DK3097086T3 - (2s)-n-[(1s)-1-cyan-2-phenylethyl]-1,4-oxazepan-2-carboxamider som dipeptidyl-peptidase i-hæmmere - Google Patents
(2s)-n-[(1s)-1-cyan-2-phenylethyl]-1,4-oxazepan-2-carboxamider som dipeptidyl-peptidase i-hæmmere Download PDFInfo
- Publication number
- DK3097086T3 DK3097086T3 DK15701577.7T DK15701577T DK3097086T3 DK 3097086 T3 DK3097086 T3 DK 3097086T3 DK 15701577 T DK15701577 T DK 15701577T DK 3097086 T3 DK3097086 T3 DK 3097086T3
- Authority
- DK
- Denmark
- Prior art keywords
- carboxamide
- ethyl
- phenyl
- oxazepan
- oxo
- Prior art date
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- KOUKXHPPRFNWPP-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid;hydrate Chemical compound O.OC(=O)C1=CN=C(C(O)=O)C=N1 KOUKXHPPRFNWPP-UHFFFAOYSA-N 0.000 description 1
- OAWXZFGKDDFTGS-UHFFFAOYSA-N pyrrolidine-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCN1C(O)=O OAWXZFGKDDFTGS-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 229950000099 quiflapon Drugs 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 229940016667 resveratrol Drugs 0.000 description 1
- 235000021283 resveratrol Nutrition 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- MNDBXUUTURYVHR-UHFFFAOYSA-N roflumilast Chemical compound FC(F)OC1=CC=C(C(=O)NC=2C(=CN=CC=2Cl)Cl)C=C1OCC1CC1 MNDBXUUTURYVHR-UHFFFAOYSA-N 0.000 description 1
- 229960002586 roflumilast Drugs 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 229950005149 setileuton Drugs 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004467 single crystal X-ray diffraction Methods 0.000 description 1
- 238000011172 small scale experimental method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000000371 solid-state nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 239000000600 sorbitol Chemical class 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 238000012306 spectroscopic technique Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- VNFWTIYUKDMAOP-UHFFFAOYSA-N sphos Chemical compound COC1=CC=CC(OC)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 VNFWTIYUKDMAOP-UHFFFAOYSA-N 0.000 description 1
- 210000000952 spleen Anatomy 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 239000008174 sterile solution Substances 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- RVUXIPACAZKWHU-UHFFFAOYSA-N sulfuric acid;heptahydrate Chemical compound O.O.O.O.O.O.O.OS(O)(=O)=O RVUXIPACAZKWHU-UHFFFAOYSA-N 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- WWEHDKRKJBWHOJ-UPVQGACJSA-N tert-butyl (2S)-2-[[(1S)-1-cyano-2-[4-(3-methylsulfonyloxyphenyl)phenyl]ethyl]carbamoyl]-1,4-oxazepane-4-carboxylate Chemical compound C(C)(C)(C)OC(=O)N1C[C@H](OCCC1)C(N[C@@H](CC1=CC=C(C=C1)C1=CC(=CC=C1)OS(=O)(=O)C)C#N)=O WWEHDKRKJBWHOJ-UPVQGACJSA-N 0.000 description 1
- SLESCLGEYKTZJO-ZEQRLZLVSA-N tert-butyl (2S)-2-[[(1S)-1-cyano-2-[4-(4-cyanophenyl)phenyl]ethyl]carbamoyl]-1,4-oxazepane-4-carboxylate Chemical compound C(C)(C)(C)OC(=O)N1C[C@H](OCCC1)C(N[C@@H](CC1=CC=C(C=C1)C1=CC=C(C=C1)C#N)C#N)=O SLESCLGEYKTZJO-ZEQRLZLVSA-N 0.000 description 1
- WBAQNCJUTMXJTK-VIFPVBQESA-N tert-butyl (2s)-2-(hydroxymethyl)-1,4-oxazepane-4-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCO[C@H](CO)C1 WBAQNCJUTMXJTK-VIFPVBQESA-N 0.000 description 1
- KDGKGIAEBNAZCD-XJDOXCRVSA-N tert-butyl 2-[[(2S)-1-amino-1-oxo-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propan-2-yl]carbamoyl]-1,4-oxazepane-4-carboxylate Chemical compound NC([C@H](CC1=CC=C(C=C1)B1OC(C(O1)(C)C)(C)C)NC(=O)C1OCCCN(C1)C(=O)OC(C)(C)C)=O KDGKGIAEBNAZCD-XJDOXCRVSA-N 0.000 description 1
- FGLIDWYLHHPLPF-NSHDSACASA-N tert-butyl n-[(2s)-1-amino-3-(4-iodophenyl)-1-oxopropan-2-yl]carbamate Chemical compound CC(C)(C)OC(=O)N[C@H](C(N)=O)CC1=CC=C(I)C=C1 FGLIDWYLHHPLPF-NSHDSACASA-N 0.000 description 1
- 229950002896 tetomilast Drugs 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000003970 toll like receptor agonist Substances 0.000 description 1
- 229940044616 toll-like receptor 7 agonist Drugs 0.000 description 1
- 229940044655 toll-like receptor 9 agonist Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 229960005294 triamcinolone Drugs 0.000 description 1
- GFNANZIMVAIWHM-OBYCQNJPSA-N triamcinolone Chemical compound O=C1C=C[C@]2(C)[C@@]3(F)[C@@H](O)C[C@](C)([C@@]([C@H](O)C4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 GFNANZIMVAIWHM-OBYCQNJPSA-N 0.000 description 1
- YNDXUCZADRHECN-JNQJZLCISA-N triamcinolone acetonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(F)[C@@H]1[C@@H]1C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O YNDXUCZADRHECN-JNQJZLCISA-N 0.000 description 1
- 229960002117 triamcinolone acetonide Drugs 0.000 description 1
- 125000005500 uronium group Chemical group 0.000 description 1
- 210000005166 vasculature Anatomy 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 229950008314 veliflapon Drugs 0.000 description 1
- 229950009860 vicriviroc Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 229960004764 zafirlukast Drugs 0.000 description 1
- MWLSOWXNZPKENC-SSDOTTSWSA-N zileuton Chemical compound C1=CC=C2SC([C@H](N(O)C(N)=O)C)=CC2=C1 MWLSOWXNZPKENC-SSDOTTSWSA-N 0.000 description 1
- 229960005332 zileuton Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/02—Seven-membered rings
- C07D267/08—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D267/10—Seven-membered rings having the hetero atoms in positions 1 and 4 not condensed with other rings
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/553—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/14—Antitussive agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A61P31/06—Antibacterial agents for tuberculosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—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
- C07D417/02—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
- 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
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- Hydrogenated Pyridines (AREA)
Claims (11)
1. Forbindelse med formlen (I) hvor
R1 e
R2 er udvalgt fra hydrogen, F, Cl, Br, OSO2C1-3-alkyl, eller Ci-3-alkyl; R3 er udvalgt fra hydrogen, F, Cl, Br, CN, CF3, SC>2Ci-3-alkyl, CONH2 eller S02NR4R5, hvor R4 og R5 sammen med det nitrogenatom, hvortil de er bundet, danner en azetidin-, pyrrolidin- eller piperidinring; eller R1 er udvalgt fra
X er udvalgt fra O, S eller CF2; Y er udvalgt fra O eller S; Q er udvalgt fra CH eller N; R6 er udvalgt fra Ci-3-alkyl, hvor Ci-3-alkyl eventuelt er substitueret med 1, 2 eller 3 F og eventuelt med én substituent udvalgt fra OH, OCi-3-alkyl, N(Ci-3-alkyl)2, cyclopropyl eller tetrahydropyran; R7 er udvalgt fra hydrogen, F, Cl eller CH3; eller et farmaceutisk acceptabelt salt deraf.
2. Forbindelse ifølge krav 1, hvor R1 er
eller et farmaceutisk acceptabelt salt deraf.
3. Forbindelse ifølge enten krav 1 eller krav 2, hvor X er O; R6 er C i-3-alkyl; og R7 er hydrogen; eller et farmaceutisk acceptabelt salt deraf.
4. Forbindelse med formlen (I) ifølge krav, der er udvalgt fra: (25)-/Y-[(15)-1 -cyan-2-(4'-cyanobiphcnyl-4-yl)cthyl]-l,4-oxazepan-2-carboxamid; (2S)-N- j( 15)-1-cyan-2-[4-(3-methyl-2-oxo-2,3-dihydro-l ,3-bcnzoxazol-5-yl)phcnyl Jethyl}-1,4 -oxazepan-2-carboxamid; (25)-iV-{( 15)-1-cyan-2-[4-(3,7-dimcthyl-2-oxo-2,3-dihydro-1 ,3-benzoxazol-5-yl)phcnyl]ethyl} -1,4-oxazepan-2-carboxamid; 4'-[(25)-2-cyan-2-{[(25)-l,4-oxazepan-2-ylcarbonyl]amino}ethyl]biphenyl-3-yl methansulfonat; (2S)-N- {(15)-1 -cyan-2-[4-(3-methyl-l ,2-benzoxazol-5-yl)phenyl]ethyl} -1,4-oxazepan-2-carbo xamid; (:2S)-N- {(1 S)-1 -cyan-2-[4'-(trifluormethyl)biphenyl-4-yl]ethyl} -1,4-oxazepan-2-carboxamid; (25)-/V-[(15)-l-cyan-2-(3',4'-difluorbiphenyl-4-yl)ethyl]-l,4-oxazepan-2-carboxamid; (2 S)-N- {(15)-1 -cyan-2-[4-(6-cyanopyridin-3-yl)phenyl]ethyl} -1,4-oxazepan-2-carboxamid; (25)-/V-{(15)-l-cyan-2-[4-(4-mcthyl-3-oxo-3,4-dihydro-2//-l,4-benzothiazin-6-yl)phenyl]ethyl } -1,4-oxazepan-2-carboxamid; (25)-/V-{(15)-l-cyan-2-[4-(3-cthyl-7-mcthyl-2-oxo-2,3-dihydro-l,3-benzoxazol-5-yl)phenyl]et hyl} -1,4-oxazepan-2-carboxamid; (25)-A'-[(15)-1 -cyan-2- (4-[3-(2-hydroxy-2-methylpropyl)-2-oxo-2,3-dihydro-1,3-benzoxazol-5 -yljphenyl} ethyl]-1,4-oxazepan-2-carboxamid; (25)-jV-[(15)-l-cyan-2-{4-[3-(2,2-difluorethyl)-7-fluor-2-oxo-2,3-dihydro-l,3-benzoxazol-5-yl] phenyl} ethyl]-l ,4-oxazepan-2-carboxamid; (25)-/Y-[( 1 5)-1 -cyan-2-(4- {3-[2-(dimethylamino)ethyl]-2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl }phenyl)ethyl]-1,4-oxazepan-2-carboxamid; (2 S)-N- {(15)-1 -cyan-2-[4-(3,3-difluor-1 -methyl-2-oxo-2,3-dihydro-1 /7-indol-6-yl)phcnyl]cthyl } -1,4-oxazepan-2-carboxamid; (2S)-N- {(1 S)-1 -cyan-2-[4-(7-fluor-3-methyl-2-oxo-2,3-dihydro-l ,3-bcnzoxazol-5-yl)phcnyl]ct hyl} -1,4-oxazepan-2-carboxamid; (25)-iV-{(15)-l-cyan-2-[4-(3-ethyl-2-oxo-2,3-dihydro-l,3-benzoxazol-5-yl)phenyl]ethyl}-l,4-o xazepan-2-carboxamid; (25)-iV-[(15)-l-cyan-2-{4-[3-(cyclopropylmethyl)-2-oxo-2,3-dihydro-l,3-benzoxazol-5-yl]phe nyl} ethyl] -1,4-oxazepan-2-carboxamid; (25)-7V-[(15)-1 -cyan-2- {4-[3-(2-methoxyethyl)-2-oxo-2,3-dihydro-1,3-benzothiazol-5-yl]pheny 1} ethyl] -1,4-oxazepan-2-carboxamid; (25)-iV-[(15)-1-cyan-2-{4-[2-oxo-3-(propan-2-yl)-2,3-dihydro-1,3-benzoxazol-5-yl]phenyl} eth yl]-1,4-oxazepan-2-carboxamid; (25)-.V-{( 15)-1-cyan-2-[4-(4-methyl-3-oxo-3,4-dihydro-2//-l,4-benzoxazin-6-yl)phenyl]ethyl} -1,4-oxazepan-2-carboxamid; (25)-7V-[(l 5)-1 -cyan-2-{4-[3-(2-mcthoxycthyl)-2-oxo-2,3-dihydro-l ,3-benzoxazol-5-yl]phcnyl } ethyl] -1,4-oxazepan-2-carboxamid; (25)-77- i (1 S)-1 -cyan-2-[4-(5-cyanothiophcn-2-yl)phcnyl]cthyl} -1,4-oxazepan-2-carboxamid; (25)-7V-[(15)-2-(4'-carbamoyl-3'-fluorbiphcnyl-4-yl)-l -cyanocthyl]-l,4-oxazepan-2-carboxami d; (2 S)-N- {(15)-1 -cyan-2-[4-(l -methyl-2-oxo-1,2-dihydroquinolin-7-yl)phenyl] ethyl} -1,4-oxazep an-2-carboxamid; (25)-7V-[(15)-1 -cyan-2- {4-[2-oxo-3-(tctrahydro-2//-pyran-4-ylmcthyl)-2,3-dihydro-1,3-benzox azol-5-yl]phenyl}ethyl]-l,4-oxazepan-2-carboxamid; (25)-.V-{(15)-2-[4-(7-chlor-3-methyl-2-oxo-2,3-dihydro-l ,3-bcnzoxazol-5-yl)phcnyl]-l-cyanoc thyl} -1,4-oxazepan-2-carboxamid; (25)-.V-[( 15)-1 -cyan-2- {4-[3-(2,2-difluorethyl)-2-oxo-2,3-dihydro-1,3-benzoxazol-5-yl]phenyl } ethyl] -1,4-oxazepan-2-carboxamid; (25)-.V-[( 15)-1 -cyan-2- {4-[2-oxo-3-(2,2,2-trifluorethyl)-2,3-dihydro-1,3-benzoxazol-5-yl]phen yl} ethyl] -1,4-oxazepan-2-carboxamid; (25)-/V-{( 15)-l-cyan-2-[4-(3-methyl-2-oxo-2,3-dihydro-l ,3-bcnzothiazol-5-yl)phcnyl]cthyl}-l, 4-oxazepan-2-carboxamid; (25)-A-{(15)-1 -cyan-2-[4'-(mcthylsulfonyl)bi phenyl-4-yl]ethyl}-l,4-oxazcpan-2-carboxam id; (2S)-N-{( 15)-2-[4'-(azetidin-1 -ylsulfonyl)biphcnyl-4-yl]-1 -cyanoethyl } -1,4-oxazcpan-2-carbox amid; (25)-7V-[( 1 S)-1 -cyan-2-(4'-fluorbiphcnyl-4-yl)cthyl]- l,4-oxazepan-2-carboxamid; (25)-./V-{(15)-2-[4-(l,3-benzothiazol-5-yl)phenyl]-l-cyanoethyl}-l,4-oxazepan-2-carboxamid; (25)-/V-[( 1 S)-1 -cyan-2-(4'-cyanbiphcnyl-4-yl)cthyl]-1,4-oxazcpan-2-carboxamid og farmaceutisk acceptable salte deraf.
5. Forbindelse ifølge krav 1, der er (25)-vV-{(15)-l-cyan-2-[4-(3-methyl-2-oxo-2,3-dihydro-l,3-benzoxazol-5-yl)phenyl]ethyl}-l,4 -oxazepan-2-carboxamid
eller et farmaceutisk acceptabelt salt deraf.
6. Forbindelse ifølge krav 1, der er (25)-/V-{(15)-l-cyan-2-[4-(3-mcthyl-2-oxo-2,3-dihydro-l,3-benzoxazol-5-yl)phenyl]ethyl}-l,4 -oxazepan-2-carboxamid
7. Farmaceutisk sammensætning, der omfatter en forbindelse med formlen (I) ifølge et hvilket som helst af kravene 1 til 6 og et farmaceutisk acceptabelt adjuvans, fortyndingsmiddel eller bærestof.
8. Forbindelse med formlen (I) ifølge et hvilket som helst af kravene 1 til 6 til anvendelse i terapi.
9. Forbindelse med formlen (I) ifølge et hvilket som helst af kravene 1 til 6, til anvendelse i behandling af obstruktive luftvejssygdomme: herunder en hvilken som helst af astma, der indbefatter bronkial, allergisk, intrinsisk, ekstrinsisk, anstrengelsesinduceret, lægemiddelinduceret (herunder aspirin- og NSAID-induceret) og støvinduceret astma, begge intermitterende og vedvarende og af enhver alvorsgrad, og andre årsager til luftvejs hyperresponsivitet; kronisk obstruktiv lungesygdom (COPD); bronkitis, herunder infektiøs og eosinofil bronkitis; emfysem; bronkiektasi; cystisk fibrose; sarkoidose; alpha-l-antitrypsindeficiens; tærskerlunge og beslægtede sygdomme; hypersensibilitetspneumonitis; lungefibrose, herunder kryptogen fibrøs alveolitis, idiopatiske interstitielle pneumonier, fibrose, der komplicerer antineoplastisk terapi og kronisk infektion, herunder tuberkulose og aspergillose og andre svampeinfektioner; komplikationer ved lungetransplantation; vaskulitiske og trombotiske forstyrrelser i lungevaskulatur, og pulmonal hypertension; hostestillende aktivitet, der indbefatter behandling af kronisk hoste forbundet med inflammatoriske og sekretoriske luftvejstilstande, og iatrogen hoste; akut og kronisk rhinitis, herunder rhinitis medicamentosa, og vasomotor rhinitis; stadig tilbagevendende og sæsonbetinget allergisk rhinitis, herunder rhinitis nervosa (høfeber); næsepolypose; akut virusinfektion, herunder almindelig forkølelse, og infektion på grund af respiratorisk syncytialvirus, influenza, coronavirus (herunder SARS) og adenovirus, akut lungelæsion, ARDS (adult respiratory distress syndrome), såvel som exacerbationer af hver af de foregående luftvejssygdomstilstande, navnlig exacerbationer af samtlige typer af astma eller COPD.
10. Forbindelse med formlen (I) til anvendelse ifølge krav 9 til anvendelse i behandling af astma eller kronisk obstruktiv lungesygdom.
11. Kombination af en forbindelse med formlen (I) ifølge et hvilket som helst af kravene 1 til 6 og ét eller flere midler, der er uafhængigt udvalgt fra: • en ikke-steroid glucocorticoidreceptoragonist; • en selektiv P2-adrenoceptoragonist; • en phosphodiesterasehæmmer; • en proteasehæmmer; • et glucocorticoid; • et anticholinergt middel; • en modulator af kemokinreceptorfunktion og • en hæmmer af kinasefunktion.
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