JP2006522118A5 - - Google Patents
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- Publication number
- JP2006522118A5 JP2006522118A5 JP2006508007A JP2006508007A JP2006522118A5 JP 2006522118 A5 JP2006522118 A5 JP 2006522118A5 JP 2006508007 A JP2006508007 A JP 2006508007A JP 2006508007 A JP2006508007 A JP 2006508007A JP 2006522118 A5 JP2006522118 A5 JP 2006522118A5
- Authority
- JP
- Japan
- Prior art keywords
- oxy
- acetic acid
- biphenyl
- trifluoromethyl
- methyl
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 5
- HLHVPJVNRURVNK-UHFFFAOYSA-N 2-(4-cyano-2-phenylphenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(C#N)C=C1C1=CC=CC=C1 HLHVPJVNRURVNK-UHFFFAOYSA-N 0.000 claims description 3
- AWOLOLKCVZPBPS-UHFFFAOYSA-N 2-(4-nitro-2-phenylphenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C([N+]([O-])=O)C=C1C1=CC=CC=C1 AWOLOLKCVZPBPS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 17
- 150000002367 halogens Chemical class 0.000 claims 14
- 125000000753 cycloalkyl group Chemical group 0.000 claims 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 10
- 125000001424 substituent group Chemical group 0.000 claims 10
- 125000003118 aryl group Chemical group 0.000 claims 8
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 8
- 239000001257 hydrogen Substances 0.000 claims 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 5
- 125000001072 heteroaryl group Chemical group 0.000 claims 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 5
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims 5
- 235000010290 biphenyl Nutrition 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 208000023504 respiratory system disease Diseases 0.000 claims 2
- 239000011734 sodium Chemical class 0.000 claims 2
- 229910052708 sodium Inorganic materials 0.000 claims 2
- UTDANZPJNOWLLZ-GFCCVEGCSA-N (2r)-2-[2-(4-ethylsulfonyl-2-methylphenyl)-4-(trifluoromethyl)phenoxy]propanoic acid Chemical compound CC1=CC(S(=O)(=O)CC)=CC=C1C1=CC(C(F)(F)F)=CC=C1O[C@H](C)C(O)=O UTDANZPJNOWLLZ-GFCCVEGCSA-N 0.000 claims 1
- UVUBPIDMHFSLPL-QMMMGPOBSA-N (2s)-2-[2-(2,4-dichlorophenyl)-4-fluorophenoxy]propanoic acid Chemical compound OC(=O)[C@H](C)OC1=CC=C(F)C=C1C1=CC=C(Cl)C=C1Cl UVUBPIDMHFSLPL-QMMMGPOBSA-N 0.000 claims 1
- GBVPNEKWRGIPPU-JTQLQIEISA-N (2s)-2-[2-(2-chloro-4-ethylsulfonylphenyl)-4-(trifluoromethyl)phenoxy]propanoic acid Chemical compound ClC1=CC(S(=O)(=O)CC)=CC=C1C1=CC(C(F)(F)F)=CC=C1O[C@@H](C)C(O)=O GBVPNEKWRGIPPU-JTQLQIEISA-N 0.000 claims 1
- LJIYOGZCGKFGDT-VIFPVBQESA-N (2s)-2-[2-(2-chloro-4-methylsulfonylphenyl)-4-(trifluoromethyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(C(F)(F)F)C=C1C1=CC=C(S(C)(=O)=O)C=C1Cl LJIYOGZCGKFGDT-VIFPVBQESA-N 0.000 claims 1
- CUQMQTKLLBWIKJ-VIFPVBQESA-N (2s)-2-[2-(2-chloro-4-methylsulfonylphenyl)-4-fluorophenoxy]propanoic acid Chemical compound OC(=O)[C@H](C)OC1=CC=C(F)C=C1C1=CC=C(S(C)(=O)=O)C=C1Cl CUQMQTKLLBWIKJ-VIFPVBQESA-N 0.000 claims 1
- DQZYOGMMSWYWDD-VIFPVBQESA-N (2s)-2-[2-(2-fluoro-4-methylsulfonylphenyl)-4-(trifluoromethyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(C(F)(F)F)C=C1C1=CC=C(S(C)(=O)=O)C=C1F DQZYOGMMSWYWDD-VIFPVBQESA-N 0.000 claims 1
- NGANXYIPATXYJN-JTQLQIEISA-N (2s)-2-[2-(3-cyanophenyl)-4-(trifluoromethyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(C(F)(F)F)C=C1C1=CC=CC(C#N)=C1 NGANXYIPATXYJN-JTQLQIEISA-N 0.000 claims 1
- RHKNWNBFQHQDBE-JTQLQIEISA-N (2s)-2-[2-(3-cyanophenyl)-4-fluorophenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(F)C=C1C1=CC=CC(C#N)=C1 RHKNWNBFQHQDBE-JTQLQIEISA-N 0.000 claims 1
- UTDANZPJNOWLLZ-LBPRGKRZSA-N (2s)-2-[2-(4-ethylsulfonyl-2-methylphenyl)-4-(trifluoromethyl)phenoxy]propanoic acid Chemical compound CC1=CC(S(=O)(=O)CC)=CC=C1C1=CC(C(F)(F)F)=CC=C1O[C@@H](C)C(O)=O UTDANZPJNOWLLZ-LBPRGKRZSA-N 0.000 claims 1
- PTMHUXOQMHNGBN-VIFPVBQESA-N (2s)-2-[2-[2-(methanesulfonamido)-4-methylpyrimidin-5-yl]-4-(trifluoromethyl)phenoxy]propanoic acid Chemical compound OC(=O)[C@H](C)OC1=CC=C(C(F)(F)F)C=C1C1=CN=C(NS(C)(=O)=O)N=C1C PTMHUXOQMHNGBN-VIFPVBQESA-N 0.000 claims 1
- MQOYNPDGKWDYIJ-JTQLQIEISA-N (2s)-2-[2-[2-chloro-4-(dimethylsulfamoyl)phenyl]-4-(trifluoromethyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(C(F)(F)F)C=C1C1=CC=C(S(=O)(=O)N(C)C)C=C1Cl MQOYNPDGKWDYIJ-JTQLQIEISA-N 0.000 claims 1
- QSQNIRJFLSUFBA-QMMMGPOBSA-N (2s)-2-[2-[2-chloro-5-(trifluoromethyl)phenyl]-4-fluorophenoxy]propanoic acid Chemical compound OC(=O)[C@H](C)OC1=CC=C(F)C=C1C1=CC(C(F)(F)F)=CC=C1Cl QSQNIRJFLSUFBA-QMMMGPOBSA-N 0.000 claims 1
- CHXYIRRYVLPDQC-LBPRGKRZSA-N (2s)-2-[2-[4-(azetidin-1-ylsulfonyl)phenyl]-4-chlorophenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(S(=O)(=O)N2CCC2)C=C1 CHXYIRRYVLPDQC-LBPRGKRZSA-N 0.000 claims 1
- GEAGOTGYCOZVOX-NSHDSACASA-N (2s)-2-[2-[4-(dimethylsulfamoyl)phenyl]-4-(trifluoromethyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(C(F)(F)F)C=C1C1=CC=C(S(=O)(=O)N(C)C)C=C1 GEAGOTGYCOZVOX-NSHDSACASA-N 0.000 claims 1
- RASODJKPCNUMHP-JTQLQIEISA-N (2s)-2-[4-chloro-2-(2-chloro-4-ethylsulfonylphenyl)phenoxy]propanoic acid Chemical compound ClC1=CC(S(=O)(=O)CC)=CC=C1C1=CC(Cl)=CC=C1O[C@@H](C)C(O)=O RASODJKPCNUMHP-JTQLQIEISA-N 0.000 claims 1
- UAVDEXAEZZZLQK-VIFPVBQESA-N (2s)-2-[4-chloro-2-(2-chloro-4-methylsulfonylphenyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(S(C)(=O)=O)C=C1Cl UAVDEXAEZZZLQK-VIFPVBQESA-N 0.000 claims 1
- JAYZYFGLBVYVHG-VIFPVBQESA-N (2s)-2-[4-chloro-2-(2-fluoro-4-methylsulfonylphenyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(S(C)(=O)=O)C=C1F JAYZYFGLBVYVHG-VIFPVBQESA-N 0.000 claims 1
- SKDYMYFZHGVKDB-JTQLQIEISA-N (2s)-2-[4-chloro-2-(3-cyanophenyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=CC(C#N)=C1 SKDYMYFZHGVKDB-JTQLQIEISA-N 0.000 claims 1
- UIRDWYDLVOOGNI-ZDUSSCGKSA-N (2s)-2-[4-chloro-2-(4-morpholin-4-ylsulfonylphenyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(S(=O)(=O)N2CCOCC2)C=C1 UIRDWYDLVOOGNI-ZDUSSCGKSA-N 0.000 claims 1
- ZCMHFUQOLQDEDX-JTQLQIEISA-N (2s)-2-[4-chloro-2-[2-chloro-4-(dimethylsulfamoyl)phenyl]phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(S(=O)(=O)N(C)C)C=C1Cl ZCMHFUQOLQDEDX-JTQLQIEISA-N 0.000 claims 1
- YYHSIEMPTBADSK-AWEZNQCLSA-N (2s)-2-[4-chloro-2-[2-methyl-4-(pyrrolidine-1-carbonyl)phenyl]phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(C(=O)N2CCCC2)C=C1C YYHSIEMPTBADSK-AWEZNQCLSA-N 0.000 claims 1
- XMIUMZJUOMARHB-JTQLQIEISA-N (2s)-2-[4-chloro-2-[4-(dimethylsulfamoyl)-2-fluorophenyl]phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(S(=O)(=O)N(C)C)C=C1F XMIUMZJUOMARHB-JTQLQIEISA-N 0.000 claims 1
- KSVZIQPZNUTVLS-NSHDSACASA-N (2s)-2-[4-chloro-2-[4-(dimethylsulfamoyl)phenyl]phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CC=C(S(=O)(=O)N(C)C)C=C1 KSVZIQPZNUTVLS-NSHDSACASA-N 0.000 claims 1
- IKSINXPRXZPOQV-NSHDSACASA-N (2s)-2-[4-chloro-2-[4-methyl-6-[methyl(methylsulfonyl)amino]pyridin-3-yl]phenoxy]propanoic acid Chemical compound OC(=O)[C@H](C)OC1=CC=C(Cl)C=C1C1=CN=C(N(C)S(C)(=O)=O)C=C1C IKSINXPRXZPOQV-NSHDSACASA-N 0.000 claims 1
- XUEHXEQKCGHAON-VIFPVBQESA-N (2s)-2-[4-cyano-2-(2,4-dichlorophenyl)phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(C#N)C=C1C1=CC=C(Cl)C=C1Cl XUEHXEQKCGHAON-VIFPVBQESA-N 0.000 claims 1
- DVEZYXONCGOUMF-VIFPVBQESA-N (2s)-2-[4-cyano-2-[2-fluoro-4-(trifluoromethyl)phenyl]phenoxy]propanoic acid Chemical class OC(=O)[C@H](C)OC1=CC=C(C#N)C=C1C1=CC=C(C(F)(F)F)C=C1F DVEZYXONCGOUMF-VIFPVBQESA-N 0.000 claims 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- FUNQKWCUODOEJV-UHFFFAOYSA-N 2-(2,4-dibromo-6-phenylphenoxy)acetic acid Chemical compound OC(=O)COc1c(Br)cc(Br)cc1-c1ccccc1 FUNQKWCUODOEJV-UHFFFAOYSA-N 0.000 claims 1
- PXZGZXHJYIRBHW-UHFFFAOYSA-N 2-(4-bromo-2-phenylphenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Br)C=C1C1=CC=CC=C1 PXZGZXHJYIRBHW-UHFFFAOYSA-N 0.000 claims 1
- UPWDVXOBZKNLLM-UHFFFAOYSA-N 2-(4-chloro-2-phenylphenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1C1=CC=CC=C1 UPWDVXOBZKNLLM-UHFFFAOYSA-N 0.000 claims 1
- ZGHICFNXOMIPLL-UHFFFAOYSA-N 2-(4-chloro-2-pyrimidin-5-ylphenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1C1=CN=CN=C1 ZGHICFNXOMIPLL-UHFFFAOYSA-N 0.000 claims 1
- DVEWANDODNREOY-UHFFFAOYSA-N 2-(4-chloro-2-quinolin-8-ylphenoxy)acetic acid Chemical compound OC(=O)COC1=CC=C(Cl)C=C1C1=CC=CC2=CC=CN=C12 DVEWANDODNREOY-UHFFFAOYSA-N 0.000 claims 1
- LCJVVYSSLAXKAG-UHFFFAOYSA-N 2-[2-(1,3-benzodioxol-5-yl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC=C(OCO2)C2=C1 LCJVVYSSLAXKAG-UHFFFAOYSA-N 0.000 claims 1
- DVJPCOUAHFSSQB-UHFFFAOYSA-N 2-[2-(1-benzofuran-2-yl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC2=CC=CC=C2O1 DVJPCOUAHFSSQB-UHFFFAOYSA-N 0.000 claims 1
- UQRPLKIQZIEQGJ-UHFFFAOYSA-N 2-[2-(2,3-dichlorophenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC=CC(Cl)=C1Cl UQRPLKIQZIEQGJ-UHFFFAOYSA-N 0.000 claims 1
- VBHCWDSHNIZODI-UHFFFAOYSA-N 2-[2-(2,4-dimethoxypyrimidin-5-yl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound COC1=NC(OC)=NC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O VBHCWDSHNIZODI-UHFFFAOYSA-N 0.000 claims 1
- LQJBEGARCXFPSB-UHFFFAOYSA-N 2-[2-(2,4-dimethylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CC(C)=CC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O LQJBEGARCXFPSB-UHFFFAOYSA-N 0.000 claims 1
- WONKNXVWKHKONP-UHFFFAOYSA-N 2-[2-(2,5-difluoro-4-methoxyphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound C1=C(F)C(OC)=CC(F)=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O WONKNXVWKHKONP-UHFFFAOYSA-N 0.000 claims 1
- HLUNPAVUYDODGZ-UHFFFAOYSA-N 2-[2-(2,5-difluoro-4-sulfamoylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound C1=C(F)C(S(=O)(=O)N)=CC(F)=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O HLUNPAVUYDODGZ-UHFFFAOYSA-N 0.000 claims 1
- JLSZZPIHSYZCJJ-UHFFFAOYSA-N 2-[2-(2,5-difluorophenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC(F)=CC=C1F JLSZZPIHSYZCJJ-UHFFFAOYSA-N 0.000 claims 1
- IETUONZSRMMZDK-UHFFFAOYSA-N 2-[2-(2,5-dimethylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CC=C(C)C(C=2C(=CC=C(C=2)C(F)(F)F)OCC(O)=O)=C1 IETUONZSRMMZDK-UHFFFAOYSA-N 0.000 claims 1
- WVZDLNVAAOUNAU-UHFFFAOYSA-N 2-[2-(2-amino-4-methylpyrimidin-5-yl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=NC(N)=NC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O WVZDLNVAAOUNAU-UHFFFAOYSA-N 0.000 claims 1
- AWGSBBHCTCZVLR-UHFFFAOYSA-N 2-[2-(2-amino-5-methylpyridin-3-yl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CN=C(N)C(C=2C(=CC=C(C=2)C(F)(F)F)OCC(O)=O)=C1 AWGSBBHCTCZVLR-UHFFFAOYSA-N 0.000 claims 1
- MOZQWBBHCHQDKF-UHFFFAOYSA-N 2-[2-(2-aminopyrimidin-5-yl)-4-chlorophenoxy]acetic acid Chemical compound C1=NC(N)=NC=C1C1=CC(Cl)=CC=C1OCC(O)=O MOZQWBBHCHQDKF-UHFFFAOYSA-N 0.000 claims 1
- BKMNDIUYMMHTDG-UHFFFAOYSA-N 2-[2-(2-chloro-4-ethylsulfonylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound ClC1=CC(S(=O)(=O)CC)=CC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O BKMNDIUYMMHTDG-UHFFFAOYSA-N 0.000 claims 1
- GIMXNRWYMAQJKM-UHFFFAOYSA-N 2-[2-(2-chloro-4-hydroxyphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC=C(O)C=C1Cl GIMXNRWYMAQJKM-UHFFFAOYSA-N 0.000 claims 1
- VAGPAMSZTPVNES-UHFFFAOYSA-N 2-[2-(2-chloro-5-methylpyridin-4-yl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CN=C(Cl)C=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O VAGPAMSZTPVNES-UHFFFAOYSA-N 0.000 claims 1
- AKJMJSFQGHRPDO-UHFFFAOYSA-N 2-[2-(2-chloro-5-sulfamoylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound NS(=O)(=O)C1=CC=C(Cl)C(C=2C(=CC=C(C=2)C(F)(F)F)OCC(O)=O)=C1 AKJMJSFQGHRPDO-UHFFFAOYSA-N 0.000 claims 1
- CFRYRSBIQVJEGG-UHFFFAOYSA-N 2-[2-(2-chlorophenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC=CC=C1Cl CFRYRSBIQVJEGG-UHFFFAOYSA-N 0.000 claims 1
- KPHTWLNCCIROCQ-UHFFFAOYSA-N 2-[2-(2-fluoro-4-methylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound FC1=CC(C)=CC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O KPHTWLNCCIROCQ-UHFFFAOYSA-N 0.000 claims 1
- AGZAFCWQOAMYMA-UHFFFAOYSA-N 2-[2-(2-fluoro-5-methylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CC=C(F)C(C=2C(=CC=C(C=2)C(F)(F)F)OCC(O)=O)=C1 AGZAFCWQOAMYMA-UHFFFAOYSA-N 0.000 claims 1
- CZRPYQXMJTVZCL-UHFFFAOYSA-N 2-[2-(2-fluoro-6-methylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CC=CC(F)=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O CZRPYQXMJTVZCL-UHFFFAOYSA-N 0.000 claims 1
- NOCGXOCSBRTPOH-UHFFFAOYSA-N 2-[2-(2-fluorophenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC=CC=C1F NOCGXOCSBRTPOH-UHFFFAOYSA-N 0.000 claims 1
- XKTKOCMSPJGZND-UHFFFAOYSA-N 2-[2-(2-methoxyphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound COC1=CC=CC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O XKTKOCMSPJGZND-UHFFFAOYSA-N 0.000 claims 1
- ARVXRFKSNMBAQY-UHFFFAOYSA-N 2-[2-(2-methyl-5-methylsulfonylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CC=C(S(C)(=O)=O)C=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O ARVXRFKSNMBAQY-UHFFFAOYSA-N 0.000 claims 1
- GYUZBMREOWMBQM-UHFFFAOYSA-N 2-[2-(2-methyl-5-sulfamoylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O GYUZBMREOWMBQM-UHFFFAOYSA-N 0.000 claims 1
- JKGLEWXFVSHOTN-UHFFFAOYSA-N 2-[2-(2-methylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=CC=CC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O JKGLEWXFVSHOTN-UHFFFAOYSA-N 0.000 claims 1
- UUBPKAKFFTVBKJ-UHFFFAOYSA-N 2-[2-(2-nitrophenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC=CC=C1[N+]([O-])=O UUBPKAKFFTVBKJ-UHFFFAOYSA-N 0.000 claims 1
- MCRYGBNSJLPWDC-UHFFFAOYSA-N 2-[2-(3,4-difluorophenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound OC(=O)COC1=CC=C(C(F)(F)F)C=C1C1=CC=C(F)C(F)=C1 MCRYGBNSJLPWDC-UHFFFAOYSA-N 0.000 claims 1
- GLSYUPIIWSOLAV-UHFFFAOYSA-N 2-[2-(3-chloro-2-methylphenyl)-4-(trifluoromethyl)phenoxy]acetic acid Chemical compound CC1=C(Cl)C=CC=C1C1=CC(C(F)(F)F)=CC=C1OCC(O)=O GLSYUPIIWSOLAV-UHFFFAOYSA-N 0.000 claims 1
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| CN102958914B (zh) | 2010-07-05 | 2015-05-27 | 埃科特莱茵药品有限公司 | 1-苯基取代的杂环衍生物及其作为前列腺素d2受体调节剂的用途 |
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2004
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- 2004-04-06 CA CA2521425A patent/CA2521425C/en not_active Expired - Fee Related
- 2004-04-06 EP EP04726044.3A patent/EP1611091B1/en not_active Expired - Lifetime
- 2004-04-06 BR BRPI0409109-4A patent/BRPI0409109A/pt not_active IP Right Cessation
- 2004-04-06 PL PL04726044T patent/PL1611091T3/pl unknown
- 2004-04-06 AU AU2004228599A patent/AU2004228599B2/en not_active Ceased
- 2004-04-06 US US10/551,783 patent/US8158820B2/en not_active Expired - Fee Related
- 2004-04-06 JP JP2006508007A patent/JP4898428B2/ja not_active Expired - Fee Related
- 2004-04-06 NZ NZ542972A patent/NZ542972A/en not_active IP Right Cessation
- 2004-04-06 DK DK04726044.3T patent/DK1611091T3/en active
- 2004-04-06 CN CN200480013447A patent/CN100575330C/zh not_active Expired - Fee Related
- 2004-04-06 PT PT47260443T patent/PT1611091E/pt unknown
- 2004-04-06 WO PCT/SE2004/000535 patent/WO2004089885A1/en not_active Ceased
- 2004-04-06 RU RU2005131732/04A patent/RU2372330C2/ru not_active IP Right Cessation
- 2004-04-06 ES ES04726044.3T patent/ES2525763T3/es not_active Expired - Lifetime
- 2004-04-06 SI SI200432206T patent/SI1611091T1/sl unknown
- 2004-04-06 MX MXPA05010682A patent/MXPA05010682A/es active IP Right Grant
- 2004-04-06 KR KR1020057018996A patent/KR101061339B1/ko not_active Expired - Fee Related
- 2004-04-07 AR ARP040101180A patent/AR043998A1/es unknown
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- 2005-10-04 CO CO05100592A patent/CO5640047A2/es not_active Application Discontinuation
- 2005-10-06 ZA ZA200508088A patent/ZA200508088B/en unknown
- 2005-10-31 IS IS8108A patent/IS8108A/is unknown
- 2005-11-04 NO NO20055219A patent/NO20055219L/no not_active Application Discontinuation
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- 2010-12-30 US US12/982,435 patent/US20110166117A1/en not_active Abandoned
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