Ki(CatS) > 100), preferably of at least 250 (Ki(CatL)/Ki(CatK) > 250 and Ki(CatL)/Ki(CatS) > 250), more preferably of at least 500 (Ki(CatL)/Ki(CatK) > 500 and Ki(CatL)/Ki(CatS) > 500) and most preferably of at least 1000 (Ki(CatL)/Ki(CatK) > 1000 and Ki(CatL)/Ki(CatS) > 1000).
- the compounds possess a selectivity to CatS and to CatK over CatB of at least 100 (Ki(CatB)/Ki(CatK) > 100 and Ki(CatB)/Ki(CatS) > 100), preferably of at least 250 (Ki(CatB)/Ki(CatK) > 250 and Ki(CatB)/Ki(CatS) > 250), more preferably of at least 500 (Ki(CatB)/Ki(CatK) > 500 and Ki(CatB)/Ki(CatS) > 500) and most preferably of at least 1000 (Ki(CatB)/Ki(CatK) > 1000 and Ki(CatB)/Ki(CatS) > 1000).
- the present invention further relates to a compound according to the present invention for modulation of both CatS and CatK, preferably for use in inhibitbion of CatS and CatK activity.
- the present invention therefore further relates to a compound according to the present invention for the prophylaxis and/or treatment of disorders and/or diseases which are mediated, at least in part, by both CatS and CatK without the inhibition of CatL and /or CatB.
- the present invention even further relates to a compound according to the present invention for the prophylaxis and/or treatment of disorders and/or diseases which are mediated, at least in part, by both CatS and CatK with a pronounced mediation by CatK without the inhibition of CatL and /or CatB.
- a compound according to the present invention in the preparation of a medicament for preventing or treating diseases in which the disease pathology may be modified by inhibiting a CatS and/or CatK.
- the invention therefore also provides pharmaceutical compositions, containing at least one compound according to the invention and optionally one or more suitable, pharmaceutically compatible auxiliaries and/or, if appropriate, one or more further
- the pharmaceutical composition according to the invention may be found as a liquid, semisolid or solid pharmaceutical form, for example in the form of injection solutions, drops, juices, syrups, sprays, suspensions, tablets, patches, capsules, plasters, suppositories, ointments, creams, lotions, gels, emulsions, aerosols or in multiparticulate form, for example in the form of pellets or granules, if appropriate pressed into tablets, decanted in capsules or suspended in a liquid, and also be administered as much.
- the pharmaceutical composition according to the invention conventionally contains further physiologically compatible pharmaceutical auxiliaries which can for example be selected from the group consisting of excipients, fillers, solvents, diluents, surface-active substances, dyes, preservatives, blasting agents, slip additives, lubricants, aromas and binders.
- physiologically compatible auxiliaries and also the amounts thereof to be used depend on whether the pharmaceutical composition is to be applied orally, subcutaneously, parenterally, intravenously, intraperitoneally, intradermally, intramuscularly, intranasally, buccally, rectally or locally, for example to infections of the skin, the mucous membranes and of the eyes.
- Preparations in the form of tablets, dragees, capsules, granules, pellets, drops, juices and syrups are preferably suitable for oral application; solutions, suspensions, easily reconstitutable dry preparations and also sprays are preferably suitable for parenteral, topical and inhalative application.
- the compounds according to the invention used in the pharmaceutical composition according to the invention in a repository in dissolved form or in a plaster, agents promoting skin penetration being added if appropriate, are suitable percutaneous application preparations. Orally or percutaneously applicable preparation forms can release the respective compound according to the invention also in a delayed manner.
- compositions according to the invention are prepared with the aid of conventional means, devices, methods and process known in the art.
- amount to be administered to the patient of the respective compounds according to the invention of the above-indicated general formula I may vary and is for example dependent on the patient's weight or age and also on the type of application, the indication and the severity of the disorder. Conventionally 0.001 to 100 mg/kg, preferably 0.05 to 75 mg kg, particularly preferably 0.05 to 50 mg of at least one such compound according to the invention are applied per kg of the patient's body weight.
- cysteine proteases function in the protein degradation in animals, including humans, e.g. in the degradation of connective tissue. Elevated levels of these cysteine proteases in the body may result in pathological conditions leading to disease.
- Cats and CatK are believed to be involved in a variety of diseases or disorders in mammals such as humans. These include pain (in particular chronic pain, inflammatory pain, mixed pain), inflammatory diseases and bone/cartilage preservation disorders.
- CatS/K dual Cats and CatK inhibitors for the treatment of rheumatoid arthritis (RA), osteoarthritis(OA), chronic obstructive pulmonary disease (COPD), atherosclerosis and
- ECM extracellular matrix
- Another embodiment of the present invention is at least one compound according the present invention for the treatment and/or prophylaxis of one or more disorders selected from the group consisting of nociceptive pain, neuropathic pain; erosive osteoarthritis (EO), in particular erosive osteoarthritis of the hand; Sjogren's Syndrom; rheumatoid arthritis (RA); psoriatic arthrithis (PsA), Psoriasis, Spondylarthritis, in particular ankylosing spondylitis; osteoporosis; Complex Regional Pain Syndrome (in particular CRPS I); Lupus erythematodes (SLE); Lupus nephritis; asthma; multiple sclerosis (MS); diabetes; chronic obstructive pulmonary disease (COPD), in particular COPD subpopoulation with osteoporosis; and asthma, in particular severe asthma subpopoulation with osteoporosis.
- EO erosive osteoarthritis
- RA rheum
- Another embodiment of the present invention therefore relates to use of at least one compound according to the present invention for the preparation of a pharmaceutical composition for the treatment and/or prophylaxis of one or more disorders or diseases, particularly selected from the group consisting of nociceptive pain, neuropathic pain; erosive osteoarthritis (EO), in particular erosive osteoarthritis of the hand; Sjogren's Syndrom; rheumatoid arthritis (RA); psoriatic arthrithis (PsA), Psoriasis, Spondylarthritis, in particular ankylosing spondylitis; osteoporosis; Complex Regional Pain Syndrome (in particular CRPS I); Lupus erythematodes (SLE); Lupus nephritis; asthma; multiple sclerosis (MS); diabetes; chronic obstructive pulmonary disease (COPD), in particular COPD subpopoulation with osteoporosis; and asthma, in particular severe asthma subpopoulation with osteoporosis.
- Another aspect of the present invention is a method of treatment and/or prophylaxis of disorders and/or diseases in a mammal, preferably of disorders and/or diseases selected from the group consisting of nociceptive pain, neuropathic pain; erosive osteoarthritis (EO), in particular erosive osteoarthritis of the hand; Sjogren's Syndrom; rheumatoid arthritis (RA); psoriatic arthrithis (PsA), Psoriasis, Spondylarthritis, in particular ankylosing spondylitis; osteoporosis; Complex Regional Pain Syndrome (in particular CRPS I); Lupus erythematodes (SLE); Lupus nephritis; asthma; multiple sclerosis (MS); diabetes; chronic obstructive pulmonary disease (COPD), in particular COPD subpopoulation with osteoporosis; and asthma, in particular severe asthma subpopoulation with osteoporosis.
- EO erosive osteoarth
- INT-1 was prepared analogously to synthetic methods known from WO2009/1 12839.
- Example 1 N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetra ydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridazin-3-yl)thiophene-2-carboxamide
- the filtrate was diluted with aqueous saturated NaHC0 3 (500 mL) and water (500 mL). The layers were separated, the aqueous layer was extracted with EtOAc (750 mL). The combined organic layer was washed with brine (2* 1 L), dried over Na 2 S0 4 and concentrated in vacuo. The aqueous layer was divided in three 1 L portions, which were extracted with EtOAc (2* 500 mL). The combined organic layer was dried over Na 2 S0 4 and concentrated in vacuo and combined with the previous organic fraction.
- DMP (0.495 g, 1.17mmol) was added to a solution of INT-2A (0.278 g, 0.584 mmol) in DCM (10 mL). The mixture was stirred at RT for 18 h. An aqueous solution of Na 2 S 2 0 3 (10%, 10 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC0 3 (50 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (30 mL). The combined organic layer was dried over Na 2 S0 . The filtrate was concentrated in vacuo.
- DMP (0.478 g, 1.13 mmol) was added to a solution of INT-3B (0.269 g, 0.564 mmol) in DCM (10 mL). The mixture was stirred at RT for 18 h. An aqueous solution of Na 2 S 2 0 3 (10%, 10 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC0 3 (50 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (30 mL). The combined organic layer was dried over Na 2 S0 . The filtrate was concentrated in vacuo.
- DMP (0.523 g, 1.23 mmol) was added to a solution of INT-4C (0.294 g, 0.616 mmol) in DCM (10 mL). The mixture was stirred at RT for 18 h. An aqueous solution of Na 2 S 2 0 3 (10%, 5 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC0 3 (10 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (10 mL). The combined organic layer was dried over Na 2 S0 4 . The filtrate was concentrated in vacuo.
- aqueous phase was acidified with aqueous HCI (2 M) until pH 4-5 and extracted with EtOAc (2x 200 mL). The combined organic layer was dried over Na 2 S0 4 and concentrated in vacuo.
- the crude product was dissolved in 1 ,4-dioxane (50 mL), hydrochloric acid (4 M in dioxane) was added. A precipitate was formed and the suspension was stirred for 2 h. The suspension was filtered and dried in vacuo to obtain INT-5A (0.500 g, 2.06 mmol, 9% ) as an off-white solid.
- DMP (0.1 16 g, 0.273 mmol) was added to a solution of INT-5B (0.065 g, 0.14 mmol) in DCM (4 mL). The mixture was stirred at RT for 72 h. An aqueous solution of Na 2 S 2 0 3 (10%, 4 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC0 3 (10 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (10 mL). The combined organic layer was dried over Na 2 S0 4 . The filtrate was concentrated in vacuo.
- DMP (0.859 g, 2.02 mmol) was added to a solution of INT-6C (0.500 g, 0.962 mmol) in DCM (8 mL). The mixture was stirred at RT for 16 h. An aqueous solution of Na 2 S 2 0 3 (10%, 25 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC0 3 (10 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (2x 10 mL). The combined organic layer was dried over Na 2 S0 4 and concentrated in vacuo. The crude was dissolved in a small amount of boiling EtOAc and cooled to RT.
- Example 7 N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-f uro[3,2-b]pyrrol-4(5H)-yl)-1 ⁇ cyclopentyl-2-oxoethyl)-5-(pyridazin-3-yl)thiazole-2-carboxamide
- NEt 3 (0.788 g, 7.80 mmol, 1.09 mL) and T3P (50% w/w in DMF, 0.694 g, 1.09 mmol, 0.649 mL) were added consecutively to a solution of INT-1 (0.254 g, 0.780 mmol) and INT-7B (0.190 g, 0.780 mmol) in dry DMF (10 mL). The reaction was stirred at RT for 16 h. The reaction was diluted with EtOAc (30 mL) and washed with aqueous saturated NaHC0 3 (30 mL). The water layer was extracted with EtOAc (2* 20 mL).
- DMP (0.555 g, 1.31 mmol) was added to a solution of INT-7C (0.200 g, 0.418 mmol) in DCM (20 mL). The mixture was stirred at RT for 16 h. An aqueous solution of Na 2 S 2 0 3 (10%, 20 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC0 3 (20 mL) was added and extracted with DCM (3* 10 mL). The combined organic layer was dried over Na 2 S0 4 and concentrated in vacuo.
- DMP (0.606 g, 1 .429 mmol) was added to a solution of INT-8A (0.340 g, 0.714 mmol) in DCM (10 mL). The mixture was stirred at RT overnight. An aqueous solution of Na 2 S 2 0 3 (10%, 10 mL) was added and the RM was stirred vigorously for 30 min. An aqueous saturated solution of NaHC0 3 (50 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (30 mL). The combined organic layer was dried over Na 2 S0 4 The filtrate was concentrated in vacuo.
- the biaryl acids can be obtained from cross coupling reactions of boronic acids or stannates with (hetero)aromatic halides (Scheme 1 ).
- tert-butyl thiazole-2-carboxylate (0.500 g, 2.70 mmol) was added to a solution of lithium bis(trimethyl- silyl)amide (2.97 mL, 1 M in THF, 2.97 mmol) in Et 2 0 (20 mL) at -100 °C. The mixture was stirred for 15 min. CBr 4 (0.985 g, 2.97 mmol) was added at -100 °C and the mixture was stirred for at this temperature for 10 min and then allowed to reach rt. The reaction was quenched with saturated aqueous NH 4 CL (20 mL). The layers were separated. The aqueous layer was extracted with Et 2 0 (3x 10 mL).
- 2-Methylpyrimidine-5-boronic acid pinacol ester (0.920 g, 4.18 mmol), ethyl 5-bromothiophene-2- carboxylate (0.568 mL, 3.80 mmol) and Na 2 C0 3 (1.21 g, 11.4 mmol) were mixed in DME (30 mL) and water (7.5 mL) and degassed with Ar. Then PdCI 2 (dppf) (0.133 g, 0.190 mmol) was added and the mixture was stirred at 100 °C for 1 h. Water (20 mL) was added and the mixture was extracted with EtOAc (3* 20 mL).
- Oxalyl chloride (0.21 mL, 2.4 mmol) was added to a solution of 5-bromothiazole-2-carboxylic acid (0.42 g, 2.0 mmol) in dry DCM (10 mL) containing a catalytic amount of dry DMF (0.05 mL) at rt and the resulting mixture was stirred for 4 h.
- MeOH (4.00 mL, 125 mmol) was added to the solution and the reaction was stirred for an additional 2 h.
- the mixture was diluted with a saturated aqueous solution of NaHC0 3 (20 mL) and extracted with DCM (3* 10 mL).
- n-butyllithium 2.5 M in hexanes, 4.75 mmol, 1.90 mL was added to a solution of ⁇ /,/V-diiso- propylamine (0.481 g, 4.75 mmol, 0.668 mL) in dry Et 2 0 (40 mL). The mixture was stirred at 0 °C for 1 h. The mixture was cooled to -100 °C (Et 2 0/Iiquid N 2 ).
- tert-butyl 5-(tributylstannyl)thiazole-2-carboxylate (1.03 g, 2.17 mmol), 5-bromo-2-(trifluoromethyl)- pyrimidine (0.493 g, 2.17 mmol), tri(furan-2-yl)phosphine (0.101 g, 0.434 mmol) and Pd 2 (dba) 3 (0.199 g, 0.217 mmol) were dissolved in dry 1 ,4-dioxane (30 mL) and the resulting solution was heated at 90 °C and stirred for 4 h. The mixture was filtered over Celite and flushed with EtOAc (100 mL). Solvents were evaporated in vacuo.
- LiOH H 2 0 (0.182 g, 4.33 mmol) was added to a suspension of ethyl 5-(5-fluoropyrimidin-4-yl)thiophene-2- carboxylate (0.364 g, 1.44 mmol) in THF (20 mL) and water (8 mL). The mixture stirred at rt for 16 h. The mixture was concentrated in vacuo. The residue was acidified to pH 3-4 using aqueous 2M HCI (2.16 mL). To this /-PrOH (15 mL) was added.
- Diisopropylamine (0.659 g, 6.51 mmol, 0.920 mL) was dissolved in dry THF (6 mL) and cooled to -78 °C under N 2 .
- a solution of n-butyllithium (1.6 M in hexanes, 6.51 mmol, 4.07 mL) was added drop wise.
- the mixture was allowed to warm to 0 °C and stirred for 30 min.
- the solution was cooled to -78 °C and a solution of feri-butyl thiophene-2-carboxylate (1.00 g, 5.43 mmol) in dry THF (6 mL) was added drop wise.
- the mixture was stirred at -78 °C for 1 h.
- LiOH H 2 0 (0.068 g, 1.6 mmol) was added to a solution of methyl 5-(6-ethylpyridazin-4-yl)thiophene-2- carboxylate (0.175 g, 0.705 mmol) in THF (5 mL) and water (1 mL).
- the RM was stirred at rt for 1 h.
- LiOH H 2 0 (0.020 g, 0.48 mmol) was added and the mixture was heated at 50 °C for 1 h.
- the RM was concentrated in vacuo. The residue was acidified to pH 4 ⁇ 5 by addition of aqueous 1 M HCI (1.9 mL) and triturated with /-PrOH (3 mL).
- tert-Butyl thiazole-2-carboxylate (1.15 g, 6.21 mmol, synthesis see above) was added to a solution of LDA (1 M in THF/heptane/ethylbenzene, 6.83 mmol, 6.83 mL) in dry THF ( 0 mL) at -78 °C and the mixture was stirred for 30 min.
- /V-Methoxy-W-methylacetamide (0.96 g, 9.3 mmol) was added and the RM was stirred for 3 h.
- the RM was quenched by adding a saturated aqueous solution of NH 4 CI (10 mL). The mixture was allowed to reach to rt.
- tert-Butyl 5-(3-(dimethylamino)acryloyl)thiazole-2-carboxylate (0.70 g) was added to a solution of formimidamide acetate (1.29 g, 12.4 mmol) in dry DMF (10 mL) and the reaction was heated up to 95 °C and stirred for 5 h. The reaction was cooled to rt and diluted with aqueous saturated NaHC0 3 (10 mL) and extracted with EtOAc (3 ⁇ 20 mL). The combined organic layer was dried over Na 2 S0 4 and concentrated in vacuo.
- Hydrazine sulfate (0.681 g, 5.24 mmol) was suspended in water (10 mL). The mixture was heated to 100°C and at this temperature 3-bromo-4-methylfuran-2,5-dione (1.00 g, 5.24 mmol) was added. The mixture was heated for 16 h at 95°C (a white precipitate forms). HBr (48% w/w in water, 0.033 g, 0.20 mmol, 0.022 mL) was added and the mixture was heated to 95°C for 2 h.
- tert-butyl 5-(3,6-dihydroxy-5-methylpyridazin-4-yl)thiophene-2-carboxylate (0.724 g, 2.348 mmol) was suspended in dry MeCN (25 mL). Tetraethylammonium chloride (1.17 g, 7.04 mmol) was added, followed by phosphorus oxychloride (1.58 g, 10.3 mmol, 0.963 mL). The mixture was stirred at reflux for 2 h. Solvents were evaporated in vacuo. The residue was stripped with DCM.
- Recombinant human cathepsins (CatS, CatK, CatL, CatB) were purchased from a Enzo Life Sciences.AII assays were carried out in 96-well format using a buffer of 50 mM KH 2 P0 4 , 50mM NaCI, 2mM EDTA, 0.5 mM DTT and 1 % Triton-X-100, pH 6.5 for Cathepsin S and a buffer of 50 mM NaOAc, 10 mM EDTA, 1 mM DTT and 0.01 % Triton-X-100, pH 5.5 for CatK/L/B.
- the enzyme (0.0007 mU/well) was incubated with fiuorogeninc substrate (Z-WR-AMC, 5 ⁇ ) at RT for 10 min.
- the enzyme (0.00175 mU/well) was incubated with fiuorogeninc substrate (Z-FR -AMC, 40 ⁇ ) at RT for 10 min.
- the enzyme (0.000874 mU/well) was incubated with fiuorogeninc substrate (Z-WR-AMC, 40 ⁇ ) at RT for 10 min.
- Flourogenic substrate turnover was detected using a microplate reader (SynergyTM H4, BioTek). Ki values were calculated using the Cheng Prusoff equation (Cheng & Prosoff 1973).
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Abstract
The invention relates to amidic oxotetrahydro-2H-furo[3.2-b]pyrrol-4(5H)-yl) derivatives as dual CatS/K inhibitors exhibiting a pronounced CatK-inhibition, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.
Description
3-Oxo-tetrahydro-furo[3,2-b]pyrrol-4(5H)-yl) derivatives II
FIELD OF THE INVENTION
The present invention relates to compounds that are dual inhibitors of the cysteine proteinases cathepsin S (CatS) and cathepsin K (CatK), pharmaceutical com positions containing said compounds, and their use in medical therapy. Such compounds are particularly useful for the therapeutic treatment of diseases which are at least partially modulated by CatS and CatK.
BACKGROUND OF THE INVENTION
Cysteine proteases represent a specific class of peptidases which bear a cysteine residue in the catalytic site of the enzyme. Many pathological disorders or diseases are the results of abnormal activity of cysteine proteases such as over expression or enhanced activation.
The cysteine cathepsins, e.g. cathepsins B, K, 0, L, S, V and F, are a class of lysosomal protease enzymes which are implicated in a multitude of house-keeping roles, but also in various disease processes and disorders including inflammation, autoimmune diseases, e.g. rheumatoid arthritis, psoriasis, asthma, osteoarthritis, osteoporosis, tumors, coronary disease, atherosclerosis, and infectious diseases.
In contrast to the ubiquitously expressed housekeeping enzymes cathepsins B, 0 and L, cathepsin S (CatS) is highly expressed in antigen presenting cells of lymphatic tissues, primarily in dendritic cells, B cells and macrophages (Wiener et al., Curr. Top. Med. Chem. , 2010, 10, 717). In the antigen presenting cells, CatS plays a major role in antigen presentation by degradation of invariant chain that is associated with the major histocompatibility class II complex.
There currently exists a major unmet need for safe orally administered medications for the treatment of inflammatory diseases such as rheumatoid arthritis, osteoarthritis, chronic obstructive pulmonary disease (COPD) and cardiovascular disease, which exhibit significant damage and remodeling of extracellular matrix (ECM).
Destruction of the ECM takes place through proteolysis of its elastin, collagen and proteoglycan constituents, which provide structure, elasticity and tensile strength to materials such as cartilage, bone, lung and vascular tissue.
US 2007/01 17785 discloses inhibitors of CatS, supporting the use of CatS inhibitors for the treatment of certain allergic conditions, such as rheumatoid arthritis or psoriasis.
CatS has also been demonstrated to mediate a pro-nociceptive effect, thereby indicating that endogenous CatS released by peripheral macrophages may contribute to the maintenance of neuropathic hyperalgesia following nerve injury (Barclay et al., Pain, 2007, 130, 225).
CatK is predominantly expressed in osteoclasts (Yasuda et al., Adv. Drug Deliv. Rev. , 2005, 57, 973). By cleavage of bone matrix proteins, CatK is involved in extracellular matrix metabolism necessary for normal bone growth and remodelling (Bossard et al., J. Biol. Chem. 1996, 271 , 12517). Hence, inhibition of CatK should result in a reduction of osteoclast mediated bone resorption. The CatK inhibitor Odanacatib has been validated in humans for the treatment of osteoporosis (Zerbini and McClung, Ther. Adv.
Musculoskel. Dis. 2013, 5(4), 199-209).
The proteolytic enzymes cathepsin S and cathepsin K are up-regulated under inflammatory conditions and have been implicated in the degradation of ECM components. For instance, CatK and CatS are found over-expressed in rheumatoid and osteoarthritic synovium. They have been shown to degrade collagen type-l and type-ll, as well as aggrecan (a multidomain proteoglycan component of articular cartilage) respectively (Yasuda et al., Adv. Drug Deliv. Rev., 2005, 57, 973).
Besides destruction of articular cartilage, CatS and CatK demonstrate potent elastinolytic activity and are involved in a broad spectrum of pathological conditions associated with elastin degradation, such as COPD and cardiovascular disease. Both enzymes are readily secreted by macrophages and smooth muscle cells and have been shown to degrade elastins from bovine aorta and lung tissue. CatS and CatK are also responsible for the vascular tissue damage associated with chronic cardiovascular disease and vascular injury.
Further, CatS and CatK have been found to play a crucial role in in atherosclerotic lesion destabilization and eventually induction of atherosclerotic plaque rupture (Sukhova et al., J. Clin. Invest., 1998, 102, 576). CatS and CatK have also been associated with vascular remodeling and causing ECM damage during the development of atherosclerosis and vascular injury-induced neointimal formation (Cheng et al. , Am. J. Pathol., 2004, 164, 243).
Thus, inhibition of CatS and CatK offer an attractive approach to prevent the tissue destruction underlying chronic inflammatory diseases such as rheumatoid arthritis, osteoarthritis, COPD and cardiovascular disease.
Since CatS and CatK appear to work in tandem and both are present in many chronic inflammatory diseases, a single compound possessing dual inhibitory activity would be a distinct advantage. There are presently no human therapeutic dual inhibitors. The use of dual CatS/K inhibitors for the treatment of conditions with inflammatory and joint-destructive components, such as rheumatoid arthritis has been suggested (Gupta et al. Expert Opin. Ther. Targets, 2008, 12, 291 ) and demonstrated in a collagen- induced murine arthritis model (Lee-Dutra et al., Expert Opin. Ther. Patents, 201 1 , 21 , 311 ).
WO 2009/1 12839 A1 describes particular 6-( iS)-chlorotetrahydrofuro[3,2-fo]pyrrol-3-ones according to general formula (I*), exhibiting potent dual inhibition versus both human CatS and CatK:
A major challenge in the development of such dual CatS/K inhibitors arises from selectivity issues towards other cathepsins. In particular, lysosomal, cytoskeletal and metabolic alterations in cardiomyopathy have been attributed to inhibition of cathepsin L (CatL) in CatL knock-out mice (Petermann et al., FASEB J. 2006, 20, 1266; Stypmann et al., PNAS, 2002, 99, 6234). Furthermore, it was shown that disruption of the cathepsin L gene leads to major abnormalities in skin and hair development and differentiation and alterations in trabecular bone deposition (Potts et al, Int. J. Exp. Path. 2004, 85, 85).
Structurally, the cathepsins K, L and S possess a high sequence homology (Lee-Dutra et al., Expert Opin. Ther. Patents 201 1 , 21 , 31 1 ; Turk et al., Biochim. Biophys. Acta, 2012. 1824, 68). Therefore, a sufficient selectivity over ubiquitously expressed CatL to avoid the undesired effects associated with inhibition of CatL is regarded to be one of the prerequisites for therapeutic suitability of CatS inhibitors (Wiener et al., Curr. Top. Med. Chem. 2010, 10, 717), but will equally refer to dual CatS/CatK inhibitors.
SUMMARY OF THE INVENTION
It was therefore an object of the invention to provide novel compounds, preferably having advantages over the prior-art compounds. The compounds should be suitable in particular as pharmacological active ingredients in pharmaceutical compositions, preferably in pharmaceutical compositions for the treatment and/or prophylaxis of disorders or diseases which are at least partially mediated by both human CatS and human CatK.
Surprisingly, it has now been found that specific 6-(7S)-chlorotetrahydrofuro[3,2-,t>]pyrrol-3-ones not only exhibit potent dual inhibition of both human CatS and human CatK, but possess an significantly increased selectivity over CatL compared to the compounds known from WO 2009/1 12839 A1.
Moreover, the compounds according to the invention have surprisingly been found not to possess an equipotent dual inhibition versus both human CatS and CatK. Instead, they exhibit a more pronounced inhibition of human CatK, while still retaining high inhibition versus human CatS. As CatK is predominantly expressed in osteoclasts, compounds with an unbalanced dual inhibition mode on human CatS and CatK may be particularly suitable for the treatment of inflammatory bone diseases, such as rheumatoid arthritis or osteoarthritis.
wherein
R1 represents H or F,
X represents S or O;
Y1 and Y2 independently represents CH or N;
Z1, Z2, Z3, Z4 and Z5 independently represents CH or N, with the proviso that 1 , 2 or 3 of Z1, Z2, Z3, Z4 and
Z5 represent N;
m denotes 0, 1 or 2;
n denotes 0, 1 , 2 or 3;
each R2 and each R3 is independently selected from the group consisting of F; CI; Br; CN; CF3; CF2H; CFH2; CF2CI; CFCI2; C1-4-alkyl; C(=0)-(C1-4-alkyl); C(=0)-NH2; C(=0)-N(H)(C1.4-alkyl); C(=0)-N(C1-4- alkyl)2; OH; 0-Ci-4-alkyl; OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; NH2; NiHXC^-alkyl); N(C1-4-alkyl)2; N(H)-C(=0)-(C1.4-alkyl); N(C1.4-alkyl)-C(=0)-(C1.4-alkyl); N(H)-S(=0)2-(C1.4-alkyl); N(H)-C(=0)-NH2; N(H)- C(=0)-N(H)(C1.4-alkyl); N(H)-C(=0)-N(C1.4-alkyl)(C1.4-alkyl); S-(d.4-alkyl); S(=0)-(C1-4-alkyl); S(=0)2-(C1-4- alkyl); S(=0)2-N(H)(C1.4-alkyl); cyclopropyl; O-cyclopropyl; NH-cyclopropyl; N(H)-C(=0)-cyclopropyl; S(=0)-(cyclopropyl) and S(=0)2-(cyclopropyl);
wherein the above-mentioned substituents Ci.4-alkyl and cyclopropyl, may in each case be unsubstituted or substituted one or more times by identical or different substituents, and the above-mentioned substituent C^-alkyl may in each case be branched or unbranched; in the form of an individual stereoisomer or a mixture thereof; in the form of a tautomer; of a free compound; of an N-oxide; or in the form of a solvate and/or of a physiologically acceptable salt.
The term "physiologically acceptable salt" preferably comprises in the sense of this invention a salt of at least one compound according to the present invention and at least one physiologically acceptable acid or base.
The term "physiologically acceptable solvate" preferably comprises in the sense of this invention an adduct of one compound according to the present invention and/or a physiologically acceptable salt of at least one compound according to the present invention with distinct molecular equivalents of one solvent or more solvents.
The term "C _4-alkyl" comprise in the sense of this invention acyclic saturated aliphatic hydrocarbon residues, which can be respectively branched or unbranched and can be unsubstituted or can be mono- or polysubstituted, e.g. mono-, di- or trisubstituted, and which contain 1 to 6 carbon atoms, i.e. 1 , 2, 3 or 4
carbon atoms. Preferred C1-4-alkyl groups are selected from the group consisting of methyl, ethyl, n-pro- pyl, 2-propyl, n-butyl, isobutyl, sec-butyl and tert-butyl.
In relation to the term "d.4-alkyl" the term "monosubstituted" or "polysubstituted" such as di- or tri-sub- stituted refers in the sense of this invention, with respect to the corresponding groups, to the single substitution or multiple substitution, e.g. disubstitution or trisubstitution, of one or more hydrogen atoms each independently of one another by at least one substituent. The term "polysubstituted" such as di- or tri- substituted with respect to polysubstituted groups such as di- or tri-substituted groups includes the poly- substitution of these groups either on different or on the same atoms, for example trisubstituted on the same carbon atom, as in the case of CF3 or CH2CF3 or at various points, as in the case of CH(OH)CHCI2. The multiple substitution can be carried out using the same or using different substituents.
In relation to the terms "C1-4-alkyl" and "cyclopropyl", the term "mono- or polysubstituted" refers in the sense of this invention, with respect to the corresponding residues or groups, to the single substitution or multiple substitution, e.g. disubstitution, trisubstitution, tetrasubstitution, or pentasubstitution, of one or more hydrogen atoms each independently of one another by at least one substituent selected from the group consisting of F; CI; Br; I; N02; CN; =0; =NH; =N(OH); =N(0-C1-4-alkyl); CF3; CF2H; CFH2; CF2CI; CFCI2; C1-4-alkyl; C(=0)-H; C(=0)-C1.4-alkyl; C(=0)-OH; C(=0)-0-C1.4-alkyl; C(=0)-N(H)(OH); C(=0)-NH2;
C(=N-0-C1.4-alkyl)-C1.4-alkyl; OH; OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; O-C^-alkyl; 0-C(=0)-C1-4- alkyl; 0-C(=0)-0-C1.4-alkyl; 0-(C=0)-N(H)(d.4-alkyl); 0-C(=0)-N(C1.4-alkyl)2; 0-S(=0)2-C1_4-alkyl; O- S(=0)2-OH; 0-S(=0)2-0-C1.4-alkyl; 0-S(=0)2-NH2; 0-S(=0)2-N(H)(d.4-alkyl); 0-S(=0)2-N(C1.4-alkyl)2; NH2; N(H)(d.4-alkyl); N(d.4-alkyl)2; N(H)-C(=0)-d.4-alkyl; N(H)-C(=0)-0-d.4-alkyl; N(H)-C(=0)-NH2; N(H)-C(=0)-N(H)(d.4-alkyl); N(H)-C(=0)-N(d.4-alkyl)2; N(C1.4-alkyl)-C(=0)-C1.4-alkyl; N(d_4-alkyl)- C(=0)-0-C1-4-alkyl; N(d.4-alkyl)-C(=0)-NH2; N(C1.4-alkyl)-C(=0)-N(H)(C1.4-alkyl); N(d.4-alkyl)-C(=0)- N(d.4-alkyl)2; N(H)-S(=0)2-OH; N(H)-S(=0)2-d.4-alkyl; N(H)-S(=0)2-0-d.4-alkyl; N(H)-S(=0)2-NH2; N(H)-S(=0)2-N(H)(C1.4-alkyl); N(H)-S(=0)2-N(d.4-alkyl)2; N(C1.4-alkyl)-S(=0)2-OH; N(d_4-alkyl)-S(=0)2- d.4-alkyl; N(d.4-alkyl)-S(=0)2-0-d.4-alkyl; N(C1.4-alkyl)-S(=0)2-NH2; N(d.4-alkyl)-S(=0)2-N(H)(d.4- alkyl); N(C1.4-alkyl)-S(=0)2-N(C1.4-alkyl)2; SH; SCF3; SCF2H; SCFH2; SCF2CI; SCFCI2; S-d.4-alkyl; S(=0)- d.4-alkyl; S(=0)2-d.4-alkyl; S(=0)2-OH; S(=0)2-0-d.4-alkyl; S(=0)2-NH2; S(=0)2-N(H)(d.4-alkyl); S(=0)2- C3.i0-cycloalkyl; 3 to 7 membered heterocyclyl; aryl or heteroaryl.
Preferred substituents of "d. -alkyl" are selected from the group consisting of F; CI; Br; CF3; C(=0)-NH2; C(=0)-N(H)(d.4-alkyl); C(=0)-N(d.6-alkyl)2; C3.6-cycloalkyl or 3 to 7 membered heterocyclyl; OH; 0-d.4- alkyl; NH2 ; N(H)(C1-4-alkyl); N(d.4-alkyl)2; N(H)-C(=0)-d.4-alkyl; N(H)-S(=0)2-C1.4-alkyl; N(d.4-alkyl)- S(=0)2-d.4-alkyl; N(H)-S(=0)2-NH2; SH; S-d.4-alkyl; S(=0)2-d.4-alkyl and S(=0)2-N(H)(d.4-alkyl).
Preferred substituents of "cycloalkyl" are selected from the group consisting of F; CI; Br; CF3; CN; =0; d. 4-alkyl; C3.6-cycloalkyl or 3 to 7 membered heterocyclyl; CHO; C(=0)-C1.4-alkyl; C02H; C(=0)0-C1.4-alkyl; C0NH2; C(=0)NH-d.4-alkyl; C(=0)N(d.4-alkyl)2; OH; 0-d.4-alkyl; OCF3; 0-C(=0)-C1.4-alkyl; NH2;
NH-C^-alkyl; N(Ci_ -alkyl)2; NH-C(=0)-C1.4-alkyl; SH; S-d^-alkyl; SCF3; S(=0)2-C1.4-alkyl; S(=0)2OH; S(=0)20-C^-alkyl and S(=0)2-NH-C1.4-alkyl.
The term "C3.10-cycloalkyl" mean for the purposes of this invention cyclic aliphatic hydrocarbons containing 3, 4, 5, 6, 7, 8, 9 or 10 carbon atoms, respectively, wherein the hydrocarbons in each case can be saturated or unsaturated (but not aromatic), unsubstituted or mono- or polysubstituted. The cycloalkyi group can be bound to the respective superordinate general structure via any desired and possible ring member of the cycloalkyi group. The cycloalkyi group can also be condensed with further saturated, (partially) unsaturated, (hetero)cyclic, aromatic or heteroaromatic ring systems, i.e. with cycloalkyi, heterocyclyl, aryl or heteroaryl residues, which in each case can in turn be unsubstituted or mono- or polysubstituted. C3.10-cycloalkyls can furthermore be singly or multiply bridged such as, for example, in the case of adamantyl, bicyclo[2.2.1]heptyl or bicyclo[2.2.2]octyl. Preferred C3- 0-cycloalkyl groups are selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclononyl, cyclodecyl, adamantly, cyclopentenyl, cyclohexenyl, cycloheptenyl, cyclooctenyl,
and . Particularly preferred C3. 0-cycloalkyl groups are
C3_6-cycloalkyl groups such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentenyl and cyclohexenyl, in particular cyclopropyl.
The terms "3 to 7-membered heterocyclyl" mean for the purposes of this invention heterocycloaliphatic saturated or unsaturated (but not aromatic) residues having 3 to 7, i.e. 3, 4, 5, 6 or 7 ring members, respectively, in which in each case at least one, if appropriate also two or three carbon atoms are replaced by a heteroatom or a heteroatom group each selected independently of one another from the group consisting of O, S, S(=0), S(=0)2, N, NH and NiC^-alkyl) such as N(CH3), wherein the ring members can be unsubstituted or mono- or polysubstituted. The cycloalkyi groups can also be condensed with further saturated or (partially) unsaturated cycloalkyi or heterocyclyl, aromatic or heteroaromatic ring systems, which in each case can in turn be unsubstituted or mono- or polysubstituted. The heterocyclyl group can be bound to the superordinate general structure via any desired and possible ring member of the heterocycloaliphatic residue if not indicated otherwise.
The term "aryl" means for the purpose of this invention aromatic hydrocarbons having 6 to 14, i.e. 6, 7, 8, 9, 10, 11 , 12, 13 or 14 ring members, preferably having 6 to 10, i.e. 6, 7, 8, 9 or 10 ring members, including phenyls and naphthyls. Each aryl residue can be unsubstituted or mono- or polysubstituted. The aryl can be bound to the superordinate general structure via any desired and possible ring member of the aryl residue. The aryl residues can also be condensed with further saturated or (partially) unsaturated cycloalkyi or heterocyclyl, aromatic or heteroaromatic ring systems, which can in turn be unsubstituted or mono- or polysubstituted. Examples of condensed aryl residues are benzodioxolanyl and benzodioxanyl. Preferably, aryl is selected from the group consisting of phenyl, 1 -naphthyl, 2-naphthyl, fluorenyl and
anthracenyl, each of which can be respectively unsubstituted or mono- or polysubstituted. A particularly preferred aryl is phenyl, unsubstituted or mono- or polysubstituted.
The term "heteroaryl" for the purpose of this invention represents a 5-, 6-, 8-, 9- or 10-membered cyclic aromatic residue containing at least 1 , if appropriate also 2, 3, 4 or 5 heteroatoms, wherein the hetero- atoms are each selected independently of one another from the group S, N and 0 and the heteroaryl residue can be unsubstituted or mono- or polysubstituted; in the case of substitution on the heteroaryl, the substituents can be the same or different and be in any desired and possible position of the heteroaryl. The binding to the superordinate general structure can be carried out via any desired and possible ring member of the heteroaryl residue if not indicated otherwise. The heteroaryl can also be part of a bi- or polycyclic system having up to 10 ring members, wherein the ring system can be formed with further saturated or (partially) unsaturated cycloalkyl or heterocyclyl, aromatic or heteroaromatic ring systems, which can in turn be unsubstituted or mono- or polysubstituted. It is preferable for the heteroaryl residue to be selected from the group consisting of benzofuranyl, benzoimidazolyl, benzothienyl, benzothiadi- azolyl, benzothiazolyl, benzotriazolyl, benzooxazolyl, benzooxadiazolyl, quinazolinyl, quinoxalinyl, carb- azolyl, quinolinyl, dibenzofuranyl, dibenzothienyl, furyl (furanyl), imidazolyl, imidazothiazolyl, indazolyl, indolizinyl, indolyl, isoquinolinyl, isoxazoyl, isothiazolyl, indolyl, naphthyridinyl, oxazolyl, oxadiazolyl, phenazinyl, phenothiazinyl, phthalazinyl, pyrazolyl, pyridyl (2-pyridyl, 3-pyridyl, 4-pyridyl), pyrrolyl, pyridazinyl, pyrimidinyl, pyrazinyl, purinyl, phenazinyl, thienyl (thiophenyl), triazolyl, tetrazolyl, thiazolyl, thiadiazolyl and triazinyl.
Within the scope of the present invention, the symbols ? or— used in the formulae denotes a link of a corresponding residue to the respective superordinate general structure.
In one embodiment of the first aspect of the invention, the compound according to general formula (I) is characterized in that R1 is H.
In another embodiment of the first aspect of the invention, the compound according to general formula (I) is characterized in that Y1 represents CH or N and Y2 represents CH; or Y1 represents CH and Y2 represents CH or N.
In yet another embodiment of the first aspect of the invention, the compound according to general formula (I) is characterized in that X represents S.
In yet another embodiment of the first aspect of the invention, the compound according to general formula (I) is characterized in that X represents S, Y represents CH and Y2 represents CH. resents CH, as given in formula (I-2):
In yet another embodiment of the first aspect of the invention, the compound according to general formula (I) is characterized in that X represents S, Y1 represents CH and Y2 represents N. resents N, as given in formula (I-3):
Yet another embodiment of the first aspect of the invention is characterized in that the compound according to general formula (I) is a compound according to general formula (la),
wherein Z represents
m denotes 0 or 1 ;
Y2 represents N or CH;
R2 is selected from the group consisting of F; CI; Br; CN; CF3; CF2H; CFH2; CF2CI; CFCI2; d_4-alkyl;
C(=0)-(C1.4-alkyl); C(=0)-NH2; C(=0)-N(H)(C1.4-alkyl); C(=0)-N(C1.4-alkyl)2; OH; 0-d.4-alkyl; OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; NH2; N(H)(d.4-alkyl), N(d-4-alkyl)2; N(H)-C(=0)-(C1.4-alkyl); N(CM- alkyl)-C(=0)-(C1.4-alkyl); N(H)-S(=0)2-(C1.4-alkyl); N(H)-C(=0)-NH2; N(H)-C(=0)-N(H)(C1.4-alkyl); N(H)-
C(=0)-N(C1.4-alkyl)(C1.4-alkyl); S-(d.4-alkyl); S(=0)-(C,.4-alkyl); S(=0)2-(C1-4-alkyl); S(=0)2-N(H)(C,.4- alkyl); cyclopropyl; O-cyclopropyl; NH-cyclopropyl; N(H)-C(=0)-cyclopropyl; S(=0)-(cyclopropyl) and
S(=0)2-(cyclopropyl);
n denotes 0, 1 or 2 and
R3 is independently selected from the group consisting of F; CI; Br; CN; CF3; CF2H; CFH2; CF2CI; CFCI2;
C1-4-alkyl; C(=0)-(d.4-alkyl); C(=0)-NH2; C(=0)-N(H)(C1.4-alkyl); C(=0)-N(C1.4-alkyl)2; OH; 0-d.4-alkyl;
OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; NH2; N(H)(d.4-alkyl); N(d.4-alkyl)2; N(H)-C(=0)-(C1.4-alkyl);
N(C1.4-alkyl)-C(=0)-(C1.4-alkyl); N(H)-S(=0)2-(C1-4-alkyl); N(H)-C(=0)-NH2; N(H)-C(=0)-N(H)(C1.4-alkyl); N(H)-C(=0)-N(C1.4-alkyl)(C1.4-alkyl); S-(d.4-alkyl); S(=0)-(d.4-alkyl); S(=0)2-(d.4-alkyl); S(=0)2-N(H)(d.
4-alkyl); cyclopropyl; O-cyclopropyl; NH-cyclopropyl; N(H)-C(=0)-cyclopropyl; S(=0)-(cyclopropyl) and
S(=0)2-(cyclopropyl).
Preferably, m denotes 0; Y2 represents N or CH; n denotes 0, 1 or 2 and
R3 is independently selected from the group consisting of F; CI; Br; CN; CF3; CF2H; CFH2; CF2CI; CFCI2; d.4-alkyl; C(=0)-(d.4-alkyl); C(=0)-NH2; C(=0)-N(H)(d.4-alkyl); C(=0)-N(d.4-alkyl)2; OH; O-C!^-alkyl;
OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; NH2; N(H)(d.4-alkyl); N(d_4-alkyl)2; N(H)-C(=0)-(d.4-alkyl);
N(d.4-alkyl)-C(=0)-(d.4-alkyl); N(H)-S(=0)2-(d.4-alkyl); N(H)-C(=0)-NH2; N(H)-C(=0)-N(H)(d.4-alkyl);
N(H)-C(=0)-N(d.4-alkyl)(d.4-alkyl); S-(d.4-alkyl); S(=0)-(d.4-alkyl); S(=0)2-(d.4-alkyl); S(=0)2-N(H)(d. 4-alkyl); cyclopropyl; O-cyclopropyl; NH-cyclopropyl; N(H)-C(=0)-cyclopropyl; S(=0)-(cyclopropyl) and
S(=0)2-(cyclopropyl).
In another embodiment of the first aspect of the invention, the compound according to general formula (la) is characterized in that m denotes 0; Y2 represents N or CH; n denotes 0, 1 or 2 and
R3 is independently selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; CH(CH3)2; C(=0)CH3; C(=0)NH2; C(=0)N(H)(CH3); C(=0)N(CH3)2; OH; OCH3; OCF3; OCF2H; OCFH2;
NH2; N(H)(CH3); N(CH3)2; N(H)-C(=0)CH3; N(H)-S(=0)2CH3; S(=0)CH3; S(=0)2CH3; S(=0)2-N(H)(CH3); cyclopropyl and O-cyclopropyl.
Preferably, m denotes 0; Y2 represents CH; n denotes 0, 1 or 2 and
R3 is independently selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; CH(CH3)2; C(=0)CH3; C(=0)NH2; C(=0)N(H)(CH3); C(=0)N(CH3)2; OH; OCH3; OCF3; OCF2H; OCFH2; NH2; N(H)(CH3); N(CH3)2; N(H)-C(=0)CH3; N(H)-S(=0)2CH3; S(=0)CH3; S(=0)2CH3; S(=0)2-N(H)(CH3); cyclopropyl and O-cyclopropyl. Yet preferably, m denotes 0; Y2 represents N; n denotes 0, 1 or 2 and
R3 is independently selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; CH(CH3)2; C(=0)CH3; C(=0)NH2; C(=0)N(H)(CH3); C(=0)N(CH3)2; OH; OCH3; OCF3; OCF2H; OCFH2; NH2; N(H)(CH3); N(CH3)2; N(H)-C(=0)CH3; N(H)-S(=0)2CH3; S(=0)CH3; S(=0)2CH3; S(=0)2-N(H)(CH3); cyclopropyl and O-cyclopropyl.
In another embodiment of the first aspect of the invention, the compound according to general formula (la) is characterized in that m denotes 0; Y2 represents N or CH;
Z represents
n denotes 0 or 1 and
R3 is independently selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; CH(CH3)2; C(=0)CH3; C(=0)NH2; C(=0)N(H)(CH3); C(=0)N(CH3)2; OH; OCH3; OCF3; OCF2H; OCFH2; NH2; N(H)(CH3); N(CH3)2; N(H)-C(=0)CH3; N(H)-S(=0)2CH3; S(=0)CH3; S(=0)2CH3; S(=0)2-N(H)(CH3); cyclopropyl and O-cyclopropyl. In another embodiment of the first aspect of the invention, the compound according to general formula (la) is characterized in that m denotes 0; Y2 represents N or CH;
n denotes 0 or 1 and
R3 is independently selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; CH(CH3)2; C(=0)CH3; C(=0)NH2; C(=0)N(H)(CH3); C(=0)N(CH3)2; OH; OCH3; OCF3; OCF2H; OCFH2; NH2; N(H)(CH3); N(CH3)2; N(H)-C(=0)CH3; N(H)-S(=0)2CH3; S(=0)CH3; S(=0)2CH3; S(=0)2-N(H)(CH3); cyclopropyl and O-cyclopropyl.
Yet another embodiment of the first aspect of the invention is characterized in that the compound
eral formula (lb),
wherein Y2 represents CH
Z3, Z4 and Z5 each represent CH and Z1 represents N or
Z1, Z4 and Z5 each represent CH and Z3 represents N or,
Z Z3 and Z5 each represent CH and Z4 represents N or
Z1, Z3 and Z4 each represent CH and Z5 represents N;
n denotes 0 or 1 and
R3 is selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; OCH3 cyclopropyl and OCF3.
Yet another embodiment of the first aspect of the invention is characterized in that the compound
eral formula (lc):
wherein Y2 represents CH or N;
Z1, Z2, Z4 and Z5 each represent CH or
Z2, Z4 and Z5 each represent CH and Z1 represents N or
z Z4 and Z5 each represent CH and Z2 represents N;
n denotes 0 or 1 or 2 and
R3 is selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; OCH3; cyclopropyl and OCF3.
Preferably, the compound according to general formula (lb) or (Ic) is characterized in that Y2 represents CH. Yet preferably, the compound according to general formula (lb) or (Ic) is characterized in that Y2 represents N.
In another embodiment of the first aspect of the invention, the compound according to general formula (lb) is characterized in that Y2 represents CH;
Z3, Z4 and Z5 each represent CH and Z1 represents N or
Z1 , Z4 and Z5 each represent CH and Z3 represents N and n denotes 0.
Particularly preferred compounds according to the invention are selected from the group consisting of N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2-
1
oxoethyl)-5-(pyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyridin-3-y()thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- ^ oxoethyl)-5-(pyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2-
4
oxoethyl)-5-(pyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyrazin-2-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(5-fluoropyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyridazin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyridine-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- ^ oxoethyl)-5-(pyrimidin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyridazin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-methylpyrimidin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 1 ^ oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2-
14
oxoethyl)-5-(5-fluoropyrimidin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-methylpyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyrazin-2-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(6-methylpyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(3-fluoropyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyrimidin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-methylpyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(6-chloropyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-cyclopropylpyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-cyclopropylpyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-(trifluoromethyl)pyrirriidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(6-(trifluoromethyl)pyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(6-cyclopropylpyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-methylpyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(5-met ylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(6-cyclopropylpyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(pyridazin-4-yl)furan-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(2-(trifluoromethyl)pyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(6-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- oxoethyl)-5-(5-ethylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2-
37
oxoethyl)-5-(5-methoxypyridazir)-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 38
oxoethyl)-5-(5-cyclopropylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 39
oxoethyl)-5-(6-methylpyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 40
oxoethyl)-5-(6-methoxypyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 41
oxoethyl)-5-(2-methoxypyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 42
oxoethyl)-5-(2-cyclopropylpyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 43
oxoethyl)-5-(2,4-dimethylpyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1-cyclopentyl-2- 44
oxoethyl)-5-(2-cyclopropylpyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 45
oxoethyl)-5-(2-methylpyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 46
oxoethyl)-5-(4-methylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 47
oxoethyl)-5-(6-ethylpyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 48
oxoethyl)-5-(6-methylpyridazin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 49
oxoethyl)-5-(2-ethylpyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 50
oxoethyl)-5-(2-ethylpyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 51
oxoethyl)-5-(2,5-dimethylpyridin-4-yl)thiopriene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 52
oxoethyl)-5-(5-methylpyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -cyclopentyl-2- 53
oxoethyl)-5-(3,6-dimethylpyridazin-4-yl)thiophene-2-carboxamide
optionally in the form of a single stereoisomer or a mixture of stereoisomers, in the form of the free compound and/or a physiologically acceptable salt or solvate thereof.
Compounds of general formula (I) are useful for the in vivo treatment or prevention of diseases participation of a cysteine protease is implicated.
Preferably, the compound of general formula (I) is a dual inhibitor of CatS and CatK (CatS/K inhibitors). More preferably, the compound of general formula (I) is a dual inhibitor of Cats and CatK with a pronounced effect on CatK (CatS/K inhibitors with preference for CatK). The term "dual for Cats and CatK" is to be understood that the inhibitor is a potent inhibitor of both CatS and CatK. Furthermore, preference may be given to compounds according to the invention that cause at least a 50% inhibition at a concentration of 3 μΜ in a functional enzyme assay for both CatS as well as CatK, preferably less than 1000 nM for both CatS and CatK, particularly preferably less than 500 nM for both CatS and CatK, more preferably less than 400 nM for both CatS and CatK, even more preferably less than 300 nM for both CatS and CatK, even more preferably less than 200 nM for both CatS and CatK, even more preferably less than 150 nM for both CatS and CatK, even more preferably less than 100 nM for both CatS and CatK, and most preferably less than 50 nM for both CatS and CatK.
For these purposes functional enzyme assays using co-incubations of commercially available recombinant human cathepsines and respective fluorogenic substrates were conducted, as described hereinafter.
Preferably, the compounds according to present invention possess a high activity in both CatS enzyme assay and CatK enzyme assay, but exhibit a preference for the CatK enzyme assay. Preferably, the Ki value of CatK enzyme assay is significantly lower than the Ki value of CatS enzyme assay, while still retaining high inhibition in both CatS and CatK enzyme assays. Preferably the preference in activity for CatK over Cat S is at least 20 fold (relating to Ki(CatS)/Ki(CatK) > 20), preferably at least 50 fold (relating to Ki(CatS)/Ki(CatK) > 50), more preferably at least 100 fold (relating to Ki(CatS)/Ki(CatK) > 100), even more preferably at least 150 fold (relating to Ki(CatS)/Ki(CatK) > 150), and most preferably at least 200 fold (relating to Ki(CatS)/Ki(CatK) > 200), while in each case the compound still causes at least a 50% inhibition at a concentration of 1000 nM in a functional enzyme assay for CatS, preferably less than 500 nM for CatS, more preferably less than 400 nM for CatS, even more preferably less than 300 nM for CatS, even more preferably less than 200 nM for CatS, even more preferably less than 150 nM for CatS, even more preferably less than 100 nM for CatS, and most preferably less than 50 nM for CatS.
Furthermore, preference may be given to compounds according to the invention that do not inhibit CatL significantly. This means that the compounds cause preferably less than 50% inhibition at a concentration of 31.6 μΜ in afunctional CatL enzyme assay. Additionally, the compounds according to present invention exhibit a significant selectivity for both CatS as well as CatK over CatL. Preferably, the compounds possess a selectivity to CatS and to CatK over CatL of at least 100 (Ki(CatL)/Ki(CatK) > 00 and Ki(CatL)/Ki(CatS) > 100), preferably of at least 250 (Ki(CatL)/Ki(CatK) > 250 and Ki(CatL)/Ki(CatS) > 250), more preferably of at least 500 (Ki(CatL)/Ki(CatK) > 500 and Ki(CatL)/Ki(CatS) > 500) and most preferably of at least 1000 (Ki(CatL)/Ki(CatK) > 1000 and Ki(CatL)/Ki(CatS) > 1000).
Furthermore, preference may be given to compounds according to the invention that do not inhibit CatB significantly. This means that the compounds cause preferably less than 50% inhibition at a concentration of 31.6 μΜ in a functional CatB enzyme assay. Additionally, the compounds according to present invention exhibit a significant selectivity for both CatS as well as CatK over CatB. Preferably, the compounds possess a selectivity to CatS and to CatK over CatB of at least 100 (Ki(CatB)/Ki(CatK) > 100 and Ki(CatB)/Ki(CatS) > 100), preferably of at least 250 (Ki(CatB)/Ki(CatK) > 250 and Ki(CatB)/Ki(CatS) > 250), more preferably of at least 500 (Ki(CatB)/Ki(CatK) > 500 and Ki(CatB)/Ki(CatS) > 500) and most preferably of at least 1000 (Ki(CatB)/Ki(CatK) > 1000 and Ki(CatB)/Ki(CatS) > 1000).
The present invention further relates to a compound according to the present invention for modulation of both CatS and CatK, preferably for use in inhibitbion of CatS and CatK activity. The present invention therefore further relates to a compound according to the present invention for the prophylaxis and/or treatment of disorders and/or diseases which are mediated, at least in part, by both CatS and CatK without the inhibition of CatL and /or CatB. The present invention even further relates to a compound according to the present invention for the prophylaxis and/or treatment of disorders and/or diseases which are mediated, at least in part, by both CatS and CatK with a pronounced mediation by CatK without the inhibition of CatL and /or CatB.
According to a further aspect of the invention, there is provided the use of a compound according to the present invention in the preparation of a medicament for preventing or treating diseases in which the disease pathology may be modified by inhibiting a CatS and/or CatK.
In another aspect of the present invention, the invention therefore also provides pharmaceutical compositions, containing at least one compound according to the invention and optionally one or more suitable, pharmaceutically compatible auxiliaries and/or, if appropriate, one or more further
pharmacologically active compounds.
The pharmaceutical composition according to the invention may be found as a liquid, semisolid or solid pharmaceutical form, for example in the form of injection solutions, drops, juices, syrups, sprays, suspensions, tablets, patches, capsules, plasters, suppositories, ointments, creams, lotions, gels, emulsions, aerosols or in multiparticulate form, for example in the form of pellets or granules, if appropriate pressed into tablets, decanted in capsules or suspended in a liquid, and also be administered as much.
In addition to at least one compound according to the invention, if appropriate in the form of one of its pure stereoisomers, in particular enantiomers or diastereomers, its racemate or in the form of mixtures of the stereoisomers, in particular the enantiomers or diastereomers, in any desired mixing ratio, or if appropriate in the form of a corresponding salt or respectively in the form of a corresponding solvate, the pharmaceutical composition according to the invention conventionally contains further physiologically compatible pharmaceutical auxiliaries which can for example be selected from the group consisting of excipients, fillers, solvents, diluents, surface-active substances, dyes, preservatives, blasting agents, slip additives, lubricants, aromas and binders.
The selection of the physiologically compatible auxiliaries and also the amounts thereof to be used depend on whether the pharmaceutical composition is to be applied orally, subcutaneously, parenterally, intravenously, intraperitoneally, intradermally, intramuscularly, intranasally, buccally, rectally or locally, for example to infections of the skin, the mucous membranes and of the eyes. Preparations in the form of tablets, dragees, capsules, granules, pellets, drops, juices and syrups are preferably suitable for oral application; solutions, suspensions, easily reconstitutable dry preparations and also sprays are preferably suitable for parenteral, topical and inhalative application. The compounds according to the invention used in the pharmaceutical composition according to the invention in a repository in dissolved form or in a plaster, agents promoting skin penetration being added if appropriate, are suitable percutaneous application preparations. Orally or percutaneously applicable preparation forms can release the respective compound according to the invention also in a delayed manner.
The pharmaceutical compositions according to the invention are prepared with the aid of conventional means, devices, methods and process known in the art. The amount to be administered to the patient of the respective compounds according to the invention of the above-indicated general formula I may vary and is for example dependent on the patient's weight or age and also on the type of application, the indication and the severity of the disorder. Conventionally 0.001 to 100 mg/kg, preferably 0.05 to 75 mg kg, particularly preferably 0.05 to 50 mg of at least one such compound according to the invention are applied per kg of the patient's body weight.
In the normal physiological process certain cysteine proteases function in the protein degradation in animals, including humans, e.g. in the degradation of connective tissue. Elevated levels of these cysteine proteases in the body may result in pathological conditions leading to disease. Cats and CatK are believed to be involved in a variety of diseases or disorders in mammals such as humans. These include pain (in particular chronic pain, inflammatory pain, mixed pain), inflammatory diseases and bone/cartilage preservation disorders.
Particularly useful are dual Cats and CatK (CatS/K) inhibitors for the treatment of rheumatoid arthritis (RA), osteoarthritis(OA), chronic obstructive pulmonary disease (COPD), atherosclerosis and
cardiovascular diseases which exhibit significant damage and remodeling of extracellular matrix (ECM) and chronic pain.
Another embodiment of the present invention is at least one compound according the present invention for the treatment and/or prophylaxis of one or more disorders selected from the group consisting of nociceptive pain, neuropathic pain; erosive osteoarthritis (EO), in particular erosive osteoarthritis of the hand; Sjogren's Syndrom; rheumatoid arthritis (RA); psoriatic arthrithis (PsA), Psoriasis, Spondylarthritis, in particular ankylosing spondylitis; osteoporosis; Complex Regional Pain Syndrome (in particular CRPS I); Lupus erythematodes (SLE); Lupus nephritis; asthma; multiple sclerosis (MS); diabetes; chronic obstructive pulmonary disease (COPD), in particular COPD subpopoulation with osteoporosis; and asthma, in particular severe asthma subpopoulation with osteoporosis.
Another embodiment of the present invention therefore relates to use of at least one compound according to the present invention for the preparation of a pharmaceutical composition for the treatment and/or prophylaxis of one or more disorders or diseases, particularly selected from the group consisting of nociceptive pain, neuropathic pain; erosive osteoarthritis (EO), in particular erosive osteoarthritis of the hand; Sjogren's Syndrom; rheumatoid arthritis (RA); psoriatic arthrithis (PsA), Psoriasis, Spondylarthritis, in particular ankylosing spondylitis; osteoporosis; Complex Regional Pain Syndrome (in particular CRPS I); Lupus erythematodes (SLE); Lupus nephritis; asthma; multiple sclerosis (MS); diabetes; chronic obstructive pulmonary disease (COPD), in particular COPD subpopoulation with osteoporosis; and asthma, in particular severe asthma subpopoulation with osteoporosis.
Another aspect of the present invention is a method of treatment and/or prophylaxis of disorders and/or diseases in a mammal, preferably of disorders and/or diseases selected from the group consisting of nociceptive pain, neuropathic pain; erosive osteoarthritis (EO), in particular erosive osteoarthritis of the hand; Sjogren's Syndrom; rheumatoid arthritis (RA); psoriatic arthrithis (PsA), Psoriasis, Spondylarthritis, in particular ankylosing spondylitis; osteoporosis; Complex Regional Pain Syndrome (in particular CRPS I); Lupus erythematodes (SLE); Lupus nephritis; asthma; multiple sclerosis (MS); diabetes; chronic obstructive pulmonary disease (COPD), in particular COPD subpopoulation with osteoporosis; and asthma, in particular severe asthma subpopoulation with osteoporosis.
All preferred embodiments of the first aspect of the invention are preferred vice versa for the other aspects and embodiments.
EXAMPLES
The compounds according to the invention can be prepared in the manner described below. The following examples further illustrate the invention but are not to be construed as limiting its scope.
All starting materials which are not explicitly described were either commercially available (the details of suppliers such as for example Acros, Avocado, Aldrich, Apollo, Bachem, Fluka, FluoroChem, Lancaster, Manchester Organics, MatrixScientific, Maybridge, Merck, Rovathin, Sigma, TCI, Oakwood, etc. can be found in the Symyx® Available Chemicals Database of MDL, San Ramon, US or the SciFinder® Database of the ACS, Washington DC, US, respectively, for example) or the synthesis thereof has already been described precisely in the specialist literature (experimental guidelines can be found in the Reaxys® Database of Elsevier, Amsterdam, NL or the SciFinder® Database of the ACS, Washington DC, US, repspectively, for example) or can be prepared using the conventional methods known to the person skilled in the art.
All reactions were conducted under nitrogen unless stated otherwise and monitored by TLC on silica gel coated glass plates or aluminium sheets. Flash column chromatography was performed on pre-packed silica gel columns (GraceResolvetm) using the indicated solvents mixtures. All solvents were used without prior drying. Dry solvents were dried on molecular sieves (4A).
The NMR spectra were determined in DMSO-d6 solutions, using a Bruker 400-UltraShield. Spectra are reported in " units (ppm) and J values (Hz) with Me4Si as the internal standard.
Acid HPLC analyses were conducted using an Agilent system, column: Waters XSelect (C18, 50x2.1 mm, 3.5μ), flow: 0.8 ml/min, column temp: 35°C, Eluent A: 0.1 % Formic acid in MeCN, Eluent B: 0.1 % Formic acid in water, lin. gradient: t=0 min 2% A, t=3.5 min 98% A, t=6 min 98%A, detection: DAD (220 - 320 nm), detection: MSD (ESI pos/neg) mass range: 00 - 800.
Basic HPLC analyses were conducted using an Agilent system, column: Waters XSelect (C18, 50x2.1 mm, 3.5μ), flow: 0.8 ml/min, column temp: 35°C, Eluent A: 95% MeCN + 5% 10 mM NH4HC03 in water, Eluent B: 10 mM NH4HC03 in water (pH=9.0), lin. gradient: t=0 min 2% A, t=3.5 min 98% A, t=6 min 98%A, detection: DAD (220 - 320 nm), detection: MSD (ESI pos/neg) mass range: 100 - 800.
The indication ..equivalents" ("eq." or "eq" or "equiv.") means molar equivalents,„RT" or "rt" means RTT (23 ± 7 °C),„M" are indications of concentration in mol/l,„aq." means aqueous,„sat." means saturated, „sol." means solution, "cone." means concentrated. The mixing ratios of solvents are usually stated in the volume / volume ratio, "calc." means "calculated", "fd." means" found".
Further abbreviations:
DME = 1 ,2-dimethoxyethane; DCM = dichloromethane; DMF = N,N-Dimethylformamide; DMP = Dess- Martin periodinane; EDCI: N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride; Et20 = diethyl ether; EtOAc = ethyl acetate; EtOH = ethanol; FC = flash chromatography; h = hour(s); HOAt = 1 - hydroxy-7-azabenzotriazole; /-PrOH = isopropanol; LDA = lithium diisopropylamine; MeCN = aceto- nitrile; MeOH = methanol; PdCI2(dppf) = 1 ,1 '-bis(diphenylphosphino)ferrocene]palladium(ll) dichloride; Pd2(dba)3 = tris(dibenzylideneacetone)dipalladium; RM = reaction mixture; rt / RT = room temperature; NEt3 = triethylamine; T3P = propylphosphonic anhydride; TFA = trifluoroacetic acid; THF =
tetrahydrofuran.
INT-1 was prepared analogously to synthetic methods known from WO2009/1 12839.
Example 1 : N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetra ydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridazin-3-yl)thiophene-2-carboxamide
INT-1B
(i) Phosphorous oxybromide (158 g, 552 mmol) was heated to 80°C under mechanical stirring until molten. 3-Hydroxypyridazine (30.5 g, 317 mmol) was added in one portion to the orange liquid, which
afforded immediately a yellow, then a black solid. This was heated to 120°C and left at this temperature for 3 h. After cooling to 0°C, small portions of ice water (in total: 300 mL) were slowly added and an exothermic reaction was observed (white smoke). During stirring, some solids did not dissolve, 2 N aqueous NaOH (180 mL) was added at RT and stirred for 45 min until all solids were dissolved. The dark red/brown solution was poured into a mechanically stirred ice/water bath, which contained 2 N aqueous NaOH solution (910 mL). The internal temperature was kept below 25°C during the addition. The pH was adjusted to ~9.5 by addition of 2 N aqueous NaOH (50 mL). The brown solution was extracted with DCM (5* 250 mL). The combined yellow organic layer was dried over Na2S04, filtered and concentrated in vacuo to obtain a grey/brown solid. The crude material was coated on silica (98 g) and filtered with heptane/EtOAc (1 :1 ) over a plug of silica (200 g). Product containing fractions were combined and concentrated in vacuo to afford INT-1A (34.7 g 216 mmol, 69%) as a green/grey solid. GCMS: >99% pure.
(ii) Diisopropylamine (21.8 g, 215 mmol, 30.4 mL) was dissolved in dry THF (200 mL) and cooled to -78°C under N2. A solution of n-butyllithium (1.6 M in hexanes, 215 mmol, 134 mL) was added drop wise. The mixture was allowed to warm to 0°C and stirred for 30 min. The solution was cooled to -78°C and a solution of ethyl thiophene-2-carboxylate (33.6 g, 215 mmol, 29.0 mL) in dry THF (50 mL) was added drop wise. The mixture was stirred at -78°C for 1 h. A solution of tributyltinchloride (70.0 g, 215 mmol, 58.3 mL) in dry THF (50 mL) was added dropwise and the solution was stirred at -78°C for 1 h, then allowed to warm up to RT and stirred for 1 h. The mixture was poured into 1 L aqueous saturated NH4CI and extracted with EtOAc (2* 750 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to obtain a brown oil. Filtration over silica (~500 g, eluted with EtOAc/heptane 1 :19) afforded INT-1B (86.8 g, 95 mmol, 91 %) as a clear orange/brown liquid.
(iii) A solution of INT-1A (28.2 g, 177 mmol) and INT-1B (86.8 g, 195 mmol) was degassed with Ar. CsF (81.0 g, 532 mmol), CuCI (2.28 g, 23.0 mmol) and PdCI2(dppf) (6.96 g, 9.51 mmol) were added and the mixture was heated at 100°C for 3 h. A solution of KF (25.0 g, 430 mmol) in 200 mL of water was added and the mixture was stirred vigorously for 3 h. The mixture was filtered over celite, rinsed with EtOAc (3 * 400 mL). The filtrate was diluted with aqueous saturated NaHC03 (500 mL) and water (500 mL). The layers were separated, the aqueous layer was extracted with EtOAc (750 mL). The combined organic layer was washed with brine (2* 1 L), dried over Na2S04 and concentrated in vacuo. The aqueous layer was divided in three 1 L portions, which were extracted with EtOAc (2* 500 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo and combined with the previous organic fraction. The product was purified by gravity column chromatography (~1 kg of silica, product loaded on Isolute, eluted with 5 L (EtOAc/heptane 1 :4), 4 L (EtOAc/heptane 2:3), 4 L (EtOAc/heptane 3:2), 5 L (EtOAc/ heptane 4:1 ), then pure EtOAc) to obtain INT-1C (15.6 g, 66.4 mmol, 38%) as a yellow solid. LCMS: calc. for [M+H]+=235.05, fd. 235.1.
(iv) LiOH H20 (5.70 g, 136 mmol) was added to a suspension of INT-1C (15.6 g, 66.4 mmol) in THF (200 mL) and water (150 mL). The mixture was heated to 65°C for 1 h. The mixture was concentrated in vacuo. The residue was acidified to pH 3-4 (range) using aqueous 2 M HCI (~70 mL). /'-PrOH (100 mL)
was added. The solids were filtered off and washed with Et20, dried in vacuo to obtain INT-1 D (13.1 g, 63.5 mmol, 96%) as a yellow solid. LCMS: calc. for [M+H]+=207.01 , fd. 207.2.
(v) A suspension of INT-1 (0.180 g, 0.553 mmol), INT-1 D (0.1 14 g, 0.553 mmol), EDCI (0.127 g, 0.663 mmol), NEt3 (0.269 mL, 1.94 mmol) and HOAt (0.0075 g, 0.055 mmol) in DMF (2 mL) was stirred at RT for 16 h (TLC, EtOAc/heptane 9:1 ). The mixture was diluted with aqueous saturated NaHC03 (10 mL) and extracted with EtOAc (3* 10 mL). The combined organic layer was washed with brine (10 mL), dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 1 :9 to 1 :0) afforded INT-1 E (0.128 g, 0.268 mmol, 49%). LCMS: calc. for [M+H]+=477.14, fd. 477.2.
(vi) DMP (0.228 g, 0.537 mmol) was added to a solution of INT-1 E (0.128 g, 0.268 mmol) in DCM (4 mL). The mixture was stirred at RT for 18 h. An aqueous solution of Na2S203 (10%, 10 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (10 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (10 mL). The combined organic layer was dried over Na2S04. The filtrate was concentrated in vacuo. Purified by basic preparative HPLC (C18, MeCN (1 % 10mM NH4HC03), 10 mM NH4HC03 in H20) and lyophilized to obtain 1 (0.100 g, 0.21 1 mmol, 78%). LCMS: calc. for [M+Hf =475.12, fd. 475.2. 1H NMR (400 MHz, DMSO-d6) as a mixture of hydrates and rotamers δ 9.25-8.90 (m, 2H), 8.41-8.22 (m, 1 H), 8.21-7.93 (m, 2H), 7.90-7.71 (m, 1 H), 6.77 (s, 0.48H), 6.49 (s, 0.33H), 6.41 (s, 0.48H), 5.78 (s, 0.33H), 5.21-3.46 (m, 8H), 2.48-2.30 (m, 1 H), 1.90-1.07 (m, 8H) ppm.
Example 2: N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1- cyclopentyl-2-oxoethyl)-5-(pyridin-3-yl)thiophene-2-carboxamide
(i) A suspension of INT-1 (0.300 g, 0.922 mmol), 5-(pyridin-3-yl)thiophene-2-carboxylic acid (0.189 g, 0.922 mmol), EDCI (0.212 g, 1 .11 mmol), NEt3 (0.449 mL, 3.23 mmol) and HOAt (0.013 g, 0.092 mmol) in DMF (4 mL) was stirred at RT for 96 h. The mixture was diluted with aqueous saturated NaHC03 (10 mL) and extracted with EtOAc (3* 10 mL). The combined organic layer was washed with brine (10 mL), dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1 to 1 :0) afforded INT-2A (0.278 g, 0.584 mmol, 63%). LCMS: calc. for [M+H]+=476.14, fd. 476.2.
(ii) DMP (0.495 g, 1.17mmol) was added to a solution of INT-2A (0.278 g, 0.584 mmol) in DCM (10 mL). The mixture was stirred at RT for 18 h. An aqueous solution of Na2S203 (10%, 10 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (50 mL) was added
and the layers were separated. The aqueous layer was extracted with DCM (30 mL). The combined organic layer was dried over Na2S0 . The filtrate was concentrated in vacuo. Purified by basic preparative HPLC (C18, MeCN (1 % 10 mM NH4HC03), 10 mM NH4HC03 in H20) and lyophilized to obtain 2 (0.1 16 g, 0.245 mmol, 42%). LCMS: calc. for [M+H]+=474.14, fd. 474.1. 1H NMR (400 MHz, DMSO-d6) as a mixture of hydrates and rotamers δ 9.17-8.85 (m, 2H), 8.64-8.46 (m, 1 H), 8.21-7.92 (m, 2H), 7.78-7.60 (m, 1 H), 7.58-7.40 (m, 1 H), 6.74 (s, 0.38H), 6.48 (s, 0.28H), 6.38 (s, 0.38H), 5.77 (s, 0.28H), 5.21 -3.44 (m, 8H), 2.46-2.23 (m, 1 H), 1.89-1.05 (m, 8H) ppm.
Example 3: N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1■ cyclopentyl-2-oxoethyl)-5-(pyrimidin-5-yl)thiophene-2-carboxamide
INT-3A
(i) A suspension of 5-boronothiophene-2-carboxylic acid (2.00 g, 11 .6 mmol), K2C03 (1.46 g, 10.6 mmol) and 5-bromopyrimidine (1.68 g, 10.6 mmol) in DME (80 mL) and water (20 mL) was degassed with Ar and tetrakis(triphenylphosphine)palladium(0) (0.61 1 g, 0.529 mmol) and stirred for 16 h at 100°C. Upon completion the reaction mixture was poured into H20 (150 mL) and washed with EtOAc (150 mL). The aqueous phase was acidified with aqueous 1 M HCI until pH 2-3 and extracted with EtOAc (3x 200 mL). The three last organic layers were combined, washed with brine, dried with Na2S04 and concentrated in vacuo. Trituration with Et20 and filtration afforded INT-3A (1.69 g, 7.79 mmol, 74%) as an off white solid. LCMS: calc. for [M+H]+=207.01 , fd. 207.2.
(ii) A suspension of INT-1 (0.300 g, 0.922 mmol), INT-3A (0.190 g, 0.922 mmol), EDCI (0.212 g, 1 .1 1 mmol), NEt3 (0.449 mL, 3.23 mmol) and HOAt (0.013 g, 0.092 mmol) in DMF (4 mL) was stirred at RT for 96 h. The mixture was diluted with aqueous saturated NaHC03 (10 mL) and extracted with EtOAc (3* 10 mL). The combined organic layer was washed with brine (10 mL), dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1 to 1 :0) afforded INT-3B (0.269 g, 0.564 mmol, 61 %). LCMS: calc. for [M+H]+=477.14, fd. 477.2.
(iii) DMP (0.478 g, 1.13 mmol) was added to a solution of INT-3B (0.269 g, 0.564 mmol) in DCM (10 mL). The mixture was stirred at RT for 18 h. An aqueous solution of Na2S203 (10%, 10 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (50 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (30 mL). The combined organic layer was dried over Na2S0 . The filtrate was concentrated in vacuo. Purified by basic preparative HPLC (C18, MeCN (1 % 10 mM NH4HC03), 10 mM NH4HC03 in H20) and lyophilized to obtain 3 (0.136 g, 0.286 mmol, 51 %). LCMS: calc. for [M+Hf =475.12, fd. 475.1 . 1H NMR (400 MHz, DMSO-d6) as a mixture of hydrates and rotamers δ 9.20-9.14 (m, 3H), 9.13-8.96 (m, 1 H), 8.40-8.01 (m, 1 H), 7.82-7.74 (m, 1 H),
6.73 (s, 0.28H), 6.48 (s, 0.21 H), 6.35 (s, 0.28H), 5.77 (s, 0.21 H), 5.21 -3.44 (m, 8H), 2.48-2.25 (m, 1 H), 1.85-1.08 (m, 8H) ppm.
Example 4: N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridazin-4-yl)thiophene-2-carboxamide
(i) A mixture of the methyl 5-bromothiophene-2-carboxylate (0.350 g, 1.58 mmol), CsF (0.480 g, 3.16 mmol) and the 4-(tributylstannyl)pyridazine (0.642 g, 1.74 mmol) was dissolved in DMF (4 mL). Tetrakis(triphenylphosphine)palladium(0) (0.183 g, 0.158 mmol) and Cul (0.060 g, 0.32 mmol) were added and the mixture was degassed with Ar. The mixture was stirred at 80°C for 2 h and diluted with DCM (50 mL) and H20 (20 mL). The organic layer was dried with Na2S04 and filtered through celite. The filter cake was washed with DCM/EtOAc (100 mL, 1 :1 ). The mixture was concentrated in vacuo and the residue triturated with Et20. The solvent was filtered off affording INT-4A (0.396 g, 1.71 mmol, quantitative) as a white solid. LCMS: calc. for [M+Hf=221.03, fd. 221.0.
(ii) To a mixture of INT-4A (0.396 g, 1.80 mmol) in THF (20 mL) and water (20 mL) was added LiOH H20 (0.226 g, 5.39 mmol). The reaction mixture was stirred at RT for 16 h. The mixture was concentrated in vacuo. Reversed phase chromatography (MeCN/H20 (+0.1 % HCOOH) 1 : 19 to 1 :0) afforded INT-4B
(iii) A suspension of INT-1 (0.276 g, 0.849 mmol), INT-4B (0.175 g, 0.849 mmol), EDCI (0.195 g, 1.02 mmol), NEt3 (0.413 mL, 2.97 mmol) and HOAt (0.012 g, 0.085 mmol) in DMF (4 mL) was stirred at RT for 72 h. The mixture was diluted with aqueous saturated NaHC03 (10 mL) and extracted with EtOAc (3* 10 mL). The combined organic layer was washed with brine (10 mL), dried over Na2S04 and concentrated in vacuo. FC (MeCN/EtOAc 0: 1 to 1 :0) afforded INT-4C (0.294 g, 0.616 mmol, 73%). LCMS: calc. for [M+H]+=477.14, fd. 477.2.
(iv) DMP (0.523 g, 1.23 mmol) was added to a solution of INT-4C (0.294 g, 0.616 mmol) in DCM (10 mL). The mixture was stirred at RT for 18 h. An aqueous solution of Na2S203 (10%, 5 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (10 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (10 mL). The combined organic layer was dried over Na2S04. The filtrate was concentrated in vacuo. Purified by basic preparative HPLC (C18, MeCN (1 % 10 mM NH4HC03), 10 mM NH4HC03 in H20) and lyophilized to obtain 4 (0.146 g, 0.307 mmol, 50%). LCMS: calc. for [M+H]+=475.12, fd. 475.1. 1H NMR (400 MHz, DMSO-d6) as a mixture of hydrates and rotamers <5 9.70-9.60 (m, 1 H), 9.30-9.21 (m, 1 H), 9.21-8.98 (m, 1 H), 8.50-7.87 (m, 3H),
6.72 (s, 0.39H), 6.48 (s, 0.31 H), 6.32 (s, 0.39H), 5.76 (s, 0.31 H), 5.19-3.43 (m, 8H), 2.48-2.26 (m, 1 H), 1.89-1.05 (m, 8H) ppm.
Example 5: N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1- cyclopentyl-2-oxoethyl)-5-(pyrazin-2-yl)thiophene-2-carboxamide
INT-5A
(i) 5-Boronothiophene-2-carboxylic acid (4.50 g, 26.2 mmol), 2-chloropyrazine (2.72 g, 23.8 mmol, 2.13 mL) and Na2C03 (7.56 g, 71.4 mmol) were combined in water (30 mL) and DME (120 mL) and degassed with Ar. Tetrakis(triphenylphosphine)palladium(0) (1.20 g, 1.04 mmol) was added and the mixture was stirred at reflux under Ar for 18 h. The reaction mixture was poured into H20 (200 mL) and washed with EtOAc (100 mL). The aqueous phase was acidified with aqueous HCI (2 M) until pH 4-5 and extracted with EtOAc (2x 200 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo. The crude product was dissolved in 1 ,4-dioxane (50 mL), hydrochloric acid (4 M in dioxane) was added. A precipitate was formed and the suspension was stirred for 2 h. The suspension was filtered and dried in vacuo to obtain INT-5A (0.500 g, 2.06 mmol, 9% ) as an off-white solid.
(ii) A suspension of INT-1 (0.300 g, 0.922 mmol), INT-5A (0.190 g, 0.922 mmol), EDCI (0.212 g, 1.1 1 mmol), NEt3 (0.449 mL, 3.23 mmol) and HOAt (0.013 g, 0.092 mmol) in DMF (4 mL) was stirred at RT for 144 h. The mixture was diluted with aqueous saturated NaHC03 (10 mL) and extracted with EtOAc (3χ 10 mL). The combined organic layer was washed with brine (10 mL), dried over Na2S04 and concentrated in vacuo. FC (MeCN (with 1 % HCOOH)/H20 1 :0 to 0:1 , silica C-18) and lyophilisation gave INT-5B (0.065 g, 0.14 mmol, 15%). LCMS: calc. for [M+H]+=477.14, fd. 477.1.
(iii) DMP (0.1 16 g, 0.273 mmol) was added to a solution of INT-5B (0.065 g, 0.14 mmol) in DCM (4 mL). The mixture was stirred at RT for 72 h. An aqueous solution of Na2S203 (10%, 4 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (10 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (10 mL). The combined organic layer was dried over Na2S04. The filtrate was concentrated in vacuo. Purified by basic preparative HPLC (C 8, MeCN (1 % 10 mM NH4HC03), 10 mM NH4HC03 in H20) and lyophilized to obtain 5 (0.045 g, 0.095 mmol, 37%). LCMS: calc. for [M+H]+=475.12, fd. 475.1. 1H NMR (400 MHz, DMSO-d6) as a mixture of hydrates and rotamers δ 9.37-9.23 (m, 1 H), 9.15-8.95 (m, 1 H), 8.72-8.54 (m, 2H), 8.22-7.89 (m, 2H), 6.76 (s, 0.28H), 6.48 (s, 0.19H), 6.39 (s, 0.28H), 5.77 (s, 0.19H), 5.20-3.43 (m, 8H), 2.47-2.24 (m, 1 H), 1.88-1.00 (m, 8H) ppm.
Example 6: N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclop
(i) A suspension of methyl 5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate (0.500 g, 1.87 mmol), Cs2C03 (1.66 g, 5.09 mmol) and 5-bromo-3-fluoropyridine (0.298 g, 1 .70 mmol) was degassed with Ar and PdCI2(dppf) (0.077 g, 0.085 mmol) and stirred for 16 h at 100°C. An aqueous saturated solution of NaHC03 (20 mL) was added and the mixture was extracted with EtOAc (3* 30 mL). The combined organic layer was washed with brine (10 mL), dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1 to 1 :0) afforded INT-6A (0.331 g, 1.33 mmol, 78%) as a white solid. LCMS: calc. for [M+H]+=238.03, fd. 238.2.
(ii) At RT, LiOH-H20 (0.179 g, 4.19 mmol) was added to a mixture of INT-6A (0.331 g, 1.33 mmol) in THF (20 mL) and water (8 mL). The reaction was stirred at RT for 16 h. The reaction was acidified with aqueous 1 M HCI pH 2-3 (10 mL). The mixture was extracted with EtOAc (3* 20 mL). The collected organic layer was washed with brine (20 mL), dried over Na2S04 and concentrated in vacuo to give INT- +=224.01 , fd. 224.2.
(iii) A suspension of INT-1 (0.322 g, 0.990 mmol), INT-6B (0.221 g, 0.990 mmol), EDCI (0.228 g, 1 .19 mmol), NEt3 (0.401 g, 3.96 mmol, 0.552 mL) and HOAt (0.027 g, 0.20 mmol) in DMF (8 mL) was stirred at RT for 16 h. The mixture was diluted with EtOAc (20 mL) and washed with aqueous saturated solution of NaHC03 (20 mL) and brine (10 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1 to 1 :0) afforded INT-6C (0.500 g, 0.962 mmol, 97%). LCMS: calc. for [M+H]+=494.12, fd. 494.2.
(iv) DMP (0.859 g, 2.02 mmol) was added to a solution of INT-6C (0.500 g, 0.962 mmol) in DCM (8 mL). The mixture was stirred at RT for 16 h. An aqueous solution of Na2S203 (10%, 25 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (10 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (2x 10 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo. The crude was dissolved in a small amount of boiling EtOAc and cooled to RT. Heptane was added until a precipitate formed and the mixture was reheated at boiling temperature until a clear solution was formed. The solution was left for 16 h standing at RT and the solids formed were filtered off. Lyophilisation (MeCN/H20) afforded 6 (0.267 g, 0.516 mmol, 51 %). LCMS: calc. for [M+H]+=492.11 , fd. 492.2. 1H NMR (400 MHz, DMSO-d6) as a mixture of hydrates and rotamers δ 9.18-8.92 (m, 1 H), 8.91-8.76 (m, 1 H), 8.65-8.52 (m, 1 H), 8.39-8.10 (m,
1.4H), 8.08-7.97 (m, 0.6H), 7.83-7.71 (m, 1 H), 6.74 (s, 0.38H), 6.48 (s, 0.28H), 6.36 (s, 0.38H), 5.77 (s, 0.28H), 5.29-3.40 (m, 8H), 2.47-2.30 (m, 1 H), 1.88-1.04 (m, 8H) ppm.
Example 7: N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-f uro[3,2-b]pyrrol-4(5H)-yl)-1■ cyclopentyl-2-oxoethyl)-5-(pyridazin-3-yl)thiazole-2-carboxamide
(i) 3-Bromopyridazine (1.02 g, 6.41 mmol), 5-(tributylstannyl)thiazole (2.00 g, 5.35 mmol), tri(furan-2- yl)phosphine (0.250 g, 1.07 mmol) and bis(dibenzylideneacetone) palladium (0.49 g, 0.53 mmol) were dissolved in dry dioxane (5 mL) and the resulting solution was heated at 90°C and stirred for 16 h. The reaction was cooled to RT and filtered using a phase separator and the solvent was evaporated. FC (EtOAc) afforded INT-7A (0.550 g, 3.37 mmol, 63%). LCMS: calc. for [M+H]+=164.02, fd. 164.0.
(ii) Thiazole INT-7A (0.550 g, 3.37 mmol) was added to a solution of Lithium diisopropylamine (1 M in THF/heptane/ethylbenzene, 26 mmol, 26 mL) in dry THF (10 mL) at -78°C and the mixture was stirred for 30 min. C02 (solid) (14.8 g, 336 mmol) was added and the reaction was stirred for 2 h. The reaction was allowed to reach RT and the solvent was evaporated in vacuo. The crude was dissolved in water (10 mL) and washed with EtOAc (10 mL). The aqueous layer was acidified using a 1 N HCI pH 4-5 solution and INT-7B (0.35 g) precipitated out as a yellow solid and was collected. LCMS: calc. for [M+H]+=208.01 , fd.
(iii) NEt3 (0.788 g, 7.80 mmol, 1.09 mL) and T3P (50% w/w in DMF, 0.694 g, 1.09 mmol, 0.649 mL) were added consecutively to a solution of INT-1 (0.254 g, 0.780 mmol) and INT-7B (0.190 g, 0.780 mmol) in dry DMF (10 mL). The reaction was stirred at RT for 16 h. The reaction was diluted with EtOAc (30 mL) and washed with aqueous saturated NaHC03 (30 mL). The water layer was extracted with EtOAc (2* 20 mL). The combined organic layer was washed with brine (20 mL), dried over Na2S04 and concentrated in vacuo. The crude product was purified by FC (MeOH/DCM 5:95) to afford INT-7C (0.200 g, 0.418 mmol, 54%). LCMS: calc. for [M+H]+=478.12, fd. 478.2.
(iv) DMP (0.555 g, 1.31 mmol) was added to a solution of INT-7C (0.200 g, 0.418 mmol) in DCM (20 mL). The mixture was stirred at RT for 16 h. An aqueous solution of Na2S203 (10%, 20 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (20 mL) was added and extracted with DCM (3* 10 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo. The crude product was purified by basic preparative HPLC (C18, MeCN (1 % 10 mM NH4HCO3), 10 mM NH4HC03 in H20) and lyophilization (MeCN/H20) afforded 7 (0.100 g, 0.210 mmol, 50%). LCMS: calc. for [M+H]+=476.11 , fd. 476.2. H-NMR (400 MHz, DMSO-d6) as a mixture of
hydrates and rotamers δ 9.35-9.24 (m, 1 H), 8.97-8.80 (m, 1.46H), 8.59-8.32 (m, 1.40H), 8.18-8.10 (m, 0.14H), 7.99-7.87 (m, 1 H), 6.74 (s, 0.37H), 6.57 (s, 0.37H), 6.53 (s, 0.15H), 5.85 (s, 0.15H), 5.42-3.46 (m, 8H), 2.54-2.30 (m, 1 H), 1.92-1.17 (m, 8H) ppm.
INT-1 INT-8A
(i) A suspension of INT-1 (0.300 g, 0.922 mmol), 5-(pyridin-4-yl)thiophene-2-carboxylic acid (0.189 g, 0.922 mmol), EDO (0.212 g, 1.1 1 mmol), NEt3 (0.449 mL, 3.23 mmol) and HOAt (0.013 g, 0.092 mmol) in DMF (4 mL) was stirred at RT until completion. The RM was diluted with aqueous saturated NaHC03 (10 mL) and extracted with EtOAc (3* 10 mL). The combined organic layer was washed with brine (10 mL), dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1 to 1 :0) afforded INT-8A (0.340 g, 0.714 mmol, 77%). LCMS: calc. for [M+H]+=476.14, fd. 476.1.
(ii) DMP (0.606 g, 1 .429 mmol) was added to a solution of INT-8A (0.340 g, 0.714 mmol) in DCM (10 mL). The mixture was stirred at RT overnight. An aqueous solution of Na2S203 (10%, 10 mL) was added and the RM was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 (50 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (30 mL). The combined organic layer was dried over Na2S04 The filtrate was concentrated in vacuo. Purified by basic preparative HPLC (C18, MeCN (1 % 10mM NH4HC03), 10 mM NH4HC03 in H20) and lyophilized to obtain 8 (0.092 g, 0.196 mmol, 28%). LCMS: calc. for [M+H]+=474.14, fd. 474.2. 1H NMR (400 MHz, DMSO-d6) as a mixture of hydrates and rotamers δ 9.17-8.93 (m, 1 H), 8.70-8.55 (m, 2H), 8.41-7.98 (m, 1 H), 7.91-7.78 (m, 1 H), 7.78-7.39 (m, 2H), 6.73 (s, 0.29H), 6.48 (s, 0.21 H), 6.36 (s, 0.29H), 5.77 (s, 0.21 H), 5.18-3.43 (m, 8H), 2.48-2.26 (m, 1 H), 1.86-1.03 (m, 8H) ppm.
Comparative Example C1 : N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol- 4(5H)-yl)-1-cyclopentyl-2-oxoethyl)-3-(pyridin-3-yl)benzamide
C1
corresponds to example 17 of WO 2009/1 2839.
Biaryl acids A
In general, the biaryl acids can be obtained from cross coupling reactions of boronic acids or stannates with (hetero)aromatic halides (Scheme 1 ).
X = CI, Br, I
M = SnR3, B(OR)2
Synthesis of 5-(2-methylpyrimidin-5-yl)thiazole-2-carboxylic acid trifluoroacetate (A1 )
Synthesis of tert-butyl thiazole-2-carboxylate
Thiazole-2-carboxylic acid (5.00 g, 38.7 mmol) was dissolved in 500 ml DCM (500 mL). DMF (0.1 mL) was added, followed by oxalyl chloride (4.98 mL, 58.1 mmol). The mixture was stirred at rt for 5 h.
Potassium 2-methylpropan-2-olate (5.65 g, 50.3 mmol) was added. The mixture was stirred at rt for 1 h. Water (200 mL) and saturated aqueous NH CI (200 mL) were added and the layers were separated. The aqueous layer was extracted with DCM (3χ 200 mL). The combined organic layer was dried on Na2S0 and concentrated under reduced pressure. The residue was dissolved in Et20 and filtered over Celite. The filtrate was concentrated under reduced pressure. FC (EtOAc/heptane 0: 1→ 3:7) afforded tert-butyl thiazole-2-carboxylate (4.80 g, 25.9 mmol, 67%). LCMS: cal for [M+H]+ = 186.05, fd 186.1 .
Synthesis of tert-butyl 5-bromothiazole-2-carboxylate
tert-butyl thiazole-2-carboxylate (0.500 g, 2.70 mmol) was added to a solution of lithium bis(trimethyl- silyl)amide (2.97 mL, 1 M in THF, 2.97 mmol) in Et20 (20 mL) at -100 °C. The mixture was stirred for 15 min. CBr4 (0.985 g, 2.97 mmol) was added at -100 °C and the mixture was stirred for at this temperature for 10 min and then allowed to reach rt. The reaction was quenched with saturated aqueous NH4CL (20 mL). The layers were separated. The aqueous layer was extracted with Et20 (3x 10 mL). The combined organic layer was dried on Na2S04 and concentrated under reduced pressure. FC (EtOAc/heptane 0:1→ 3:17) afforded tert-butyl 5-bromothiazole-2-carboxylate (0.580 g, 2.20 mmol, 81 %). LCMS: cal for [M+H]+ = 263.69, fd 264.1.
Synthesis of tert-butyl 5-(2-methylpyrimidin-5-yl)thiazole-2-carboxylate
A solution of 2-methyl-5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)pyrimidine (0.156 g, 0.708 mmol), tert-butyl 5-bromothiazole-2-carboxylate (0.170 g, 0.644 mmol) and Na2C03 (0.205 g, 1 .93 mmol) in dioxane (10 mL) and water (3 mL) was degassed with Ar. Tetrakis(triphenylphosphine)palladium (0.037 g, 0.032 mmol) was added and the mixture was heated at 90 °C for 1 h. The mixture was poured into saturated aqueous NH4CI (30 mL) and extracted with EtOAc (2* 20 mL). The combined organic layer was washed with water (20 mL) and brine (10 mL), dried on Na2S04 and concentrated under reduced pressure. Purification by FC (EtOAc/heptane 1 :9→ 1 :0) afforded tert-butyl 5-(2-methylpyrimidin-5-yl)- thiazole-2-carboxylate (0.156 g, 0.562 mmol, 87%) as a white solid. LCMS: cal for [M+H]+ = 278.09, fd 278.2.
5-(2-methylpyrimidin-5-yl)thiazole-2-carboxylic acid trifluoroacetate (A1 )
A solution of tert-butyl 5-(2-methylpyrimidin-5-yl)thiazole-2-carboxylate (0.156 g, 0.562 mmol) in DCM (3 mL) was cooled to -15 °C. TFA (3 mL) was slowly added. After addition, the mixture was allowed to warm up to rt and stirred for 4 h. The mixture was concentrated under reduced pressure and co-evaporated with DCM to obtain 5-(2-methylpyrimidin-5-yl)thiazole-2-carboxylic acid as its TFA salt (A1). LCMS: cal for [M+H]+ = 222.03, fd 222.0.
The following biaryls were synthesized as described for A1
Synthesis of 5-(2-methylpyrimidin-5-yl)thiophene-2-carboxylic acid (A6)
Synthesis of ethyl 5-(2-methylpyrimidin-5-vnthiophene-2-carboxylate
2-Methylpyrimidine-5-boronic acid pinacol ester (0.920 g, 4.18 mmol), ethyl 5-bromothiophene-2- carboxylate (0.568 mL, 3.80 mmol) and Na2C03 (1.21 g, 11.4 mmol) were mixed in DME (30 mL) and water (7.5 mL) and degassed with Ar. Then PdCI2(dppf) (0.133 g, 0.190 mmol) was added and the mixture was stirred at 100 °C for 1 h. Water (20 mL) was added and the mixture was extracted with EtOAc (3* 20 mL). The combined organic layer was washed with brine (20 mL), dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1 -> 1 :0) afforded ethyl 5-(2-methylpyrimidin-5-yl)thiophene- 2-carboxylate (0.740 g, 2.98 mmol, 78%). LCMS: cal for [M+Hf = 249.07, fd 249.1.
Synthesis of 5-(2-methylpyrimidin-5-yl)thiophene-2-carboxylic acid (A6)
At rt, LiOH H20 (0.500 g, 1 .9 mmol) was added to a mixture of ethyl 5-(2-methylpyrimidin-5-yl)thiophene- 2-carboxylate (0.740 g, 2.98 mmol) in THF (7.5 mL) and water (7.5 mL). The reaction was stirred at rt for 3 h. The reaction was acidified with aqueous 1 M HCI (1 1.9 mL). The solids were filtered, washed with /- PrOH (5 mL) and dried in vacuo to give to give 5-(2-methylpyrimidin-5-yl)thiophene-2-carboxylic acid (A6, 0.625 g, 2.84 mmol, 95%) as a white solid. LCMS: cal for [M+Hf = 221 .04, fd 221.1.
The following biaryls were synthesized as described for A8
Biaryl acid A Starting materials analytical data
5-(2-methylpyridin-4- A7 ethyl 5-bromothiophene-2-carboxylate, LC-MS [M+hf] =
yl)thiophene-2-carboxylic acid (2-methylpyridin-4-yl)boronic acid 220.1
5-(2-methoxypyridin-4-yl)thio- methyl 5-bromothiophene-2-carboxylate, LC-MS [M+H*] =
A8
phene-2-carboxylic acid (2-methoxypyridin-4-yl)boronic acid 236.0
5-(6-(trifluoromethyl)pyridin-3- ethyl 5-bromothiophene-2-carboxylate, (6- LC-MS [M+Ff] =
A9
yl)thiophene-2-carboxylic acid (trifluoromethyl)pyridin-3-yl)boronic acid 274.0
5-(6-cyclopropylpyridin-3- ethyl 5-bromothiophene-2-carboxylate, LC-MS [M+Ff] = yl)thiophene-2-carboxylic acid A10 2-cyclopropyl-5-(4,4,5,5-tetramethyl-1 ,3,2- 246.1
dioxaborolan-2-yl)pyridine
5-(2-cyclopropylpyridin-4- ethyl 5-bromothiophene-2-carboxylate, LC-MS [M+l-f] =
A11
yl)thiophene-2-carboxylic acid (2-cyclopropylpyridin-4-yl)boronic acid 246.0
Synthesis of 5-(pyridin-3-yl)thiazole-2-carboxylic acid (A12)
Synthesis of 5-bromothiazole-2-carboxylic acid
Thiazole-2-carboxylic acid (1 .60 g, 12.4 mmol) was added to a solution of LDA (1 M in THF/heptane/ ethylbenzene, 26.0 mmol, 26 mL) in dry THF (100 mL) at -78 °C and the mixture was stirred for 30 min. CBr4 (4.52 g, 13.6 mmol) was added and the reaction was stirred for 2 h. The RM was quenched by adding water (30 mL). The mixture was allowed to reach rt and diluted by adding an aqueous saturated solution of NaHC03 (50 mL). The mixture was filtered through a pad of Celite and extracted with EtOAC (50 mL). The organic layer was discarded and the aqueous layer acidified using a 1 M solution of HCI until pH acidic. The solution was then extracted with EtOAc (3* 30 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to leave 5-bromothiazole-2-carboxylic acid (0.42 g, 2.0 mmol, 16%). LCMS: cal for [M+H]+ = 207.90, fd 208.0.
Synthesis of methyl 5-bromothiazole-2-carboxylate
Oxalyl chloride (0.21 mL, 2.4 mmol) was added to a solution of 5-bromothiazole-2-carboxylic acid (0.42 g, 2.0 mmol) in dry DCM (10 mL) containing a catalytic amount of dry DMF (0.05 mL) at rt and the resulting mixture was stirred for 4 h. MeOH (4.00 mL, 125 mmol) was added to the solution and the reaction was stirred for an additional 2 h. The mixture was diluted with a saturated aqueous solution of NaHC03 (20 mL) and extracted with DCM (3* 10 mL). The combined organic layer was washed with water (20 mL) and brine (2* 20 mL), dried over Na2S04 and concentrated in vacuo. FC (EtO Ac/heptane 0:1→ 3:7) afforded methyl 5-bromothiazole-2-carboxylate (0.23 g, 1.03 mmol, 51 %). LCMS: cal for [M+H]+ = 221.91 , fd 221.9.
Synthesis of methyl 5-(pyridin-3-yl)thiazole-2-carboxylate
A solution of methyl 5-bromothiazole-2-carboxylate (0.340 g, 1.53 mmol) and 3-(tributylstannyl)pyridine (0.564 g, 1.53 mmol) in dioxane (7 mL) was degassed with N2. Tri-2-furylphosphine (0.071 g, 0.306 mmol) and Pd2(dba)3 (0.140 g, 0.153 mmol) were added and the mixture was heated at 90 °C for 16 h. The mixture was filtered over Celite. The filtrate was concentrated and purified by FC (EtOAc/heptane 0: 1 → 1 :0) to obtain methyl 5-(pyridin-3-yl)thiazole-2-carboxylate (0.143 g, 0.518 mmol, 46%) as a yellow solid. LCMS: cal for [M+H]+ = 221 .03, fd 221.2.
Synthesis of 5-(pyridin-3-yl)thiazole-2-carboxylic acid (A12)
LiOH H20 (0.102 g, 2.43 mmol) was added to a solution of methyl 5-(pyridin-3-yl)thiazole-2-carboxylate (0.349 g, 1 .59 mmol) in THF (6 mL) and water (2 mL). The RM was stirred at rt for 1.5 h. The RM was concentrated in vacuo. The residue was acidified to pH ~4 by addition of aqueous 2 M HCI (~1.3 mL) and triturated with /-PrOH (5 mL). The resulting solid was obtained by filtration, washed with cold /-PrOH (2 mL) and pentane (2* 5 mL) and dried to afford 5-(pyridin-3-yl)thiazole-2-carboxylic acid (A13, 0.308 g, 1.49 mmol, 94%) as a yellow solid. LCMS: cal for [M+H]+ = 207.01 , fd 207.2.
The following biaryls were synthesized as described for A12
Synthesis 5-(pyrazin-2-yl)thiazole-2-carboxylic acid trifluoroacetate (A15)
Synthesis of tert-butyl 5-(pyrazin-2-yl)thiazole-2-carboxylate
A solution of tert-butyl 5-bromothiazole-2-carboxylate (0.500 g, 1.89 mmol) and 2-(tributylstannyl)pyrazine (0.734 g, 1 .99 mmol) in dioxane (10 mL) was degassed with N2. Tri-2-furylphosphine (0.0880 g, 0.379 mmol) and Pd2(dba)3 (0.173 g, 0.189 mmol) were added and the mixture was heated at 85 °C for 16 h. The mixture was filtered over Celite. The filtrate was concentrated and purified by FC (EtOAc/heptane 0:1 → 8:2) to obtain tert-butyl 5-(pyrazin-2-yl)thiazole-2-carboxylate (0.291 g, 0.818 mmol, 43%) as a yellow solid. LCMS: cal for [M+Hf = 264.07, fd 264.2. Synthesis of 5-(pyrazin-2-yl)thiazole-2-carboxylic acid trifluoroacetate (A15)
A solution of tert-butyl 5-(pyrazin-2-yl)thiazole-2-carboxylate (0.310 g, 0.836 mmol) in DCM (5 mL) was cooled to -15 °C. TFA (4.0 mL, 54.0 mmol) was added dropwise in 5 min. After addition, the mixture was allowed to warm up to rt and stirred for 3 h. The mixture was concentrated under reduced pressure and co-evaporated with DCM (2 x 10 mL) and Et20 (2 x 10 mL) to obtain 5-(pyrazin-2-yl)thiazole-2-carboxylic acid as its TFA salt (A15). LCMS: cal for [M+H]+ = 208.01 , fd 208.0.
The following biaryls were synthesized as described for A15
Biaryl acid A Starting materials analytical data
5-(pyridin-4-yl)thiazole-2- tert-butyl 5-bromothiazole-2-carboxylate, LC-MS [M+l-f ]
A16
carboxylic acid trifluoroacetate 4-(tributylstannyl)pyridine = 207.2
5-(2-methylpyridin-4- tert-butyl 5-bromothiazole-2-carboxylate, LC-MS [M+hf] yl)thiazole-2-carboxylic acid A17 2-methyl-4-(tributylstannyl)pyridine = 221 .2 trifluoroacetate
5-(6-chloropyridin-3- tert-butyl 5-bromothiazole-2-carboxylate, LC-MS [M+l-f] yl)thiazole-2-carboxylic acid A18 2-chloro-5-(tributylstannyl)pyridine = 297.2 trifluoroacetate
5-(pyrimidin-5-yl)thiazole-2- tert-butyl 5-bromothiazole-2-carboxylate, LC-MS [M+hf]
A19
carboxylic acid trifluoroacetate 5-(tributylstannyl)pyrimidine = 208.0
Synthesis of 5-(2-(trifluoromethyl)pyrimidin-5-yl)thiazole-2-carboxylic acid trifluoroacetate (A20)
Synthesis of tert-butyl 5-(tributylstannvDthiazole-2-carboxylate
At -78 °C, n-butyllithium (2.5 M in hexanes, 4.75 mmol, 1.90 mL) was added to a solution of Λ/,/V-diiso- propylamine (0.481 g, 4.75 mmol, 0.668 mL) in dry Et20 (40 mL). The mixture was stirred at 0 °C for 1 h. The mixture was cooled to -100 °C (Et20/Iiquid N2). A solution of tert-butyl thiazole-2-carboxylate (0.800 g, 4.32 mmol, synthesis see above) in dry Et20 (40 mL) was added drop wise at -100 °C and the mixture was stirred for 15 min. Tributylchlorostannane (1.55 g, 4.75 mmol, 1.29 mL) was added and the RM was stirred for 10 min at -100 °C, 1 h at -78 °C and then allowed to reach to rt. The reaction was quenched by adding aqueous NH4CI (50 mL). The aqueous layer extracted three times with E20 (3* 25 ml). The combined organic layers was dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1→ 1 :1 ) gave tert-butyl 5-(tributylstannyl)thiazole-2-carboxylate (1.03 g, 2.17 mmol, 50%) as a clear oil.
Synthesis of tert-butyl 5-(2-(trifluoromethyl)pyrimidin-5-yl)thiazole-2-carboxylate
tert-butyl 5-(tributylstannyl)thiazole-2-carboxylate (1.03 g, 2.17 mmol), 5-bromo-2-(trifluoromethyl)- pyrimidine (0.493 g, 2.17 mmol), tri(furan-2-yl)phosphine (0.101 g, 0.434 mmol) and Pd2(dba)3 (0.199 g, 0.217 mmol) were dissolved in dry 1 ,4-dioxane (30 mL) and the resulting solution was heated at 90 °C and stirred for 4 h. The mixture was filtered over Celite and flushed with EtOAc (100 mL). Solvents were evaporated in vacuo. FC (EtOAc/heptane 0:1 -» 1 :1 ) afforded tert-butyl 5-(2-(trifluoromethyl)pyrimidin-5- yl)thiazole-2-carboxylate (0.597 g, 1.80 mmol, 83%) as a yellow solid. LCMS: cal for [M+H]+ = 332.06, fd 276.0 (-ffiu).
Synthesis of 5-(,2-(trifluoromethyl)pyrimidin-5-yl)thiazole-2-carboxylic acid trifluoroacetate (A20)
TFA (10 mL) was added to a solution of tert-butyl 5-(2-(trifluoromethyl)pyrimidin-5-yl)thiazole-2- carboxylate (0.597 g, 1.80 mmol) in DCM (10 mL) at - 0 °C. The RM was allowed to warm to rt and stirred for 3 h. The solvent was evaporated in vacuo and the residue was stripped with DCM (2* 5 mL) to give 5-(2-(trifluoromethyl)pyrimidin-5-yl)thiazole-2-carboxylic acid trifluoroacetate (A20). LCMS: cal for [M+Hf = 276.00, fd 276.0.
The following biaryls were synthesized as described for A20
Synthesis of 5-(2-ethylpyridin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A24)
Synthesis of 2-ethylpyridine 1 -oxide
H202 (35.0 mL, 343 mmol, 30% w/v) was added to a solution of 2-ethylpyridine (10.0 g, 93.0 mmol) in acetic acid (40 mL). The mixture was heated at 80 °C for 6 h. The mixture was allowed to cool to rt. Water (250 mL) was added and the mixture was extracted with DCM (8* 100 mL). The combined organic layer was washed with brine (400 mL), dried on Na2S04 and concentrated under reduced pressure. The residue was dissolved in DCM (100 mL) and washed with saturated aqueous NaHC03 (100 mL). The aqueous layer was extracted with DCM ( 0x 50 mL). The combined organic layer was dried over Na2S0 and concentrated under reduced pressure to obtain 2-ethylpyridine 1 -oxide (9.50 g, 77.0 mmol, 83%) as an oil.
Synthesis of 2-ethyl-4-nitropyridine 1 -oxide
A solution of 2-ethylpyridine 1 -oxide (9.50 g, 77.0 mmol) in sulphuric acid (20 mL) was cooled to 0 °C. Nitric acid (20 mL, 70%) was added drop wise. After addition, the mixture was heated at 95 °C for 18 h. The mixture was allowed to cool to rt and slowly poured into 300 mL ice water. Aqueous 1 M NaOH (175 mL) was added to obtain pH 9-10. The mixture was extracted with DCM (4* 100 mL). The combined organic layer was dried over Na2S04 and concentrated under reduced pressure. Et20 (30 mL) was added and the solids were filtered off to obtain 2-ethyl-4-nitropyridine 1 -oxide (5.02 g, 29.8 mmol, 39%). The filtrate was dissolved in sulphuric acid (10 mL) and cooled to 0 °C. Nitric acid (10 mL, 70%) was added drop wise. After addition, the mixture was heated at 1 10 °C for 18 h. The mixture was allowed to cool to rt and slowly poured into 200 mL ice water. Aqueous 1 M NaOH (1 10 mL) was added to obtain pH 9-10. The mixture was extracted with DCM (3* 100 mL). The combined organic layer was dried over Na2S04 and concentrated under reduced pressure. Et20 (20 mL) was added and the solids were filtered off to obtain 2-ethyl-4-nitropyridine 1-oxide (3.31 g, 19.7 mmol, 26% / combined yield: 8.33 g, 49.5 mmol, 64% pale yellow solid). LCMS: cal for [M+Hf = 169.05, fd 169.2.
Synthesis of 4-bromo-2-ethylpyridine 1 -oxide
A solution of 2-ethyl-4-nitropyridine 1 -oxide (8.33 g, 49.5 mmol) in HBr in acetic acid (80 mL, 457 mmol, 33% w/w) was heated at 100 °C for 5 days. The mixture was allowed to cool to rt and slowly poured into 200 mL ice water. Aqueous 1 M NaOH was added to obtain pH 9-10. The mixture was extracted with DCM (3* 150 mL). The combined organic layer was dried over Na2S04 and concentrated under reduced pressure. FC (EtOAc/heptane 1 :4→ 1 :0) afforded 4-bromo-2-ethylpyridine 1 -oxide (5.49 g, 27.2 mmol, 55%) as a crystalline solid.
Synthesis of 4-(2-(tert-butoxycarbonyl)thiazol-5-vn-2-ethylpyridine 1 -oxide
A solution of 4-bromo-2-ethylpyridine 1 -oxide (0.503 g, 2.49 mmol), tert-butyl 5-(tributylstannyl)thiazole-2- carboxylate (1.18 g, 2.49 mmol, synthesis see above) and CsF (1.13 g, 7.46 mmol) in 1 ,4-dioxane (40 mL) was degassed with Ar. PdCI2(dppf) (0.091 g, 0.12 mmol) and CuCI (0.032 g, 0.32 mmol) were added and the mixture was heated at 80 °C for 3 h. KF (0.50 g, 8.6 mmol) in 20 mL water was added and the mixture was stirred at rt for 18 h. The mixture was filtered over Celite and rinsed with EtOAc (60 mL). The filtrate was washed with water (25 mL) and brine (25 mL), dried over Na2S04 and concentrated under reduced pressure. FC (EtOAc/heptane 1 :9→ 1 :0) afforded 4-(2-(tert-butoxycarbonyl)thiazol-5-yl)-2-ethyl-
pyridine 1 -oxide (0.560 g (89% w/w), 1.63 mmol, 65%) as a solid. LCMS: cal for [M+H]+ = 307.10, fd 307.1.
Synthesis of tert-butyl 5-(2-ethylpyridin-4-v0thiazole-2-carboxylate
Under N2, palladium (10% on activated carbon, 0.173 g, 0.163 mmol) was added to a solution of 4-(2- (tert-butoxycarbonyl)thiazol-5-yl)-2-ethylpyridine 1 -oxide (0.560 g (89% w/w), 1 .63 mmol) in EtOH (35 mL). H2 was applied (balloon) and the mixture was stirred at rt overnight. The mixture was filtered over Celite and the filtrate was concentrated under reduced pressure to obtain tert-butyl 5-(2-ethylpyridin-4- yl)thiazole-2-carboxylate (0.375 g, 1.29 mmol, 79%). LCMS: cal for [M+H]+ = 291.1 1 , fd 291.1.
Synthesis of 5-(2-ethylpyridin-4-vDthiazole-2-carboxylic acid trifluoroacetate (A24)
TFA (10 mL) was added to a solution of tert-butyl 5-(2-ethylpyridin-4-yl)thiazole-2-carboxylate (0.375 g, 1.29 mmol) in DCM (10 mL) at -10 °C. The RM was allowed to warm to rt and stirred for 4 h. The solvent was evaporated in vacuo and the residue was co-evaporated with DCM (2* 5 mL) to give 5-(2-ethyl- pyridin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A24). LCMS: cal for [M+H]+ = 235.05, fd 235.2.
Synthesis of 5-(6-methylpyridazin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A22)
Synthesis of 6-methylpyridazine 1 -oxide
To a solution of 3-methylpyridazine (4.60 g, 48.9 mmol) in acetic acid (30.0 mL) was added H202 (29.4 g, 259 mmol, 29.4 mL, 30% (w/w) in water). The mixture was heated at 120 °C for 6 h. The mixture was allowed to cool to rt and poured in aqueous saturated NaHC03 (500 mL) and extracted with DCM (5* 50 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to afford 6-methyl- pyridazine 1 -oxide (2.22 g, 20.2 mmol, 41 %). LCMS: cal for [M+H]+ = 1 1.05, fd 1 11.2. 1H NMR shows a 1 :1 mixture of both possible /V-oxides.
Synthesis of 6-methyl-4-nitropyridazine 1 -oxide
To a solution of 6-methylpyridazine 1 -oxide (2.10 g, 19.1 mmol) in sulphuric acid (37.5 g, 383 mmol, 20.4 mL) at 0 °C under N2 was added fuming nitric acid (10.8 g, 172 mmol, 7.31 mL) drop wise. The mixture was heated at 1 10 °C for 4 h and stirred at rt for 16 h. The mixture was slowly poured in ice-water (200 mL). This mixture was poured in 1 M NaOH (100 mL) and aqueous saturated NaHC03 (80 mL) was added to give pH: 7-8. The water layer was extracted with EtOAc (3* 100 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to afford an orange solid. The water layer was extracted with DCM (5* 50 mL). The combined organic layer was dried over Na2S04, combined with the earlier obtained orange solid and concentrated in vacuo to afford crude product. The crude product was purified by FC (acetone/ DCM 2:98 isocratic) and FC (acetone/ DCM 2:98 isocratic) to obtain 6-methyl-4- nitropyridazine 1 -oxide (0.940 g, 6.06 mmol, 32%), as a yellow solid. LCMS: cal for [M+H]+ = 156.03, fd 156.2.
Synthesis of 4-bromo-6-methylpyridazine 1 -oxide
HBr in acetic acid (21 .3 g, 86.9 mmol, 15.0 mL, 33%) was added to 6-methyl-4-nitropyridazine 1 -oxide (0.759 g, 4.89 mmol). The mixture was heated at 100 °C for 2 h. This mixture was poured in ice-water (50
mL) and basified by addition of 6 M NaOH (45 mL). The water layer was extracted with DCM (3* 50 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to afford crude product. The crude product was purified by FC (acetone/ DCM 3:97) and FC (acetone/ DCM 2:98) to obtain 4- bromo-6-methylpyridazine 1 -oxide (0.689 g, 3.66 mmol, 75%) as a yellow solid. LCMS: cal for [M+H]+ = 188.96, fd 189.0.
Synthesis of 4-(2-(tert-butoxycarbonyl)thiazol-5-yl)-6-methylpyridazine 1 -oxide
A solution of 4-bromo-6-methylpyridazine 1 -oxide (0.386 g, 2.04 mmol) and tert-butyl 5-(tributylstannyl)- thiazole-2-carboxylate (0.970 g, 2.04 mmol, synthesis see above) in dry 1 ,4-dioxane (25 mL) was degassed with N2. Tri(furan-2-yl)phosphine (0.095 g, 0.41 mmol) and Pd2(dba)3 (0.187 g, 0.205 mmol) were added and the resulting solution was heated at 90 °C and stirred for 4 h. The mixture was filtered over Celite and flushed with EtOAc (50 mL). Solvents were evaporated in vacuo. FC (EtOAc/heptane 0:1 → 3:7) and FC (acetone/ DCM 5:95) afforded 4-(2-(tert-butoxycarbonyl)thiazol-5-yl)-6-methylpyridazine 1 - oxide (0.288 g, 0.982 mmol, 48%) as a yellow solid. LCMS: cal for [M+Hf = 294.08, fd 294.2.
Synthesis of tert-butyl 5-(6-methylpyridazin-4-yl)thiazole-2-carboxylate
A solution of 4-(2-(tert-butoxycarbonyl)thiazol-5-yl)-6-methylpyridazine 1 -oxide (0.286 g, 0.975 mmol) in ammonium hydroxide (8 mL, 32% in water), MeOH (5 mL) and DCM (5 mL) was degassed with N2. Palladium (0.300 g, 2.82 mmol, 10% on activated carbon) was added. The mixture was saturated with H2 by alternating vacuum/ H2 purges. H2 was then bubbled through the mixture for 1.5 h. The RM was purged with N2 and filtered over Celite. The filter layer was rinsed with warm MeOH (2* 10 mL) and DCM (2x 10 mL). The filtrate was concentrated and redissolved in MeOH (5 mL) and DCM (5 mL). To the mixture NEt3 (2.00 mL, 14.4 mmol) and palladium (10% on activated carbon, catalytic spatula tip) were added. The mixture was saturated with H2 by alternating vacuum/ H2 purges. H2 was then bubbled through the mixture for 20 h. Additional palladium (10% on activated carbon, catalytic spatula tip) was added and stirring was continued for 6 h. The RM was purged with N2 and filtered over Celite. The filter layer was rinsed with warm MeOH (3* 20 mL). The filtrate was concentrated. The residue was diluted with DCM (20 mL) and poured in saturated NH4CI (30 mL). The water layer was extracted with DCM (2* 10 mL). The combined organic layer was washed with brine (30 mL), dried over Na2S04 and
concentrated in vacuo. FC (MeOH/ DCM 2:98→ 4:96) and FC (MeOH/ DCM 2:98) afforded tert-butyl 5- (6-methylpyridazin-4-yl)thiazole-2-carboxylate (0.1 10 g, 0.397 mmol, 41 %). LCMS: cal for [M+H]+ = 278.09, fd 278.2.
Synthesis of 5-(6-methylpyridazin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A22)
A solution of tert-butyl 5-(6-methylpyridazin-4-yl)thiazole-2-carboxylate (0.109 g, 0.393 mmol) in DCM (4 mL) was cooled to -15 °C. TFA (1.5 mL, 20.3 mmol) was added dropwise. After addition, the mixture was stirred at -15 °C for 15 min and then allowed to warm up to rt and stirred for 4 h. The RM was cooled to - 15 °C. TFA (0.5 mL, 6.75 mmol) was added dropwise. After addition, the mixture was stirred at -15 °C for 15 min and then allowed to warm up to rt and stirred for 2.5 h. The mixture was concentrated under reduced pressure and co-evaporated with DCM (2* 0 mL) and Et20 (3x 10 mL) to obtain 5-(6-methyl- pyridazin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A22). LCMS: cal for [M+H]+ = 222.03, fd 222.0.
Synthesis of 5-(5-fluoropyrimidin-4-yl)thiophene-2-carboxylic acid (A26)
Synthesis of ethyl 5-(tributylstannyl)thiophene-2-carboxylate
Diisopropylamine (3.89 g, 38.4 mmol, 5.43 mL) was dissolved in dry THF (20 mL) and cooled to -78 °C under N2. A solution of n-butyllithium (1.6 M in hexanes, 38.4 mmol, 24.0 mL) was added drop wise. The mixture was allowed to warm to 0 °C and stirred for 30 min. The solution was cooled to -78 °C and a solution of ethyl thiophene-2-carboxylate (5.00 g, 32.1 mmol, 4.30 mL) in dry THF (10 mL) was added drop wise. The mixture was stirred at -78 °C for 1 h. A solution of tributyltinchloride (10.9 g, 33.6 mmol, 9.12 mL) in dry THF (10 mL) was added drop wise and the solution was stirred at -78 °C for 1 h, then allowed to warm up to rt and stirred for 1 h. The mixture was poured into 200 mL aqueous saturated NH4CI and extracted with EtOAc (3* 100 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to obtain a brown oil. FC (EtOAc/heptane (+1 % NEt3) 0: 1→ 1 :20, 40 g silica) afforded ethyl 5-(tributylstannyl)thiophene-2-carboxylate (13.2 g, 29.7 mmol, 93%) as a clear orange/brown solution.
Synthesis of ethyl 5-(5-fluoropyrimidin-4-yl)thiophene-2-carboxylate
A solution of ethyl 5-(tributylstannyl)thiophene-2-carboxylate (1.38 g, 3.1 1 mmol) and 4-bromo-5-fluoro- pyrimidine (0.500 g, 2.83 mmol) in DMF (10 mL) was degassed with Ar. CsF (1.29 g, 8.48 mmol), CuCI (0.036 g, 0.367 mmol) and PdCI2(dppf) (0.257 g, 0.283 mmol) were added and the mixture was heated at 100 °C for 16 h. The mixture was diluted with EtOAc (100 mL) and water (100 mL). The layers were separated; the aqueous layer was extracted with EtOAc (2x 100 mL). The combined organic layer was washed with brine (25 mL), dried over Na2S04, filtered over Celite and concentrated in vacuo. FC (EtOAc/heptane 0:1→ 1 :0) afforded ethyl 5-(5-fluoropyrimidin-4-yl)thiophene-2-carboxylate (0.364 g, 1.30 mmol, 46%) as a pale yellow solid. LCMS: cal for [M+H]+ = 253.04, fd 253.2.
Synthesis of 5-(5-fluoropyrimidin-4-vDthiophene-2-carboxylic acid (A26)
LiOH H20 (0.182 g, 4.33 mmol) was added to a suspension of ethyl 5-(5-fluoropyrimidin-4-yl)thiophene-2- carboxylate (0.364 g, 1.44 mmol) in THF (20 mL) and water (8 mL). The mixture stirred at rt for 16 h. The mixture was concentrated in vacuo. The residue was acidified to pH 3-4 using aqueous 2M HCI (2.16 mL). To this /-PrOH (15 mL) was added. The solids were filtered off and washed with Et20, dried in vacuo to obtain 5-(5-fluoropyrimidin-4-yl)thiophene-2-carboxylic acid (A26, 0.231 g, 0.927 mmol, 64%) as a yellow solid. LCMS: cal for [M+H]+ = 225.01 , fd 225.2.
The following biaryls were synthesized as described for A26
Biaryl acid A Starting materials analytical data
5-(5-methylpyridazin-3- ethyl thiophene-2-carboxylate,
A37
yl)thiophene-2-carboxylic acid 3-chloro-5-methylpyridazine
5-(2-(trifluoromethyl)pyrimidin-5- ethyl thiophene-2-carboxylate, LC-MS [M+H÷]
A28
yl)thiophene-2-carboxylic acid 5-bromo-2-(trifluoromethyl)pyrimidine = 275.0
5-(2,4-dimethylpyrimidin-5- methyl thiophene-2-carboxylate, LC-MS [Μ+ΗΊ
A31
yl)thiophene-2-carboxylic acid 5-bromo-2,4-dimethylpyrimidine = 235.2
5-(2-methylpyridin-3-yl)thiophene- methyl thiophene-2-carboxylate, LC-MS [M+H+]
A32
2-carboxylic acid 3-bromo-2-methylpyridine = 220.0
5-(4-methylpyridazin-3- methyl thiophene-2-carboxylate, LC-MS [M+l-f ]
A33
yl)thiophene-2-carboxylic acid 3-chloro-4-methylpyridazine = 221.2
5-(2,5-dimethylpyridin-4- methyl thiophene-2-carboxylate, 4- LC-MS [M+H*]
A35
yl)thiophene-2-carboxylic acid chloro-2,5-dimethylpyridine = 234.2
Synthesis of 5-(2-cyclopropylpyrimidin-5-yl)thiophene-2-carboxylic acid trifluoroacetate (A27)
Synthesis of tert-butyl 5-(tributylstannyl)thiophene-2-carboxylate
Diisopropylamine (0.659 g, 6.51 mmol, 0.920 mL) was dissolved in dry THF (6 mL) and cooled to -78 °C under N2. A solution of n-butyllithium (1.6 M in hexanes, 6.51 mmol, 4.07 mL) was added drop wise. The mixture was allowed to warm to 0 °C and stirred for 30 min. The solution was cooled to -78 °C and a solution of feri-butyl thiophene-2-carboxylate (1.00 g, 5.43 mmol) in dry THF (6 mL) was added drop wise. The mixture was stirred at -78 °C for 1 h. A solution of tributyltinchloride (1 .86 g, 5.70 mmol, 1.55 mL) in dry THF (5 mL) was added drop wise and the solution was stirred at -78 °C for 1 h, then allowed to warm up to rt and stirred for 1 h. The mixture was poured into aqueous saturated NH4CI (40 mL) and extracted with EtOAc (2* 20 mL). The combined organic layer was washed with brine (20 mL), dried over Na2S04 and concentrated in vacuo. Crude product was purified by silica column chromatography (NEt3/EtOAc/ heptane 1 :40:500) to afford tert-butyl 5-(tributylstannyl)thiophene-2-carboxylate (2.20 g, 4.65 mmol, 86%) as a colorless oil.
Synthesis of tert-butyl 5-(2-cvclopropylpyrimidin-5-yl)thiophene-2-carboxylate
A solution of 5-bromo-2-cyclopropylpyrimidine (0.365 g, 1.83 mmol) and tert-butyl 5-(tributylstannyl)- thiophene-2-carboxylate (0.868 g, 1.83 mmol) in DMF (4.0 mL) was degassed with N2. CsF (1.1 1 g, 7.33 mmol), CuCI (0.0182 g, 0.183 mmol) and tetrakis(triphenylphosphine) palladium (0.212 g, 0.183 mmol) were added and the mixture was heated at 110 °C under microwave conditions for 30 min. The mixture was diluted with EtOAc (40 mL) and filtered over Celite. The filter cake was washed with EtOAc (2 x 10 mL). The filtrate was poured in water (120 mL). The water layer was extracted with EtOAc (30 mL). The combined organic layer was washed with water (3* 100 mL) and brine (2* 50 mL), dried over Na2S04 and concentrated in vacuo. The crude product was purified by FC (EtOAc/heptane 0:1→ 1 :0) and gave tert-butyl 5-(2-cyclopropylpyrimidin-5-yl)thiophene-2-carboxylate (0.438 g, 1.45 mmol, 79%) as a yellow solid. LCMS: cal for [M+H]+ = 303.11 , fd 303.2.
Synthesis of 5-(2-cvclopropylpyrimidin-5-yl)thiophene-2-carboxylic acid trifluoroacetate (A27)
A solution of tert-butyl 5-(2-cyclopropylpyrimidin-5-yl)thiophene-2-carboxylate (0.437 g, 1.45 mmol) in DCM (18 mL) was cooled to 0 °C. TFA (8.32 g, 72.9 mmol, 5.40 mL) was added drop wise. After addition, the mixture was allowed to warm to rt and stirred for 3 h. The mixture was concentrated under reduced pressure and co-evaporated with toluene/ DCM 1 :1 , (3* 30 mL) and Et20 (2* 30 mL) to afford 5-(2- cyclopropylpyrimidin-5-yl)thiophene-2-carboxylic acid as its TFA salt (A27). LCMS: cal for [M+H]+ = 247.05, fd 247.0.
The following biaryl was synthesized as described for A38
Synthesis of 5-(5-ethylpyridazin-3-yl)thiophene-2-carboxylic acid (A30)
Synthesis of ethyl 5-(5-chloropyridazin-3-yl)thiophene-2-carboxylate
A solution of 3,5-dichloropyridazine (2.68 g, 18.0 mmol) and ethyl 5-(tributylstannyl)thiophene-2- carboxylate (8.0 g, 18 mmol, synthesis see above) in 1 ,4-dioxane (25 mL) was degassed with Ar. CsF (8.19 g, 53.9 mmol), CuCI (0.18 g, 1 .80 mmol) and PdCI2(dppf) (0.66 g, 0.90 mmol) were added and the mixture was heated at 70 °C for 2 h. KF (4.0 g, 70.0 mmol) in 50 mL water was added and the mixture was stirred at rt for 2 h. The mixture was filtered over Celite and the filter rinsed with DCM (15 mL) and brine (15 mL). The organic layer was dried over Na2S0 , filtered and concentrated in vacuo. FC (EtOAc/ heptane 0:1→ 1 :1 ) afforded ethyl 5-(5-chloropyridazin-3-yl)thiophene-2-carboxylate (1.80 g, 6.70 mmol, 37%). LCMS: cal for [M+H]+ = 269.01 , fd 269.0.
Synthesis of ethyl 5-(5-ethylpyridazin-3-vDthiophene-2-carboxylate
A suspension of ethyl 5-(5-chloropyridazin-3-yl)thiophene-2-carboxylate (0.500 g, 1.86 mmol) in THF (15 mL) was degassed with Ar. PdCI2(dppf) (0.136 g, 0.186 mmol) was added, followed by drop wise addition of diethylzinc (1 M in hexane) (1.82 g, 2.50 mmol, 2.5 mL). After complete addition, the mixture was heated at 70 °C for 4 h. The mixture was diluted with water (30 mL) and extracted with DCM (2χ 20 mL). The combined organic layer was washed with brine (10 mL), dried on Na2S04 and concentrated in vacuo. FC (EtOAc/ DCM 0:1→ 3:1 ) afforded ethyl 5-(5-ethylpyridazin-3-yl)thiophene-2-carboxylate (0.274 g, 1.04 mmol, 56%). LCMS: cal for [M+H]+ = 263.08, fd 263.1.
Synthesis of 5-(5-ethylpyridazin-3-yl)thiophene-2-carboxylic acid (A30)
LiOH H20 (0.110 g, 2.62 mmol) was added to a solution of ethyl 5-(5-ethylpyridazin-3-yl)thiophene-2- carboxylate (0.274 g, 1.04 mmol) in THF (10 mL) and water (2 mL). The reaction was stirred at rt for 6 h. The mixture was concentrated under reduced pressure. The residue was acidified to pH 3-4 using aqueous 2 M HCI. The solids were filtered off to obtain 5-(5-ethylpyridazin-3-yl)thiophene-2-carboxylic acid (A30, 0.202 g, 0.862 mmol, 83%). LCMS: cal for [M+H]+ = 235.05, fd 235.0.
Synthesis of 5-(2-ethylpyridin-4-yl)thiophene-2-carboxylic acid (A34)
Synthesis of methyl 5-(tributylstannyl)thiophene-2-carboxylate
Diisopropylamine (4.27 g, 42.2 mmol, 5.96 mL) was dissolved in dry THF (50 mL) and cooled to -78 °C under N2. A solution of n-butyllithium (1 .6 M in hexanes, 42.2 mmol, 26.4 mL) was added drop wise. The mixture was allowed to warm to 0 °C and stirred for 30 min. The solution was cooled to -78 °C and a solution of methyl thiophene-2-carboxylate (5.00 g, 35.2 mmol) in dry THF (50 mL) was added drop wise. The mixture was stirred at -78 °C for 1 h. A solution of tributyltinch loride (12.0 g, 36.9 mmol, 10.0 mL) in dry THF (50 mL) was added drop wise and the solution was stirred at -78 °C for 1 h, then allowed to
warm up to rt and stirred for 16 h. The mixture was poured into 250 mL aqueous saturated NH4CI and extracted with EtOAc (3* 150 mL). The combined organic layer was washed with brine (400 mL), dried over Na2S04 and concentrated in vacuo. FC (EtOAc (+8% NEt3)/heptane 0:1→ 1 :40) afforded methyl 5- (tributylstannyl)thiophene-2-carboxylate (1 1.2 g, 25.9 mmol, 74%) as a brown oil.
Synthesis of 2-ethyl-4-(5-(methoxycarbonyl)thiophen-2-vnDyridine 1 -oxide
A solution of 4-bromo-2-ethylpyridine 1 -oxide (0.937 g, 4.64 mmol, synthesis see above), methyl 5-(tri- butylstannyl)thiophene-2 -carboxylate (2.00 g, 4.64 mmol) and cesium fluoride (2.1 1 g, 13.9 mmol) in 1 ,4- dioxane (40 mL) was degassed with Ar. PdCI2(dppf) (0.170 g, 0.232 mmol) and CuCI (0.060 g, 0.60 mmol) were added and the mixture was heated at 80 °C for 4 h. KF (0.50 g, 8.6 mmol) in 20 mL water was added and the mixture was stirred at rt for 18 h. The mixture was filtered over Celite and rinsed with EtOAc (100 mL). The filtrate was washed with water (40 mL) and brine (40 mL), dried over Na2S04 and concentrated under reduced pressure. FC (EtOAc/heptane 1 :9→ 1 :0) afforded 2-ethyl-4-(5-(methoxy- carbonyl)thiophen-2-yl)pyridine 1 -oxide (0.960 g, 3.65 mmol, 79%) as a solid. LCMS: cal for [M+H]+ = 264.06, fd 264.1 .
Synthesis of methyl 5-(2-ethylpyridin-4-ylHhior->hene-2-carboxylate
Under N2, palladium (10% on activated carbon, 0.190 g, 0.789 mmol) was added to a solution of 2-ethyl- 4-(5-(methoxycarbonyl)thiophen-2-yl)pyridine 1 -oxide (0.470 g, 1.79 mmol) in EtOH (35 mL). H2 was applied (balloon) and the mixture was stirred at rt overnight. The mixture was filtered over Celite and the filtrate was concentrated under reduced pressure to obtain methyl 5-(2-ethylpyridin-4-yl)thiophene-2- carboxylate (0.439 g, 1.78 mmol, 99%). LCMS: cal for [M+H]+ = 248.07, fd 248.1.
Synthesis of 5-(2-ethylpyridin-4-yl)thiophene-2-carboxylic acid (A34)
LiOH H20 (0.163 g, 3.88 mmol) was added to a solution of methyl 5-(2-ethylpyridin-4-yl)thiophene-2- carboxylate (0.439 g, 1.78 mmol) in THF (15 mL) and water (10 mL). The reaction was stirred at rt for 2 h. The mixture was concentrated under reduced pressure. /-PrOH (5 mL) was added and the mixture was acidified to pH 3-4 using aqueous 1 M HCI. The solids were filtered off and washed with Et20 to obtain 5- (2-ethylpyridin-4-yl)thiophene-2-carboxylic acid (A34, 0.316 g, 1.36 mmol, 76%) as a solid. LCMS: cal for [M+Hf = 234.05, fd 234.2.
Synthesis of 5-(5-cyclopropylpyridazin-3-yl)thiophene-2-carboxylic acid (A36)
Synthesis of ethyl 5-(5-cvclopropylpyridazin-3-yl)thiophene-2-carboxylate
A suspension of ethyl 5-(5-chloropyridazin-3-yl)thiophene-2-carboxylate (0.600 g, 2.23 mmol, synthesis see above), cyclopropylboronic acid (0.29 g, 3.4 mmol) and potassiumphosphate, tribasic (1 .42 g, 6.70 mmol) in toluene (75 mL) and water (7.5 mL) was degassed with Ar. Palladium acetate (0.025 g, 0.112 mmol) and tricyclohexylphosphine (0.063 g, 0.223 mmol) were added and the mixture was heated at 100 °C for 16 h. The mixture was filtered over Celite, washed with EtOAc. The filtrate was concentrated under reduced pressure. FC (EtOAc/ DCM 0:1→ 3:1 ) afforded ethyl 5-(5-cyclopropylpyridazin-3- yl)thiophene-2-carboxylate (0.485 g, 1 .68 mmol, 75%). LCMS: cal for [M+H]+ = 275.08, fd 275.1.
Synthesis of 5-(5-cvclopropylpyridazin-3-yl)thiophene-2-carboxylic acid (A36)
LiOH H20 (0.220 g, 5.30 mmol) was added to a solution of ethyl 5-(5-cyclopropylpyridazin-3-yl)thiophene- 2-carboxylate (0.485 g, 1.68 mmol) in THF (10 mL) and water (4 mL). The reaction was stirred at rt for 16 h. The mixture was concentrated under reduced pressure. The residue was acidified to pH 3-4 using aqueous 2 M HCI. /'-PrOH (5 mL) was added and the solids were filtered off and washed with Et20 to obtain 5-(5-cyclopropylpyridazin-3-yl)thiophene-2-carboxylic acid (A36, 0.325 g, 1 .25 mmol, 71 %) as a solid. LCMS: cal for [M+H]+ = 247.05, fd 247.0.
Synthesis of 5-(6-methylpyridazin-4-yl)thiophene-2-carboxylic acid (A38)
Synthesis of 6-methylpyridazine 1 -oxide
To a solution of 3-methylpyridazine (4.60 g, 48.9 mmol) in acetic acid (30.0 mL) was added H202 (29.4 g, 259 mmol, 29.4 mL, 30%, w/w, in water). The mixture was heated at 120 °C for 6 h. The mixture was allowed to cool to rt and poured in aqueous saturated NaHC03 (500 mL) and extracted with DCM (5* 50 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to afford 6-methylpyridazine 1 -oxide (2.22 g, 20.2 mmol, 41 %). LCMS: cal for [M+H]+ = 1 1 1.05, fd 1 11.2. 1H NMR shows a 1 :1 mixture of both possible /V-oxides.
Synthesis of 6-methyl-4-nitropyridazine 1 -oxide
To a solution of 6-methylpyridazine 1 -oxide (2.10 g, 19.1 mmol) in sulphuric acid (37.5 g, 383 mmol, 20.4 mL) at 0 °C under N2 was added fuming nitric acid (10.8 g, 172 mmol, 7.31 mL) drop wise. The mixture was heated at 110 °C for 4 h and stirred at rt for 16 h. The mixture was slowly poured in ice-water (200 mL). This mixture was poured in 1 M NaOH (100 mL) and aqueous saturated NaHC03 (80 mL) was added to give pH 7-8. The water layer was extracted with EtOAc (3* 100 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to afford an orange solid. The water layer was extracted with DCM (5* 50 mL). The combined organic layer was dried over Na2S04, combined with the earlier obtained orange solid and concentrated in vacuo to afford crude product. The crude product was purified by FC (acetone/ DCM 2:98 isocratic) and FC (acetone/ DCM 2:98 isocratic) to obtain 6-methyl-4- nitropyridazine 1 -oxide (0.940 g, 6.06 mmol, 32%), the pure /V-oxide, as a yellow solid. LCMS: cal for [M+Hf = 156.03, fd 156.2.
Synthesis of 4-bromo-6-methylpyridazine 1 -oxide
HBr in acetic acid (21.3 g, 86.9 mmol, 15.0 mL, 33%) was added to 6-methyl-4-nitropyridazine 1 -oxide (0.759 g, 4.89 mmol). The mixture was heated at 100 °C for 2 h. This mixture was poured in ice-water (50 mL) and basified by addition of 6 M NaOH (45 mL). The water layer was extracted with DCM (3* 50 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo to afford crude product. The crude product was purified by FC (acetone/ DCM 3:97) and FC (acetone/ DCM 2:98) to obtain 4- bromo-6-methylpyridazine 1 -oxide (0.689 g, 3.66 mmol, 75%) as a yellow solid. LCMS: cal for [M+H]+ = 188.96, fd 189.0.
Synthesis of 4-(5-(methoxycarbonyl)thiophen-2-yl)-6-methylpyridazine 1 -oxide
A solution of 4-bromo-6-methylpyridazine 1 -oxide (0.565 g, 2.99 mmol), methyl 5-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate (0.802 g, 2.99 mmol) and cesium carbonate (1.95 g, 5.98 mmol) in 1 ,4-dioxane (15 mL) and water (3 mL) was degassed with N2. To this was added
PdCI2(dppf) (0.244 g, 0.299 mmol) and the mixture was heated at 110 °C for 1.5 h. The mixture was diluted with EtOAc (20 mL) and filtered over Celite. The filter layer was rinsed with EtOAc (3* 10 mL). The filtrate was poured in saturated NaHC03 solution (50 mL). The water layer was extracted with EtOAc (3x 20 mL). The combined organic layer was washed with water (50 mL) and brine (50 mL), dried over Na2S04 and concentrated in vacuo. FC (acetone/ DCM 5:95) afforded 4-(5-(methoxycarbonyl)thiophen-2- yl)-6-methylpyridazine 1 -oxide (0.31 1 g, 1.24 mmol, 42%) as a yellow solid. LCMS: cal for [M+H]+ = 251 .04, fd 251.0.
Synthesis of methyl 5-(6-methylpyridazin-4-yl)thiophene-2-carboxylate
A solution of 4-(5-(methoxycarbonyl)thiophen-2-yl)-6-methylpyridazine 1 -oxide (0.305 g, 1.22 mmol) in ammonium hydroxide (10 mL, 32% in water), MeOH (5 mL) and DCM (5 mL) was degassed with N2. Palladium (10% on activated carbon, catalytic spatula tip) was added. The mixture was saturated with H2 by alternating vacuum/H2 purges. H2 was then bubbled through the mixture for 1 .5 h. The RM was purged with N2 and filtered over Celite. The filter layer was rinsed with warm MeOH (2* 10 mL) and DCM (2x 10 mL). To the filtrate palladium (10% on activated carbon, catalytic spatula tip) was added. The mixture was saturated with H2 by alternating vacuum/ H2 purges. H2 was then bubbled through the mixture for 5.5 h. The RM was purged with N2 and filtered over Celite. The filter layer was rinsed with warm MeOH (2x 10 mL) and DCM (2x 0 mL). The filtrate was concentrated. The residue was dissolved DCM (20 mL) and poured in saturated NH4CI (20 mL). The water layer was extracted with DCM (3χ 10 mL). The combined organic layer was washed with water (20 mL) and brine (20 mL), dried over Na2S04 and concentrated in vacuo. FC (MeOH/ DCM 1 :99→ 5:95) and FC (MeOH/ DCM 1 :99) afforded methyl 5-(6-methylpyridazin- 4-yl)thiophene-2-carboxylate (0.102 g, 0.435 mmol, 36%). LCMS: cal for [M+H]+ = 235.05, fd 235.0.
Synthesis of 5-(6-methylpyridazin-4-yl)thiophene-2-carboxylic acid (A38)
LiOH H20 (0.036 g, 0.86 mmol) was added to a solution of methyl 5-(6-methylpyridazin-4-yl)thiophene-2- carboxylate (0.099 g, 0.42 mmol) in THF (3 mL) and water (0.6 mL). The RM was stirred at rt for 2 h. The RM was concentrated in vacuo. The residue was acidified to pH 4-5 by addition of aqueous 1 M HCI (~0.9 mL) and triturated with /-PrOH (2.5 mL). The resulting solid was obtained by filtration, washed with cold i- PrOH (2x 1.5 mL) and pentane (3x 1.5 mL) and dried to afford 5-(6-methylpyridazin-4-yl)thiophene-2- carboxylic acid (A38, 0.080 g, 0.36 mmol, 86%) as a beige solid. LCMS: cal for [M+H]+ = 221.03, fd 221 .0.
Synthesis of 5-(6-methoxypyridazin-4-yl)thiophene-2-carboxylic acid (A39)
Synthesis of methyl 5-(6-chloropyridazin-4-yl)thiophene-2-carboxylate
A suspension of 3,5-dichloropyridazine (0.400 g, 2.68 mmol), methyl 5-(4,4,5,5-tetramethyl-1 ,3,2-dioxa- borolan-2-yl)thiophene-2-carboxylate (0.720 g, 2.68 mmol) and KF (0.390 g, 6.71 mmol) in toluene (15 mL) and water (3 mL) was degassed with Ar for 10 min. Palladium(ll) acetate (0.030 g, 0.13 mmol) and 1 ,2,3,4,5-pentaphenyl-1 '-(di-ferf-butylphosphino)ferrocene (0.095 g, 0.13 mmol) were added and the
mixture was degassed with Ar for 3 more min, then heated at 70 °C for 18 h. The mixture was filtered over Celite. The filtrate was concentrated under reduced pressure and purified by FC (EtOAc/heptane 1 :19→ 2:3) to obtain methyl 5-(6-chloropyridazin-4-yl)thiophene-2-carboxylate (0.300 g, 85%, w/w, 1.00 mmol, 37%). LCMS: cal for [M+H]+ = 254.99, fd 255.0.
Synthesis of 5-(6-methoxypyridazin-4-yl)thiophene-2-carboxylic acid (A39)
A solution of sodium hydride (0.220 g, 60% (w/w), 5.50 mmol) in MeOH (10 mL) was added to a solution of methyl 5-(6-chloropyridazin-4-yl)thiophene-2-carboxylate (0.300 g, 85% (w/w), 1.00 mmol) in MeOH (10 mL). The mixture was heated at 50 °C for 3 h. The mixture was concentrated under reduced pressure. The residue was suspended in isopropanol (5 mL) and acidified to pH ~3-4 with 1 M aqueous HCI The solids were filtered off to obtain 5-(6-methoxypyridazin-4-yl)thiophene-2-carboxylic acid (A58, 0.105 g, 0.444 mmol, 44%) as a brown solid. LCMS: cal for [M+Hf = 237.03, fd 237.0.
Synthesis of 5-(6-ethylpyridazin-4-yl)thiophene-2-carboxylic acid hydrochloride (A40)
Synthesis of methyl 5-(6-ethylpyridazin-4-yl)thiophene-2-carboxylate
A solution of methyl 5-(6-chloropyridazin-4-yl)thiophene-2-carboxylate (0.380 g, 1.39 mmol, synthesis see above) in THF (2.4 mL) was degassed with N2 for 5 min. Then PdCI2(dppf) (0.072 g, 0.088 mmol) and diethylzinc (1 M in hexanes, 5.40 mmol, 5.40 mL) were added. The mixture was heated at 70 °C for 1.5 h. The mixture was poured in water (40 mL) and extracted with DCM (4* 20 mL). The combined organic layer was washed with brine (50 mL), dried over Na2S04 and concentrated in vacuo. The crude product was purified by FC (EtOAc/ DCM 1 :99→ 2:8) and by reversed phase chromatography (MeCN/H20 (+0.1 % HCOOH) 1 :19→ 1 :0) and co-evaporated with toluene (3* 25 mL) to obtain methyl 5-(6-ethyl- pyridazin-4-yl)thiophene-2-carboxylate (0.177 g, 0.713 mmol, 51 %) as a beige solid. LCMS: cal for
[M+H]+ = 249.06, fd 249.2.
Synthesis of 5-(6-ethylpyridazin-4-yl)thiophene-2-carboxylic acid hydrochloride (A40)
LiOH H20 (0.068 g, 1.6 mmol) was added to a solution of methyl 5-(6-ethylpyridazin-4-yl)thiophene-2- carboxylate (0.175 g, 0.705 mmol) in THF (5 mL) and water (1 mL). The RM was stirred at rt for 1 h. LiOH H20 (0.020 g, 0.48 mmol) was added and the mixture was heated at 50 °C for 1 h. The RM was concentrated in vacuo. The residue was acidified to pH 4Γ5 by addition of aqueous 1 M HCI (1.9 mL) and triturated with /-PrOH (3 mL). The resulting semi-solid could not be obtained by filtration. The mixture was concentrated in vacuo to afford Synthesis of 5-(6-ethylpyridazin-4-yl)thiophene-2-carboxylic acid hydrochloride (A40) as a yellow solid. LCMS: cal for [M+H]+ = 235.05, fd 235.1 .
Synthesis of 5-(pyrimidin-4-yl)thiophene-2-carboxylic acid (A41 )
Synthesis of methyl 5-acetylthiophene-2-carboxylate
To a solution of 5-acetylthiophene-2-carboxylic acid (5.00 g, 29.4 mmol) in dry DMF (24 mL) were added K2C03 (12.2 g, 88 mmol) and iodomethane (5.00 g, 35.3 mmol, 2.20 ml) and the mixture was stirred at rt over the weekend. Upon completion the mixture was acidified with 1 M HCI (50 mL) and extracted with EtOAc (3* 20 mL). The combined organic layers were washed with aqueous saturated solution of NaHC03 (20 mL), dried with Na2S04, filtered and concentrated in vacuo. Trituration with Et20 and
filtration afforded methyl 5-acetylthiophene-2-carboxylate (4.1 1 g, 21 .2 mmol, 72%) as a brown solid. LCMS: cal for [M+H]+ = 185.02, fd 185.2.
Synthesis of (E)-methyl 5-(3-(dimethylamino)aci^lov0thiophene-2-carboxylate
A mixture of methyl 5-acetylthiophene-2-carboxylate (3.03 g, 16.5 mmol) and DMF dimethyl acetal (7.85 g, 65.8 mmol, 8.75 mL) was stirred at 75 °C overnight. Upon completion the mixture was concentrated in vacuo. Trituration with Et20 and filtering afforded (E)-methyl 5-(3-(dimethylamino)- acryloyl)thiophene-2-carboxylate (3.58 g, 14.2 mmol, 86%) as a light brown solid. LCMS: cal for [M+H]+ = 240.06, fd 240.2.
Synthesis of methyl 5-(pyrimidin-4-vDthiophene-2-carboxylate
A mixture of (E)-methyl 5-(3-(dimethylamino)acryloyl)thiophene-2-carboxylate (3.58 g, 15.0 mmol) and formamidine acetate (9.35 g, 90.00 mmol) was heated to 200 °C for 4 h. The mixture was cooled to rt and EtOAc (50 mL) and brine (50 mL) were added. The organic phase was separated, dried with Na2S04 and concentrated in vacuo. Crystallization from EtOH and filtration afforded methyl 5-(pyrimidin-4-yl)thio- phene-2-carboxylate (1 .01 g, 3.53 mmol, 24%) as a creambrown solid. LCMS: cal for [M+H]+ = 221.03, fd 221.0.
Synthesis of S-fpyrimidin^-vQthiophene^-carboxylic acid (A41 )
To a mixture of methyl 5-(pyrimidin-4-yl)thiophene-2-carboxylate (1.01 g, 4.59 mmol) in THF (20 mL) and water (20 mL) was added LiOH H20 (0.58 g, 13.8 mmol). The RM was stirred at rt overnight. The mixture was diluted with aqueous 1 M HCI until acidic. The water layer was extracted with EtOAc (3* 40 mL). The aqueous layer was concentrated in vacuo and the solids redissolved in 2 mL H20 and filtered off to give 5-(pyrimidin-4-yl)thiophene-2-carboxylic acid (A41 , 0.875 g, 3.82 mmol, 83%) as an offwhite solid. LCMS: cal for [M+H]+ = 207.01 , fd 207.0.
Synthesis of 5-(2-methylpyrimidin-4-yl)thiophene-2-carboxylic acid (A42)
Synthesis of (E)-methyl 5-(3-(dimethylamino)acryloyl)thiophene-2-carboxylate
A solution of 5-acetylthiophene-2-carboxylic acid (1.00 g, 5.88 mmol) in DMF dimethyl acetal (5 mL, 37.3 mmol) was heated at reflux temperature until completion. The mixture was concentrated under reduced pressure. Trituration from Et20 afforded (E)-methyl 5-(3-(dimethylamino)acryloyl)thiophene-2-carboxylate as a yellow solid. LCMS: cal for [M+Hf = 240.06, fd 240.2.
Synthesis of methyl 5-(2-methylpyrimidin-4-yl)thiophene-2-carboxylate
A suspension of (E)-methyl 5-(3-(dimethylamino)acryloyl)thiophene-2-carboxylate, acetamidine hydrochloride (1.11 g, 11.7 mmol) and potassium carbonate (1.94 g, 14.1 mmol) in DMF (40 mL) was heated at 120 °C until completion. The mixture was diluted with EtOAc (200 mL) and washed with water (100 mL) and brine (2* 75 mL), dried on Na2S04 and concentrated under reduced pressure. FC (EtOAc/heptane 1 :9→ 1 :0) afforded methyl 5-(2-methylpyrimidin-4-yl)thiophene-2-carboxylate (0.838 g, 3.58 mmol, 61 % yield over 2 steps) as a white solid. LCMS: cal for [M+H]+ = 235.05, fd 235.0.
Synthesis of 5-(2-methylpyrimidin-4-yl)thiophene-2-carboxylic acid (A42)
LiOH H20 (0.320 g, 7.63 mmol) was added to a solution of methyl 5-(2-methylpyrimidin-4-yl)thiophene-2- carboxylate (0.838 g, 3.58 mmol) in THF (15 mL) and water (10 mL). The reaction was stirred at rt until completion. The RM was acidified to pH ~2 using aqueous 1 M HCI. /-PrOH (10 mL) was added and the solids were filtered off and washed with Et20 to obtain 5-(2-methylpyrimidin-4-yl)thiophene-2-carboxylic acid (A42, 0.677 g, 3.07 mmol, 86%) as a solid. LCMS: cal for [M+H]+ = 221.03, fd 221.0.
Synthesis of 5-(pyrimidin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A43)
Synthesis of tert-butyl 5-acetylthiazole-2-carboxylate
tert-Butyl thiazole-2-carboxylate (1.15 g, 6.21 mmol, synthesis see above) was added to a solution of LDA (1 M in THF/heptane/ethylbenzene, 6.83 mmol, 6.83 mL) in dry THF ( 0 mL) at -78 °C and the mixture was stirred for 30 min. /V-Methoxy-W-methylacetamide (0.96 g, 9.3 mmol) was added and the RM was stirred for 3 h. The RM was quenched by adding a saturated aqueous solution of NH4CI (10 mL). The mixture was allowed to reach to rt. The aqueous layer was extracted with EtOAC (2* 10 ml). The combined organic layer was dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 0:1→ 1 :4) afforded tert-butyl 5-acetylthiazole-2-carboxylate (0.40 g, 1 .76 mmol, 28%). LCMS: cal for [M+H]+ = 228.06, fd 228.1 .
Synthesis of tert-butyl 5-(3-(dimethylamino)acryloyl)thiazole-2-carboxylate
tert-Butyl 5-acetylthiazole-2-carboxylate (0.50 g, 2.20 mmol) was dissolved in 1 ,1 -dimethoxy-/V,/V-di- methylmethanamine (5.24 g, 44.0 mmol, 6.55 mL) and the mixture was warmed up to 70 °C and stirred for 2 h. The reaction was allowed to reach rt and the solvent evaporated to leave tert-butyl 5-(3-(dimethyl- amino)acryloyl)thiazole-2-carboxylate (0.70 g). LCMS: cal for [M+H]+ = 283.10, fd 283.2.
Synthesis of tert-butyl 5-(pyrimidin-4-yl)thiazole-2-carboxylate
tert-Butyl 5-(3-(dimethylamino)acryloyl)thiazole-2-carboxylate (0.70 g) was added to a solution of formimidamide acetate (1.29 g, 12.4 mmol) in dry DMF (10 mL) and the reaction was heated up to 95 °C and stirred for 5 h. The reaction was cooled to rt and diluted with aqueous saturated NaHC03 (10 mL) and extracted with EtOAc (3χ 20 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo. FC (DCM) afforded tert-butyl 5-(pyrimidin-4-yl)thiazole-2-carboxylate (0.30 g, 1.1 mmol, 46% yield over 2 steps). LCMS: cal for [M+H]+ = 264.07, fd 264.1.
Synthesis of 5-(pyrimidin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A43)
TFA (5 mL) was added to a solution of tert-butyl 5-(pyrimidin-4-yl)thiazole-2-carboxylate (0.30 g, 1.1 mmol) in DCM at -10 °C. The RM was allowed to warm to rt and stirred until completion. The solvent was evaporated in vacuo to give 5-(pyrimidin-4-yl)thiazole-2-carboxylic acid trifluoroacetate (A43, 0.36 g, 1.1 mmol, 100%). LCMS: cal for [M+H]+ = 208.01 , fd 208.0.
Synthesis of 5-(5-methylpyridazin-4-yl)thiophene-2-carboxylic acid hydrochloride (A44)
Synthesis of 3-bromo-4-methylfuran-2,5-dione
3-Methylfuran-2,5-dione (6.24 g, 55.6 mmol, 5.00 mL) was placed in a closed pressure vial. Under N2 AIBr3 (0.178 g, 0.668 mmol) was added, followed by Br2 (8.89 g, 55.6 mmol, 2.87 mL). The mixture was stirred at 120°C for 16 h. The vial was cooled to 0 °C. Solids were removed from the vial and recrys- tallized from toluene/heptane, washed with heptane and dried in vacuo to obtain 3-bromo-4-methylfuran-
2.5- dione (7.80 g, 40.8 mmol, 73%) as a brown crystalline solid. LCMS: cal for [M+H]+=190.93, fd 191.0.
Synthesis of 4-bromo-5-methylpyridazine-3,6-diol
Hydrazine sulfate (0.681 g, 5.24 mmol) was suspended in water (10 mL). The mixture was heated to 100°C and at this temperature 3-bromo-4-methylfuran-2,5-dione (1.00 g, 5.24 mmol) was added. The mixture was heated for 16 h at 95°C (a white precipitate forms). HBr (48% w/w in water, 0.033 g, 0.20 mmol, 0.022 mL) was added and the mixture was heated to 95°C for 2 h. The mixture was cooled and the precipitate was filtered, washed with water (20 mL) and dried in vacuo to obtain 4-bromo-5-methyl- pyridazine-3,6-diol (0.960 g, 4.68 mmol, 89%) as a white solid. LCMS: cal for [M+H]+=204.95, fd 205.0.
Synthesis of tert-butyl 5-(3,6-dihvdroxy-5-methylpyridazin-4-yl)thiophene-2-carboxylate
(5-(ferf-Butoxycarbonyl)thiophen-2-yl)boronic acid (0.763 g, 3.34 mmol) and 4-bromo-5-methylpyridazine-
3.6- diol (0.754 g, 3.68 mmol) were dissolved in 1 ,4-dioxane (28 mL) and water (7 mL). Cs2C03 (2.18 g, 6.69 mmol) was added. The mixture was degassed with Ar for 5 min. PdCI2(dppf) (0.304 g, 0.334 mmol) was added. The mixture was heated at 110 °C (hot start) for 1.5 h. The mixture was cooled and acidified to pH 5-6 with aqueous 2 M HCI. Solvents were evaporated in vacuo. FC (CH2CI2/MeOH 1 :0→ 9:1 ) afforded tert-butyl 5-(3,6-dihydroxy-5-methylpyridazin-4-yl)thiophene-2-carboxylate (0.874 g, 1.98 mmol, 59%, 70% purity). LCMS: cal for [M+H]+=309.35, fd 309.2.
Synthesis of 5-(3.6-dichloro-5-methylpyridazin-4-yl)thiophene-2-carboxylic acid
tert-butyl 5-(3,6-dihydroxy-5-methylpyridazin-4-yl)thiophene-2-carboxylate (0.724 g, 2.348 mmol) was suspended in dry MeCN (25 mL). Tetraethylammonium chloride (1.17 g, 7.04 mmol) was added, followed by phosphorus oxychloride (1.58 g, 10.3 mmol, 0.963 mL). The mixture was stirred at reflux for 2 h. Solvents were evaporated in vacuo. The residue was stripped with DCM. FC (EtO Ac/heptane 1 :9→ 1 :0) afforded 5-(3,6-dichloro-5-methylpyridazin-4-yl)thiophene-2-carboxylic acid (0.355 g, 1.23 mmol, 52%) as a white solid. LCMS: cal for [M+H]+ =288.95, fd 289.0.
Synthesis of methyl 5-(5-methylpyridazin-4-yl)thiophene-2-carboxylate
5-(3,6-dichloro-5-methylpyridazin-4-yl)thiophene-2-carboxylic acid (0.324 g, 1.12 mmol) was dissolved in MeOH (20 mL). Palladium/carbon (0.162 g, 0.152 mmol, 10 %w/w) was added, followed by triethyl amine (0.340 g, 3.36 mmol, 0.469 mL). The mixture was brought under H2 and was stirred at RT for 1 h. The mixture was filtered over Celite and flushed with MeOH (80 mL). Solvents were evaporated in vacuo. The residue was diluted with CH2CI2 (50 mL) and half saturated NaHC03 (50 mL). The water layer was extracted with DCM (2 * 50 mL). The organic layer was dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 1 :9→ 1 :0) afforded methyl 5-(5-methylpyridazin-4-yl)thiophene-2-carboxylate (0.175 g, 0.747 mmol, 67%) as a yellowish solid. LCMS: cal for [M+H]+=235.27, fd 235.2.
Synthesis of 5-(5-methylpyridazin-4-yl)thiophene-2-carboxylic acid hydrochloride (A44)
LiOH H20 (0.125 g, 2.99 mmol) was added to a suspension of methyl 5-(5-methylpyridazin-4-yl)thio- phene-2-carboxylate (0.175 g, 0.747 mmol) in tetrahydrofuran (5 mL) and water (5 mL). The mixture was stirred at RT for 2 h. The mixture was concentrated in vacuo. The residue was acidified to pH 2-3 using aqueous 2M HCI. /-PrOH (15 mL) was added. Solvents were evaporated in vacuo. The solid was stripped with toluene (2 *) and DIPE (2 x), and dried in vacuo to obtain 5-(5-methylpyridazin-4-yl)thiophene-2- carboxylic acid hydrochloride (A44) as a yellow solid as its HCI salt. LCMS: cal for [M+H]+ =221.03, fd 221 .2.
Synthesis of 5-(3,6-dimethylpyridazin-4-yl)thiophene-2-carboxylic acid (A45)
Synthesis of methyl 5-(6-chloro-3-methylpyridazin-4-yl)thiophene-2-carboxylate
solution of 4,6-dichloro-3-methylpyridazine (0.851 g, 5.22 mmol), methyl 5-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)thiophene-2-carboxylate (1.40 g, 5.22 mmol) and KF (0.758 g, 13.1 mmol) in toluene (9.6 mL) and water (2.4 mL) was degassed with N2. Palladium acetate (0.059 g, 0.26 mmol) and
1 ,2,3,4,5-pentaphenyl-1 '-(di-fe/ -butylphosphino)ferrocene (Q-phos) (0.184 g, 0.261 mmol) were added and the mixture was heated at 70 °C for 16 h. The mixture was diluted with EtOAc (40 mL) and filtered over Celite. The filter layer was rinsed with EtOAc (2 * 40 mL). The filtrate was concentrated and purified by FC (EtOAc/heptane 0:1→ 4:6), FC (EtOAc/heptane 0:1→ 3:7) and FC (EtOAc/heptane 0:1→ 3:7) to obtain methyl 5-(6-chloro-3-methylpyridazin-4-yl)thiophene-2-carboxylate (0.414 g, 1 .45 mmol, 28%) as a pink solid. LCMS cal for [M+Hf = 269.01 , fd 269.0.
Synthesis of methyl 5-(3,6-dimethylpyridazin-4-yl)thiophene-2-carboxylate
To a solution of methyl 5-(6-chloro-3-methylpyridazin-4-yl)thiophene-2-carboxylate (0.333 g, 1.24 mmol) and Cs2C03 (0.808 g, 2.48 mmol) in dioxane (8.0 mL) and water (0.2 mL) was added trimethylboroxine (3.5 M solution in tetrahydrofuran, 0.933 g, 3.72 mmol, 1.04 mL). The mixture was degassed with N2 for 5 min and PdCI2(dppf) (0.051 g, 0.062 mmol) was added. The mixture was heated at 100 °C for 4 h and stirred at RT for 16 h. The mixture was filtered over Celite. The filter cake was washed with warm EtOAc (2 x 20 mL). The filtrate was poured in aqueous saturated NaHC03 (30 mL) and extracted with EtOAc (2 χ 20 mL). The combined organic layer was washed with brine (30 mL), dried over Na2S04 and concentrated in vacuo. The crude product was purified by FC (EtOAc/heptane 1 :1→ 1 :0) to obtain methyl 5-(3,6-dimethylpyridazin-4-yl)thiophene-2-carboxylate (0.303 g, 1.15 mmol, 93%) as a yellow solid.
LCMS: cal for [M+H]+= 249.06, fd 249.2.
Synthesis of 5-(3.6-dimethylpyridazin-4-yl)thiophene-2-carboxylic acid (A45)
LiOH H20 (0.130 g, 3.10 mmol) was added to a solution of methyl 5-(3,6-dimethylpyridazin-4-yl)thio- phene-2-carboxylate (0.297 g, 1.13 mmol) in THF (10 mL) and water (2 mL). The RM was stirred at 30 °C for 2.5 h. The RM was concentrated in vacuo. The residue was acidified to pH 3-4 by addition of aqueous 2 M HCI (1.6 mL) and triturated with a mixture of /-PrOH (2 mL) and pentane (3 mL). The resulting solid was obtained by filtration, washed with cold /-PrOH (1 mL) and pentane (3 x 3 mL) and dried to afford 5- (3,6-dimethylpyridazin-4-yl)thiophene-2-carboxylic acid (A45, 0.202 g, 0.855 mmol, 76%) as a brown solid. LCMS: cal for [M+H]+= 235.05, fd 235.2.
Synthesis of final compounds
Final compound can be obtained by coupling the biaryl acids A with amine INT-1 , (synthesis:
WO2008/007127, p. 104f). This yields the alcohols INT-A, that are oxidized to give final compounds B (Scheme 2).
Scheme 2: Synthesis of final compounds
Synthesis of N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2-carboxamide (Example 13)
Synthesis of N-((S)-2-((3R.3aR.6S.6aS)-6-chloro-3-hvdroxytetrahvdro-2H-furo[3.2-blpyrrol-4(5H)-yl)-1 - cvclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2-carboxamide
A suspension of (S)-2-amino-1-((3R,3aR,6S,6aS)-6-chloro-3-hydroxytetrahydro-2H-furo[3,2-b]pyrrol- 4(5H)-yl)-2-cyclopentylethanone hydrochloride (1 , 0.446 g, 1.37 mmol), 5-(2-methylpyrimidin-5-yl)thio- phene-2-carboxylic acid (A6, 0.302 g, 1.37 mmol), EDCI (0.315 g, 1 .65 mmol), NEt3 (0.667 mL, 4.80 mmol, 0.486 g) and HOAt (0.019 g, 0.14 mmol) in DMF (5 mL) was stirred at rt for 18 h. The mixture was diluted with EtOAc (10 mL) and washed with aqueous saturated solution of NaHC03 (10 mL) and brine (10 mL). The organic layer was dried over Na2S04 and concentrated in vacuo. FC (EtOAc/heptane 1 :1 -> 1 :0) afforded N-((S)-2-((3R,3aR,6S,6aS)-6-chloro-3-hydroxytetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2-carboxamide (0.492 g, 1.00 mmol, 73%). LCMS: cal for [M+H]+ = 491 .15, fd 491.2.
Synthesis of N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahvdro-2H-furof3.2-blpyrrol-4(5H)-yl)-1 -cvclo- pentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2-carboxamide (Example 13)
DMP (0.850 g, 2.00 mmol) was added to a solution of N-((S)-2-((3R,3aR,6S,6aS)-6-chloro-3-hydroxy- tetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1-cyclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2- carboxamide (0.492 g, 1.00 mmol) in DCM (10 mL). The mixture was stirred at rt for 18 h. An aqueous solution of sodium thiosulfate ( 0%, 0 mL) was added and the mixture was stirred vigorously for 30 min. An aqueous saturated solution of NaHC03 ( 0 mL) was added and the layers were separated. The aqueous layer was extracted with DCM (3* 10 mL). The combined organic layer was dried over Na2S04 and concentrated in vacuo. Purification by FC (EtOAc(1 % NEt3)/ heptane(1 % NEt3) 1 : 1→ 1 :0) and lyophilization (MeCN/H20) afforded N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-
4(5H)-yl)-1 -cyclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2-car^^ (Example 13,
0.242 g, 0.495 mmol, 49%). LCMS: cal for [M+H]+ = 489.14, fd 489.2. 1H NMR (400 MHz, DMSO-<¾) as a mixture of hydrates and rotamers δ 9.21-8.90 (m, 3H), 8.22-7.94 (m, 1 H), 7.81-7.64 (m, 1 H), 6.73 (s, 0.47H), 6.48 (s, 0.34H), 6.35 (s, 0.47H), 5.76 (s, 0.34H), 5.17-3.39 (m, 8H), 2.69-2.57 (m, 3H), 1.86-0.93 (m, 8H) ppm.
The following final compounds (table 1 ) were synthesized as described for Example 13.
Table 1.
/ 0 dimethylpyridazin-4-yl)thiophene-2-carboxamide
The compounds were prepared according to the procedure for Example 13 using the appropriate biaryl acid A (Table 2).
LCMS
Yield 1H NMR (400 MHz, DMSO-c/6) as a mixture of
Nr Purification Acid [M+H]+
[%] hydrates and rotamers
cal / fd
Trituration from
9.83-9.55 (m, 1 H), 9.41 -9.18 (m, 1 H), 9.00- heptane/EtOAc (3:4).
7.88 (m, 3H), 6.66 (s, 0.43H), 6.49 (s, 0.43H), 475.1 1 ,
9 The precipitate was 71 A41
6.47 (s, 0.18H), 5.78 (s, 0.18H), 5.47- 3.46 (m, 475.2 obtained by filtration,
8H), 2.49-2.18 (m, 1 H), 1.86-1 .04 (m, 8H)
washed with pentane
9.16-9.06 (m, 0.4H), 9.05-8.95 (m, 0.6H), 8.80- basic preparative 8.69 (m, 1 H), 8.41 -8.33 (m, 0.03H), 8.18-8.10
HPLC (C18, MeCN (m, 0.4H), 8.10-8.06 (m, 0.4H), 8.06-7.97 (m,
476.1 1 ,
10 (1 % 10mM 61 A14 1.2H), 7.90-7.79 (m, 1 H), 6.75 (s, 0.37H), 6.48
476.1 NH4HCO3), 10 mM (s, 0.27H), 6.35 (s, 0.37H), 5.77 (s, 0.27H),
NH4HCO3 in H20) 5.26-3.44 (m, 8H), 2.66-2.60 (m, 3H), 2.48- 2.25 (m, 1 H), 1.86-1.05 (m, 8H)
9.31 -9.25 (m, 2H), 9.24-9.18 (m, 1 H), 8.93- 8.85 (m, 0.07H), 8.84-8.76 (m, 0.30H), 8.70-
Crystallization from 8.61 (m, 1 H), 8.36-8.26 (m, 0.60H), 8.08-8.01 489.13,
1 1 71 A42
EtOAc (m, 0.03H), 6.68 (s, 0.57H), 6.50 (s, 0.57H), 489.1
6.48 (s, 0.25H), 5.79 (s, 0.25H), 5.34-3.44 (m,
8H), 2.48-2.20 (m, 1 H), 1.85-1.15 (m, 8H)
9.21 -8.90 (m, 3H), 8.22-7.94 (m, 1 H), 7.81 -
Crystallization from 7.64 (m, 1 H), 6.73 (s, 0.47H), 6.48 (s, 0.34H), 476.1 ,
12 60 A19
EtOAc and heptane 6.35 (s, 0.47H), 5.76 (s, 0.34H), 5.17-3.39 (m, 476.2
8H), 2.69-2.57 (m, 3H), 1.86-0.93 (m, 8H)
9.09-8.98 (m, 1 H), 8.86-8.48 (m, 2.42H), 8.34- 7.98 (m, 1.58H), 7.62-7.45 (m, 1 H), 6.67 (s,
Crystallization from 493.10,
14 68 A26 0.36H), 6.49 (s, 0.36H), 6.47 (s, 0.17H), 5.78
EtOAc and heptane 493.2
(s, 0.17H), 5.34-3.41 (m, 8H), 2.40-2.23 (m,
1 H), 1.86-1.07 (m, 8H)
9.13 (s, 2H), 8.86 (d, J = 8.3 Hz, 0.34H), 8.77
(d, J = 8.7 Hz, 0.20H), 8.67-8.53 (m, 1 H), 8.29
(d, J = 8.2 Hz, 0.34H), 8.03 (d, J = 8.6 Hz, 475.1 1 ,
- 84 A12
0.12H), 6.69 (s, 0.25H), 6.62-6.41 (m, 0.34H), 475.2 5.79 (s, 0.09H), 5.32-3.43 (m, 8H), 2.68 (s,
3H), 2.41 -2.23 (m, 1 H), 1.90-1.07 (m, 8H)
basic preparative 9.50-9.36 (m, 1 H), 8.93-8.58 (m, 3.40H), 8.39- HPLC (C18, MeCN 8.27 (m, 0.51 H), 8.10-8.01 (m, 0.09H), 6.67 (s,
490.12,
(1 % 10mM 56 A1 0.48H), 6.50 (s, 0.48H), 6.47 (s, 0.21 H), 5.79
490.2 NH4HCO3), 10 mM (s, 0.21 H), 5.35-3.40 (m, 8H), 2.48-2.20 (m,
NH4HCO3 in H20) 1 H), 1.86-1.03 (m, 8H)
8.91 -8.84 (m, 0.3H), 8.83-8.76 (m, 0.2H), 8.74- 8.62 (m, 3H), 8.35-8.26 (m, 0.35H), 8.09-8.01
(m, 0.15H), 7.84-7.74 (m, 2H), 6.67 (s, 0.35H), 476.1 1 ,
81 A15
6.50 (s, 0.35H), 6.48 (s, 0.15H), 5.79 (s, 476.2 0.15H), 5.39-3.38 (m, 8H), 2.47-2.38 (m,
0.5H), 2.38-2.24 (m, 0.5H), 1.86-1.10 (m, 8H)
8.90-8.82 (m, 1 H), 8.80-8.73 (m, 0.2H), 8.71 - 8.64 (m, 0.2H), 8.54-8.44 (m, 1 H), 8.30-8.22
(m, 0.5H), 8.13-8.05 (m, 1 H), 8.03-7.95 (m,
Crystallization from 475.1 1 ,
46 A16 0.1 H), 7.43-7.34 (m, 1 H), 6.68 (s, 0.45H), 6.50
EtOAc and heptane 475.2
(s, 0.2H), 6.47 (s, 0.45H), 5.78 (s, 0.2H), 5.39- 3.38 (m, 8H), 2.46-2.38 (m, 0.4H), 2.37-2.23
(m, 0.6H), 1.84-1.1 1 (m, 8H)
8.98-8.91 (m, 0.2H), 8.89-8.83 (m, 0.2H), 8.81 - 8.72 (m, 2H), 8.60-8.52 (m, 1 H), 8.38-8.30 (m,
0.4H), 8.13-8.07 (m, 0.2H), 8.07-8.01 (m, 1 H),
Crystallization from 489.13,
73 A2 6.68 (s, 0.42H), 6.50 (s, 0.42H), 6.48 (s,
EtOAc and heptane 489.2
0.18H), 5.79 (s, 0.18H), 5.35-3.36 (m, 8H),
2.49-2.38 (m, 0.5H), 2.37-2.25 (m, 0.5H), 1.85- 1.12 (m, 8H)
9.27-9.18 (m, 0.92H), 9.00-8.78 (m, 2.44H),
8.39-8.06 (m, 1 .64H), 6.67 (s, 0.51 H), 6.50 (s,
Crystallization from 493.10,
68 A3 0.51 H), 6.47 (s, 0.23H), 5.79 (s, 0.23H), 5.34- EtOAc and heptane 493.1
3.40 (m, 8H), 2.48-2.23 (m, 1 H), 1.88-1.05 (m,
8H)
8.89-8.81 (m, 0.25H), 8.81 -8.73 (m, 0.2H),
8.72-8.62 (m, 1 H), 8.58-8.48 (m, 1 H), 8.33-
476.1 1 ,
- 81 A43 8.25 (m, 0.4H), 8.07-7.98 (m, 0.15H), 7.72- 476.2
7.63 (m, 1 H), 7.62-7.53 (m, 1 H), 6.67 (s,
0.39H), 6.49 (s, 0.17H), 6.47 (s, 0.39H), 5.78
9.12-9.04 (m, 0.5H), 9.02-8.91 (m, 0.5H), 8.51 - 8.42 (m, 1 H), 8.17-8.10 (m, 0.45H), 8.04-7.97
(m, 0.55H), 7.84-7.80 (m, 0.45H), 7.80-7.74
Crystallization from (m, 0.55H), 7.61 -7.54 (m, 1 H), 7.53-7.44 (m, 514.15,
70 A10
EtOAc and heptane 1 H), 6.74 (s, 0.42H), 6.48 (s, 0.30H), 6.36 (s, 514.2
0.42H), 5.77 (s, 0.30H), 5.17-3.43 (m, 8H),
2.50-2.49 (m, 3H), 2.46-2.30 (m, 1 H), 1.84- 1.09 (m, 8H)
9.18-8.88 (m, 2H), 8.21 -8.08 (m, 1 H), 8.39-
8.00 (m, 1 H), 7.98-7.83 (m, 1 H), 6.77 (s,
Crystallisation from 488.13,
87 A7 0.07H), 6.49 (s, 0.05H), 6.41 (s, 0.07H), 5.77
EtOAc and heptane 488.2
(s, 0.05H), 5.23-3.44 (m, 8H), 2.47-2.28 (m,
1 H), 2.38 (s, 3H), 1.92-0.93 (m, 8H)
8.81 (s, 1 H), 8.75 (d, J = 8.6 Hz, 0.2H), 8.67
(d, J = 8.6 Hz, 0.2H), 8.57-8.41 (m, 1 H), 8.25
FC, (d, J = 8.3 Hz, 0.5H), 8.12-8.02 (m, 1 H), 7.98
(EtOAc(1 %Et3N)/hep (d, J = 8.0 Hz, 0.1 H), 7.52-7.38 (m, 1 H), 6.70 489.14,
43 A37
tane(1 %Et3N) 1 :1→ (s, 0.4H), 6.52 (s, 0.4H), 6.49 (s, 0.2H), 5.80 489.2 1 :0) (s, 0.2H), 5.44-3.42 (m, 8H), 2.39-2.25 (m,
1 H), 2.25-2.08 (m, 1 H), 2.05-1.16 (m, 8H),
1.16-0.84 (m, 4H)
9.89-9.78 (m, 1 H), 9.38-9.27 (m, 1 H), 9.16- acidic preparative 9.04 (m, 0.95H), 8.45-8.08 (m, 1 .05H), 7.70- HPLC (C18, MeCN 7.53 (m, 1 H), 7.49-7.31 (m, 1 H), 6.71 (s, 515.14,
56 A4
(0.1 % HCOOC), H20 0.32H), 6.49 (s, 0.25H), 6.34 (s, 0.32H), 5.79 515.2 (0.1 % HCOOC)) (s, 0.25H), 5.24-3.44 (m, 8H), 2.46-2.35 (m,
1 H), 1.92-1.05 (m, 8H)
9.56-9.47 (m, 2H), 8.97 (d, J = 8.4 Hz, 0.33H),
8.89 (d, J = 8.7 Hz, 0.11 H), 8.81 -8.72 (m,
1.16H), 8.34 (d, J = 8.3 Hz, 0.24H), 8.09 (d, J
459.14,
- 85 A13 = 8.6 Hz, 0.16H), 6.68 (s, 0.24H), 6.51 (s,
459.2
0.24H), 6.48 (s, 0.12H), 5.79 (s, 0.12H), 5.35-
3.37 (m, 8H), 2.47-2.24 (m, 1 H), 1.87-1 .12 (m,
8H)
acidic preparative 9.23 (s, 1 H), 8.91 (d, J = 8.3 Hz, 0.25H), 8.82
544.10, HPLC (C18, MeCN 44 A20 (d, J = 8.6 Hz, 0.25H), 8.77-8.67 (m, 1 H), 8.50
544.0 (0.1 % HCOOC), H20 (d, J = 8.2 Hz, 1 H), 8.32 (d, J = 8.3 Hz, 0.5H),
(0.1 % HCOOQ) 8.10-8.01 (m, 1 H), 6.69 (s, 0.35H), 6.58-6.44
(m, 0.5H), 5.80 (s, 0.15H), 5.37-3.42 (m, 8H),
2.36-2.24 (m, 1 H), 2.01 -1.13 (m, 8H)
9.13-9.03 (m, 1.4H), 9.00-8.92 (m, 0.6H), 8.34- basic preparative 8.29 (m, 0.03H), 8.19-8.1 1 (m, 1.4H), 8.06- HPLC (C18, MeCN 7.98 (m, 1 H), 7.98-7.92 (m, 0.6H), 6.77 (s,
543.10,
(1 % 10mM 55 A5 0.39H), 6.49 (s, 0.26H), 6.41 (s, 0.39H), 5.78
543.2 NH4HCO3), 10 mM (s, 0.26H), 5.23-3.41 (m, 8H), 2.75-2.65 (m,
NH4HCO3 in H20) 2H), 2.48-2.30 (m, H), 1.86-1.31 (m, 8H),
1.30-1.21 (m, 3H)
9.1 1 -9.02 (m, 0.5H), 9.00-8.86 (m, 1.5H), 8.21 - 8.14 (m, 0.5H), 8.12-8.06 (m, 0.5H), 8.06-7.99
Crystallization from (m, 1 H), 7.89-7.78 (m, 1 H), 6.77 (s, 0.35H), 503.14,
61 A30
EtOAc and heptane 6.48 (s, 0.25H), 6.40 (s, 0.35H), 5.77 (s, 503.2
0.25H), 5.18-3.40 (m, 1 1 H), 2.44-2.30 (m, 1 H),
1.90-1.10 (m, 8H)
9.09-8.98 (m, 1.4H), 8.97-8.90 (m, 0.6H), 8.54- 8.52 (m, 0.01 H), 8.32-8.26 (m, 0.04H), 8.18- 8.11 (m, 0.4H), 8.06-8.00 (m, 1 H), 7.99-7.94
Crystallisation from (m, 0.6H), 7.92-7.84 (m, 1 H), 6.77 (s, 0.32H), 505.12,
50 A29
EtOAc/pentane 6.49 (s, 0.21 H), 6.41 (s, 0.32H), 5.78 (s, 505.1
0.21 H), 5.24-3.42 (m, 8H)] 2.47-2.32 (m, 1 H),
2.06-1.97 (m, 1 H), 1.86-1.22 (m, 8H), 1.21 - 1.11 (m, 2H), 1.09-0.98 (m, 2H)
9.54-9.40 (m, 1 H), 9.21 -8.97 (m, 1 H), 8.25-
Crystallization from 7.78 (m, 3H), 6.73 (s, 0.36H), 6.48 (s, 0.28H), 515.14,
55 A36
EtOAc and heptane 6.33 (s, 0.36H), 5.77 (s, 0.28H), 5.18-3.45 (m, 515.1
8H), 2.45-2.27 (m, 1 H), 1.86-1.00 (m, 8H)
9.36-9.24 (m, 1 H), 9.1 1 -9.02 (m, 0.3H), 9.00- 8.87 (m, 0.6H), 8.36-8.28 (m, 0.1 H), 8.22-8.14
(m, 0.3H), 8.06 (m, 0.7H), 8.03-7.89 (m, 1 H),
489.13,
- 79 A38 7.52-7.43 (m, 1 H), 6.72 (s, 0.25H), 6.47 (s,
489.2 0.15H), 6.29 (s, 0.25H), 5.84 (s, 0.15H), 5.10-
3.46 (m, 1 1 H), 2.01 -1.47 (m, 6H), 1.06 (dd,
5H)
basic preparative
9.19-8.86 (m, 1 H), 8.38-7.68 (m, 3H), 7.38- HPLC (C18, MeCN
7.04 (m, 2H), 6.73 (s, 0.38H), 6.48 (s, 0.28H), 519.14,
(1 % 10mM 59 A39
11 H), 2.49-2.28 (m, 1 H), 1.87-1.02 (m, 8H)
NH4HCO3 in H20)
9.24-8.85 (m, 1 H), 8.55-8.29 (m, 1 H), 8.29- 7.18 (m, 4H), 6.73 (s, 0.32H), 6.48 (s, 0.24H),
504.13,
- 76 A8 6.36 (s, 0.32H), 5.77 (s, 0.24H), 5.21 -3.44 (m,
504.0
8H), 2.46-2.28 (m, 1 H), 2.23-2.06 (m, 1 H),
1.95-1.06 (m, 8H), 1.07-0.75 (m, 4H)
9.19-9.04 (m, 0.4H), 9.04-8.91 (m, 0.6H), 8.72- 8.57 (m, 1 H), 8.22-8.12 (m, 0.4H), 8.11 -7.99
(m, 0.6H), 7.47-7.34 (m, 1 H), 6.74 (s, 0.35H),
514.15,
- 80 A11 6.49 (s, 0.24H), 6.36 (s, 0.34H), 5.77 (s,
514.2 0.24H), 5.22-3.43 (m, 8H), 2.65-2.59 (m, 3H),
2.59-2.55 (m, 3H), 2.47-2.34 (m, 1 H), 1.88- 1.08 (m, 8H)
8.90-8.83 (m, 0.16H), 8.81 -8.75 (m, 0.24H),
8.71 -8.64 (m, 1 H), 8.51 -8.43 (m, 1 H), 8.33- 8.26 (m, 0.52H), 8.07-8.00 (m, 0.08H), 7.75-
7.68 (m, 1 H), 7.55-7.47 (m, 1 H), 6.67 (s, 503.14,
- 77 A31
0.48H), 6.50 (s, 0.48H), 6.47 (s, 0.21 H), 5.78 503.0 (s, 0.21 H), 5.38-3.43 (m, 8H), 2.47-2.24 (m,
1 H), 2.24-2.12 (m, 1 H), 1 .87-1 .10 (m, 8H),
1.10-0.87 (m, 4H)
9.13-8.89 (m, 1 H), 8.53-8.43 (m, 1 H), 8.30 (d,
J = 7.8 Hz, 0.05H), 8.14 (d, J = 3.9 Hz, 0.26H),
8.07-7.95 (m, 0.69H), 7.88-7.77 (m, 1 H), 7.42-
515.14,
- 88 A23 7.28 (m, 2H), 6.75 (s, 0.26H), 6.49 (s, 0.17H),
515.2 6.39 (s, 0.26H), 5.78 (s, 0.17H), 5.19-3.48 (m,
8H), 2.60 (s, 3H), 2.49-2.30 (m, 1 H), 1.87-1.10
(m, 8H)
9.16-8.94 (m, 2H), 8.35 (d, J = 8.4 Hz, 0.05H),
8.16 (d, J = 4.1 Hz, 0.23H), 8.09-8.00 (m,
0.72H), 7.80-7.63 (m, 2H), 6.79 (s, 0.19H), 488.13,
- 80 A32
6.51 (s, 0.12H), 6.42 (s, 0.19H), 5.80 (s, 488.2 0.12H), 5.21 -3.47 (m, 8H), 2.65-2.55 (m, 3H),
2.49-2.30 (m, 1 H), 1.86-1.1 1 (m, 8H)
9.55-9.43 (m, 1 H), 9.27-9.22 (m, 0.02H), 9.20- 9.10 (m, 0.42H), 9.10-9.00 (m, 0.54H), 8.46- basic preparative
8.41 (m, 0.02H), 8.25-8.16 (m, 0.42H), 8.12- HPLC (C18, MeCN
8.04 (m, 0.58H), 8.04-7.99 (m, 0.42H), 7.99- 489.13,
(1 % 10mM 62 A33
7.94 (m, 0.58H), 7.92-7.82 (m, 1 H), 6.73 (s, 489.2 NH4HC03), 10 mM
0.42H), 6.49 (s, 0.33H), 6.33 (s, 0.42H), 5.77
(s, 0.33H), 5.18-3.41 (m, 8H), 3.04-2.89 (m,
2H), 2.45-2.30 (m, 1 H), 1.92-1 .06 (m, 1 1 H)
9.64-9.30 (m, 1.03H), 9.04-8.71 (m, 1.50H),
8.42-8.20 (m, 0.29H), 8.14-7.82 (m, 1.18H),
6.66 (s, 0.27H), 6.49 (s, 0.27H), 6.47 (s, 503.14,
87 A40
0.13H), 5.78 (s, 0.13H), 5.34-3.41 (m, 8H), 503.2 2.80-2.60 (m, 3H), 2.44-2.23 (m, 1H), 1.93- 1.09 (m, 8H)
9.14-9.03 (m, 0.35H), 9.03-8.92 (m, 0.65H),
8.56-8.43 (m, 1H), 8.22-8.10 (m, 0.35H), 8.03- 7.99 (m, 0.65H), 7.89-7.72 (m, 1H), 7.61-7.54
490.12,
81 A22 (m, H), 7.54-7.46 (m, 1H), 6.74 (s, 0.29H),
490.2
6.48 (s, 0.21 H), 6.36 (s, 0.29H), 5.77 (s,
0.21 H), 5.21-3.45 (m, 8H), 2.84-2.74 (m, 2H),
2.46-2.36 (m, 1H), 1.88-1.05 (m, 11H)
8.86 (d, 0.25H), 8.78 (d, 0.20H), 8.73-8.64 (m,
1H), 8.63-8.51 (m, 1H), 8.30 (d, 0.40H), 8.04
(d, 0.15H), 7.72-7.65 (m, 1H), 7.65-7.55 (m,
502. 5,
48 A34 1H), 6.67 (s, 0.41H), 6.50 (s, 0.41H), 6.47 (s,
502.2
0.17H), 5.78 (s, 0.17H), 5.34-3.41 (m, 8H),
2.86-2.75 (m, 2H), 2.36 (ddd, H), 1.84-1.31
(m, 8H), 1.30-1.22 (m, 3H)
9.14-9.04 (m, 0.20H), 9.03-8.92 (m, 0.70H),
8.45-8.36 (m, 1H), 8.36-8.29 (m, 0.10H), 8.20- 8.12 (m, 0.20H), 8.10-7.97 (m, 0.80H), 7.52- 7.49 (m, 0.20H), 7.48-7.45 (m, 0.80H), 7.38- 503.14,
80 A24
7.35 (m, 1H), 6.75 (s, 0.15H), 6.51 (s, 0.10H), 503.2 6.37 (s, 0.15H), 5.79 (s, 0.10H), 5.21-3.46 (m,
8H), 2.48-2.44 (m, 3H), 2.44-2.34 (m, 4H),
• 1.85-1.07 (m, 8H)
basic preparative
9.83-9.55 (m, 1H), 9.41-9.18 (m, 1H), 9.00- HPLC (C18, MeCN
7.88 (m, 3H), 6.66 (s, 0.43H), 6.49 (s, 0.43H), 502.15,
(1% 10mM 46 A35
6.47 (s, 0.18H), 5.78 (s, 0.18H), 5.47- 3.46 (m, 502.2 8H), 2.49-2.18 (m, 1H), 1.86-1.04 (m, 8H)
9.33-9.26 (m, 1H), 9.20-9.14 (m, 1H), 9.13- basic preparative 8.91 (m, 0.79H), 8.41-8.36 (m, 0.07H), 8.21- HPLC (C18, MeCN 8.15 (m, 0.14H), 8.11-8.02 (m, 1H), 7.74-7.63
489.1,
(1% 10mM 35 A44 (m, 1H), 6.69 (s, 0.14H), 6.44 (s, 0.10H), 6.30
489.2 NH4HCO3), 10 mM (s, 0.14H), 5.72 (s, 0.10H), 5.22-3.36 (m, 8H),
NH4HCO3 in H20) 2.50 (s, 3H), 2.46-2.30 (m, 1H), 1.85-1.06 (m,
8H)
9.20-9.11 (m, 0.40H), 9.09-8.99 (m, 0.55H),
8.45-8.38 (m, 0.03H), 8.24-8.16 (m, 0.40H),
8.12-8.02 (m, 0.62H), 7.73-7.56 (m, 2H), 6.73
503.1 ,
53 - 79 A45 (s, 0.39H), 6.49 (s, 0.29H), 6.34 (s, 0.39H),
503.2 5.77 (s, 0.29H), 5.21 -3.45 (m, 8H), 2.88-2.72
(m, 3H), 2.66-2.58 (m, 3H), 2.46-2.30 (m, 1 H),
1.94-1.03 (m, 8H)
2. Biological characterization -Cat S/K/L functional enzyme assays
Reference and test compounds were assayed for inhibitory potency (IC50) against human cathepsins using the following assay setups:
Recombinant human cathepsins (CatS, CatK, CatL, CatB) were purchased from a Enzo Life Sciences.AII assays were carried out in 96-well format using a buffer of 50 mM KH2P04, 50mM NaCI, 2mM EDTA, 0.5 mM DTT and 1 % Triton-X-100, pH 6.5 for Cathepsin S and a buffer of 50 mM NaOAc, 10 mM EDTA, 1 mM DTT and 0.01 % Triton-X-100, pH 5.5 for CatK/L/B. For Cats, the enzyme (0.0007 mU/well) was incubated with fiuorogeninc substrate (Z-WR-AMC, 5 μΜ) at RT for 10 min. For CatK the enzyme (0.00175 mU/well) was incubated with fiuorogeninc substrate (Z-FR -AMC, 40 μΜ) at RT for 10 min. For CatL, the enzyme (0.000874 mU/well) was incubated with fiuorogeninc substrate (Z-WR-AMC, 40 μΜ) at RT for 10 min. Flourogenic substrate turnover was detected using a microplate reader (Synergy™ H4, BioTek). Ki values were calculated using the Cheng Prusoff equation (Cheng & Prosoff 1973).
Table 3. -Cat S/K/L functional enzyme assays
Compound hCatK, Selectivity hCatL
hCatS, Ki [μΜ]
(Examlpe#) Ki [μΜ] Ki(hCatS) / Ki(hCatK) inhibition [%] at 31 .6μΜ
1 0.151 0.0015 99 72
2 0.308 0.0007 453 45
3 0.11 1 0.002 53 73
4 0.040 0.002 22 73
5 0.355 0.002 169 81
6 0.174 0.003 55 42
7 0.263 0.003 50 62
8 0.160 0.0008 210 50
9 0.208 0.002 104 67
10 0.1 12 0.006 19 65
11 0.279 0.002 140 59
12 0.080 0.006 13 51
13 0.071 0.001 71 72
14 1.358 0.003 453 44
15 0.303 0.002 152 56
16 0.191 0.005 38 66
18 0.212 0.003 71 50
19 0.296 0.002 148 50
20 0.513 0.003 171 42
21 0.900 0.003 300 43
22 0.558 0.027 21 56
23 0.100 0.0015 67 52
24 0.543 0.006 99 44
25 0.127 0.002 64 41
26 0.246 0.009 27 39
27 0.552 0.012 46 39
28 0.463 0.004 110 20
29 0.707 0.001 728 22
30 0.086 0.0006 151 57
31 0.056 0.003 17 68
32 0.951 0.003 283 24
33 0.047 0.026 2 48
34 0.362 0.001 355 21
35 0.655 0.007 93 9
36 0.036 0.003 10 58
37 0.061 0.008 8 70
38 0.014 0.003 5 51
39 0.017 0.002 9 74
40 0.052 0.002 26 58
41 0.321 0.0003 1070 2
42 0.087 0.0002 435 4
43 0.304 0.001 304 61
44 0.296 0.0004 740 28
45 0.451 0.0005 902 45
46 0.881 0.005 186 52
47 0.012 0.004 3 71
48 0.044 0.004 11 67
49 0.051 0.0001 563 38
50 0.171 0.0004 388 67
51 0.111 0.0002 697 40
52 0.138 0.0005 276 60
53 0.023 0.0006 38 54
Comparative
Example C1
0.0824 0.0148 6 0.925 (Ki) (ex. 17 of
2009/112839)
Claims
Claims:
1 . A compound of the general formula (I)
wherein
R1 represents H or F.
X represents S or O;
Y1 and Y2 independently represents CH or N;
Z1. Z2. Z3. Z4 and Z5 independently represents CH or N.
with the proviso that 1 . 2 or 3 of Z Z2. Z3. Z4 and Z5 represent N;
m denotes 0. 1 or 2;
n denotes 0. 1. 2. or 3;
each R2 and each R3 is independently selected from the group consisting of F; CI; Br; CN; CF3; CF2H; CFH2; CF2CI; CFCI2; d.4-alkyl;
C(=0)-N(C1.4-alkyl)2; OH; 0-CM-alkyl; OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; NH2; N(H)(d.4- alkyl); N(d-4-alkyl)2;
N(d.4-alkyl)-C(=0)-(d-4-alkyl);
alkyl); N(H)-C(=0)-NH2; N(H)-C(=0)-N(H)(d.4-aikyl); N(H)-C(=0)-N(C1.4-alkyl)(C1.4-alkyl); S-(d.4 alkyl); S(=0)-(C1.4-alkyl); S(=0)2-(C1.4-alkyl); S(=0)2-N(H)(d.4-alkyl); cyclopropyl; O-cyclopropyl; NH-cyclopropyl; N(H)-C(=0)-cyclopropyl; S(=0)-(cyclopropyl) and S(=0)2-(cyclopropyl); wherein the above-mentioned substituents C1-4-alkyl and cyclopropyl. may in each case be unsubstituted or substituted one or more times by identical or different substituents. and the above-mentioned substituent d.4-alkyl may in each case be branched or unbranched; in the form of an individual stereoisomer or a mixture thereof; in the form of a tautomer; of a free compound; of an N-oxide; or in the form of a solvate and/or of a physiologically acceptable salt.
A compound according to claim 1 , characterized in that R1 is H.
A compound according to claim 1 or 2, characterized in that
Y represents CH or N and Y2 represents CH; or
Y1 represents CH and Y2 represents CH or N.
A compound according to any of the preceding claims, characterized in that
X represents S.
5. A compound according to claims to claims 1 to 4, characterized in that
X represents S. Y1 represents CH and Y2 represents CH.
6. A compound according to claims 1 to 4, characterized in that
X represents S. Y1 represents CH and Y2 represents N.
7. A compound according to any of the preceding claims, characterized in that the compound of the
Y2 represents N or CH;
R2 is selected from the group consisting of F; CI; Br; CN; CF3; CF2H; CFH2; CF2CI; CFCI2; d.4- alkyl; C(=0)-(C1.4-alkyl); C(=0)-NH2; C(=0)-N(H)(C1.4-alkyl); C(=0)-N(C1.4-alkyl)2; OH; 0-C1-4- alkyl; OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; NH2; N(H)(d.4-alkyl); N(d-4-alkyl)2; N(H)-C(=0)- (d.4-alkyl); N(C1.4-alkyl)-C(=0)-(C1.4-alkyl); N(H)-S(=0)2-(C1.4-alkyl); N(H)-C(=0)-NH2; N(H)- C(=0)-N(H)(C1.4-alkyl); N(H)-C(=0)-N(C1.4-alkyl)(C1.4-alkyl); S-(d-4-alkyl); S(=0)-(d.4-alkyl); S(=0)2-(d_4-alkyl); S(=0)2-N(H)(d.4-alkyl); cyclopropyl; O-cyclopropyl; NH-cyclopropyl; N(H)- C(=0)-cyclopropyl; S(=0)-(cyclopropyl) and S(=0)2-(cyclopropyl);
n denotes 0, 1 or 2 and
R3 is independently selected from the group consisting of F; CI; Br; CN; CF3; CF2H; CFH2; CF2CI; CFCI2; d.4-alkyl; C(=0)-(d.4-alkyl); C(=0)-NH2; C(=0)-N(H)(d.4-alkyl); C(=0)-N(d.4-alkyl)2; OH; 0-d.4-alkyl; OCF3; OCF2H; OCFH2; OCF2CI; OCFCI2; NH2; N(H)(d.4-alkyl); N(C1-4-alkyl)2; N(H)- C(=0)-(C1-4-alkyl); N(d.4-alkyl)-C(=0)-(d.4-alkyl); N(H)-S(=0)2-(d.4-alkyl); N(H)-C(=0)-NH2;
S(=0)-(d.4-alkyl);
S(=0)2-(C1.4-alkyl); S(=0)2-N(H)(C1.4-alkyl); cyclopropyl; O-cyclopropyl; NH-cyclopropyl; N(H)- C(=0)-cyclopropyl; S(=0)-(cyclopropyl) and S(=0)2-(cyclopropyl).
8. A compound according to claim 7, characterized in that
m denotes 0;
n denotes 0, 1 or 2 and
R3 is independently selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; CH(CH3)2; C(=0)CH3; C(=0)NH2; C(=0)N(H)(CH3); C(=0)N(CH3)2; OH; OCH3; OCF3; OCF2H; OCFH2; NH2; N(H)(CH3); N(CH3)2; N(H)-C(=0)CH3; N(H)-S(=0)2CH3; S(=0)CH3;
S(=0)2CH3; S(=0)2-N(H)(CH3); cyclopropyl and O-cyclopropyl.
m denotes 0;
n denotes 0 or 1 or 2 and
R3 is independently selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; CH(CH3)2; C(=0)CH3; C(=0)NH2; C(=0)N(H)(CH3); C(=0)N(CH3)2; OH; OCH3; OCF3; OCF2H; OCFH2; NH2; N(H)(CH3); N(CH3)2; N(H)-C(=0)CH3; N(H)-S(=0)2CH3; S(=0)CH3;
S(=0)2CH3; S(=0)2-N(H)(CH3); cyclopropyl and O-cyclopropyl.
10. A compound according to any of the preceding claims, characterized in that the compound of the general formula (I) is a compound according to general formula (lb).
Z1, Z3 and Z5 each represent CH and Z4 represents N or
Z1 , Z3 and Z4 each represent CH and Z5 represents N;
n denotes 0 or 1 or 2 and
R3 is selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; OCH3; cyclopropyl and OCF3. A compound according to any of the preceding claims, characterized in that the compound of the general formula (I) is a compound according to general formula (Ic).
wherein Y2 represents CH or N;
Z Z2, Z4 and Z5 each represent CH or
Z2, Z4 and Z5 each represent CH and Z1 represents N or
Z Z4 and Z5 each represent CH and Z2 represents N;
n denotes 0 or 1 or 2 and
R3 is selected from the group consisting of F; CI; CN; CF3; CF2H; CFH2; CH3; CH2CH3; OCH3 cyclopropyl and OCF3.
A compound according to claim 10 or 1 1 , characterized in that
Y2 represents CH.
A compound according to any of the preceding claims, selected from the group consisting of N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -
Ί
cyclopentyl-2-oxoethyl)-5-(pyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - ^ cyclopentyl-2-oxoethyl)-5-(pyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - ^ cyclopentyl-2-oxoethyl)-5-(pyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - ^ cyclopentyl-2-oxoethyl)-5-(pyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - ^ cyclopentyl-2-oxoethyl)-5-(pyrazin-2-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -
6 cyclopentyl-2-oxoethyl)-5-(5-fluoropyridin-3-yl)thiophene-2-carboxamide
7 N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -
cyclopentyl-2-oxoethyl)-5-(pyridazin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridine-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyrimidin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridazin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-c loro-3-oxotetra ydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1- cyclopentyl-2-oxoethyl)-5-(pyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(5-fluoropyrimidin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyrazin-2-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-methylpyridin-3-yl)thiazole-2-carboxanrijde
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(3-fluoropyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyrimidin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-chloropyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-cyclopropylpyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-cyclopropylpyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-(trifluoromethyl)pyrimidin-5-yl)thiophene-2-carboxami^
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetra ydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1- cyclopentyl-2-oxoethyl)-5-(6-(trifluoromethyl)pyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-cyclopropylpyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(5-methylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-cyclopropylpyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(pyridazin-4-yl)furan-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-(trifluoromethyl)pyrimidin-5-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-(trifluoromethyl)pyridin-3-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1- cyclopentyl-2-oxoethyl)-5-(5-ethylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(5-methoxypyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(5-cyclopropylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-methylpyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-methoxypyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methoxypyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-cyclopropylpyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoet yl)-5-(2,4-dimet ylpyrimidin-5-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-cyclopropylpyridin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-methylpyridin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6~chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(4-methylpyridazin-3-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-ethylpyridazin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(6-methylpyridazin-4-yl)thiazole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - cyclopentyl-2-oxoethyl)-5-(2-ethylpyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 -
50
cyclopentyl-2-oxoethyl)-5-(2-etriylpyridin-4-yl)thia2ole-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - 51
cyclopentyl-2-oxoethyl)-5-(2,5-dimethylpyridin-4-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - 52
cyclopentyl-2-oxoethyl)-5-(5-methylpyridazin^-yl)thiophene-2-carboxamide
N-((S)-2-((3aS,6S,6aS)-6-chloro-3-oxotetrahydro-2H-furo[3,2-b]pyrrol-4(5H)-yl)-1 - 53
cyclopentyl-2-oxoethyl)-5-(3,6-dimethylpyridazin-4-yl)thiophene-2-carboxamide in the form of an individual stereoisomer or a mixture thereof; in the form of a tautomer; of a free compound; of an N-oxide; or in the form of a solvate and/or of a physiologically acceptable salt.
A pharmaceutical composition comprising at least one compound according to one or more of claims 1 to 13.
A compound according to one or more of claims 1 to 13 for the treatment and/or prophylaxis of a disorder selcetd from the group consisting of nociceptive pain; neuropathic pain; erosive osteoarthritis (EO). in particular erosive osteoarthritis of the hand; Sjogren's Syndrom; rheumatoid arthritis ( A); psoriatic arthrithis (PsA); Psoriasis; Spondylarthritis, in particular ankylosing spondylitis; osteoporosis; Complex Regional Pain Syndrome (in particular CRPS I); Lupus erythematodes (SLE); Lupus nephritis; asthma; multiple sclerosis (MS); diabetes; chronic obstructive pulmonary disease (COPD), in particular COPD subpopoulation with osteoporosis; and asthma, in particular severe asthma subpopoulation with osteoporosis.
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CA2946618A CA2946618A1 (en) | 2014-04-23 | 2015-04-23 | 3-oxo-tetrahydro-furo[3,2-b]pyrrol-4(5h)-yl) derivatives ii |
EP15718776.6A EP3134414A1 (en) | 2014-04-23 | 2015-04-23 | 3-oxo-tetrahydro-furo[3,2-b]pyrrol-4(5h)-yl) derivatives ii |
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EP14001458 | 2014-04-23 | ||
EP14001458.0 | 2014-04-23 |
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WO2015161924A1 true WO2015161924A1 (en) | 2015-10-29 |
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PCT/EP2015/000839 WO2015161924A1 (en) | 2014-04-23 | 2015-04-23 | 3-oxo-tetrahydro-furo[3,2-b]pyrrol-4(5h)-yl) derivatives ii |
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US (1) | US9802947B2 (en) |
EP (1) | EP3134414A1 (en) |
AR (1) | AR100177A1 (en) |
CA (1) | CA2946618A1 (en) |
TW (1) | TW201620915A (en) |
WO (1) | WO2015161924A1 (en) |
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WO2019185875A1 (en) | 2018-03-30 | 2019-10-03 | Syngenta Participations Ag | Herbicidal compounds |
Citations (1)
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WO2009112839A1 (en) * | 2008-03-13 | 2009-09-17 | Amura Therapeutics Limited | Compounds |
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US20070117785A1 (en) | 2000-08-14 | 2007-05-24 | Butler Christopher R | Substituted pyrazoles and methods of treatment with substituted pyrazoles |
GB0614052D0 (en) | 2006-07-14 | 2006-08-23 | Amura Therapeutics Ltd | Compounds |
-
2015
- 2015-04-23 TW TW104112968A patent/TW201620915A/en unknown
- 2015-04-23 CA CA2946618A patent/CA2946618A1/en not_active Abandoned
- 2015-04-23 US US14/693,975 patent/US9802947B2/en not_active Expired - Fee Related
- 2015-04-23 EP EP15718776.6A patent/EP3134414A1/en not_active Withdrawn
- 2015-04-23 WO PCT/EP2015/000839 patent/WO2015161924A1/en active Application Filing
- 2015-04-24 AR ARP150101236A patent/AR100177A1/en unknown
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WO2009112839A1 (en) * | 2008-03-13 | 2009-09-17 | Amura Therapeutics Limited | Compounds |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2019185875A1 (en) | 2018-03-30 | 2019-10-03 | Syngenta Participations Ag | Herbicidal compounds |
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TW201620915A (en) | 2016-06-16 |
CA2946618A1 (en) | 2015-10-29 |
US20150307506A1 (en) | 2015-10-29 |
US9802947B2 (en) | 2017-10-31 |
EP3134414A1 (en) | 2017-03-01 |
AR100177A1 (en) | 2016-09-14 |
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