WO2017144483A1 - Novel pyrrolidine derivatives - Google Patents

Novel pyrrolidine derivatives Download PDF

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Publication number
WO2017144483A1
WO2017144483A1 PCT/EP2017/053967 EP2017053967W WO2017144483A1 WO 2017144483 A1 WO2017144483 A1 WO 2017144483A1 EP 2017053967 W EP2017053967 W EP 2017053967W WO 2017144483 A1 WO2017144483 A1 WO 2017144483A1
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WO
WIPO (PCT)
Prior art keywords
trifluoromethyl
pyrrolidine
cyclopropanecarbonyl
cyanocyclopropyl
carboxamide
Prior art date
Application number
PCT/EP2017/053967
Other languages
French (fr)
Inventor
Wolfgang Haap
Bernd Kuhn
Thomas Luebbers
Jens-Uwe Peters
Original Assignee
F. Hoffmann-La Roche Ag
Hoffmann-La Roche Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to MA43667A priority Critical patent/MA43667B1/en
Priority to CR20180404A priority patent/CR20180404A/en
Application filed by F. Hoffmann-La Roche Ag, Hoffmann-La Roche Inc. filed Critical F. Hoffmann-La Roche Ag
Priority to RU2018133640A priority patent/RU2736498C1/en
Priority to SG11201807074VA priority patent/SG11201807074VA/en
Priority to AU2017224343A priority patent/AU2017224343B2/en
Priority to DK17705662.9T priority patent/DK3419970T3/en
Priority to LTEP17705662.9T priority patent/LT3419970T/en
Priority to SI201730195T priority patent/SI3419970T1/en
Priority to CN201780013397.XA priority patent/CN108699044B/en
Priority to UAA201809397A priority patent/UA122084C2/en
Priority to CA3011652A priority patent/CA3011652C/en
Priority to EP17705662.9A priority patent/EP3419970B1/en
Priority to MX2018009638A priority patent/MX2018009638A/en
Priority to KR1020187024347A priority patent/KR20180111862A/en
Priority to ES17705662T priority patent/ES2775781T3/en
Priority to PL17705662T priority patent/PL3419970T3/en
Priority to JP2018541661A priority patent/JP6952044B2/en
Priority to MYPI2018001465A priority patent/MY196560A/en
Priority to RS20200183A priority patent/RS59938B1/en
Publication of WO2017144483A1 publication Critical patent/WO2017144483A1/en
Priority to IL260130A priority patent/IL260130B/en
Priority to ZA2018/04120A priority patent/ZA201804120B/en
Priority to PH12018501585A priority patent/PH12018501585B1/en
Priority to CONC2018/0007756A priority patent/CO2018007756A2/en
Priority to US16/111,721 priority patent/US10689339B2/en
Priority to HRP20200307TT priority patent/HRP20200307T1/en

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    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4192—1,2,3-Triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4196—1,2,4-Triazoles
    • A—HUMAN NECESSITIES
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    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
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    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • the present invention relates to organic compounds useful for therapy and/or prophylaxis in a mammal, and in particular to compounds that are preferential inhibitors of the cysteine protease cathepsin, in particular of the cysteine protease cathepsin S.
  • the invention relates in particular to a compound of formula (I)
  • R is hydrogen, alkyl, haloalkyl, halogen or triazolyl
  • R is (halo)(oxy)pyridinyl, (alkyl)(oxy)pyridinyl, (alkyl)(haloalkyl)pyrazolyl,
  • haloalkoxyphenyl alkoxyphenyl, cycloalkyloxyphenyl, cycloalkyloxy, alkyltetrazolyl, triazolyl, alkyltriazolyl, dialkyltriazolyl, halotriazolyl, haloalkylpyrazolyl, formylphenyl, aminopyrimidinyl, cyanophenyl, (alkoxy)(dihalo)phenyl, hydroxyalkylphenyl, benzo[l,3]dioxolyl, dialkylthiazolyl, alkylthiazolyl, alkoxypyrimidinyl, dialkylisoxazolyl or (halo)(haloalkyl)triazolyl; or a pharmaceutically acceptable salt or ester thereof.
  • the compounds of the invention are preferential inhibitors of the cysteine protease Cathepsin (Cat), in particular Cathepsin S and are therefore useful to treat metabolic diseases like diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease and diabetic nephropathy.
  • Cat cysteine protease Cathepsin
  • immune mediated diseases like rheumatoid arthritis, multiple sclerosis, sjorgen syndrome, lupus erythematosus, neuropathic pain, diabetes type I, asthma and allergy and skin related immune disease are suitable diseases to be treated with a cathepsin S inhibitor.
  • Objects of the present invention are the compounds of formula (I) and their aforementioned salts per se and their use as therapeutically active substances, a process for the manufacture of the said compounds, intermediates, pharmaceutical compositions, medicaments containing the said compounds, their pharmaceutically acceptable salts, the use of the said compounds and salts for the prophylaxis and/or therapy of illnesses, especially in the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease and diabetic nephropathy, and the use of the said compounds and salts for the production of medicaments for the treatment or prophylaxis of diabetes,
  • Atherosclerosis atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease and diabetic nephropathy.
  • Mammalian cathepsins are cysteine-type proteases involved in key steps of biological and pathological events. Cathepsins are considered tractable drug targets as it is feasible to inhibit enzymatic activity with small molecules and are therefore of interest to the pharmaceutical industry (Bromme, D. (2001), 'Papain-like cysteine proteases', Curr Protoc Protein Sci, Chapter 21, Unit 21 2; Roberts, R. (2005), 'Lysosomal cysteine proteases: structure, function and inhibition of cathepsins', Drug News Perspect, 18 (10), 605-14).
  • Cathepsin S is prominently expressed in antigen presenting cells like macrophages and dendritic cells and smooth muscle cells.
  • Cathepsin S is only weakly expressed in normal arterial tissue, strong upregulation is seen in atherosclerotic arteries (Liu, J., et al.
  • Cathepsin S deficient mice have a reduced atherosclerosis-phenotype when tested in appropriate mouse models.
  • LDL-Rec deficient mice reduced lipid accumulation, elastin- fibre breakdown and chronic arterial inflammation is reported.
  • APO E deficient mice a significant reduction of acute plaque rupture events was reported.
  • chronic renal disease is introduced into CatS/In APO-E deficient mice a strong reduction of accelerated calcification is seen on top of the anti atherosclerotic activity in arteries and heart valves (Aikawa, E., et al.
  • Cathepsin S is involved in the degradation of extracellular matrix that stabilises the plaque.
  • Cathepsin S has potent elastinolytic activity and can exert this at neutral pH, a feature that distinguishes Cathepsin S from all other Cathepsins.
  • Cathepsin S is the major protease involved in antigen processing, in particular cleavage of the invariant chain in antigen presenting cells, resulting in reduced contribution of Tcells to the chronic inflammation of the
  • Atherosclerotic tissue Elevated inflammation results in further oxidative and proteolytic tissue damage and subsequently plaque destabilisation (Cheng, X. W., et al. (2004), 'Increased expression of elastolytic cysteine proteases, cathepsins S and K, in the neointima of balloon-injured rat carotid arteries', Am J Pathol, 164 (1), 243-51; Driessen, C, et al.
  • Cathepsin S plays also a role in the reduction of tumor growth and tumor cell invasion as described by Roberta E. Burden in Clin Cancer Res 2009;15(19).
  • nephrectomized Cathepsin S knock out mice showed a significant reduction of arterial calcification when compared to nephrectomized wild type mice. This indicates that inhibition of Cathepsin S may have a beneficial effect on the reduction of cardiovascular events in chronic kidney disease patients (Elena Aikawa, Circulation, 2009, 1785-1794).
  • alkyl signifies a straight-chain or branched-chain alkyl group with 1 to 8 carbon atoms, particularly a straight or branched-chain alkyl group with 1 to 6 carbon atoms and more particularly a straight or branched-chain alkyl group with 1 to 4 carbon atoms.
  • Examples of straight- chain and branched-chain Q-Cg alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl, the isomeric pentyls, the isomeric hexyls, the isomeric heptyls and the isomeric octyls, particularly methyl, ethyl, propyl, butyl and pentyl more particularly methyl, ethyl, propyl, isopropyl, isobutyl, tert.-butyl and isopentyl.
  • a particular example of alkyl is methyl.
  • cycloalkyl signifies a cycloalkyl ring with 3 to 8 carbon atoms and particularly a cycloalkyl ring with 3 to 6 carbon atoms.
  • Examples of cycloalkyl are cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl, cycloheptyl and cyclooctyl.
  • a particular example of “cycloalkyl” is cyclopropyl.
  • (oxy)pyridinyl refers to py + -0 " , wherein py represents pyridine.
  • alkoxy signifies a group of the formula alkyl-O- in which the term “alkyl” has the previously given significance, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy.
  • Particular "alkoxy” are methoxy and ethoxy, and in particular methoxy.
  • cycloalkyloxy alone or in combination, signifies a group of the formula cycloalkyl-O- in which the term “cycloalkyl” has the previously given significance.
  • a particular cycloalkyloxy is cyclopropyloxy.
  • halogen or "halo", alone or in combination, signifies fluorine, chlorine, bromine or iodine and particularly fluorine, chlorine or bromine, more particularly fluorine and chlorine.
  • halo in combination with another group, denotes the substitution of said group with at least one halogen, particularly substituted with one to five halogens, particularly one to four halogens, i.e. one, two, three or four halogens.
  • a particular "halogen” is chlorine.
  • haloalkyl denotes an alkyl group substituted with at least one halogen, particularly substituted with one to five halogens, particularly one to three halogens.
  • Particular "haloalkyl” are trifluoromethyl and difluoromethyl, in particular trifluoromethyl.
  • haloalkoxy denotes an alkoxy group substituted with at least one halogen, particularly substituted with one to five halogens, particularly one to three halogens. Particular "haloalkoxy” is trifluoromethoxy.
  • carbonyl alone or in combination, signifies the -C(O)- group.
  • amino alone or in combination, signifies the primary amino group (-NH 2 ), the secondary amino group (-NH-), or the tertiary amino group (-N-).
  • pharmaceutically acceptable salts refers to those salts which retain the biological effectiveness and properties of the free bases or free acids, which are not biologically or otherwise undesirable.
  • the salts are formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, particularly hydrochloric acid, and organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, N-acetylcy stein.
  • inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, particularly hydrochloric acid
  • organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succin
  • salts derived from an inorganic base include, but are not limited to, the sodium, potassium, lithium, ammonium, calcium, magnesium salts.
  • Salts derived from organic bases include, but are not limited to salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, lysine, arginine, N-ethylpiperidine, piperidine, polyamine resins.
  • the compound of formula (I) can also be present in the form of zwitterions.
  • Particularly preferred pharmaceutically acceptable salts of compounds of formula (I) are the salts of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid and methanesulfonic acid.
  • “Pharmaceutically acceptable esters” means that the compound of general formula (I) may be derivatised at functional groups to provide derivatives which are capable of conversion back to the parent compounds in vivo. Examples of such compounds include physiologically acceptable and metabolically labile ester derivatives, such as
  • esters methoxymethyl esters, methylthiomethyl esters and pivaloyloxymethyl esters.
  • any physiologically acceptable equivalents of the compound of general formula (I), similar to the metabolically labile esters, which are capable of producing the parent compound of general formula (I) in vivo, are within the scope of this invention.
  • one of the starting materials or compounds of formula (I) contain one or more functional groups which are not stable or are reactive under the reaction conditions of one or more reaction steps
  • appropriate protecting groups as described e.g. in "Protective Groups in Organic Chemistry” by T. W. Greene and P. G. M. Wuts, 3 rd Ed., 1999, Wiley, New York
  • Such protecting groups can be removed at a later stage of the synthesis using standard methods described in the literature.
  • protecting groups are tert-butoxycarbonyl (Boc), 9-fluorenylmethyl carbamate (Fmoc), 2-trimethylsilylethyl carbamate (Teoc), carbobenzyloxy (Cbz) and p-methoxybenzyloxycarbonyl (Moz).
  • the compound of formula (I) can contain several asymmetric centers and can be present in the form of optically pure enantiomers, mixtures of enantiomers such as, for example, racemates, mixtures of diastereoisomers, diastereoisomeric racemates or mixtures of diastereoisomeric racemates.
  • asymmetric carbon atom means a carbon atom with four different substituents. According to the Cahn-Ingold-Prelog Convention an asymmetric carbon atom can be of the "R” or "S" configuration.
  • the invention further relates to: A compound of formula (I) wherein R 1 is alkyl, haloalkyl or halogen;
  • R is (alkyl)(haloalkyl)pyrazolyl, alkyltetrazolyl, triazolyl, alkyltriazolyl, dialkyltriazolyl, halotriazolyl, haloalkylpyrazolyl, dialkylthiazolyl, alkylthiazolyl or dialkylisoxazolyl;
  • the invention further relates to a compound of formula (I) selected from:
  • the invention particularly relates to a compound of formula (I) selected from:
  • the invention particularly relates to a compound of formula (I) which is (2S,4R)-4- [4-(5-Methyl-tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide.
  • ACN Acetonitrile
  • boc ie/t-Butyloxycarbonyl
  • BOP Benzotriazolyl-N-oxy-tris(dimethylamino)-phosphonium hexafluorophosphate
  • BOP-C1 Bis-(2-oxo-3-oxazolidinyl)-phosphinic acid chloride
  • CDI 1 , 1 ' -Carbonyldiimidazole
  • EDCI N-(3-Dimetylaminopropyl)-N' -ethyl-carbodiimide hydrochloride
  • HATU 0-(7-azabenzotriazol- 1 -yl)- 1 , 1 ,3,3-tetramethyluronium hexafluorophosphate;
  • HOBT 1-Hydroxybenzotriazole;
  • Hunig's Base Ethyl-diisopropyl-amine;
  • mCPBA or MCPBA meta-Chloroperoxybenzoic acid; MeOH: Methanol;
  • Mes-Cl Mesyl chloride; min: minute; Na 2 S0 4 : Sodium sulfate;
  • Nos-Cl 3-Nitrobenzenesulfonyl chloride
  • Pd 2 (dba) 3 Tris(dibenzylideneacetone)dipalladium
  • PyB OP Benzotriazol- 1 -yl- oxy tripyrrolidinepho sphonium hexafluoropho sphate ;
  • TBTU 0-(Benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium terafluoroborate
  • THF Tetrahydrofurane
  • TFA Trifluoroacetic acid
  • Tos-Cl Toluene-4-sulfonyl chloride.
  • Acid e.g. methane sulfonic acid, phenyl sulfonic acid, trifluoromethyl sulfonic acid, HCl, HBr, sulfuric acid,TFA, formic acid
  • X OH, CI, O-SO 2 -LG 1
  • LG 1 Leaving group such as phenyl, methyl, ethyl, 3-nitrophenyl, 4-methylphenyl, 4- bromophenyl, trifluoromethyl
  • LG 2 F, CI, Br, I, B(OH) 2 , B(OR 3 ) 2 ; e) R 1 as defined above;
  • R 3 Methyl, ethyl or both R 3 form together with the oxygen and boron atoms to which they are attached a ring such as 4,4,5, 5-tetramethyl-[l,3,2]dioxaborolane
  • Oxidation e.g. methane sulfonic acid, phenyl sulfonic
  • Boc-protected compound 1 is deprotected with an appropriate acid such as TFA, HCl, formic acid, sulfuric acid etc. to yield after crystallization the salt 2.
  • Reaction of salt 2 with 1-trifluoromethyl-cyclopropanecarboxylic acid in the presence of a base such as triethyl amine, Hunig's Base or N-methyl morpholine and an appropriate amide coupling reagent such as HATU, PyBop, TBTU, CDI, EDCI, BOP or Bop-Cl yields amide 3.
  • Reaction of alcohol 4 with a sulfonylchloride derivative such as methane sulfonylchloride, phenyl sulfonylchloride, tosylchloride, nosylchloride, brosylchloride or anhydrides such as triflic anhydride yields compound 5.
  • Thioether 6 is obtained by reaction of sulfonate 5 with thiophenol 5b in the presenece of an appropriate base such as Hunig's base, triethyl amine, pyridine, lutidine, Na 2 C0 3 , K 2 C0 3 or Cs 2 C0 3 .
  • sulfone 7 can be either directly reacted with heterocyclic compounds in a S Ar fashion in the presence of a base such as Hunig's base, triethyl amine, pyridine, lutidine, Na 2 C0 3 , K 2 C0 3 or Cs 2 C0 3 or via a Suzuki reaction with boronic acids or esters thereof using metal catalysts and bases known in the art such as e.g. Pd(PPh 3 ) 4 , Pd 2 (dba) 3 or a Pd-source with a phosphine ligand to yield the final compounds 8.
  • a peroxide source such as hydrogen peroxide, mCPBA, oxone or metal complexes of hydrogen peroxide such as M0O 2 CI 2 /H 2 O 2 or Na x W y O z /H 2 0 2 systems.
  • a base such as Hunig's base, triethyl amine, pyridine, lutidine, Na 2 C0 3
  • Oxidation of pyridine derivatives to the corresponding N-oxide can be accomplished by using an oxidation reagent such as hydrogen peroxide, mCPBA or oxone.
  • an oxidation reagent such as hydrogen peroxide, mCPBA or oxone.
  • the invention thus also relates to a process for the manufacture of a compound of formula (I) comprising:
  • R 1 and R2 are as defined in any one of claims 1 to 6 and wherein LG 1 is F, CI, Br, I, B(OH) 2 or B(OR 3 ) 2 , LG 2 is H, B(OH) 2 , B(OR 3 ) 2 , Br or I and each R 3 is independently selected from methyl, ethyl and both R together with the oxygen and boron atoms to which they are attached form an organoboron ring; or
  • R is as defined in any one of claims 1 to 6 and R 4 is halogen or alkyl.
  • oxidation reagents are e.g. hydrogen peroxide, mCPBA or oxone.
  • 4,4,5, 5-tetramethyl-l,3,2-dioxaborolane is an example of organoboron ring.
  • the invention further relates to a compound of formula (I) when manufactured according to the above process.
  • compositions or medicament containing a compound of the invention and a therapeutically inert carrier, diluent or excipient, as well as a method of using the compounds of the invention to prepare such composition and medicament.
  • the compound of formula (I) may be formulated by mixing at ambient temperature at the appropriate pH, and at the desired degree of purity, with physiologically acceptable carriers, i.e., carriers that are non- toxic to recipients at the dosages and concentrations employed into a galenical
  • the pH of the formulation depends mainly on the particular use and the concentration of compound, but preferably ranges anywhere from about 3 to about 8.
  • a compound of formula (I) is formulated in an acetate buffer, at pH 5.
  • the compound of formula (I) is sterile.
  • the compound may be stored, for example, as a solid or amorphous composition, as a lyophilized formulation or as an aqueous solution.
  • compositions are formulated, dosed, and administered in a fashion consistent with good medical practice.
  • Factors for consideration in this context include the particular disorder being treated, the particular mammal being treated, the clinical condition of the individual patient, the cause of the disorder, the site of delivery of the agent, the method of administration, the scheduling of administration, and other factors known to medical practitioners.
  • the compounds of the invention may be administered by any suitable means, including oral, topical (including buccal and sublingual), rectal, vaginal, transdermal, parenteral, subcutaneous, intraperitoneal, intrapulmonary, intradermal, intrathecal and epidural and intranasal, and, if desired for local treatment, intralesional administration.
  • Parenteral infusions include intramuscular, intravenous, intraarterial, intraperitoneal, or subcutaneous administration.
  • the compounds of the invention may be administered in particular by intravitreal administration.
  • the compounds of the present invention may be administered in any convenient administrative form, e.g., tablets, powders, capsules, solutions, dispersions, suspensions, syrups, sprays, suppositories, gels, emulsions, patches, etc.
  • Such compositions may contain components conventional in pharmaceutical preparations, e.g., diluents, carriers, pH modifiers, sweeteners, bulking agents, and further active agents.
  • a typical formulation is prepared by mixing a compound of the present invention and a carrier or excipient. Suitable carriers and excipients are well known to those skilled in the art and are described in detail in, e.g., Ansel, Howard C, et al., Ansel's
  • the formulations may also include one or more buffers, stabilizing agents, surfactants, wetting agents, lubricating agents, emulsifiers, suspending agents,
  • the invention thus also relates to:
  • a compound of formula (I) for use as therapeutically active substance is a compound of formula (I) for use as therapeutically active substance
  • a pharmaceutical composition comprising a compound of formula (I) and a therapeutically inert carrier;
  • a compound of formula (I) for the preparation of medicaments for the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic rethinopathy or age related macular degeneration;
  • a method for the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic rethinopathy or age related macular degeneration which method comprises administering an effective amount of a compound of formula (I) to a patient in need thereof.
  • the mixture was stirred for 20 h at room temperature, before it was poured onto an aqueous citric acid solution (10 % in water, 1.6 L) and the phases were separated.
  • the aqueous phase was extracted with ethyl acetate (3 x 500 mL).
  • the combined organic extracts were washed with 20 brine (500 mL), dried over sodium sulfate, and concentrated in vacuo.
  • the crude product (245 g, brown oil) was dissolved in dichloromethane (330 mL) before ethyl acetate (130 mL) and heptane (660 mL) were added and dichloromethane was carefully distilled off in vacuo. The product started to crystallize.
  • tetrahydrofuran (880 mL) was added and the mixture was acidified by addition of concentrated hydrochloric acid (37% m/m, 47 mL), followed by the addition of sodium chloride (440 g). After extraction with ethyl acetate (1 x 1.4 L, 3 x 550 mL), the combined organic extracts were dried over sodium sulfate and concntrated in vacuo. At a volume of ca. 1.5 L, the product started to crystallize upon addition of seed crystals. The volume of the suspension was further reduced to ca. 500 mL and cooled to 2°C (ice bath).
  • Example 3d) (7.03 g, 14.9 mmol, Eq: 1.00) was dissolved in propionitrile (80 mL) and 4- bromo-2-trifluoromethyl-benzenethiol CAS 1208075-10-8 (5.75 g, 22.4 mmol, Eq: 1.50) was added. Now, triethylamine (3.02 g, 4.16 mL, 29.8 mmol, Eq: 2.00) was carefully added and the reaction mixture was stirred at reflux for 18 h. The reaction mixture was extracted with 10% aqueous Na 2 C0 3 solution/ AcOEt. The organic layers were dried over Na 2 S0 4 , filtered and evoporated.
  • Example 3f (500 mg, 830 ⁇ , Eq: 1.00), l-methyl-5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)-3-(trifluoromethyl)-lH-pyrazole (275 mg, 996 ⁇ , Eq: 1.20) and triphenylphosphine (43.5 mg, 166 ⁇ , Eq: 0.20) were dissolved in 1,2-dimethoxyethane (6 mL). Pd(OAc) 2 (18.6 mg, 83.0 ⁇ , Eq: 0.10) and 2M aqueous Na 2 C0 3 solution (1.5 mL) were added to the solution. The reaction mixture was stirred at 60°C for 8 h.
  • Example 6
  • example 7a In a 250 mL round-bottomed flask, example 7a) (5.85 g, 11.5 mmol, Eq: 1.00) was combined with dichloromethane (80 mL) to give a white suspension. 3-chloroperoxy- benzoic acid (5.15 g, 29.9 mmol, Eq: 2.60) was added. The reaction mixture was stirred for 48 h at 22° C. After that, 3-chloroperoxybenzoic acid (991 mg, 5.74 mmol, Eq: 0.5) was added and the reaction mixture was strirred for additional 72 h.
  • example 7b (100.0 mg, 185 ⁇ , Eq: 1.00) was combined with DMA (1.5 mL) to give a light yellow solution.
  • the reaction mixture was stirred for 18 h at 25 °C.
  • additional cyclobutanol (13.3 mg, 14.5 ⁇ , 185 ⁇ , Eq: 1.00) was added and the reaction mixture was stirred at 25 °C for 18 h.
  • the crude material was purified by preparative HPLC to yield the title compound as an amorphous colorless solid (31 mg; 28%).
  • m/z 592.3 [M-
  • the reaction mixture was heated to 80 °C and stirred for 3h.
  • the reaction mixture was poured into water and extracted with EtOAc (2x).
  • the organic layers were combined, washed with saturated aqueous NaHC0 3 solution (lx), water (3x) and brine (lx).
  • the organic layers were dried over Na 2 S0 4 and concentrated in vacuo.
  • Example 12
  • Example 28
  • Example 3f (100 mg, 166 ⁇ , Eq: 1.00), 2,2-difluorobenzo[d][l,3]dioxol-5-ylboronic acid (50.3 mg, 249 ⁇ , Eq: 1.50) were dissolved in dioxane (2 mL).
  • Aqueous 2M Na 2 C0 3 solution (415 ⁇ , 830 ⁇ , Eq: 5.00) and 1,1 '-bis (diphenylphosphino)- ferrocenepalladium(II) dichloride dichloromethane complex (6.78 mg, 8.3 ⁇ , Eq: 0.05) were added to the solution and stirred at 85°C for 13 h.
  • the crude material was filtered and purified by preparative HPLC to yield the title compound as light yellow foam (83 mg; 74%).
  • m/z 680.2 [M+H] + .
  • example 3f In a 5 mL microwavetube, example 3f (100 mg, 166 ⁇ , Eq: 1.00), potassium acetate (24.4 mg, 249 ⁇ , Eq: 1.50) and tetrakis(triphenylphosphine)palladium (0) (9.59 mg, 8.3 ⁇ , Eq: 0.05) were dissolved in DMA (1 mL). Now 2,4-dimethylthiazole (94.0 mg, 89.0 ⁇ , 830 ⁇ , Eq: 5.00) was added. The tube was sealed and the mixture was stirred for 30 min at 170° C in the microwave oven.
  • Example 49 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -
  • Example 50 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
  • Example 55 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
  • Example 3f (100 mg, 166 ⁇ , Eq: 1.00), l-(difluoromethyl)-4-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)-lH-pyrazole (60.8 mg, 249 ⁇ mol, Eq: 1.50) were dissolved in dioxane (2 mL).
  • Example 60 was prepared in analogy to example 48 starting from (2S,4R)-4-(4-bromo-2- methylphenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -
  • Example 61 was prepared in analogy to example 48 starting from (2S,4R)-4-(4-bromo-2- methylphenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -
  • example 3f In a 5 mL microwavetube, example 3f (lOOmg, 166 ⁇ , Eq: 1.00), potassium acetate (24.4 mg, 249 ⁇ , Eq: 1.50) and tetrakis(triphenylphosphine)palladium (0) (9.59 mg, 8.3 ⁇ , Eq: 0.05) were combined with DMA (1 mL). 2-Methylthiazole (82.3 mg, 74.2 ⁇ , 830 ⁇ , Eq: 5.00) was added. The tube was sealed and the mixture was stirred for 30 minutes at 160° C in the microwave oven. The reaction mixture was poured into EtOAc (15 mL) and extracted with 0.1 M aqueous HC1 solution (1 x 20 mL).
  • Example 64 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
  • reaction mixture was stirred over 5 days and was subsequently heated to 140°C for 30 min in a microwave oven.
  • the reaction mixture was then poured into water (40 mL) and extracted with ethyl acetate (2 x 40 mL).
  • Enzyme activity is measured by observing the increase in fluorescence intensity caused by cleavage of a peptide substrate containing a fluorophore whose emission is quenched in the intact peptide.
  • Assay buffer 100 mM potassium phosphate pH 6.5, EDTA-Na 5 mM, Triton X-100 0.001%, DTT 5 mM.
  • Enzymes (all at 1 nM): human and mouse Cathepsin S, Cat K, Cat B, Cat L.
  • Enzyme is added to the substance dilutions in 96-well microtitre plates and the reaction is started with substrate. Fluorescence emission is measured over 20 minutes, during which time a linear increase is observed in the absence of inhibitor. IC 50 are calculated by standard methods.
  • Example ICso Example ICso
  • the compounds of the invention are preferential inhibitors of Cathepsin-S over Cathepsin- L, K and B.
  • the compounds according to the invention have, in the foregoing assay, an IC 50 at Cat S which is between 0.00001 and 100 ⁇ , in particular between 0.00001 and 50 ⁇ , more particularly between 0.00001 and 20 ⁇ .
  • the particular compounds of the invention have an IC 50 in the foregoing assay below 0.09 ⁇ .
  • Film coated tablets containing the following ingredients can be manufactured in a conventional manner:
  • the active ingredient is sieved and mixed with microcrystalline cellulose and the mixture is granulated with a solution of polyvinylpyrrolidone in water. The granulate is then mixed with sodium starch glycolate and magnesium stearate and compressed to yield kernels of 120 or 350 mg respectively. The kernels are lacquered with an aq. solution / suspension of the above mentioned film coat.
  • Capsules containing the following ingredients can be manufactured in a conventional manner:
  • the components are sieved and mixed and filled into capsules of size 2.
  • Injection solutions can have the following composition:
  • Water for injection solutions ad 1.0 ml
  • the active ingredient is dissolved in a mixture of Polyethylene glycol 400 and water for injection (part).
  • the pH is adjusted to 5.0 by addition of acetic acid.
  • the volume is adjusted to 1.0 ml by addition of the residual amount of water.
  • the solution is filtered, filled into vials using an appropriate overage and sterilized.

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Abstract

The invention relates to a compound of formula (I) wherein R1 and R2 are defined as in the description and in the claims. The compound of formula (I) can be used as a medicament against diabetes, atherosclerosis and other conditions linked to cathepsin.

Description

Novel pyrrolidine derivatives
The present invention relates to organic compounds useful for therapy and/or prophylaxis in a mammal, and in particular to compounds that are preferential inhibitors of the cysteine protease cathepsin, in particular of the cysteine protease cathepsin S.
The invention relates in particular to a compound of formula (I)
Figure imgf000003_0001
wherein
R is hydrogen, alkyl, haloalkyl, halogen or triazolyl; and
R is (halo)(oxy)pyridinyl, (alkyl)(oxy)pyridinyl, (alkyl)(haloalkyl)pyrazolyl,
haloalkoxyphenyl, alkoxyphenyl, cycloalkyloxyphenyl, cycloalkyloxy, alkyltetrazolyl, triazolyl, alkyltriazolyl, dialkyltriazolyl, halotriazolyl, haloalkylpyrazolyl, formylphenyl, aminopyrimidinyl, cyanophenyl, (alkoxy)(dihalo)phenyl, hydroxyalkylphenyl, benzo[l,3]dioxolyl, dialkylthiazolyl, alkylthiazolyl, alkoxypyrimidinyl, dialkylisoxazolyl or (halo)(haloalkyl)triazolyl; or a pharmaceutically acceptable salt or ester thereof.
The compounds of the invention are preferential inhibitors of the cysteine protease Cathepsin (Cat), in particular Cathepsin S and are therefore useful to treat metabolic diseases like diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease and diabetic nephropathy. In addition, immune mediated diseases like rheumatoid arthritis, multiple sclerosis, sjorgen syndrome, lupus erythematosus, neuropathic pain, diabetes type I, asthma and allergy and skin related immune disease are suitable diseases to be treated with a cathepsin S inhibitor. Objects of the present invention are the compounds of formula (I) and their aforementioned salts per se and their use as therapeutically active substances, a process for the manufacture of the said compounds, intermediates, pharmaceutical compositions, medicaments containing the said compounds, their pharmaceutically acceptable salts, the use of the said compounds and salts for the prophylaxis and/or therapy of illnesses, especially in the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease and diabetic nephropathy, and the use of the said compounds and salts for the production of medicaments for the treatment or prophylaxis of diabetes,
atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease and diabetic nephropathy.
Mammalian cathepsins are cysteine-type proteases involved in key steps of biological and pathological events. Cathepsins are considered tractable drug targets as it is feasible to inhibit enzymatic activity with small molecules and are therefore of interest to the pharmaceutical industry (Bromme, D. (2001), 'Papain-like cysteine proteases', Curr Protoc Protein Sci, Chapter 21, Unit 21 2; Roberts, R. (2005), 'Lysosomal cysteine proteases: structure, function and inhibition of cathepsins', Drug News Perspect, 18 (10), 605-14).
Cathepsin S is prominently expressed in antigen presenting cells like macrophages and dendritic cells and smooth muscle cells. (Hsing, L. C. and Rudensky, A. Y. (2005), 'The lysosomal cysteine proteases in MHC class Π antigen presentation', Immunol Rev, 207, 229-41; Rudensky, A. and Beers, C. (2006), 'Lysosomal cysteine proteases and antigen presentation', Ernst Schering Res Found Workshop, (56), 81-95). While Cathepsin S is only weakly expressed in normal arterial tissue, strong upregulation is seen in atherosclerotic arteries (Liu, J., et al. (2006), 'Increased serum cathepsin S in patients with atherosclerosis and diabetes', Atherosclerosis, 186 (2), 411-9; Sukhova, G. K., et al. (1998) , 'Expression of the elastolytic cathepsins S and K in human atheroma and regulation of their production in smooth muscle cells', J Clin Invest, 102 (3), 576-83).
Preclinical data suggest that the function of Cathepsin S is critical for atherosclerosis as Cathepsin S deficient mice have a reduced atherosclerosis-phenotype when tested in appropriate mouse models. In LDL-Rec deficient mice reduced lipid accumulation, elastin- fibre breakdown and chronic arterial inflammation is reported. In APO E deficient mice a significant reduction of acute plaque rupture events was reported. When chronic renal disease is introduced into CatS/In APO-E deficient mice a strong reduction of accelerated calcification is seen on top of the anti atherosclerotic activity in arteries and heart valves (Aikawa, E., et al. (2009), 'Arterial and aortic valve calcification abolished by elastolytic cathepsin S deficiency in chronic renal disease', Circulation, 119 (13), 1785-94; de Nooijer, R., et al. (2009), 'Leukocyte cathepsin S is a potent regulator of both cell and matrix turnover in advanced atherosclerosis', Arterioscler Thromb Vase Biol, 29 (2), 188- 94; Rodgers, K. J., et al. (2006), 'Destabilizing role of cathepsin S in murine
atherosclerotic plaques', Arterioscler Thromb Vase Biol, 26 (4), 851-6; Sukhova, G. K., et al. (2003), 'Deficiency of cathepsin S reduces atherosclerosis in LDL receptor-deficient mice', J Clin Invest, 111 (6), 897-906). This suggests a potential inhibitor of Cathepsin S would stabilise atherosclerotic plaque by reducing extracellular matrix breakdown, by reducing the proinflammatory state and by reducing accelerated calcification and subsequently its clinical manifestations.
These phenotypes described in atherosclerosis models are in agreement with known cellular functions of Cathepsin S. Firstly, Cathepsin S is involved in the degradation of extracellular matrix that stabilises the plaque. In particular, Cathepsin S has potent elastinolytic activity and can exert this at neutral pH, a feature that distinguishes Cathepsin S from all other Cathepsins. Secondly, Cathepsin S is the major protease involved in antigen processing, in particular cleavage of the invariant chain in antigen presenting cells, resulting in reduced contribution of Tcells to the chronic inflammation of the
atherosclerotic tissue. Elevated inflammation results in further oxidative and proteolytic tissue damage and subsequently plaque destabilisation (Cheng, X. W., et al. (2004), 'Increased expression of elastolytic cysteine proteases, cathepsins S and K, in the neointima of balloon-injured rat carotid arteries', Am J Pathol, 164 (1), 243-51; Driessen, C, et al.
(1999) , 'Cathepsin S controls the trafficking and maturation of MHC class Π molecules in dendritic cells', J Cell Biol, 147 (4), 775-90; Rudensky, A. and Beers, C. (2006),
'Lysosomal cysteine proteases and antigen presentation', Ernst Schering Res Found Workshop, (56), 81-95).
The anti-inflammatory and anti-elastinolytic properties of a Cat S inhibitor make it also a prominent target for chronic obstructive pulmonary disease (Williams, A. S., et al. (2009), 'Role of cathepsin S in ozone-induced airway hyperresponsiveness and
inflammation', Pulm Pharmacol Ther, 22 (1), 27-32). Furthermore due to its extracellular functions in matrix degradation, inhibition of cathepsin S will impact neointima formation and angiogenesis (Burns-Kurtis, C. L., et al. (2004), 'Cathepsin S expression is up- regulated following balloon angioplasty in the hypercholesterolemic rabbit', Cardiovasc Res, 62 (3), 610-20; Cheng, X. W., et al. (2004), 'Increased expression of elastolytic cysteine proteases, cathepsins S and K, in the neointima of balloon-injured rat carotid arteries', Am J Pathol, 164 (1), 243-51; Shi, G. P., et al. (2003), 'Deficiency of the cysteine protease cathepsin S impairs microvessel growth', Circ Res, 92 (5), 493-500; Wang, B., et al. (2006), 'Cathepsin S controls angiogenesis and tumor growth via matrix-derived angiogenic factors', J Biol Chem, 281 (9), 6020-9). An inhibitor of Cathepsin S might therefore be useful in several different disease settings.
Cathepsin S plays also a role in the reduction of tumor growth and tumor cell invasion as described by Roberta E. Burden in Clin Cancer Res 2009;15(19). In addition, nephrectomized Cathepsin S knock out mice showed a significant reduction of arterial calcification when compared to nephrectomized wild type mice. This indicates that inhibition of Cathepsin S may have a beneficial effect on the reduction of cardiovascular events in chronic kidney disease patients (Elena Aikawa, Circulation, 2009, 1785-1794).
In the present description the term "alkyl", alone or in combination, signifies a straight-chain or branched-chain alkyl group with 1 to 8 carbon atoms, particularly a straight or branched-chain alkyl group with 1 to 6 carbon atoms and more particularly a straight or branched-chain alkyl group with 1 to 4 carbon atoms. Examples of straight- chain and branched-chain Q-Cg alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl, the isomeric pentyls, the isomeric hexyls, the isomeric heptyls and the isomeric octyls, particularly methyl, ethyl, propyl, butyl and pentyl more particularly methyl, ethyl, propyl, isopropyl, isobutyl, tert.-butyl and isopentyl. A particular example of alkyl is methyl.
The term "cycloalkyl", alone or in combination, signifies a cycloalkyl ring with 3 to 8 carbon atoms and particularly a cycloalkyl ring with 3 to 6 carbon atoms. Examples of cycloalkyl are cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl, cycloheptyl and cyclooctyl. A particular example of "cycloalkyl" is cyclopropyl.
The term "oxy", alone or in combination, signifies the -O- group.
As an exception, "(oxy)pyridinyl" refers to py+-0", wherein py represents pyridine.
The term "alkoxy", alone or in combination, signifies a group of the formula alkyl-O- in which the term "alkyl" has the previously given significance, such as methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy. Particular "alkoxy" are methoxy and ethoxy, and in particular methoxy.
The term "cycloalkyloxy", alone or in combination, signifies a group of the formula cycloalkyl-O- in which the term "cycloalkyl" has the previously given significance. A particular cycloalkyloxy is cyclopropyloxy.
The terms "halogen" or "halo", alone or in combination, signifies fluorine, chlorine, bromine or iodine and particularly fluorine, chlorine or bromine, more particularly fluorine and chlorine. The term "halo", in combination with another group, denotes the substitution of said group with at least one halogen, particularly substituted with one to five halogens, particularly one to four halogens, i.e. one, two, three or four halogens. A particular "halogen" is chlorine.
The term "haloalkyl", alone or in combination, denotes an alkyl group substituted with at least one halogen, particularly substituted with one to five halogens, particularly one to three halogens. Particular "haloalkyl" are trifluoromethyl and difluoromethyl, in particular trifluoromethyl.
The term "haloalkoxy", alone or in combination, denotes an alkoxy group substituted with at least one halogen, particularly substituted with one to five halogens, particularly one to three halogens. Particular "haloalkoxy" is trifluoromethoxy.
The terms "hydroxyl" and "hydroxy", alone or in combination, signify the -OH group.
The term "carbonyl", alone or in combination, signifies the -C(O)- group.
The term "formyl", alone or in combination, signifies the -CH(O) group
The term "amino", alone or in combination, signifies the primary amino group (-NH2), the secondary amino group (-NH-), or the tertiary amino group (-N-). The term "pharmaceutically acceptable salts" refers to those salts which retain the biological effectiveness and properties of the free bases or free acids, which are not biologically or otherwise undesirable. The salts are formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, particularly hydrochloric acid, and organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, N-acetylcy stein. In addition these salts may be prepared form addition of an inorganic base or an organic base to the free acid. Salts derived from an inorganic base include, but are not limited to, the sodium, potassium, lithium, ammonium, calcium, magnesium salts. Salts derived from organic bases include, but are not limited to salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, lysine, arginine, N-ethylpiperidine, piperidine, polyamine resins. The compound of formula (I) can also be present in the form of zwitterions. Particularly preferred pharmaceutically acceptable salts of compounds of formula (I) are the salts of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid and methanesulfonic acid.
"Pharmaceutically acceptable esters" means that the compound of general formula (I) may be derivatised at functional groups to provide derivatives which are capable of conversion back to the parent compounds in vivo. Examples of such compounds include physiologically acceptable and metabolically labile ester derivatives, such as
methoxymethyl esters, methylthiomethyl esters and pivaloyloxymethyl esters.
Additionally, any physiologically acceptable equivalents of the compound of general formula (I), similar to the metabolically labile esters, which are capable of producing the parent compound of general formula (I) in vivo, are within the scope of this invention.
If one of the starting materials or compounds of formula (I) contain one or more functional groups which are not stable or are reactive under the reaction conditions of one or more reaction steps, appropriate protecting groups (as described e.g. in "Protective Groups in Organic Chemistry" by T. W. Greene and P. G. M. Wuts, 3rd Ed., 1999, Wiley, New York) can be introduced before the critical step applying methods well known in the art. Such protecting groups can be removed at a later stage of the synthesis using standard methods described in the literature. Examples of protecting groups are tert-butoxycarbonyl (Boc), 9-fluorenylmethyl carbamate (Fmoc), 2-trimethylsilylethyl carbamate (Teoc), carbobenzyloxy (Cbz) and p-methoxybenzyloxycarbonyl (Moz).
The compound of formula (I) can contain several asymmetric centers and can be present in the form of optically pure enantiomers, mixtures of enantiomers such as, for example, racemates, mixtures of diastereoisomers, diastereoisomeric racemates or mixtures of diastereoisomeric racemates.
The term "asymmetric carbon atom" means a carbon atom with four different substituents. According to the Cahn-Ingold-Prelog Convention an asymmetric carbon atom can be of the "R" or "S" configuration.
The invention further relates to: A compound of formula (I) wherein R1 is alkyl, haloalkyl or halogen;
A compound of formula (I) wherein R1 is methyl, trifluoromethyl or chlorine;
A compound of formula (I) wherein R is (alkyl)(haloalkyl)pyrazolyl, alkyltetrazolyl, triazolyl, alkyltriazolyl, dialkyltriazolyl, halotriazolyl, haloalkylpyrazolyl, dialkylthiazolyl, alkylthiazolyl or dialkylisoxazolyl;
A compound of formula (I) wherein R is (methyl)(trifluoromethyl)pyrazolyl, methyltetrazolyl, triazolyl, methyltriazolyl, dimethyltriazolyl, chlorotriazolyl,
trifluoromethylpyrazolyl, difluoromethylpyrazolyl, dimethylthiazolyl, methylthiazolyl or dimethylisoxazolyl;
The invention further relates to a compound of formula (I) selected from:
(2S ,4R)-4- [4- (2-Chloro- 1 -oxy-pyridin-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S ,4R)-4- [4- (2-Methyl- 1 -oxy-pyridin-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(2-Methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S,4R)-4-(2'-Trifluoromethoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(2'-Ethoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide;
(2S,4R)-4-(2'-Cyclopropoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(4-Cyclobutoxy-2-trifluoromethyl-benzenesulfonyl)-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide; (2S,4R)-4-(2-chloro-4-(5-methyl-2H-tetrazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-tetrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-( 1 -cyanocyclopropyl)-4-(2,4-di( 1H- 1 ,2,4-triazol- 1 -yl)phenylsulfonyl)- 1 - (l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2-chloro-4-(2H-l,2,3-triazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(lH-l,2,3-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3,5-dimethyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-(trifluoromethyl)-lH-pyrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifhioromethyl)
cyclopropanecarbonyl)pyrrolidine-2-carboxamide; (2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(trif uoromethoxy)biphenyl-4-ylsulfonyl)-l- (l-(trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2-chloro-4-cyclobutoxyphenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 - (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(3-methyl-2'-(trifluoromethoxy)biphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-[4-(5-Methyl-3-trifluoromethyl-pyrazol -yl)-2-trif uoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ;
(2S,4R)-4-(4-( 1H- 1 ,2,4-triazol- l-yl)-2-(trifluoromethyl)phenylsulfonyl)-N-( 1- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
(2S ,4R)-4- [4- (3 ,5-Dimethyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 -( 1 -trif uoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(l-methyl-3-(trifluoromethyl)-lH-pyrazol-5- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-formyl-3-methylbiphenyl-4-ylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide; (2S ,4R)-4- [4- (3-Chloro- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-lH-l,2,4-triazol-l-yl)-2- (trif uoromethyl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)
cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(l-methyl-3-(trifluoromethyl)-lH- pyrazol-5-yl)phenylsulfonyl)- 1 -( 1 -(trif uoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethyl-lH-l,2,4-triazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-( 1H- 1 ,2,3-triazol- 1 -yl)phenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 - (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(1 -cyanocyclopropyl) -4-(4-(3 - (trifluoromethyl) - 1 H-pyrazol- 1 - yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-formylbiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxybiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(4-(2-aminopyrimidin-5-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxy-3-methylbiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2'-cyano-3-methylbiphenyl-4-ylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide; (2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxy-4',5'-difluoro-3-methylbiphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(hydroxymethyl)biphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(4-(2-aminopyrimidin-5-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(2,2-Difluoro-benzo[l,3]dioxol-5-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(4- trifluoromethyl-pyrazol- 1 -yl)-benzenesulfonyl] -pyrrolidine-2-carboxylic acid ( 1 - cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (5-Methyl-tetrazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(2,4-Dimethyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)phenylsulfonyl)-l- (l-(trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methylthiazol-5-yl)phenylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methoxypyrimidin-5-yl)phenylsulfonyl)-l- (l-(trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-[l,2,3]Triazol-2-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ; (2S,4R)-4-(4-[l,2,3]Triazol-l-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)phenylsulfonyl)-l- (l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-[4-(l-Difluoromethyl-lH-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (5-Methyl-tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(3- trifluoromethyl- lH-pyrazol-4-yl)-benzenesulfonyl]-pyrrolidine-2-carboxylic acid (1- cyano-cyclopropyl)-amide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(hydroxymethyl)-3-methylbiphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(2-methylthiazol-5- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methoxypyrimidin-5-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(2-Methyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide; (2S,4R)-4-(4-Tetrazol- 1 -yl-2-trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide;
(2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2R,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(l-Methyl-3-trifluoromethyl-lH-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide; and
(2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide.
The invention particularly relates to a compound of formula (I) selected from:
(2S,4R)-4-[4-(2-Methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S,4R)-4-(2-chloro-4-(5-methyl-2H-tetrazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-tetrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(2H-l,2,3-triazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide; (2S,4R)-4-(2-chloro-4-(lH-l,2,3-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3,5-dimethyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-(trifluoromethyl)-lH-pyrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifhioromethyl)
cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(5-Methyl-3-trifluoromethyl-pyrazol-l-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ; (2S,4R)-4-(4-( 1H- 1 ,2,4-triazol- l-yl)-2-(trifluoromethyl)phenylsulfonyl)-N-( 1- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S ,4R)-4- [4- (3 ,5-Dimethyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 -( 1 -trif uoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S ,4R)-4- [4- (3-Chloro- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-lH-l,2,4-triazol-l-yl)-2- (trif uoromethyl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(l-methyl-3-(trifluoromethyl)-lH- pyrazol-5-yl)phenylsulfonyl)- 1 -( 1 -(trif uoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide;
(2S,4R)-l-(l-Trif uoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(4- trifluoromethyl-pyrazol- 1 -yl)-benzenesulfonyl] -pyrrolidine-2-carboxylic acid ( 1 - cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (5-Methyl-tetrazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(2,4-Dimethyl-thiazol-5-yl)-2-trif uoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-[l,2,3]Triazol-2-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ; (2S,4R)-4-(4-[l,2,3]Triazol-l-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(l-Difluoromethyl-lH-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (5-Methyl-tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(3- trifluoromethyl- lH-pyrazol-4-yl)-benzenesulfonyl]-pyrrolidine-2-carboxylic acid (1- cyano-cyclopropyl)-amide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(2-methylthiazol-5- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(2-Methyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-Tetrazol- 1 -yl-2-trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide;
(2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2R,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide; and (2S,4R)-4-[4-(l-Methyl-3-trifluoromethyl H-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide.
The invention particularly relates to a compound of formula (I) which is (2S,4R)-4- [4-(5-Methyl-tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide.
The following abbreviations are used in the present application:
AcOEt: Ethyl acetate;
ACN: Acetonitrile; boc: ie/t-Butyloxycarbonyl
BOP: Benzotriazolyl-N-oxy-tris(dimethylamino)-phosphonium hexafluorophosphate;
BOP-C1: Bis-(2-oxo-3-oxazolidinyl)-phosphinic acid chloride;
Cbz: Carbobenzyloxy
CDI: 1 , 1 ' -Carbonyldiimidazole;
DCM : Dichloromethane;
DIEA: Diisopropyl ethyl amine;
DMAP: 4-Dimethylaminopyridine;
DMF: N,N-Dimethylformamide;
EDCI: N-(3-Dimetylaminopropyl)-N' -ethyl-carbodiimide hydrochloride;
EtOAc: Ethyl acetate;
Fmoc : 9-Fluorenylmethyloxycarbonyl h: hour;
HATU: 0-(7-azabenzotriazol- 1 -yl)- 1 , 1 ,3,3-tetramethyluronium hexafluorophosphate; HOBT: 1-Hydroxybenzotriazole; Hunig's Base: Ethyl-diisopropyl-amine; mCPBA or MCPBA: meta-Chloroperoxybenzoic acid; MeOH: Methanol; Mes-Cl: Mesyl chloride; min: minute; Na2S04: Sodium sulfate;
Nos-Cl: 3-Nitrobenzenesulfonyl chloride; Pd2(dba)3: Tris(dibenzylideneacetone)dipalladium;
PyB OP : Benzotriazol- 1 -yl- oxy tripyrrolidinepho sphonium hexafluoropho sphate ;
TBTU: 0-(Benzotriazol-l-yl)-N,N,N',N'-tetramethyluronium terafluoroborate; THF: Tetrahydrofurane;
TFA: Trifluoroacetic acid; and
Tos-Cl: Toluene-4-sulfonyl chloride.
The compound of formula (I) can be manufacture by known procedures or according to the procedures described in schemes 1 and 2 below. Scheme 1
Figure imgf000021_0001
Definitions: a) Acid: e.g. methane sulfonic acid, phenyl sulfonic acid, trifluoromethyl sulfonic acid, HCl, HBr, sulfuric acid,TFA, formic acid; b) X: OH, CI, O-SO2-LG1; c) LG1: Leaving group such as phenyl, methyl, ethyl, 3-nitrophenyl, 4-methylphenyl, 4- bromophenyl, trifluoromethyl; d) LG2: F, CI, Br, I, B(OH)2, B(OR3)2; e) R1 as defined above; f) R 3 : Methyl, ethyl or both R 3 form together with the oxygen and boron atoms to which they are attached a ring such as 4,4,5, 5-tetramethyl-[l,3,2]dioxaborolane; g) Oxidation: oxidation is performed with one of the oxidizing agents known in the art such as hydrogen peroxide or metal complexes of hydrogen peroxide, oxone or mCPBA; h) R as defined above; i) LG3: H, B(OH)2, B(OR3)2, Br or I.
Boc-protected compound 1 is deprotected with an appropriate acid such as TFA, HCl, formic acid, sulfuric acid etc. to yield after crystallization the salt 2. Reaction of salt 2 with 1-trifluoromethyl-cyclopropanecarboxylic acid in the presence of a base such as triethyl amine, Hunig's Base or N-methyl morpholine and an appropriate amide coupling reagent such as HATU, PyBop, TBTU, CDI, EDCI, BOP or Bop-Cl yields amide 3.
Alternatively, 2 is reacted with 1-trifluoromethyl-cyclopropanecarboxylic acid in the presence of e.g. oxalyl chloride, thionyl chloride, phosphoryl chloride, phosgene or triphosgene to yield amide 3. Ring opening of the lactam 3 with 1-amino- cyclopropanecarbonitrile or salts therefore, e.g. hydrochloride salt, is accommodated in the presence of an appropriate base such as e.g. Hunig's base, triethyl amine, sodium 2- ethylhexanoate, pyridine or lutidine at elevated tempereature between 30°C - 80°C to yield alcohol 4. Reaction of alcohol 4 with a sulfonylchloride derivative such as methane sulfonylchloride, phenyl sulfonylchloride, tosylchloride, nosylchloride, brosylchloride or anhydrides such as triflic anhydride yields compound 5. Thioether 6 is obtained by reaction of sulfonate 5 with thiophenol 5b in the presenece of an appropriate base such as Hunig's base, triethyl amine, pyridine, lutidine, Na2C03, K2C03 or Cs2C03. Subsequent oxidation of thioether 6 with a peroxide source such as hydrogen peroxide, mCPBA, oxone or metal complexes of hydrogen peroxide such as M0O2CI2/H2O2 or NaxWyOz/H202 systems yields sulfone 7. Compound 7 can be either directly reacted with heterocyclic compounds in a S Ar fashion in the presence of a base such as Hunig's base, triethyl amine, pyridine, lutidine, Na2C03, K2C03 or Cs2C03 or via a Suzuki reaction with boronic acids or esters thereof using metal catalysts and bases known in the art such as e.g. Pd(PPh3)4, Pd2(dba)3 or a Pd-source with a phosphine ligand to yield the final compounds 8.
Scheme 2
Figure imgf000022_0001
Definitions: a) R 1 as defined above; b) R 3 : methyl, chloro.
Oxidation of pyridine derivatives to the corresponding N-oxide can be accomplished by using an oxidation reagent such as hydrogen peroxide, mCPBA or oxone. The invention thus also relates to a process for the manufacture of a compound of formula (I) comprising:
(a) The reaction of a compound of formula (A)
Figure imgf000023_0001
in the presence of a compound of formula R2-LG 2 wherein R 1 and R2 are as defined in any one of claims 1 to 6 and wherein LG1 is F, CI, Br, I, B(OH)2 or B(OR3)2, LG2 is H, B(OH)2, B(OR 3 )2, Br or I and each R 3 is independently selected from methyl, ethyl and both R together with the oxygen and boron atoms to which they are attached form an organoboron ring; or
(b) The reaction of a compound of formula (B)
Figure imgf000023_0002
in the presence of an oxidation reagent, wherein R is as defined in any one of claims 1 to 6 and R4 is halogen or alkyl.
Examples of oxidation reagents are e.g. hydrogen peroxide, mCPBA or oxone. 4,4,5, 5-tetramethyl-l,3,2-dioxaborolane is an example of organoboron ring.
The invention further relates to a compound of formula (I) when manufactured according to the above process.
Another embodiment of the invention provides a pharmaceutical composition or medicament containing a compound of the invention and a therapeutically inert carrier, diluent or excipient, as well as a method of using the compounds of the invention to prepare such composition and medicament. In one example, the compound of formula (I) may be formulated by mixing at ambient temperature at the appropriate pH, and at the desired degree of purity, with physiologically acceptable carriers, i.e., carriers that are non- toxic to recipients at the dosages and concentrations employed into a galenical
administration form. The pH of the formulation depends mainly on the particular use and the concentration of compound, but preferably ranges anywhere from about 3 to about 8. In one example, a compound of formula (I) is formulated in an acetate buffer, at pH 5. In another embodiment, the compound of formula (I) is sterile. The compound may be stored, for example, as a solid or amorphous composition, as a lyophilized formulation or as an aqueous solution.
Compositions are formulated, dosed, and administered in a fashion consistent with good medical practice. Factors for consideration in this context include the particular disorder being treated, the particular mammal being treated, the clinical condition of the individual patient, the cause of the disorder, the site of delivery of the agent, the method of administration, the scheduling of administration, and other factors known to medical practitioners.
The compounds of the invention may be administered by any suitable means, including oral, topical (including buccal and sublingual), rectal, vaginal, transdermal, parenteral, subcutaneous, intraperitoneal, intrapulmonary, intradermal, intrathecal and epidural and intranasal, and, if desired for local treatment, intralesional administration. Parenteral infusions include intramuscular, intravenous, intraarterial, intraperitoneal, or subcutaneous administration. The compounds of the invention may be administered in particular by intravitreal administration. The compounds of the present invention may be administered in any convenient administrative form, e.g., tablets, powders, capsules, solutions, dispersions, suspensions, syrups, sprays, suppositories, gels, emulsions, patches, etc. Such compositions may contain components conventional in pharmaceutical preparations, e.g., diluents, carriers, pH modifiers, sweeteners, bulking agents, and further active agents. A typical formulation is prepared by mixing a compound of the present invention and a carrier or excipient. Suitable carriers and excipients are well known to those skilled in the art and are described in detail in, e.g., Ansel, Howard C, et al., Ansel's
Pharmaceutical Dosage Forms and Drug Delivery Systems. Philadelphia: Lippincott, Williams & Wilkins, 2004; Gennaro, Alfonso R., et al. Remington: The Science and Practice of Pharmacy. Philadelphia: Lippincott, Williams & Wilkins, 2000; and Rowe, Raymond C. Handbook of Pharmaceutical Excipients. Chicago, Pharmaceutical Press, 2005. The formulations may also include one or more buffers, stabilizing agents, surfactants, wetting agents, lubricating agents, emulsifiers, suspending agents,
preservatives, antioxidants, opaquing agents, glidants, processing aids, colorants, sweeteners, perfuming agents, flavoring agents, diluents and other known additives to provide an elegant presentation of the drug (i.e., a compound of the present invention or pharmaceutical composition thereof) or aid in the manufacturing of the pharmaceutical product (i.e., medicament). The invention thus also relates to:
A compound of formula (I) for use as therapeutically active substance;
A pharmaceutical composition comprising a compound of formula (I) and a therapeutically inert carrier;
The use of a compound of formula (I) for the preparation of medicaments for the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic rethinopathy or age related macular degeneration;
A compound of formula (I) for use in the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic
rethinopathy or age related macular degeneration; and
A method for the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic rethinopathy or age related macular degeneration, which method comprises administering an effective amount of a compound of formula (I) to a patient in need thereof.
The invention will now be illustrated by the following examples which have no limiting character. Examples
Example 1
(2S,4R)-4-[4-(2-Chloro-l-oxy-pyridin-4-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Chiral
Figure imgf000026_0001
In a 10 mL round-bottomed flask CAS 1252637-43-6 (0.05 g, 78.7 μπιοΐ, Eq: 1.00) was combined with dichloromethane (1 mL) to give a colorless solution. 3- Chlorobenzoperoxoic acid (20.4 mg, 118 μιηοΐ, Eq: 3 x 1.5 each after 24 h, 48 h, 72 h) was added. The reaction mixture was heated to 22 °C and stirred for totally 168 h. The crude material was purified by preparative HPLC to yield the title compound as a colorless amorphous solid (25 mg; 50%). m/z = 651.2 [M+H]+.
Example 2
(2S,4R)-4-[4-(2-Methyl-l-oxy-pyridin-4-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide hiral
Figure imgf000027_0001
In a 10 mL round-bottomed flask, CAS 1252637-46-9 (50 mg, 81.4 μπιοΐ, Eq: 1.00) was combined with dichloromethane (1 mL) to give a colorless solution. mCPBA (21.1 mg, 122 μιηοΐ, Eq: 1.5) was added. The reaction mixture was heated to 22 °C and stirred for totally 20 h. The crude material was purified by preparative HPLC to yield the title compound as a colorless amorphous solid (40 mg; 78%). m/z = 631.3 [M+H]+.
Example 3
(2S,4R)-4-[4-(2-Methyl-5-trifluoromethyl-2Hpyrazol-3-yl)-2-trifluoromethyl- benzenesulfonyl]-l-(l-trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide
Chiral
Figure imgf000027_0002
a) (lS,4S)-3-Oxo-2-oxa-5-azonia-bicyclo[2.2.1]heptane methanesulfonate
Figure imgf000027_0003
(lS,4S)-3-Oxo-2-oxa-5-aza-bicyclo[2.2.1]heptane-5-carboxylic acid tert-b tyl ester (100.0 g, 469 mmol) was dissolved in ethyl acetate (970 mL) and methanesulfonic acid (43.5 mL, 659 mmol) was added at 45°C. The mixture was stirred for 16 h at 45°C. The suspension was cooled to room temperature, filtered, and the precipitate was washed with ethyl acetate (240 mL) and dried in vacuo to yield the title compound as a white crystalline solid (94.2 g, 96%). m/z = 113 [M-H]~. b) (lS,4S)-5-(l-Trifluoromethyl-cyclopropanecarbonyl)-2-oxa-5-aza-bicyclo[2.2.1 ]heptan- 3-one
Figure imgf000028_0001
1-Trifluoromethyl-cyclopropanecarboxylic acid (167.0 g, 1084 mmol) was suspended in toluene (500 mL) and then dimethylformamide (3.6 mL, 47 mmol) was added. The mixture was cooled to 2°C (ice bath) and a solution of oxalyl chloride (90 mL, 1037 mmol) in toluene (167 mL) was added drop wise (within 25 min). The mixture was then stirred for additional 30 min, followed by 4 h at room temperature. Subsequently, it was cooled to 0°C again (dry ice / methanol bath) and (15,,4lS')-3-oxo-2-oxa-5-azonia- bicyclo[2.2.1]heptane methanesulfonate (200 g, 956 mmol), tetrahydrofuran (330 mL) and triethylamine (500 mL, 3.59 mol) were slowly added, keeping the reaction temperature below 5°C. Especially after addition of 50% of triethylamine, the reaction becomes strongly exothermic and efficient cooling is essential. The mixture was stirred for 20 h at room temperature, before it was poured onto an aqueous citric acid solution (10 % in water, 1.6 L) and the phases were separated. The aqueous phase was extracted with ethyl acetate (3 x 500 mL). The combined organic extracts were washed with 20 brine (500 mL), dried over sodium sulfate, and concentrated in vacuo. The crude product (245 g, brown oil) was dissolved in dichloromethane (330 mL) before ethyl acetate (130 mL) and heptane (660 mL) were added and dichloromethane was carefully distilled off in vacuo. The product started to crystallize. The suspension was cooled to 2°C (ice bath) and stirred for 1 h, before it was filtered. The precipitate was washed with ethyl acetate / heptane 1:9 (v/v, 300 mL) and dried in vacuo to afford the title compound as a light brown powder (219 g, 92%). 1H NMR (CDC13, 400 MHz): d 1.17-1.25 (m, 1H), 1.30 (dd, / = 5.3 Hz, 8.3 Hz, 1H), 1.37-1.46 (m, 2H), 2.13 and 2.37 (AB, JAB = 10.7 Hz, each 1H), 3.63 and 3.73 (AB, JAB = 12.1 Hz, each 1H), 4.99 (s, 1H), 5.21 (s, 1H). c) ( 2S,4S)-4-Hydroxy-l -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide
Figure imgf000029_0001
(15,,4lS,)-5-(l-Trifluoromethyl-cyclopropanecarbonyl)-2-oxa-5-aza-bicyclo[2.2.1]heptan-3- one (220 g, 883 mmol), 1-amino-cyclopropanecarbonitrile hydrochloride (140 g, 1.18 mol) and sodium 2-ethylhexanoate (97%, 230 g, 1.34 mol) were dissolved in water (1.32 L). The mixture was stirred for 20 h at 53°C. After cooling to room temperature,
tetrahydrofuran (880 mL) was added and the mixture was acidified by addition of concentrated hydrochloric acid (37% m/m, 47 mL), followed by the addition of sodium chloride (440 g). After extraction with ethyl acetate (1 x 1.4 L, 3 x 550 mL), the combined organic extracts were dried over sodium sulfate and concntrated in vacuo. At a volume of ca. 1.5 L, the product started to crystallize upon addition of seed crystals. The volume of the suspension was further reduced to ca. 500 mL and cooled to 2°C (ice bath). After stirring for 60 min, the crystals were filtered off, washed with ethyl acetate / heptane 1 : 1 (v/v, 600 mL) and heptane (300 mL), and dried in vacuo to provide the title compound as off-white crystals (255.0 g, 87%). 1H NMR (CDC13, 400 MHz):d 1.18-1.29 (m,4H), 1.30- 1.42 (m, 2H), 1.50-1.59 (m, 2H), 2.17-2.26 (m, 1H), 2.29 (d, / = 14.5 Hz, 1H), 3.73 and 3.96 (ABX, JAB = 11.8 Hz, JAX = 4.3 Hz, JBX = 0 Hz, each 1H), 4.43-4.53 (m, 2H), 4.81 (bid, / = 8.3 Hz, 1H), 7.73 (s, 1H). d) Benzenesulfonic acid (3S,5S)-5-(l-cyano-cyclopropylcarbamoyl)-l-(l-trifl oromethyl- cyclopropanecarbonyl)-pyrrolidin-3-yl ester
Figure imgf000029_0002
(2lS,,45')-4-Hydroxy- 1 - ( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (l-cyano-cyclopropyl)-amide (100.0 g, 301.8 mmol) was dissolved in tetrahydrofuran (500 mL). The mixture was cooled to 2°C (ice bath), benzenesulfonyl chloride (99%, 48 mL, 370.5 mmol), 4-(dimethylamino)pyridine (98%, 2.0 g, 16.0 mmol), and triethylamine (75.0 mL, 539 mmol) were added subsequently and the mixture was stirred for 15 min. The reaction was allowed to warm to room temperature and stirred for 20 h. After cooling to 2°C (ice bath), water (150 mL) and methanol (350 mL) were added. Tetrahydrofuran was distilled off carefully in vacuo (ca. 500 mL) and water (500 mL) was added slowly. After addition of 300 mL water, crystallization was induced by addition of seed crystals. The resulting suspension was stirred for 30 min at 2°C (ice bath) and filtered. The solid was washed with methanol / water 1:2 (v/v, 300 mL) and heptane (300 mL) and dried in vacuo to afford the title compound as off-white crystals (140.8 g, 99%). 1H NMR (CDC13, 400 MHz): d 1.06-1.27 (m, 4H), 1.28-1.41 (m, 2H), 1.44-1.54 (m, 2H), 2.26 (ddd, / = 5.9 Hz, 9.4 Hz, 14.2 Hz, 1H), 2.59 (ddd, / = 3.8 Hz, 3.8 Hz, 14.2 Hz, 1H), 3.90 and 4.03 (ABX, JAB = 12.5 Hz, JAX = 4.0 Hz, JBX = 5.2 Hz, each 1H), 4.57 (br d, / = 5.1 Hz, 1H), 5.02-5.09 (m, 1H), 7.08 (br s, 1H), 7.61 (t, 7 = 7.8 Hz, 2H), 7.71 (t, 7 = 7.5 Hz, 1H), 7.95 (d, 7 = 7.2 Hz, 2H). e) ( 2S,4R )-4-( 4-Bromo-2-trifluoromethyl-phenylsulfanyl)-l -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide
Figure imgf000030_0001
Example 3d) (7.03 g, 14.9 mmol, Eq: 1.00) was dissolved in propionitrile (80 mL) and 4- bromo-2-trifluoromethyl-benzenethiol CAS 1208075-10-8 (5.75 g, 22.4 mmol, Eq: 1.50) was added. Now, triethylamine (3.02 g, 4.16 mL, 29.8 mmol, Eq: 2.00) was carefully added and the reaction mixture was stirred at reflux for 18 h. The reaction mixture was extracted with 10% aqueous Na2C03 solution/ AcOEt. The organic layers were dried over Na2S04, filtered and evoporated. The crude material was purified by flash chromatography (silica gel, 120 g, 0% to 50% EtOAc in heptane) to yield the title compound as a white foam (8.14 g; 96%). m/z = 571.9/570.1 [M+H]+. (Br isotopes) f) ( 2S,4R )-4-( 4-Bromo-2-trifluoromethyl-benzenesulfonyl)-l -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (l-cyano-cyclopropyl)-amide
Figure imgf000031_0001
Example 3e) (8.14 g, 14.3 mmol, Eq: 1.00) was dissolved in dichloromethane (50 mL) and mCPBA (5.17 g, 30.0 mmol, Eq: 2.10) was carefully added portionwise .The reaction mixture was stirred over night at 25°C. The reaction mixture was extracted with 10% aqueous Na2C03 solution and aqueous Na2S203 saturated solution. The organic layers were dried over Na2S04 and Na2S03 for 2 h, filtered and evaporated ( attention peroxide!) to yield the title compound as a white foam (8.6 g; 100%). m/z = 602.0/604.0 [M+H]+. (Br isotopes) g) (2S,4R)-4-[4-(2-Methyl-5-trifl oromethyl-2Hpyrazol-3-yl)-2-trifl oromethyl- benzenesulfonyl] -1 -(1 -trifluoromethyl-cyclopropanecarbonyl)-pyrroUdine-2-carboxylic acid (l-cyano-cyclopropyl)-amide
Chiral
Figure imgf000031_0002
Example 3f) (500 mg, 830 μιηοΐ, Eq: 1.00), l-methyl-5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)-3-(trifluoromethyl)-lH-pyrazole (275 mg, 996 μιηοΐ, Eq: 1.20) and triphenylphosphine (43.5 mg, 166 μιηοΐ, Eq: 0.20) were dissolved in 1,2-dimethoxyethane (6 mL). Pd(OAc)2 (18.6 mg, 83.0 μπιοΐ, Eq: 0.10) and 2M aqueous Na2C03 solution (1.5 mL) were added to the solution. The reaction mixture was stirred at 60°C for 8 h. The reaction mixture was poured into 0.1 M aqueous HCl solution (100 mL) and extracted with DCM. The aqueous layer was washed with DCM (3 x 50 mL). The organic layers were dried over Na2S04 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 20 g, 0% to 80% EtOAc in heptane) to yield the title compound as light yellow foam (410 mg; 74%). m/z = 670.1169 [M-H]~. Example 4
(2S,4R)-4-(2,-Trifluoromethoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Chiral
Figure imgf000032_0001
Example 3f) (50 mg, 83.0 μιηοΐ, Eq: 1.00), 2-(trifluoromethoxy)phenylboronic acid (20.5 mg, 99.6 μιηοΐ, Eq: 1.20) and triphenylphosphine (4.35 mg, 16.6 μιηοΐ, Eq: 0.20) were dissolved in 1,2-dimethoxyethane (1 mL). Pd(OAc)2 (1.86 mg, 8.3 μιηοΐ, Eq: 0.10) and aqueous 2M Na2C03 solution (250 μΐ) were added to the solution and stirred at 50°C for 8 h. The crude material was filtered and purified by preparative HPLC to yield the title compound as a white solid (41 mg; 72%). m/z = 684.0 [M+H]+.
Example 5
(2S,4R)-4-(2'-Ethoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (l-cyano-cyclopropyl)-amide
Chiral
Figure imgf000032_0002
Example 5 was prepared in analogy to example 4 starting from example 3f) and 2- ethoxyphenylboronic acid to yield the title compound as a white solid (40 mg; 75%). m/z = 644.1[M+H]+. Example 6
(2S,4R)-4-(2'-Cyclopropoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000033_0001
Example 6 was prepared in analogy to example 4 starting from example 3f) and 2- cyclopropoxyphenylboronic acidto yield the title compound as a white solid (39 mg; 72%). m/z = 656.3 [M+H]+.
Example 7 (2S,4R)-4-(4-Cyclobutoxy-2-trifluoromethyl-benzenesulfonyl)-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (l-cyano-cyclopropyl)-amide
Figure imgf000033_0002
a) ( 2S,4R )-4-( 4-Fluoro-2-trifluoromethyl-phenylsulfanyl)-l -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (l-cyano-cyclopropyl)-amide
Figure imgf000034_0001
In a 250 mL four-necked flask, example 3d) (7 g, 14.8 mmol, Eq: 1.00) and 4-fluoro-2- trifluoromethyl-benzenethiol (CAS 1208077-00-2) (4.08 g, 20.8 mmol, Eq: 1.40) were combined with propionitrile (70 mL) to give a yellow solution. Triethylamine (5.38 mL, Eq: 2.60) was added at 22° C.The reaction mixture was heated to 110 °C and stirred for 3 h. The reaction mixture was poured into ethylacetate (300 mL) and extracted with aqueous 10% Na2C03 solution (2 x 100 mL).The aqueous layer was back-extracted with EtOAc (2 x 250 mL). The organic layers were combined, washed with saturated aqueous NaCl solution (1 x 75 mL).The organic layers were dried over Na2S04 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 120 g , 20% to 70% EtOAc in heptane) to yiled the title compound as a colorless foam (6.83 g; 90 %). m/z = 510.0 [M+H]+. b) ( 2S,4R )-4-( 4-Fluoro-2-trifluoromethyl-benzenesulfonyl)-l -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide
Figure imgf000034_0002
In a 250 mL round-bottomed flask, example 7a) (5.85 g, 11.5 mmol, Eq: 1.00) was combined with dichloromethane (80 mL) to give a white suspension. 3-chloroperoxy- benzoic acid (5.15 g, 29.9 mmol, Eq: 2.60) was added.The reaction mixture was stirred for 48 h at 22° C. After that, 3-chloroperoxybenzoic acid (991 mg, 5.74 mmol, Eq: 0.5) was added and the reaction mixture was strirred for additional 72 h. The reaction mixture was poured into 200 mL dichloromethane and extracted with aqueous 10% Na2C03 solution (3 x 150mL ).The aqueous layer was back-extracted with dichloromethane (3 x 150mL).The organic layers were combined, washed with saturated aqueous Na2S203-solution (4 x 100 mL)->(Peroxide Test), brine (1 x 100 mL), dried over Na2S04 and concentrated in vacuo to yield the title compound as a white solid (6.36 g; 100%). m/z = 542.3 [M+H]+. m/z = 540.3 [M-H]~. c) ( 2S,4R )-4-( 4-Cyclobutoxy-2-trifluoromethyl-benzenesulfonyl)-l -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1 -cyano-cyclopropyl)-amide
Figure imgf000035_0001
In a 10 mL round-bottomed flask, example 7b) (100.0 mg, 185 μιηοΐ, Eq: 1.00) was combined with DMA (1.5 mL) to give a light yellow solution.cesium carbonate (72.2 mg, 222 μιηοΐ, Eq: 1.20) and cyclobutanol (20.0 mg, 21.7 μΐ, 277 μιηοΐ, Eq: 1.5) were added.The reaction mixture was stirred for 18 h at 25 °C. After that, additional cyclobutanol (13.3 mg, 14.5 μΐ, 185 μιηοΐ, Eq: 1.00) was added and the reaction mixture was stirred at 25 °C for 18 h. The crude material was purified by preparative HPLC to yield the title compound as an amorphous colorless solid (31 mg; 28%). m/z = 592.3 [M-
Example 8
(2S,4R)-4-(2-chloro-4-(5-methyl-2H-tetrazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000035_0002
a) ( 2S,4R )-4-(2-Chloro-4-fluoro-phenylsulfanyl)-l -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide
Figure imgf000036_0001
Example 8a) was prepared in analogy to example 7a) starting from example 3d) and 2- chloro-4-fluoro-benzenethiol to yield the title compound as a colorless gum (6.35 g; 96%). m/z = 476.1 [M+H]+. b) ( 2S,4R )-4-(2-Chloro-4-fluoro-benzenesulfonyl)-l -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide
Figure imgf000036_0002
Example 8b) was prepared in analogy to example 7b) starting from example 8a) the title compound as a white foam (6.55 g; 97%). m/z = 508.3 [M+H]+. c) (2S,4R)-4-(2-chloro-4-(5-methyl-2H-tetrazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyi i -( 1 -( trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000036_0003
In a 10 mL round-bottomed flask, (2S,4R)-4-(2-chloro-4-fluorophenylsulfonyl)-N-(l- cyanocyclopropyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 8b)) (400 mg, 788 μιηοΐ, Eq: 1.00) was combined with DMA (5 mL) to give a colorless solution. 5-methyl-lH-tetrazole (132 mg, 1.58 mmol, Eq: 2.00) and cesium carbonate (513 mg, 1.58 mmol, Eq: 2.00) were added. The reaction mixture was heated to 80 °C and stirred for 3h. After that, 5-methyl-lH-tetrazole (13.2 mg, 0.158 mmol, Eq: 0.20) was added and the mixture was stirred at 80 °C for additional 2 h. The reaction mixture was poured into water and extracted with EtOAc (2x). The organic layers were combined, washed with saturated aqueous NaHC03 solution (lx), water (3x) and brine (lx). The organic layers were dried over Na2S04 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 20g, Heptan/AcOEt 2/1, 1/1, 1/2, 1/3) to yield the title compound as a light brown foam (183 mg; 41%). m/z = 572.2 [M+H]+.
Example 9
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-tetrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000037_0001
Example 9 was obtained as a regioisomer during the synthesis of example 8 as a white foam (198 mg; 44%). m/z = 572.2 [M+H]+.
Example 10
(2S,4R)-4-(2-chloro-4-(lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)- l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000037_0002
In a 10 mL round-bottomed flask, (2S,4R)-4-(2-chloro-4-fluorophenylsulfonyl)-N-(l- cyanocyclopropyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 8b)) (400 mg, 788 μιηοΐ, Eq: 1.00) was combined with DMA (5 mL) to give a colorless solution. lH-l,2,4-triazole (111 mg, 1.58 mmol, Eq: 2.00) and cesium carbonate (513 mg, 1.58 mmol, Eq: 2.00) were added. The reaction mixture was heated to 80 °C and stirred for 3h. The reaction mixture was poured into water and extracted with EtOAc (2x). The organic layers were combined, washed with saturated aqueous NaHC03 solution (lx), water (3x) and brine (lx). The organic layers were dried over Na2S04 and concentrated in vacuo. The crude material was purified twice by flash chromatography (silica gel, 20g, DCM/MeOH 98/2, 19/1) and (silica gel, 20g, Heptan/AcOEt 1/2, 1/3, 1/4) to yield the title compound as a white foam (264 mg; 60%). m/z = 557.1[M+H]+.
Example 11 (2S,4R)-N-(l-cyanocyclopropyl)-4-(2,4-di(lH-l,2,4-triazol-l-yl)phenylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000038_0001
Example 11 was obtained as a byproduct during the synthesis of example 10 as a white solid (34 mg; 7%). m/z = 590.1[M+H]+. Example 12
(2S,4R)-4-(2-chloro-4-(2H-l,2,3-triazol-2-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)- l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000038_0002
Example 12 was prepared in analogy to example 10 starting from (2S,4R)-4-(2-chloro-4- fluorophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifluoromethyl)cyclopropane- carbonyl)pyrrolidine-2-carboxamide (example 8b)) and lH-l,2,3-triazole to yield the title compound as a off-white solid (189 mg; 43%). m/z = 557.1[M+H]+.
Example 13
(2S,4R)-4-(2-chloro-4-(lH-l,2,3-triazol-l-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)- l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000039_0001
Example 13 was obtained as a regioisomer during the synthesis of example 12 as an white solid (170 mg; 39%). m/z = 557.1 [M+H]+.
Example 14
(2S,4R)-4-(2-chloro-4-(3-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000039_0002
Example 14 was prepared in analogy to example 10 starting from (2S,4R)-4-(2-chloro-4- fluorophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifluoromethyl)cyclopropane- carbonyl)pyrrolidine-2-carboxamide (example 8b)) and 3-methyl-lH-l,2,4-triazole by stirring the reaction mixture at 22°C for 16 h to yield the title compound as a white foam (212 mg; 47 %). m/z = 571.2 [M+H]+.
Example 15 (2S,4R)-4-(2-chloro-4-(3,5-dimethyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000040_0001
Example 15 was prepared in analogy to example 10 starting from (2S,4R)-4-(2-chloro-4- fluorophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifluoromethyl)cyclopropane- carbonyl)pyrrolidine-2-carboxamide (example 8b)) and 3,5-dimethyl-lH-l,2,4-triazole by stirring the reaction mixture at 22°C for 16 h to yield the title compound as a white foam (400 mg; 76 %). m/z = 585.2[M+H]+.
Example 16
(2S,4R)-4-(2-chloro-4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000040_0002
Example 16 was prepared in analogy to example 10 starting from (2S,4R)-4-(2-chloro-4- fluorophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifluoromethyl)cyclopropane- carbonyl)pyrrolidine-2-carboxamide (example 8b)) and 3-chloro-lH-l,2,4-triazole by stirring the reaction mixture at 22°C for 16 h to yield the title compound as a white foam (432 mg; 81 %). m/z = 591.2 [M+H]+.
Example 17
(2S,4R)-4-(2-chloro-4-(3-(trifluoromethyl)-lH-pyrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide Chiral
Figure imgf000041_0001
Example 17 was prepared in analogy to example 10 starting from (2S,4R)-4-(2-chloro-4- fluorophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifluoromethyl)cyclopropane- carbonyl)pyrrolidine-2-carboxamide (example 8b)) and 3-(trifluoromethyl)-lH-pyrazole by stirring the reaction mixture at 22°C for 16 h to yield the title compound as a white foam (419 mg; 76 %). m/z = 624.1 [M+H]+.
Example 18
(2S,4R)-4 2-chloro-4 5-methyl-3-(trifluoromethyl)-lH-pyrazol-l-yl)phenylsulfonyl)- N-(l-cyanocyclopropyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000041_0002
Example 18 was prepared in analogy to example 10 starting from (2S,4R)-4-(2-chloro-4- fluorophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifluoromethyl)cyclopropane- carbonyl)pyrrolidine-2-carboxamide (example 8b)) and 5-methyl-3-(trifluoromethyl)-lH- pyrazole by stirring the reaction mixture at 22°C for 16 h to yield the title compound as a white foam (411 mg; 73 %). m/z = 638.1 [M+H]+.
Example 19
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide Chiral
Figure imgf000042_0001
a) ( 2S,4R )-N-( 1 -cyanocyclopropyl)-4-( 4-fluoro-2-methylphenylthio )-l -( 1 - ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000042_0002
The title compound was prepared in analogy to example 3, step e), using 4-fluoro-2- methylbenzenethiol, and obtained as a light brown gum (3.47 g, 97%). m/z = 456.4 [M+H]+. b) ( 2S,4R )-N-( 1 -cyanocyclopwpyl)-4-( 4-fluoro-2-methylphenylsulfonyl)
( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000042_0003
The title compound was prepared in analogy to example 3, step f) from (2S,4R)-N-(1- cyanocyclopropyl)-4-(4-fluoro-2-methylphenylthio)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 19a) and obtained as a white foam (2.84 g, 76%). m/z = 487.1202 [M+]. c) (2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulfonyl)-l -( 1 -( trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Figure imgf000043_0001
(2S,4R)-N-(l-Cyanocyclopropyl)-4-(4-fluoro-2-methylphenylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 19b, 70 mg, 144 μιηοΐ), 3-(trifluoromethyl)-lH-pyrazole (39.1 mg, 287 μιηοΐ) and cesium carbonate (93.6 mg, 287 μιηοΐ) were combined with N,N-dimethylacetamide (1.00 mL) in a sealed tube to give a white suspension. The reaction was stirred over the weekend at ambient temperature. After filtration, the title compound was isolated from the reaction mixture by preparative HPLC (zorbax CI 8 21.2x50mm; flow: 20 mL/min; gradient: acetonitrile / water (+0.1% formic acid) = (95%-5% to 5%-95%) in 7.5 min; collected by 254 nm detector; 28.8mg, 33.2%). m/z = 604.14 [M+H+]. Example 20
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(trifluoromethoxy)biphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000043_0002
a) ( 2S,4R )-4-( 4-bromophenylthio )-N-( 1 -cyanocyclopropyl)-! -( 1 - ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000044_0001
The title compound was prepared in analogy to example 3, step e), using 4- bromobenzenethiol, and obtained as a colorless foam (952 mg, 95 %). m/z
[M+H]+. b) ( 2S,4R )-4-( 4-bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)-! -( 1 - ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000044_0002
The title compound was prepared in analogy to example 3, step f) from (2S,4R)-4-(4- bromophenylthio)-N- ( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20a) and obtained as a white powder (918 mg, 91%). m/z = 532.0/534.0 [M-H]". c) ( 2S,4R )-N-( 1 -cyanocyclopropyl)-4-( 2 '-( trifluoromethoxy)biphenyl-4-ylsulfonyl)-l -( 1 - ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000044_0003
To a solution of (2S,4R)-4-(4-bromophenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b, 321 mg, 0.6 mmol) and 2-(trifluoromethoxy)phenylboronic acid (185 mg, 900 μιηοΐ) in dioxan (6 mL) and sodium carbonate 2M in water (1.5 mL, 3.00 mmol) was added under stirring and under an athmosphere of nitrogen l,l'-bis)diphenylphosphino)-ferrocene- palladiuim(II)dichloride dichloromethane complex (24.5 mg, 30.0 μιηοΐ). The reaction was heated to 85°C over night. After cooling water was added and the reaction was extracted twice with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel using heptane : ethyl acetate (9: 1 to 1:4) as the eluent. The crude product was stirred with hptane/diethyl ether, filtered and dried to yield the title compound as a white powder (272.4 mg, 74 %). m/z = 614.1 [M-H]~.
Example 21 (2S,4R)-4-(2-chloro-4-cyclobutoxyphenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000045_0001
Example 21 was prepared in analogy to example 10 starting from (2S,4R)-4-(2-chloro-4- fluorophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifluoromethyl)cyclopropane- carbonyl)pyrrolidine-2-carboxamide (example 8b)) and cyclobutanol by stirring the reaction mixture at 22°C for 16 h to yield the title compound as a white foam (166 mg; 60%). m/z = 560.2 [M+H]+.
Example 22
(2S,4R)-N-(l-cyanocyclopropyl)-4-(3-methyl-2'-(trifluoromethoxy)biphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide Chiral
Figure imgf000046_0001
a) ( 2S,4R )-4-( 4-bromo-2-methylphenylthio )-N-( 1 -cyanocyclopropyl)-! -( 1 - ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000046_0002
The title compound was prepared in analogy to example 3, step e), using 4- bromobenzenethiol, and obtained as a colorless oil (1087 mg, 89 ). m/z = 516.1/518.3 [M+H]+. b) ( 2S,4R )-4-( 4-bromo-2-methylphenylsulfonyl)-N-( 1 -cyanocyclopropyl)-l -( 1 - ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000046_0003
The title compound was prepared in analogy to example 3, step f) from (2S,4R)-4-(4- bromo-2-methylphenylthio)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22a) and 2- (trifluoromethoxy)phenylboronic acid and obtained as a colorless waxy solid (1.05 g, 93%). m/z = 550.2 / 548.2 [M+H]+. c) ( 2S,4R )-N-( 1 -cyanocyclopropyl)-4-( 3-methyl-2 '-( trifluoromethoxy)biphenyl-4- ylsulfonyi i -( 1 -( trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Figure imgf000047_0001
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l-
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22a) and obtained as a off-white foam (179 mg, 57%). m/z = 630.3 [M+H]+.
Example 23
(2S,4R)-4-[4-(5-Methyl-3-trifluoromethyl-pyrazol-l-yl)-2-trifluoromethyl- benzenesulfonyl]-l-(l-trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide
Figure imgf000047_0002
Example 23 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and 5-methyl-3- (trifluoromethyl)-lH-pyrazole by stirring the reaction mixture at 22°C for 72 h to yield the title compound as a colorless foam (104 mg; 84%). m/z = 672.1325 [M+H]+.
Example 24 (2S,4R)-4-[4-(3-Methyl-[l,2,4]triazol-l-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000048_0001
Example 24 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and 3-methyl-lH- 1,2,4- triazole by stirring the reaction mixture at 22°C for 72 h to yield the title compound as a colorless amorphous solid (26 mg; 23%). m/z = 605.1390 [M+H]+.
Example 25
(2S,4R)-4-[4 3-Methyl-[l,2,4]triazol-4-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000048_0002
Example 25 was obtained as a regioisomer during the synthesis of example 24 to yield the title compound as a colorless amorphous solid (1.5 mg; 1.3 %). m/z = 605.1398 [M+H]+.
Example 26 (2S,4R)-4-(4-(lH-l,2,4-triazol-l-yl)-2-(trifluoromethyl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000049_0001
Example 26 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and lH-l,2,4-triazole by stirring the reaction mixture at 22°C for 4 h to yield the title compound as a colorless amorphous solid (68 mg; 31%). m/z = 589.1110 [M+H]+.
Example 27
(2S,4R)-4-[4-(3,5-Dimethyl-[l,2,4]triazol-l-yl)-2-trifluoromethyl-benzenesulfonyl]-l- (l-trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000049_0002
Example 27 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and 3,5-dimethyl-lH- 1,2,4- triazole by stirring the reaction mixture at 22°C for 4 h to yield the title compound as a colorless foam (122 mg; 53%). m/z = 619.1553 [M+H]+. Example 28
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(l-methyl-3-(trifluoromethyl)-lH-pyrazol-5- yl)phenylsulf onyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000050_0001
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 1- methyl-5-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)- IH-pyrazole and obtained as a white solid (31 mg, 8%) after purification on preparative HPLC. m/z = 602.2 [M-H]~.
Example 29
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-formyl-3-methylbiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Figure imgf000050_0002
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulf onyl)-N- ( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2- formylphenylboronic acid and obtained as a white solid (146 mg, 51%). m/z = 574.2 [M+H]+.
Example 30 (2S,4R)-4-[4-(3-Chloro-[l,2,4]triazol-l-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000051_0001
Example 30 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and 3-chloro-lH- 1,2,4- triazole by stirring the reaction mixture at 22°C for 4 h to yield the title compound as a colorless foam (135 mg; 59%). m/z = 623.0708 [M+H]+.
Example 31
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-lH-l,2,4-triazol-l-yl)-2-
(trifluoromethyl)phenylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide
Figure imgf000051_0002
Example 31 was obtained as a regioisomer during the synthesis of example 24 to yield the title compound as a colorless amorphous solid (26 mg; 23 %). m/z = 605.1397 [M+H]+.
Example 32 (2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(l-methyl-3-(trifluoromethyl)-lH- pyrazol-5-yl)phenylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide
Chiral
Figure imgf000052_0001
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulf onyl)-N- ( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 1- methyl-5-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)- IH-pyrazole and obtained as a off-white solid (16 mg, 5%) after purification on preparative HPLC. m/z = 618.3 [M+H]+.
Example 33
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethyl-lH-l,2,4-triazol-l- yl)phenylsulf onyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000052_0002
a) ( 2S,4R )-N-( 1 -cyanocyclopropyl)-4-( 4-fluorophenylthio )-!-(!- ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide Chiral
Figure imgf000053_0001
The title compound was prepared in analogy to example 3, step e), using 4- fluorobenzenethiol, and obtained as a off-white foam (2.72 g, 72%). m/z = 442.2 [M+H+]. b) ( 2S,4R )-N-( 1 -cyanocyclopropyl)-4-( 4-fluorophenylsulfonyl)-l -( 1 - ( trifluoromethyl)cyclopropanecarbonyl )pyrrolidine-2-carboxamide
Figure imgf000053_0002
The title compound was prepared in analogy to example 3, step f) from (2S,4R)-N-(1- cyanocyclopropyl)-4-(4-fluorophenylthio)-l-(l-(trifluoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide (example 33a) and obtained as a white foam (840 mg, 29%). m/z = 474.11 [M+H+]. c) (2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethyl-lH-l,2,4-triazol-l- yl)phenylsulfonyl)-l -( 1 -( trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Figure imgf000053_0003
Under an atmosphere of argon, (2S,4R)-N-(l-cyanocyclopropyl)-4-(4- fluorophenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide (example 33, step b, 0.1 g, 211 μιηοΐ) was combined with N,N- dimethylacetamide (2.00 mL) to give a colorless suspension. 3,5-Dimethyl-lH- 1,2,4- triazole (41.0 mg, 422 μιηοΐ) and cesium carbonate (138 mg, 422 μιηοΐ) were added.The reaction mixture was stirred over the weekend at ambient temperature. The crude material was purified by preparative HPLC (Zorbax Eclipse XDB-C18; 21,2x50mm; flow: 25 mL/min; gradient: acetonitrile / water (+0.1% formic acid) = (95%-5% to 5%-95%) in 6 min; collected by 254 nm detector ) to yield the title compound as a colorless viscous oil (13.2 mg, 11.4 %). m/z = 551.17 [M+H+].
Example 34 (2S,4R)-4-(4-(lH-l,2,3-triazol-l-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Figure imgf000054_0001
The title compound was prepared in analogy to example 33, using lH-l,2,3-triazole in step c), and was obtained as a colorless viscous oil (2.5 mg, 2.83 %). m/z = 523.13 [M+H+]). Example 35
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000055_0001
The title compound was prepared in analogy to example 33, using 3-(trif uoromethyl)-lH- pyrazole in step c), and was obtained as a white solid (38.2 mg, 38.3 %). m/z = 590.13 [M+H+].
Example 36
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000055_0002
The title compound was prepared in analogy to example 33, using 5-methyl-3- (trif uoromethyl)-lH-pyrazole in step c), and was obtained as a white solid (22.1 mg, 21.7 %). m/z = 604.14 [M+H+]).
Example 37
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-formylbiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide Chiral
Figure imgf000056_0001
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 2- formylphenylboronic acid and obtained as a white powder (57.6 mg, 52%). m/z = 558.2 [M-H]~.
Example 38
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxybiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000056_0002
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 2- ethoxyphenylboronic acid and obtained as a pink powder (86.1 mg, 75%). m/z = 574.2 [M-
Example 39
(2S,4R)-4-(4-(2-aminopyrimidin-5-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide Chiral
Figure imgf000057_0001
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 2- aminopyrimidin-5-ylboronic acid and obtained as a white powder (72 mg, 66%). m/z = 547.2 [M-H ].
Example 40
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxy-3-methylbiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000057_0002
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulf onyl)-N- ( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2- ethoxyphenylboronic acid and obtained as a off-white solid (255 mg, 87%). m/z = 590.4 [M+H]+.
Example 41
(2S,4R)-4-(2'-cyano-3-methylbiphenyl-4-ylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide Chiral
Figure imgf000058_0001
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l-
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2- (4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzonitrile and obtained as a off-white solid (43.2 mg, 12%) after purification on preparative HPLC. m/z = 571.2 [M+H]+.
Example 42
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxy-4',5'-difluoro-3-methylbiphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000058_0002
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulf onyl)-N- ( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2- ethoxy-4,5-difluorophenylboronic acid and obtained as a off-white solid (235.5 mg, 75%) after purification on preparative HPLC. m/z = 626.3 [M+H]+.
Example 43
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(hydroxymethyl)biphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide Chiral
Figure imgf000059_0001
To a solution of (2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-formylbiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 37, 35.6 mg, 63.6 μιηοΐ) in methanol (1 mL) was added under stirring and under an athmosphere of nitrogen sodium borohydride (2.41 mg, 63.6 μιηοΐ). The reaction was stirred at room temperature over night. Water was added and the reaction was extracted twice with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The residue was stirred with heptane for 15 minutes, filtered and dried to yield the title compound as a white powder (26.4 mg, 74%). m/z = 560.2 [M-H]~.
Example 44
(2S,4R)-4-(4-(2-aminopyrimidin-5-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000059_0002
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulf onyl)-N- ( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2- aminopyrimidin-5-ylboronic acid and obtained as a off-white solid (78.8 mg, 70%) after purification on preparative HPLC. m/z = 563.4 [M+H]+.
Example 45 (2S,4R)-4-[4-(2,2-Difluoro-benzo[l,3]dioxol-5-yl)-2-trifluoromethyl-benzenesulfonyl]- l-(l-trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Chiral
Figure imgf000060_0001
Example 3f) (100 mg, 166 μιηοΐ, Eq: 1.00), 2,2-difluorobenzo[d][l,3]dioxol-5-ylboronic acid (50.3 mg, 249 μιηοΐ, Eq: 1.50) were dissolved in dioxane (2 mL). Aqueous 2M Na2C03 solution (415 μΐ, 830 μιηοΐ, Eq: 5.00) and 1,1 '-bis (diphenylphosphino)- ferrocenepalladium(II) dichloride dichloromethane complex (6.78 mg, 8.3 μιηοΐ, Eq: 0.05) were added to the solution and stirred at 85°C for 13 h. The crude material was filtered and purified by preparative HPLC to yield the title compound as light yellow foam (83 mg; 74%). m/z = 680.2 [M+H]+.
Example 46
(2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(4- trifluoromethyl-pyrazol-l-yl)-benzenesulfonyl]-pyrrolidine-2-carboxylic acid (1- cyano-cyclopropyl)-amide
Figure imgf000060_0002
Example 46 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and 4-(trifluoromethyl)-lH- pyrazole by stirring the reaction mixture at 22°C for 24 h to yield the title compound as a colorless foam (75 mg; 62%). m/z = 657.1103 [M+H]+.
Example 47
(2S,4R)-4-[4-(5-Methyl-tetrazol-l-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000061_0001
Example 47 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and 5-methyl-lH-tetrazole by stirring the reaction mixture at 22°C for 24 h to yield the title compound as a colorless amorphous solid (63 mg; 28%). m/z = 605.1289 [M+H]+.
Example 48
(2S,4R)-4-[4-(2,4-Dimethyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Chiral
Figure imgf000061_0002
In a 5 mL microwavetube, example 3f) (100 mg, 166 μιηοΐ, Eq: 1.00), potassium acetate (24.4 mg, 249 μιηοΐ, Eq: 1.50) and tetrakis(triphenylphosphine)palladium (0) (9.59 mg, 8.3 μηιοΐ, Eq: 0.05) were dissolved in DMA (1 mL). Now 2,4-dimethylthiazole (94.0 mg, 89.0 μΐ, 830 μιηοΐ, Eq: 5.00) was added. The tube was sealed and the mixture was stirred for 30 min at 170° C in the microwave oven. After that, 2,4-dimethylthiazole (94.0 mg, 89.0 μΐ, 830 μιηοΐ, Eq: 5.00) was added to the reaction mixture. The reaction mixture was heated in the microwave oven at 170° C for 30 min. Now, the reaction mixture was poured into EtOAc (15 mL) and extracted with 0.1M aqueous HCI solution (20 mL). The aqueous layer was back-extracted with EtOAc (2 x 15mL). The organic layers were combined, then dried over Na2S04, filtered and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 4 g, 0% to 60% EtOAc in DCM). The roughly purified material was in addition purified by preparative HPLC to yield the title compound as a colorless solid (11 mg; 10%). m/z = 635.1210 [M+H]+.
Example 49
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)phenylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000062_0001
Example 49 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 2,4- dimethylthiazole to yield the title compound as a white powder (44 mg, 39%) after purification on preparative HPLC. m/z = 565.2 [M-H]~.
Example 50
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methylthiazol-5-yl)phenylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide Chiral
Figure imgf000063_0001
Example 50 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 2- methylthiazole to yield the title compound as a white powder (42 mg, 38%) after purification on preparative HPLC. m/z = 551.3 [M-H]~.
Example 51
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methoxypyrimidin-5-yl)phenylsulfonyl)-l-(l (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000063_0002
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-phenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 2- methoxypyrimidin-5-ylboronic acid and obtained as a white powder (67.2 mg, 60%). m/z 562.1 [M-H]~.
Example 52
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000064_0001
Example 52 was obtained as a regioisomer during the synthesis of example 14 to yield the title compound as a white solid (69 mg; 15 %). m/z = 571.2 [M+H]+.
Example 53
(2S,4R)-4-(4-[l,2,3]Triazol-2-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000064_0002
Example 53 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and lH-l,2,3-triazole by stirring the reaction mixture at 22°C for 24 h to yield the title compound as a colorless foam (89 mg; 41%). m/z = 590.1175 [M+H]+.
Example 54
(2S,4R)-4-(4-[l,2,3]Triazol-l-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000065_0001
Example 54 was obtained as regioisomer during the synthesis of example 53 to yield the title compound as a colorless foam (38 mg; 36%). m/z = 590.1175 [M+H]+.
Example 55
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)phenylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000065_0002
Example 55 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 3,5- dimethylisoxazole to yield the title compound as a colorless solid (10 mg, 9%) after purification on preparative HPLC. m/z = 549.2 [M-H]~.
Example 56
(2S,4R)-4-[4-(l-Difluoromethyl-lHpyrazol-4-yl)-2-trifluoromethyl-benzenesulfonyl]- l-(l-trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide hiral
Figure imgf000066_0001
Example 3f) (100 mg, 166 μιηοΐ, Eq: 1.00), l-(difluoromethyl)-4-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)-lH-pyrazole (60.8 mg, 249 μmol, Eq: 1.50) were dissolved in dioxane (2 mL). Aqueous 2M Na2C03 solution (415 μΐ, 830 μιηοΐ, Eq: 5.00) and Ι,Γ-bis (diphenylphosphino)ferrocene.palladium(II) dichloride dichloromethane complex (6.78 mg, 8.3 μιηοΐ, Eq: 0.05) were added to the solution and stirred at 85°C for 14 h. The crude material was filtered and purified by preparative HPLC. After that, the material was purified by flash chromatography (silica gel, 4 g, 0% to 66% EtOAc in heptane) to yield the title compound as light yellow foam (90 mg; 85%). m/z = 638.1113 [M-H]~.
Example 57
(2S,4R)-4-[4-(5-Methyl-tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Figure imgf000066_0002
Example 57 was obtained as a regioisomer during the synthesis of example 47 to yield the title compound as a colorless amorphous solid (34 mg; 15%). m/z = 604.2 [M-H]".
Example 58 (2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(3- trifluoromethyl-lHpyrazol-4-yl)-benzenesulfonyl]-pyrrolidine-2-carboxylic acid (1- cyano-cyclopropyl)-amide
Figure imgf000067_0001
Example 58 was prepared in analogy to example 56 starting from example 3f) and 4- (4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)- lH-pyrazole to yield title compound as a white solid (6.0 mg; 5.5 %). m/z = 658.5[M+H]+.
Example 59
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(hydroxymethyl)-3-methylbiphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000067_0002
Example 59 was prepared in analogy to example 43 starting from (2S,4R)-N-(1- cyanocyclopropyl)-4-(2'-formyl-3-methylbiphenyl-4-ylsulfonyl)-l-(l- (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 29) to yield the title compound as a off-white solid (36.1 mg, 45%) after purification on preparative HPLC. m/z = 574.2 [M-H]~.
Example 60
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)-2- methylphenylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000068_0001
Example 60 was prepared in analogy to example 48 starting from (2S,4R)-4-(4-bromo-2- methylphenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2,4 dimethylthiazole to yield the title compound as a off-white solid (44.9 mg, 39%) after purification on preparative HPLC. m/z = 581.2 [M+H]+.
Example 61
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(2-methylthiazol-5-yl)phenylsulfonyl) l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Chiral
Figure imgf000068_0002
Example 61 was prepared in analogy to example 48 starting from (2S,4R)-4-(4-bromo-2- methylphenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2- methylthiazole to yield the title compound as a off-white solid (55.9 mg, 49%) after purification on preparative HPLC. m/z = 567.2 [M+H]+.
Example 62
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methoxypyrimidin-5-yl)-2- methylphenylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide Chiral
Figure imgf000069_0001
The title compound was prepared in analogy to example 20, step c) from (2S,4R)-4-(4- bromo-2-methylphenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l-
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 22b) and 2- methoxypyrimidin-5-ylboronic acid and obtained as a light brown solid (72 mg, 62%). m/z
= 578.2 [M+H+].
Example 63
(2S,4R)-4-[4-(2-Methyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (1-cyano- cyclopropyl)-amide
Chiral
Figure imgf000069_0002
In a 5 mL microwavetube, example 3f) (lOOmg, 166 μιηοΐ, Eq: 1.00), potassium acetate (24.4 mg, 249 μιηοΐ, Eq: 1.50) and tetrakis(triphenylphosphine)palladium (0) (9.59 mg, 8.3 μιηοΐ, Eq: 0.05) were combined with DMA (1 mL). 2-Methylthiazole (82.3 mg, 74.2 μΐ, 830 μιηοΐ, Eq: 5.00) was added. The tube was sealed and the mixture was stirred for 30 minutes at 160° C in the microwave oven. The reaction mixture was poured into EtOAc (15 mL) and extracted with 0.1 M aqueous HC1 solution (1 x 20 mL). The aqueous layer was back-extracted with EtOAc (2 x 10 mL). The organic layers were dried over Na2S04 and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 4 g, 0% to 60% EtOAc in DCM) to yield the title compound as an off-white solid (8 mg; 8%). m/z = 621.1064 [M+H]+.
Example 64 (2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)-2- methylphenylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Chiral
Figure imgf000070_0001
Example 64 was prepared in analogy to example 48 starting from (2S,4R)-4-(4- bromophenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 -
(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (example 20b) and 3,5- dimethylisoxazole to yield the title compound as a a off-white solid (28.5 mg, 25%) after purification on preparative HPLC. m/z = 565.3 [M+H]+.
Example 65
(2S,4R)-4-(4-Tetrazol-l-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid (l-cyano-cyclopropyl)-amide
Figure imgf000070_0002
Example 65 was prepared in analogy to example 10 starting from (2S,4R)-4-(4-fluoro-2- trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine- 2-carboxylic acid (l-cyano-cyclopropyl)-amide (example 7b)) and lH-tetrazole by stirring the reaction mixture at 22°C for 48 h to yield the title compound as an amorphous colorless solid (29 mg; 13%). m/z = 591.113 [M+H]+.
Example 66 (2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000071_0001
Under an atmosphere of argon, (2S,4R)-N-(l-cyanocyclopropyl)-4-(4-fluoro-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide (example 19, step b, 0.2 g, 410 μιηοΐ) was combined with N,N- dimethylacetamide (8.00 mL) to give a colorless suspension. 3-Chloro-lH-l,2,4-triazole (86.7 mg, 821 μιηοΐ) and cesium carbonate (267 mg, 821 μιηοΐ) were added. The reaction mixture was stirred over 5 days and was subsequently heated to 140°C for 30 min in a microwave oven. The reaction mixture was then poured into water (40 mL) and extracted with ethyl acetate (2 x 40 mL). The crude material was purified by preparative HPLC and obtained as a light yellow, viscuous oil (12 mg, 5.1%). m/z = 571.11 [M+H+].
Example 67 (2R,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - (1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
Figure imgf000071_0002
The title compound was obtained as a by-product in the preparation of example 66 and was obtained as a light yellow viscous oil (13.9 mg, 5.9%, stereochemistry assigned by
NOESY-NMR). m/z = 571.1137 [M+H+].
Example 68
(2S,4R)-4-[4-(l-Methyl-3-trifluoromethyl-lHpyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl]-l-(l-trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide
Figure imgf000072_0001
Example 68 was prepared in analogy to example 56 starting from example 3f) and 1- methyl-4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)- IH-pyrazole to yield the title compound as a white foam (167 mg; 75%). m/z = 689.1581 [M+NH4]+.
Example 69
(2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)- l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide
Figure imgf000072_0002
Under an atmosphere of argon, (2S,4R)-N-(l-cyanocyclopropyl)-4-(4- fluorophenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide (example 33, step b, 0.3 g, 634 μιηοΐ) was combined with N,N- dimethylacetamide (12 mL) to give a colorless suspension. 3-Chloro-lH-l,2,4-triazole (134 mg, 1.27 mmol) and cesium carbonate (413 mg, 1.27 mmol, Eq: 2) were added. The reaction mixture was stirred over the weekend at ambient temperature, and was
subsequently heated to 140°C for 30 min in a microwave oven. The reaction mixture was poured into water (50 mL) and extracted with ethyl acetate (2 x 50 mL). The crude material was purified by preparative HPLC to yield the title compound as a colorless viscous oil (93.9mg, 26.6 %). m/z = 557.09 [M+H+].
Example 70 Cathepsin enzyme inhibition assay
Enzyme activity is measured by observing the increase in fluorescence intensity caused by cleavage of a peptide substrate containing a fluorophore whose emission is quenched in the intact peptide.
Assay buffer: 100 mM potassium phosphate pH 6.5, EDTA-Na 5 mM, Triton X-100 0.001%, DTT 5 mM.
Enzymes (all at 1 nM): human and mouse Cathepsin S, Cat K, Cat B, Cat L.
Substrate (20 μΜ): Z-Val-Val-Arg-AMC, except for Cat K which uses Z-Leu-Arg-AMC (both from Bachem).
Z = Benzyloxycarbonyl. AMC = 7-Amino-4-Methyl-Coumarin.
DTT = dithiothreitol.
Final volume: 100 μΐ^.
Excitation 360 nm, Emission 465 nm.
Enzyme is added to the substance dilutions in 96-well microtitre plates and the reaction is started with substrate. Fluorescence emission is measured over 20 minutes, during which time a linear increase is observed in the absence of inhibitor. IC50 are calculated by standard methods.
Inhibition of human Cat S, mouse Cat S, human Cat K, human Cat B, human Cat L and mouse Cat L have been measured separately. The results obtained for human Cat S for representative compounds of the invention are expressed in the following table in μΜ. Example ICso Example ICso
1 0.000968 36 0.002597
2 0.00077 37 0.001894
3 0.001018 38 0.003208
4 0.000978 39 0.000483
5 0.000836 40 0.001208
6 0.001062 41 0.00086
7 0.00091 42 0.001458
8 0.000533 43 0.003572
9 0.000683 44 0.00051
10 0.000686 45 0.00107
11 0.012625 46 0.000752
12 0.00056 47 0.000349
13 0.000568 48 0.001167
14 0.000529 49 0.000909
15 0.00061 50 0.000728
16 0.000563 51 0.000882
17 0.000704 52 0.000486
18 0.00098 53 0.000506
19 0.001431 54 0.000382
20 0.005716 55 0.001436
21 0.001071 56 0.000526
22 0.001136 57 0.000564
23 0.001123 58 0.002421
24 0.000772 59 0.000943
25 0.00327 60 0.000614
26 0.000391 61 0.000613
27 0.000558 62 0.000592
28 0.00233 63 0.000585
29 0.000811 64 0.00065
30 0.000625 65 0.000584
31 0.00054 66 0.2227
32 0.000955 67 0.54225
33 0.001568 68 0.000829
34 0.001062 69 0.49675 35 0.00102
The compounds of the invention are preferential inhibitors of Cathepsin-S over Cathepsin- L, K and B.
The compounds according to the invention have, in the foregoing assay, an IC50 at Cat S which is between 0.00001 and 100 μΜ, in particular between 0.00001 and 50 μΜ, more particularly between 0.00001 and 20 μΜ. The particular compounds of the invention have an IC50 in the foregoing assay below 0.09 μΜ.
Example A
Film coated tablets containing the following ingredients can be manufactured in a conventional manner:
Ingredients Per tablet
Kernel:
Compound of formula (I) 10.0 mg 200.0 mg
Microcrystalline cellulose 23.5 mg 43.5 mg
Lactose hydrous 60.0 mg 70.0 mg
Povidone K30 12.5 mg 15.0 mg
Sodium starch glycolate 12.5 mg 17.0 mg
Magnesium stearate 1.5 mg 4.5 mg
(Kernel Weight) 120.0 mg 350.0 mg
Film Coat:
Hydroxypropyl methyl cellulose 3.5 mg 7.0 mg
Polyethylene glycol 6000 0.8 mg 1.6 mg
Talc 1.3 mg 2.6 mg Iron oxide (yellow) 0.8 mg 1.6 mg
Titan dioxide 0.8 mg 1.6 mg
The active ingredient is sieved and mixed with microcrystalline cellulose and the mixture is granulated with a solution of polyvinylpyrrolidone in water. The granulate is then mixed with sodium starch glycolate and magnesium stearate and compressed to yield kernels of 120 or 350 mg respectively. The kernels are lacquered with an aq. solution / suspension of the above mentioned film coat.
Example B
Capsules containing the following ingredients can be manufactured in a conventional manner:
Figure imgf000076_0001
The components are sieved and mixed and filled into capsules of size 2.
Example C
Injection solutions can have the following composition:
Compound of formula (I) 3.0 mg
Polyethylene glycol 400 150.0 mg
Acetic acid q.s. ad pH 5.0
Water for injection solutions ad 1.0 ml The active ingredient is dissolved in a mixture of Polyethylene glycol 400 and water for injection (part). The pH is adjusted to 5.0 by addition of acetic acid. The volume is adjusted to 1.0 ml by addition of the residual amount of water. The solution is filtered, filled into vials using an appropriate overage and sterilized.

Claims

A compound of formula (I)
Figure imgf000078_0001
wherein
R1 is hydrogen, alkyl, haloalkyl, halogen or triazolyl; and
R is (halo)(oxy)pyridinyl, (alkyl) (oxy)pyridinyl, (alkyl) (haloalkyl)pyrazolyl,
haloalkoxyphenyl, alkoxyphenyl, cycloalkyloxyphenyl, cycloalkyloxy, alkyltetrazolyl, triazolyl, alkyltriazolyl, dialkyltriazolyl, halotriazolyl, haloalkylpyrazolyl, formylphenyl, aminopyrimidinyl, cyanophenyl,
(alkoxy)(dihalo)phenyl, hydroxyalkylphenyl, benzo[l,3]dioxolyl,
dialkylthiazolyl, alkylthiazolyl, alkoxypyrimidinyl, dialkylisoxazolyl or (halo)(haloalkyl)triazolyl; or a pharmaceutically acceptable salt or ester thereof.
A compound according to claim 1, wherein R1 is alkyl, haloalkyl or halogen.
A compound according to claim 1 or 2, wherein R1 is methyl, trifluoromethyl or chlorine.
A compound according to any one of claims 1 to 3, wherein R is
(alkyl) (haloalkyl)pyrazolyl, alkyltetrazolyl, triazolyl, alkyltriazolyl, dialkyltriazolyl, halotriazolyl, haloalkylpyrazolyl, dialkylthiazolyl, alkylthiazolyl or dialkylisoxazolyl.
A compound according to any one of claims 1 to 4, wherein R is
(methyl) (trifluoromethyl)pyrazolyl, methyltetrazolyl, triazolyl, methyltriazolyl, dimethyltriazolyl, chlorotnazolyl, trifluoromethylpyrazolyl, difluoromethylpyrazolyl, dimethylthiazolyl, methylthiazolyl or dimethylisoxazolyl.
A compound according to any one of claims 1 to 5 selected from
(2S ,4R)-4- [4- (2-Chloro- 1 -oxy-pyridin-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S ,4R)-4- [4- (2-Methyl- 1 -oxy-pyridin-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(2-Methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S,4R)-4-(2'-Trifluoromethoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(2'-Ethoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide;
(2S,4R)-4-(2'-Cyclopropoxy-3-trifluoromethyl-biphenyl-4-sulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(4-Cyclobutoxy-2-trifluoromethyl-benzenesulfonyl)-l-(l-trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide;
(2S,4R)-4-(2-chloro-4-(5-methyl-2H-tetrazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-tetrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide; (2S,4R)-N-( 1 -cyanocyclopropyl)-4-(2,4-di( 1H- 1 ,2,4-triazol- 1 -yl)phenylsulfonyl)- 1 - (l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2-chloro-4-(2H-l,2,3-triazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(lH-l,2,3-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3,5-dimethyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-(trifluoromethyl)-lH-pyrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trifhioromethyl)
cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(trif uoromethoxy)biphenyl-4-ylsulfonyl)-l- (l-(trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2-chloro-4-cyclobutoxyphenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 - (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide; (2S,4R)-N-(l-cyanocyclopropyl)-4-(3-methyl-2'-(trifluoromethoxy)biphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-[4-(5-Methyl-3-trifluoromethyl-pyrazol-l-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(4-( 1H- 1 ,2,4-triazol- l-yl)-2-(trifluoromethyl)phenylsulfonyl)-N-( 1- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide
(2S ,4R)-4- [4- (3 ,5-Dimethyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 -( 1 -trif uoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(l-methyl-3-(trifluoromethyl)-lH-pyrazol-5- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-formyl-3-methylbiphenyl-4-ylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S ,4R)-4- [4- (3-Chloro- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-lH-l,2,4-triazol-l-yl)-2- (trif uoromethyl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)
cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(l-methyl-3-(trifluoromethyl)-lH- pyrazol-5-yl)phenylsulfonyl)- 1 -( 1 -(trif uoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide; (2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethyl-lH-l,2,4-triazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-( 1H- 1 ,2,3-triazol- 1 -yl)phenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 - ( 1 - (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S ,4R)-N- ( 1 -cyanocyclopropyl) -4- (4- (3 - (trifluoromethyl) - 1 H-pyrazol- 1 - yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-formylbiphenyl-4-ylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxybiphenyl-4-ylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(4-(2-aminopyrimidin-5-yl)phenylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxy-3-methylbiphenyl-4-ylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2'-cyano-3-methylbiphenyl-4-ylsulfonyl)-N-(l-cyanocyclopropyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-ethoxy-4',5'-difluoro-3-methylbiphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(hydroxymethyl)biphenyl-4-ylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(4-(2-aminopyrimidin-5-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(2,2-Dif uoro-benzo[l,3]dioxol-5-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide; (2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(4- trifluoromethyl-pyrazol- 1 -yl)-benzenesulfonyl] -pyrrolidine-2-carboxylic acid ( 1 - cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (5-Methyl-tetrazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(2,4-Dimethyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)phenylsulfonyl)-l- (l-(trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methylthiazol-5-yl)phenylsulfonyl)-l-(l- (trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methoxypyrimidin-5-yl)phenylsulfonyl)-l- (l-(trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-[l,2,3]Triazol-2-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(4-[l,2,3]Triazol-l-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)phenylsulfonyl)-l- (l-(trif uoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-4-[4-(l-Difluoromethyl-lH-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide; (2S ,4R)-4- [4- (5-Methyl-tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(3- trifluoromethyl- lH-pyrazol-4-yl)-benzenesulfonyl]-pyrrolidine-2-carboxylic acid (1- cyano-cyclopropyl)-amide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2'-(hydroxymethyl)-3-methylbiphenyl-4- ylsulfonyl)-l-(l-(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(2-methylthiazol-5- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2-methoxypyrimidin-5-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(2-Methyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-Tetrazol- 1 -yl-2-trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide;
(2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2R,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide; (2S,4R)-4-[4-(l-Methyl-3-trifluoromethyl-lH-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide; and
(2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide.
A compound according to any one of claims 1 to 6 selected from
(2S,4R)-4-[4-(2-Methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S,4R)-4-(2-chloro-4-(5-methyl-2H-tetrazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-tetrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(2H-l,2,3-triazol-2-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(lH-l,2,3-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3,5-dimethyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide; (2S,4R)-4-(2-chloro-4-(3-chloro-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(3-(trifluoromethyl)-lH-pyrazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(2-chloro-4-(5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulfonyl)-N-( 1 -cyanocyclopropyl)- 1 -( 1 -(trif uoromethyl)
cyclopropanecarbonyl)pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(3-(trifluoromethyl)-lH-pyrazol-l- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(5-Methyl-3-trifluoromethyl-pyrazol -yl)-2-trif uoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ;
(2S ,4R)-4- [4- (3-Methyl- [ 1 ,2,4] triazol-4-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ;
(2S,4R)-4-(4-( 1H- 1 ,2,4-triazol- l-yl)-2-(trifluoromethyl)phenylsulfonyl)-N-( 1- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S ,4R)-4- [4- (3 ,5-Dimethyl- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 -( 1 -trif uoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ;
(2S ,4R)-4- [4- (3-Chloro- [ 1 ,2,4] triazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyanocyclopropyl)- amide ; (2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(5-methyl-lH-l,2,4-triazol-l-yl)-2- (trifluoromethyl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(l-methyl-3-(trifluoromethyl)-lH- pyrazol-5-yl)phenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl) pyrrolidine-2-carboxamide;
(2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(4- trifluoromethyl-pyrazol- 1 -yl)-benzenesulfonyl] -pyrrolidine-2-carboxylic acid ( 1 - cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (5-Methyl-tetrazol- 1 -yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(2,4-Dimethyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(2-chloro-4-(5-methyl-lH-l,2,4-triazol-l-yl)phenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-[l,2,3]Triazol-2-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-(4-[l,2,3]Triazol-l-yl-2-trifluoromethyl-benzenesulfonyl)-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-4-[4-(l-Difluoromethyl-lH-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide;
(2S ,4R)-4- [4- (5-Methyl-tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 - ( 1 - trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ; (2S,4R)-l-(l-Trifluoromethyl-cyclopropanecarbonyl)-4-[2-trifluoromethyl-4-(3- trifluoromethyl- lH-pyrazol-4-yl)-benzenesulfonyl]-pyrrolidine-2-carboxylic acid (1- cyano-cyclopropyl)-amide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(2,4-dimethylthiazol-5-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(2-methyl-4-(2-methylthiazol-5- yl)phenylsulf onyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-[4-(2-Methyl-thiazol-5-yl)-2-trifluoromethyl-benzenesulfonyl]-l-(l- trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano- cyclopropyl)- amide ;
(2S,4R)-N-(l-cyanocyclopropyl)-4-(4-(3,5-dimethylisoxazol-4-yl)-2- methylphenylsulfonyl)- 1 -( 1 -(trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2S,4R)-4-(4-Tetrazol- 1 -yl-2-trifluoromethyl-benzenesulfonyl)- 1 -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide;
(2S,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide;
(2R,4R)-4-(4-(3-chloro-lH-l,2,4-triazol-l-yl)-2-methylphenylsulfonyl)-N-(l- cyanocyclopropyl)- 1 - ( 1 - (trifluoromethyl)cyclopropanecarbonyl)pyrrolidine-2- carboxamide; and
(2S,4R)-4-[4-(l-Methyl-3-trifluoromethyl-lH-pyrazol-4-yl)-2-trifluoromethyl- benzenesulfonyl] - 1 -( 1 -trifluoromethyl-cyclopropanecarbonyl)-pyrrolidine-2- carboxylic acid (l-cyano-cyclopropyl)-amide.
A compound according to any one of claims 1 to 7 which is (2S,4R)-4-[4-(5-Methyl- tetrazol-2-yl)-2-trifluoromethyl-benzenesulfonyl] - 1 -( 1 -trifluoromethyl- cyclopropanecarbonyl)-pyrrolidine-2-carboxylic acid ( 1 -cyano-cyclopropyl)-amide.
9. A process for the manufacture of a compound according to any one of claims 1 to 8 comprising: (a) The reaction of a compound of formula (A)
Figure imgf000089_0001
in the presence of a compound of formula R2-LG 2 wherein R 1 and R2 are as defined in any one of claims 1 to 6 and wherein LG1 is F, CI, Br, I, B(OH)2 or B(OR3)2, LG2 is H, B(OH)2, B(OR 3 )2, Br or I and each R 3 is independently selected from methyl, ethyl and both R together with the oxygen and boron atoms to which they are attached form an organoboron ring; or
(b) The reaction of a compound of formula (B)
Figure imgf000089_0002
in the presence of an oxidation reaction, wherein R is as defined in any one of claims 1 to 6 and R4 is halogen or alkyl.
10. A compound according to any one of claims 1 to 8, when manufactured according to a process of claim 9.
11. A compound according to any one of claims 1 to 8 for use as therapeutically active substance. 12. A pharmaceutical composition comprising a compound in accordance with any one of claims 1 to 8 and a therapeutically inert carrier.
13. The use of a compound according to any one of claims 1 to 8 for the preparation of medicaments for the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic rethinopathy or age related macular degeneration.
14. A compound according to any one of claims 1 to 8 for use in the treatment or
prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic rethinopathy or age related macular degeneration.
15. A method for the treatment or prophylaxis of diabetes, atherosclerosis, abdominal aortic aneurysm, peripheral arterial disease, cancer, reduction of cardiovascular events in chronic kidney disease, diabetic nephropathy, diabetic rethinopathy or age related macular degeneration, which method comprises administering an effective amount of a compound as defined in any one of claims 1 to 8 to a patient in need thereof.
16. The invention as hereinbefore described.
***
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018139438A1 (en) 2017-01-24 2018-08-02 アステラス製薬株式会社 Phenyldifluoromethyl-substituted prolineamide compound
WO2020058297A1 (en) 2018-09-18 2020-03-26 F. Hoffmann-La Roche Ag Use of a cathepsin s inhibitor against the formation of anti-drug antibodies

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010121918A1 (en) * 2009-04-20 2010-10-28 F. Hoffmann-La Roche Ag Proline derivatives as cathepsin inhibitors
WO2013068434A1 (en) * 2011-11-11 2013-05-16 F. Hoffmann-La Roche Ag Process for the preparation of 1-acyl-4-phenylsulfonylprolinamide derivatives and new intermediates

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8729061B2 (en) * 2011-11-25 2014-05-20 Hoffmann-La Roche Inc. Pyrrolidine derivatives
CN104114068B (en) * 2011-12-09 2017-07-11 W.C.布拉德利公司 Cooking grate with adjustable Heating Characteristics
EP2814822B1 (en) * 2012-02-17 2016-04-20 F.Hoffmann-La Roche Ag Novel pyrrolidine derivatives
PE20150995A1 (en) * 2012-08-21 2015-06-29 Hoffmann La Roche NEW PYRIDINE DERIVATIVES

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010121918A1 (en) * 2009-04-20 2010-10-28 F. Hoffmann-La Roche Ag Proline derivatives as cathepsin inhibitors
WO2013068434A1 (en) * 2011-11-11 2013-05-16 F. Hoffmann-La Roche Ag Process for the preparation of 1-acyl-4-phenylsulfonylprolinamide derivatives and new intermediates

Non-Patent Citations (23)

* Cited by examiner, † Cited by third party
Title
AIKAWA, E. ET AL.: "Arterial and aortic valve calcification abolished by elastolytic cathepsin S deficiency in chronic renal disease", CIRCULATION, vol. 119, no. 13, 2009, pages 1785 - 94
ANSEL, HOWARD C. ET AL.: "Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems", 2004, LIPPINCOTT, WILLIAMS & WILKINS
BROMME, D.: "Curr Protoc Protein Sci", 2001, article "Papain-like cysteine proteases"
BURNS-KURTIS, C. L. ET AL.: "Cathepsin S expression is up-regulated following balloon angioplasty in the hypercholesterolemic rabbit", CARDIOVASC RES, vol. 62, no. 3, 2004, pages 610 - 20
CHENG, X. W. ET AL.: "Increased expression of elastolytic cysteine proteases, cathepsins S and K, in the neointima of balloon-injured rat carotid arteries", AM J PATHOL, vol. 164, no. 1, 2004, pages 243 - 51, XP008119922
DE NOOIJER, R. ET AL.: "Leukocyte cathepsin S is a potent regulator of both cell and matrix turnover in advanced atherosclerosis", ARTERIOSCLER THROMB VASC BIOL, vol. 29, no. 2, 2009, pages 188 - 94
DRIESSEN, C. ET AL.: "Cathepsin S controls the trafficking and maturation of MHC class ? molecules in dendritic cells", J CELL BIOL, vol. 147, no. 4, 1999, pages 775 - 90
ELENA AIKAWA, CIRCULATION, 2009, pages 1785 - 1794
GENNARO, ALFONSO R. ET AL.: "Remington: The Science and Practice of Pharmacy", 2000, LIPPINCOTT, WILLIAMS & WILKINS
HANS HILPERT ET AL: "Identification of Potent and Selective Cathepsin S Inhibitors Containing Different Central Cyclic Scaffolds", JOURNAL OF MEDICINAL CHEMISTRY, vol. 56, no. 23, 12 December 2013 (2013-12-12), pages 9789 - 9801, XP055212296, ISSN: 0022-2623, DOI: 10.1021/jm401528k *
HSING, L. C.; RUDENSKY, A. Y.: "The lysosomal cysteine proteases in MHC class ? antigen presentation", IMMUNOL REV, vol. 207, 2005, pages 229 - 41
LIU, J. ET AL.: "Increased serum cathepsin S in patients with atherosclerosis and diabetes", ATHEROSCLEROSIS, vol. 186, no. 2, 2006, pages 411 - 9, XP028071394, DOI: doi:10.1016/j.atherosclerosis.2005.08.001
ROBERTA E., BURDEN IN CLIN CANCER RES, vol. 15, no. 19, 2009
ROBERTS, R.: "Lysosomal cysteine proteases: structure, function and inhibition of cathepsins", DRUG NEWS PERSPECT, vol. 18, no. 10, 2005, pages 605 - 14
RODGERS, K. J. ET AL.: "Destabilizing role of cathepsin S in murine atherosclerotic plaques", ARTERIOSCLER THROMB VASC BIOL, vol. 26, no. 4, 2006, pages 851 - 6
ROWE, RAYMOND C.: "Handbook of Pharmaceutical Excipients", 2005, PHARMACEUTICAL PRESS
RUDENSKY, A.; BEERS, C.: "Lysosomal cysteine proteases and antigen presentation", ERNST SCHERING RES FOUND WORKSHOP, 2006, pages 81 - 95
SHI, G. P. ET AL.: "Deficiency of the cysteine protease cathepsin S impairs microvessel growth", CIRC RES, vol. 92, no. 5, 2003, pages 493 - 500, XP002624035, DOI: doi:10.1161/01.RES.0000060485.20318.96
SUKHOVA, G. K. ET AL.: "Deficiency of cathepsin S reduces atherosclerosis in LDL receptor-deficient mice", J CLIN INVEST, vol. 111, no. 6, 2003, pages 897 - 906
SUKHOVA, G. K. ET AL.: "Expression of the elastolytic cathepsins S and K in human atheroma and regulation of their production in smooth muscle cells", J CLIN INVEST, vol. 102, no. 3, 1998, pages 576 - 83, XP008119923, DOI: doi:10.1172/JCI181
T. W. GREENE; P. G. M. WUTS: "Protective Groups in Organic Chemistry", 1999, WILEY
WANG, B. ET AL.: "Cathepsin S controls angiogenesis and tumor growth via matrix-derived angiogenic factors", J BIOL CHEM, vol. 281, no. 9, 2006, pages 6020 - 9, XP055419964, DOI: doi:10.1074/jbc.M509134200
WILLIAMS, A. S. ET AL.: "Role of cathepsin S in ozone-induced airway hyperresponsiveness and inflammation", PULM PHARMACOL THER, vol. 22, no. 1, 2009, pages 27 - 32, XP025882994, DOI: doi:10.1016/j.pupt.2008.11.002

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018139438A1 (en) 2017-01-24 2018-08-02 アステラス製薬株式会社 Phenyldifluoromethyl-substituted prolineamide compound
US10322997B2 (en) 2017-01-24 2019-06-18 Astellas Pharma Inc. Phenyldifluoromethyl-substituted prolinamide compound
KR20190110549A (en) 2017-01-24 2019-09-30 아스테라스 세이야쿠 가부시키가이샤 Phenyldifluoromethyl substituted prolineamide compounds
US10532979B2 (en) 2017-01-24 2020-01-14 Astellas Pharma Inc. Phenyldifluoromethyl-substituted prolinamide compound
WO2020058297A1 (en) 2018-09-18 2020-03-26 F. Hoffmann-La Roche Ag Use of a cathepsin s inhibitor against the formation of anti-drug antibodies
CN112839716A (en) * 2018-09-18 2021-05-25 豪夫迈·罗氏有限公司 Use of cathepsin S inhibitors to combat formation of anti-drug antibodies
JP7438198B2 (en) 2018-09-18 2024-02-26 エフ． ホフマン－ラ ロシュ アーゲー Use of cathepsin S inhibitors for the formation of anti-drug antibodies

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