NO327256B1 - Inhibitorer av cytosolisk fosfolipase A2, fremgangsmate for fremstilling av og mellomprodukter ved fremstilling av slike forbindelser, farmasoytiske preparater inneholdende slike forbindelser samt anvendelse av slike forbindelser for fremstilling av farmasoytiske preparater for behandling av lidelser - Google Patents
Inhibitorer av cytosolisk fosfolipase A2, fremgangsmate for fremstilling av og mellomprodukter ved fremstilling av slike forbindelser, farmasoytiske preparater inneholdende slike forbindelser samt anvendelse av slike forbindelser for fremstilling av farmasoytiske preparater for behandling av lidelser Download PDFInfo
- Publication number
- NO327256B1 NO327256B1 NO20042679A NO20042679A NO327256B1 NO 327256 B1 NO327256 B1 NO 327256B1 NO 20042679 A NO20042679 A NO 20042679A NO 20042679 A NO20042679 A NO 20042679A NO 327256 B1 NO327256 B1 NO 327256B1
- Authority
- NO
- Norway
- Prior art keywords
- ethyl
- chloro
- indol
- benzoic acid
- benzhydryl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims description 243
- 238000011282 treatment Methods 0.000 title claims description 45
- 238000002360 preparation method Methods 0.000 title claims description 18
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title claims description 11
- 208000035475 disorder Diseases 0.000 title claims description 8
- 239000000543 intermediate Substances 0.000 title description 307
- 238000000034 method Methods 0.000 title description 273
- 230000008569 process Effects 0.000 title description 6
- 239000003112 inhibitor Substances 0.000 title description 5
- 108020002496 Lysophospholipase Proteins 0.000 title description 4
- 102100037611 Lysophospholipase Human genes 0.000 title description 3
- 239000008194 pharmaceutical composition Substances 0.000 title description 3
- 150000002148 esters Chemical class 0.000 claims description 188
- 239000002253 acid Substances 0.000 claims description 182
- -1 tetrahydropyranyl- Chemical group 0.000 claims description 158
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 114
- 239000000460 chlorine Substances 0.000 claims description 104
- 239000005711 Benzoic acid Substances 0.000 claims description 80
- 229910052736 halogen Inorganic materials 0.000 claims description 79
- 235000010233 benzoic acid Nutrition 0.000 claims description 73
- 150000002367 halogens Chemical class 0.000 claims description 71
- 238000006243 chemical reaction Methods 0.000 claims description 67
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 51
- 125000000217 alkyl group Chemical group 0.000 claims description 43
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 43
- 150000001412 amines Chemical class 0.000 claims description 38
- 150000003839 salts Chemical group 0.000 claims description 33
- 208000006673 asthma Diseases 0.000 claims description 31
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 28
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 27
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 25
- 238000004519 manufacturing process Methods 0.000 claims description 21
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 21
- 150000001299 aldehydes Chemical class 0.000 claims description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- 239000000825 pharmaceutical preparation Substances 0.000 claims description 20
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 18
- 150000004820 halides Chemical class 0.000 claims description 18
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 18
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 17
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 14
- 241000124008 Mammalia Species 0.000 claims description 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims description 12
- 229940124530 sulfonamide Drugs 0.000 claims description 12
- 150000003456 sulfonamides Chemical class 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 11
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 11
- 125000000814 indol-3-yl group Chemical group [H]C1=C([H])C([H])=C2N([H])C([H])=C([*])C2=C1[H] 0.000 claims description 11
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 208000025747 Rheumatic disease Diseases 0.000 claims description 8
- 150000001345 alkine derivatives Chemical class 0.000 claims description 8
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 8
- 150000001241 acetals Chemical class 0.000 claims description 7
- 150000003973 alkyl amines Chemical class 0.000 claims description 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- 239000012038 nucleophile Substances 0.000 claims description 6
- 125000006239 protecting group Chemical group 0.000 claims description 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 5
- WSWJZMPSIAPEKV-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(2-cyanophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=CC=C1C#N WSWJZMPSIAPEKV-UHFFFAOYSA-N 0.000 claims description 5
- 206010061218 Inflammation Diseases 0.000 claims description 5
- 230000002917 arthritic effect Effects 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 230000004054 inflammatory process Effects 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 201000008482 osteoarthritis Diseases 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- NYEVKOMTBTUYNA-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[2-(tetrazol-1-yl)ethylsulfonylamino]ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CCN1N=NN=C1 NYEVKOMTBTUYNA-UHFFFAOYSA-N 0.000 claims description 4
- 208000002193 Pain Diseases 0.000 claims description 4
- 229910006074 SO2NH2 Inorganic materials 0.000 claims description 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- OLNJUISKUQQNIM-UHFFFAOYSA-N indole-3-carbaldehyde Chemical compound C1=CC=C2C(C=O)=CNC2=C1 OLNJUISKUQQNIM-UHFFFAOYSA-N 0.000 claims description 4
- NBKQRVSGHYZUOR-UHFFFAOYSA-N indoline-3-carbaldehyde Natural products C1=CC=C2C(C=O)CNC2=C1 NBKQRVSGHYZUOR-UHFFFAOYSA-N 0.000 claims description 4
- 125000001041 indolyl group Chemical group 0.000 claims description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 3
- VLXJCZYNQNYWMD-UHFFFAOYSA-N 4-[2-[1-benzhydryl-2-[2-(benzylsulfonylamino)ethyl]-5-chloroindol-3-yl]ethylsulfonyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1S(=O)(=O)CCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=CC=C1 VLXJCZYNQNYWMD-UHFFFAOYSA-N 0.000 claims description 3
- ANTKWQZDLKJLIU-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-(2-pyrrolidin-1-ylethylsulfonylamino)ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CCN1CCCC1 ANTKWQZDLKJLIU-UHFFFAOYSA-N 0.000 claims description 3
- OFOGOAQOIPVATJ-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(2,6-difluorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethylsulfonyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1S(=O)(=O)CCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=C(F)C=CC=C1F OFOGOAQOIPVATJ-UHFFFAOYSA-N 0.000 claims description 3
- ONPHRKDEKQCHFZ-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(2-chlorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethylsulfonyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1S(=O)(=O)CCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=CC=C1Cl ONPHRKDEKQCHFZ-UHFFFAOYSA-N 0.000 claims description 3
- ASHPCYWCOXBICU-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(2-fluorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethylsulfonyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1S(=O)(=O)CCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=CC=C1F ASHPCYWCOXBICU-UHFFFAOYSA-N 0.000 claims description 3
- REFGWQMELMZPRN-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(3,4-dichlorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethylsulfonyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1S(=O)(=O)CCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=C(Cl)C(Cl)=C1 REFGWQMELMZPRN-UHFFFAOYSA-N 0.000 claims description 3
- MWALSBGPGSBGQB-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[[3-(trifluoromethyl)phenyl]methylsulfonylamino]ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=CC(C(F)(F)F)=C1 MWALSBGPGSBGQB-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 125000002541 furyl group Chemical group 0.000 claims description 3
- 230000003301 hydrolyzing effect Effects 0.000 claims description 3
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 3
- 150000003461 sulfonyl halides Chemical class 0.000 claims description 3
- 125000001984 thiazolidinyl group Chemical group 0.000 claims description 3
- 125000001544 thienyl group Chemical group 0.000 claims description 3
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims description 3
- 125000001425 triazolyl group Chemical group 0.000 claims description 3
- VQZHFZADYMVWEJ-UHFFFAOYSA-N 2-[2-[1-benzhydryl-3-[2-(4-carboxyphenoxy)ethyl]-5-chloroindol-2-yl]ethylsulfamoyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)C1=CC=CC=C1C(O)=O VQZHFZADYMVWEJ-UHFFFAOYSA-N 0.000 claims description 2
- MRSNPMBYUDTKSE-UHFFFAOYSA-N 2-[2-[2-[1-benzhydryl-3-[2-(4-carboxyphenoxy)ethyl]-5-chloroindol-2-yl]ethylsulfamoyl]ethylcarbamoyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CCNC(=O)C1=CC=CC=C1C(O)=O MRSNPMBYUDTKSE-UHFFFAOYSA-N 0.000 claims description 2
- FNXUWBAIVOTZLA-UHFFFAOYSA-N 3-[2-[1-benzhydryl-3-[2-(4-carboxyphenoxy)ethyl]-5-chloroindol-2-yl]ethylsulfamoylmethyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=CC(C(O)=O)=C1 FNXUWBAIVOTZLA-UHFFFAOYSA-N 0.000 claims description 2
- ATBZLJGREVYQGX-UHFFFAOYSA-N 3-[4-[2-[1-benzhydryl-5-chloro-2-[2-[(2,6-difluorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethylsulfonyl]phenyl]propanoic acid Chemical compound C1=CC(CCC(=O)O)=CC=C1S(=O)(=O)CCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=C(F)C=CC=C1F ATBZLJGREVYQGX-UHFFFAOYSA-N 0.000 claims description 2
- XQACXFKAHCRKRX-UHFFFAOYSA-N 3-[4-[2-[1-benzhydryl-5-chloro-2-[2-[(3,4-dichlorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethylsulfonyl]phenyl]propanoic acid Chemical compound C1=CC(CCC(=O)O)=CC=C1S(=O)(=O)CCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=C(Cl)C(Cl)=C1 XQACXFKAHCRKRX-UHFFFAOYSA-N 0.000 claims description 2
- TUVVIDHZUDAIOO-UHFFFAOYSA-N 4-[2-[1-benzhydryl-2-[2-(1,3-benzoxazol-2-ylmethylsulfonylamino)ethyl]-5-chloroindol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=NC2=CC=CC=C2O1 TUVVIDHZUDAIOO-UHFFFAOYSA-N 0.000 claims description 2
- UOKDNVVSJUDJCY-UHFFFAOYSA-N 4-[2-[1-benzhydryl-2-[2-(2,1,3-benzoxadiazol-4-ylsulfonylamino)ethyl]-5-chloroindol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)C1=CC=CC2=NON=C12 UOKDNVVSJUDJCY-UHFFFAOYSA-N 0.000 claims description 2
- WLKXBZQQXPWMRG-UHFFFAOYSA-N 4-[2-[1-benzhydryl-2-[2-(butylsulfonylamino)ethyl]-5-chloroindol-3-yl]ethoxy]benzoic acid Chemical compound C12=CC(Cl)=CC=C2N(C(C=2C=CC=CC=2)C=2C=CC=CC=2)C(CCNS(=O)(=O)CCCC)=C1CCOC1=CC=C(C(O)=O)C=C1 WLKXBZQQXPWMRG-UHFFFAOYSA-N 0.000 claims description 2
- ICHLFEFMEVEOPZ-UHFFFAOYSA-N 4-[2-[1-benzhydryl-2-[2-[(5-bromo-6-chloropyridin-3-yl)sulfonylamino]ethyl]-5-chloroindol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)C1=CN=C(Cl)C(Br)=C1 ICHLFEFMEVEOPZ-UHFFFAOYSA-N 0.000 claims description 2
- GGYXYSZVESBVHH-UHFFFAOYSA-N 4-[2-[1-benzhydryl-2-[2-[[3,5-bis(trifluoromethyl)phenyl]methylsulfonylamino]ethyl]-5-chloroindol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 GGYXYSZVESBVHH-UHFFFAOYSA-N 0.000 claims description 2
- SWXMJYPSWZZIQI-UHFFFAOYSA-N 4-[2-[1-benzhydryl-2-[3-(benzylsulfonylamino)propyl]-5-chloroindol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCCNS(=O)(=O)CC1=CC=CC=C1 SWXMJYPSWZZIQI-UHFFFAOYSA-N 0.000 claims description 2
- FSHDXZQFIRNXLR-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-(2-imidazol-1-ylethylsulfonylamino)ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CCN1C=NC=C1 FSHDXZQFIRNXLR-UHFFFAOYSA-N 0.000 claims description 2
- DKEDYGNQAGGBEB-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-(2-naphthalen-1-ylethylsulfonylamino)ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CCC1=CC=CC2=CC=CC=C12 DKEDYGNQAGGBEB-UHFFFAOYSA-N 0.000 claims description 2
- PVHNNYOGNLHHRM-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-(2-pyrazol-1-ylethylsulfonylamino)ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CCN1N=CC=C1 PVHNNYOGNLHHRM-UHFFFAOYSA-N 0.000 claims description 2
- XQQIEDNHXSGOJH-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-(cyanomethylsulfonylamino)ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C11)=C(CCNS(=O)(=O)CC#N)N1C(C=1C=CC=CC=1)C1=CC=CC=C1 XQQIEDNHXSGOJH-UHFFFAOYSA-N 0.000 claims description 2
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- SNTOFZJYIMNNMY-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-(oxan-2-ylmethylsulfonylamino)ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1OCCCC1 SNTOFZJYIMNNMY-UHFFFAOYSA-N 0.000 claims description 2
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- BQRKIASPYSGSPF-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(1-methylimidazol-4-yl)sulfonylamino]ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound CN1C=NC(S(=O)(=O)NCCC=2N(C3=CC=C(Cl)C=C3C=2CCOC=2C=CC(=CC=2)C(O)=O)C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BQRKIASPYSGSPF-UHFFFAOYSA-N 0.000 claims description 2
- XYIFJJRIOLNKSU-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(2,3-dichlorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=CC(Cl)=C1Cl XYIFJJRIOLNKSU-UHFFFAOYSA-N 0.000 claims description 2
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- QJWBAXBHYLDSEO-UHFFFAOYSA-N 4-[2-[1-benzhydryl-5-chloro-2-[2-[(2,4-dichlorophenyl)methylsulfonylamino]ethyl]indol-3-yl]ethoxy]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OCCC(C1=CC(Cl)=CC=C1N1C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1CCNS(=O)(=O)CC1=CC=C(Cl)C=C1Cl QJWBAXBHYLDSEO-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- 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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- A—HUMAN NECESSITIES
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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
- A61K31/40—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
- A61K31/403—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 condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
- C07D209/16—Tryptamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—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
- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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
- C07D413/02—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
-
- 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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Immunology (AREA)
- Neurology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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US33458801P | 2001-12-03 | 2001-12-03 | |
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US41966402P | 2002-10-18 | 2002-10-18 | |
PCT/US2002/038311 WO2003048122A2 (en) | 2001-12-03 | 2002-12-02 | Inhibitors of cytosolic phospholipase a2 |
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NO20042679L NO20042679L (no) | 2004-06-25 |
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NO20042679A NO327256B1 (no) | 2001-12-03 | 2004-06-25 | Inhibitorer av cytosolisk fosfolipase A2, fremgangsmate for fremstilling av og mellomprodukter ved fremstilling av slike forbindelser, farmasoytiske preparater inneholdende slike forbindelser samt anvendelse av slike forbindelser for fremstilling av farmasoytiske preparater for behandling av lidelser |
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EP (1) | EP1451154B1 (de) |
JP (1) | JP4657605B2 (de) |
KR (1) | KR100973665B1 (de) |
CN (1) | CN100503566C (de) |
AR (1) | AR037684A1 (de) |
AT (1) | ATE384045T1 (de) |
AU (1) | AU2002351182B2 (de) |
BR (1) | BR0214672A (de) |
CA (1) | CA2469138C (de) |
CO (1) | CO5580763A2 (de) |
CY (1) | CY1107383T1 (de) |
DE (1) | DE60224707T2 (de) |
DK (2) | DK1892239T3 (de) |
EC (1) | ECSP045131A (de) |
ES (2) | ES2300490T3 (de) |
HK (2) | HK1065799A1 (de) |
HU (1) | HUP0402577A3 (de) |
IL (2) | IL162052A0 (de) |
IN (1) | IN2005KO00312A (de) |
NO (1) | NO327256B1 (de) |
NZ (1) | NZ533269A (de) |
PL (1) | PL370445A1 (de) |
PT (1) | PT1451154E (de) |
TW (1) | TWI334778B (de) |
WO (1) | WO2003048122A2 (de) |
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US7713964B2 (en) | 2001-12-03 | 2010-05-11 | Wyeth Llc | Methods for treating asthmatic conditions |
US7605156B2 (en) | 2001-12-03 | 2009-10-20 | Wyeth | Methods for the use of inhibitors of cytosolic phospholipase A2 |
TW200510305A (en) | 2003-07-25 | 2005-03-16 | Wyeth Corp | Process for the preparation of CPLA2 inhibitors |
JP2007515403A (ja) | 2003-11-17 | 2007-06-14 | ワイス | N−置換フタルイミドの調製方法 |
HN2004000536A (es) * | 2003-12-16 | 2009-02-18 | Wyeth Corp | Un procediemiento de sintesis para la alquilacion reductiva de la posicon c-3 de indoles |
AR048239A1 (es) | 2004-02-25 | 2006-04-12 | Wyeth Corp | Procesos para la preparacion de haluros de aril- y heteroaril-alquilsulfonilo e intermediarios de sintesis de los mismos |
US20050244367A1 (en) * | 2004-05-03 | 2005-11-03 | Ilypsa, Inc. | Phospholipase inhibitors localized in the gastrointestinal lumen |
AR053410A1 (es) * | 2004-08-19 | 2007-05-09 | Wyeth Corp | Proceso para la sintesis de indoles n-alquilados c-2, c-3 sustituidos. compuestos intermediarios |
KR101355422B1 (ko) | 2005-04-13 | 2014-02-06 | 아스션 팔마 에이/에스 | 피부 결합조직질환 치료용 베타-2 아드레노리셉터 작용제 |
GT200600228A (es) * | 2005-05-27 | 2006-12-26 | Inhibidores de la fosfolipasa a2 citosolica | |
WO2007013974A2 (en) * | 2005-07-21 | 2007-02-01 | Wyeth | Process for the synthesis of sulfonyl halides and sulfonamides from sulfonic acid salts |
CA2627043A1 (en) | 2005-11-03 | 2007-05-18 | Ilypsa, Inc. | Multivalent indole compounds and use thereof as phospholipase-a2 inhibitors |
FR2899471A1 (fr) * | 2006-04-06 | 2007-10-12 | Pasteur Institut | Utilisation d'au moins un inhibiteur de la phospholipase a2 cytosolique comme medicament pour le traitement des maladies respiratoires |
WO2007140317A2 (en) * | 2006-05-26 | 2007-12-06 | Wyeth | Use of inhibitors of cytosolic ph0sph0lipase a2 in the treatment of thrombosis |
CL2007003144A1 (es) * | 2006-10-31 | 2008-06-20 | Wyeth Corp | Composicion farmaceutica que comprende a) un sistema portador o excipiente, con un agente tensioactivo desde un 50-90% en peso y un promotor de biodisponibilidad desde un 10-30% en peso y b) un agente farmacologico activo derivado de un indol; proced |
TW200824686A (en) * | 2006-10-31 | 2008-06-16 | Wyeth Corp | Formulations of phospholipase enzyme inhibitors |
JP5164972B2 (ja) * | 2007-03-29 | 2013-03-21 | 第一三共株式会社 | cPLA2阻害活性を有するインドール誘導体およびその用途並びに製造方法 |
WO2009133831A1 (ja) | 2008-04-28 | 2009-11-05 | 旭化成ファーマ株式会社 | フェニルプロピオン酸誘導体及びその用途 |
WO2011047156A1 (en) * | 2009-10-15 | 2011-04-21 | Hercules Technology Management Co V, Inc. | Sepiapterin reductase inhibitors for the treatment of pain |
WO2012031763A1 (en) | 2010-09-08 | 2012-03-15 | Twincore Zentrum Fuer Experimentelle Und Klinische Infektionsforschung Gmbh | Use of inhibitors of phospholipase a2 for the treatment or prevention of flavivirus infection |
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CA2079374C (en) * | 1991-09-30 | 2003-08-05 | Merck Frosst Canada Incorporated | (bicyclic-azaarylmethoxy)indoles as inhibitors of leukotriene biosynthesis |
US5994398A (en) * | 1996-12-11 | 1999-11-30 | Elan Pharmaceuticals, Inc. | Arylsulfonamides as phospholipase A2 inhibitors |
EE200000486A (et) * | 1998-02-25 | 2002-02-15 | Genetics Institute, Inc. | Fosfolipaasensüümide inhibiitorid, neid sisaldav farmatseutiline kompositsioon ning meetod põletikulise reaktsiooni raviks imetajal |
EP1062205A2 (de) * | 1998-02-25 | 2000-12-27 | Genetics Institute, Inc. | Inhibitoren von phospholipasen enzymen |
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2002
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