JP2009530272A5 - - Google Patents
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- JP2009530272A5 JP2009530272A5 JP2009500323A JP2009500323A JP2009530272A5 JP 2009530272 A5 JP2009530272 A5 JP 2009530272A5 JP 2009500323 A JP2009500323 A JP 2009500323A JP 2009500323 A JP2009500323 A JP 2009500323A JP 2009530272 A5 JP2009530272 A5 JP 2009530272A5
- Authority
- JP
- Japan
- Prior art keywords
- hydroxy
- ethylamino
- phenyl
- ethyl
- 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.)
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- 150000001875 compounds Chemical class 0.000 claims description 38
- 125000000217 alkyl group Chemical group 0.000 claims description 36
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- 239000001257 hydrogen Substances 0.000 claims description 33
- 150000003839 salts Chemical class 0.000 claims description 27
- -1 R 31 Chemical compound 0.000 claims description 23
- 125000001072 heteroaryl group Chemical group 0.000 claims description 23
- 125000003545 alkoxy group Chemical group 0.000 claims description 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
- 125000003107 substituted aryl group Chemical group 0.000 claims description 17
- 150000002431 hydrogen Chemical class 0.000 claims description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 8
- 239000003638 chemical reducing agent Substances 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 125000002619 bicyclic group Chemical group 0.000 claims description 4
- 125000002950 monocyclic group Chemical group 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000006239 protecting group Chemical group 0.000 claims 15
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 4
- VKCKAMBPNXKGHL-QFIPXVFZSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[(2-methoxyphenyl)methylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC=C1CNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 VKCKAMBPNXKGHL-QFIPXVFZSA-N 0.000 claims 3
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims 3
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims 3
- 208000011341 adult acute respiratory distress syndrome Diseases 0.000 claims 3
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- YBEOVDGQPYYDKC-FQEVSTJZSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(piperidin-1-ylmethyl)phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CN1CCCCC1 YBEOVDGQPYYDKC-FQEVSTJZSA-N 0.000 claims 2
- WWEHZPFFGZLBOV-QFIPXVFZSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[(2-pyridin-2-ylethylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CNCCC1=CC=CC=N1 WWEHZPFFGZLBOV-QFIPXVFZSA-N 0.000 claims 2
- CLZMZYMASUQJLW-FPOVZHCZSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[[(2r)-1-methoxy-3-methylbutan-2-yl]amino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC[C@@H](C(C)C)NCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 CLZMZYMASUQJLW-FPOVZHCZSA-N 0.000 claims 2
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 2
- 206010014561 Emphysema Diseases 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- 230000009286 beneficial effect Effects 0.000 claims 2
- 201000009267 bronchiectasis Diseases 0.000 claims 2
- 206010006451 bronchitis Diseases 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 239000003112 inhibitor Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 206010039083 rhinitis Diseases 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- JFUAWXPBHXKZGA-IBGZPJMESA-N 4-fluoro-2-[(4r)-5,5,5-trifluoro-4-hydroxy-2-methyl-4-(1h-pyrrolo[2,3-c]pyridin-2-ylmethyl)pentan-2-yl]phenol Chemical compound C([C@@](O)(CC=1NC2=CN=CC=C2C=1)C(F)(F)F)C(C)(C)C1=CC(F)=CC=C1O JFUAWXPBHXKZGA-IBGZPJMESA-N 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- OEHDDSHOAVGWRF-IBGZPJMESA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(morpholin-4-ylmethyl)phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CN1CCOCC1 OEHDDSHOAVGWRF-IBGZPJMESA-N 0.000 claims 1
- ZUHXIOJIKIPZOR-IBGZPJMESA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(piperazin-1-ylmethyl)phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CN1CCNCC1 ZUHXIOJIKIPZOR-IBGZPJMESA-N 0.000 claims 1
- QWWLVVDOGURJDF-IBGZPJMESA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-(pyrrolidin-1-ylmethyl)phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CN1CCCC1 QWWLVVDOGURJDF-IBGZPJMESA-N 0.000 claims 1
- BGLYKONMLBFSGK-SFHVURJKSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[(2-methoxyethylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COCCNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 BGLYKONMLBFSGK-SFHVURJKSA-N 0.000 claims 1
- GVJALQHQZPOADA-DEOSSOPVSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[(3-phenylpropylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CNCCCC1=CC=CC=C1 GVJALQHQZPOADA-DEOSSOPVSA-N 0.000 claims 1
- ZSMUEPQTTOFHSI-NRFANRHFSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[(3-propan-2-yloxypropylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound CC(C)OCCCNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 ZSMUEPQTTOFHSI-NRFANRHFSA-N 0.000 claims 1
- DEHYDNLJXVYLKL-NRFANRHFSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[(3-propoxypropylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound CCCOCCCNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 DEHYDNLJXVYLKL-NRFANRHFSA-N 0.000 claims 1
- IUPSVOSSHSTCNC-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[(3-pyridin-2-ylpropylamino)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CNCCCC1=CC=CC=N1 IUPSVOSSHSTCNC-QHCPKHFHSA-N 0.000 claims 1
- QLAUZPPGGRVYJJ-SANMLTNESA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[(4-phenylpiperidin-1-yl)methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CN(CC1)CCC1C1=CC=CC=C1 QLAUZPPGGRVYJJ-SANMLTNESA-N 0.000 claims 1
- XJUWVHGTDKNBLN-IBGZPJMESA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[2-(2-methoxyethylamino)ethyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COCCNCCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 XJUWVHGTDKNBLN-IBGZPJMESA-N 0.000 claims 1
- GRHZLQJHXLNCBM-QFIPXVFZSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[2-(pyridin-2-ylmethylamino)ethyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CCNCC1=CC=CC=N1 GRHZLQJHXLNCBM-QFIPXVFZSA-N 0.000 claims 1
- PLQWTOQXQJAHBY-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[2-[(2-methoxyphenyl)methylamino]ethyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC=C1CNCCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 PLQWTOQXQJAHBY-QHCPKHFHSA-N 0.000 claims 1
- UMQKUTLZAVAIQA-DEOSSOPVSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[2-[2-(2-methoxyphenyl)ethylamino]ethyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC=C1CCNCCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 UMQKUTLZAVAIQA-DEOSSOPVSA-N 0.000 claims 1
- VJPFFEYBQADOEZ-IBGZPJMESA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[(2-methoxy-2-methylpropyl)amino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC(C)(C)CNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 VJPFFEYBQADOEZ-IBGZPJMESA-N 0.000 claims 1
- PNTAECGMYJNBSW-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[(2-methoxyphenyl)methyl-methylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC=C1CN(C)CC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 PNTAECGMYJNBSW-QHCPKHFHSA-N 0.000 claims 1
- PLKYHUCBRLEYME-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[(3-methoxyphenyl)methylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC(CNCC=2C=C(CCNC[C@H](O)C=3C=4SC(=O)NC=4C(O)=CC=3)C=CC=2)=C1 PLKYHUCBRLEYME-QHCPKHFHSA-N 0.000 claims 1
- BSOHYTBASIBPHA-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[(4-methoxyphenyl)methylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C1=CC(OC)=CC=C1CNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 BSOHYTBASIBPHA-QHCPKHFHSA-N 0.000 claims 1
- XPJHOPNYYGFTFU-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[2-(2-hydroxyphenyl)ethylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CNCCC1=CC=CC=C1O XPJHOPNYYGFTFU-QHCPKHFHSA-N 0.000 claims 1
- PIQKJCGMILEGLT-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[2-(2-methoxyphenyl)ethylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC=C1CCNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 PIQKJCGMILEGLT-QHCPKHFHSA-N 0.000 claims 1
- PVUXNNHCSQZNFM-QFIPXVFZSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[3-(2-methylpropoxy)propylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound CC(C)COCCCNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 PVUXNNHCSQZNFM-QFIPXVFZSA-N 0.000 claims 1
- CISJUOJARBBEPR-LIRRHRJNSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[[(2s)-1-methoxypropan-2-yl]amino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC[C@H](C)NCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 CISJUOJARBBEPR-LIRRHRJNSA-N 0.000 claims 1
- YWYCMZFLOQQZRC-DEOSSOPVSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[3-[[methyl(2-phenylethyl)amino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C=1C=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=CC=1CN(C)CCC1=CC=CC=C1 YWYCMZFLOQQZRC-DEOSSOPVSA-N 0.000 claims 1
- DNNQRUUXWVHSRB-NDEPHWFRSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[4-[2-[(2-pyridin-2-ylethylamino)methyl]phenyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=C1)=CC=C1C1=CC=CC=C1CNCCC1=CC=CC=N1 DNNQRUUXWVHSRB-NDEPHWFRSA-N 0.000 claims 1
- XNZJTBRCBWPOTP-PBBNMVCDSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[4-[2-[[[(1r)-1-phenylethyl]amino]methyl]phenyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C1([C@H](NCC=2C(=CC=CC=2)C=2C=CC(CCNC[C@H](O)C=3C=4SC(=O)NC=4C(O)=CC=3)=CC=2)C)=CC=CC=C1 XNZJTBRCBWPOTP-PBBNMVCDSA-N 0.000 claims 1
- NYWJZLOBZHVZMI-QFIPXVFZSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[4-[[(2-methoxyphenyl)methylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC=C1CNCC(C=C1)=CC=C1CCNC[C@H](O)C1=CC=C(O)C2=C1SC(=O)N2 NYWJZLOBZHVZMI-QFIPXVFZSA-N 0.000 claims 1
- YOCAICFOALLBEO-QHCPKHFHSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[4-[[2-(2-methoxyphenyl)ethylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound COC1=CC=CC=C1CCNCC(C=C1)=CC=C1CCNC[C@H](O)C1=CC=C(O)C2=C1SC(=O)N2 YOCAICFOALLBEO-QHCPKHFHSA-N 0.000 claims 1
- HRIMLSKWGJERPD-VWLOTQADSA-N 4-hydroxy-7-[(1r)-1-hydroxy-2-[2-[4-[[2-(7-methyl-1h-indol-3-yl)ethylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C1([C@@H](O)CNCCC2=CC=C(C=C2)CNCCC=2C=3C=CC=C(C=3NC=2)C)=CC=C(O)C2=C1SC(=O)N2 HRIMLSKWGJERPD-VWLOTQADSA-N 0.000 claims 1
- KKHJTNLHISNRCZ-UHFFFAOYSA-N 4-hydroxy-7-[1-hydroxy-2-[2-[3-[[(2-hydroxyphenyl)methylamino]methyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound C=1C=C(O)C=2NC(=O)SC=2C=1C(O)CNCCC(C=1)=CC=CC=1CNCC1=CC=CC=C1O KKHJTNLHISNRCZ-UHFFFAOYSA-N 0.000 claims 1
- KIXKMKREZOCTDI-UHFFFAOYSA-N 4-hydroxy-7-[1-hydroxy-2-[2-[4-[2-[(3-propan-2-yloxypropylamino)methyl]phenyl]phenyl]ethylamino]ethyl]-3h-1,3-benzothiazol-2-one Chemical compound CC(C)OCCCNCC1=CC=CC=C1C(C=C1)=CC=C1CCNCC(O)C1=CC=C(O)C2=C1SC(=O)N2 KIXKMKREZOCTDI-UHFFFAOYSA-N 0.000 claims 1
- WONPWDMMWFWEFC-ODOSRFNGSA-N 7-[(1r)-2-[1-[3-[[2-(2,6-dichlorophenyl)ethylamino]methyl]phenyl]propan-2-ylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NC(C)CC(C=1)=CC=CC=1CNCCC1=C(Cl)C=CC=C1Cl WONPWDMMWFWEFC-ODOSRFNGSA-N 0.000 claims 1
- XXPNWYXHQVWMTB-QHCPKHFHSA-N 7-[(1r)-2-[2-[2-[[2-(2-fluorophenyl)ethylamino]methyl]phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC1=CC=CC=C1CNCCC1=CC=CC=C1F XXPNWYXHQVWMTB-QHCPKHFHSA-N 0.000 claims 1
- PURQGWJEQYPHEZ-NRFANRHFSA-N 7-[(1r)-2-[2-[3-(azepan-1-ylmethyl)phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CN1CCCCCC1 PURQGWJEQYPHEZ-NRFANRHFSA-N 0.000 claims 1
- XLPXMNLCZGSYPS-LJAQVGFWSA-N 7-[(1r)-2-[2-[3-[(2,2-diphenylethylamino)methyl]phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CNCC(C=1C=CC=CC=1)C1=CC=CC=C1 XLPXMNLCZGSYPS-LJAQVGFWSA-N 0.000 claims 1
- GLCDQTGVYSDVBW-QFIPXVFZSA-N 7-[(1r)-2-[2-[3-[2-(azepan-1-yl)ethyl]phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CCN1CCCCCC1 GLCDQTGVYSDVBW-QFIPXVFZSA-N 0.000 claims 1
- RCUOEZMFFUESSQ-QFIPXVFZSA-N 7-[(1r)-2-[2-[3-[2-(cyclohexylamino)ethyl]phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CCNC1CCCCC1 RCUOEZMFFUESSQ-QFIPXVFZSA-N 0.000 claims 1
- UZNMXZFHPXULMI-DEOSSOPVSA-N 7-[(1r)-2-[2-[3-[2-[2-(2-fluorophenyl)ethylamino]ethyl]phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1CCNCCC1=CC=CC=C1F UZNMXZFHPXULMI-DEOSSOPVSA-N 0.000 claims 1
- HXHAEKRMZXMRER-NDEPHWFRSA-N 7-[(1r)-2-[2-[3-[3-[(benzylamino)methyl]phenyl]phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound C([C@H](O)C=1C=2SC(=O)NC=2C(O)=CC=1)NCCC(C=1)=CC=CC=1C(C=1)=CC=CC=1CNCC1=CC=CC=C1 HXHAEKRMZXMRER-NDEPHWFRSA-N 0.000 claims 1
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- VKISKXWEKUKQJG-QHCPKHFHSA-N 7-[(1r)-2-[2-[3-[[(2-ethoxyphenyl)methylamino]methyl]phenyl]ethylamino]-1-hydroxyethyl]-4-hydroxy-3h-1,3-benzothiazol-2-one Chemical compound CCOC1=CC=CC=C1CNCC1=CC=CC(CCNC[C@H](O)C=2C=3SC(=O)NC=3C(O)=CC=2)=C1 VKISKXWEKUKQJG-QHCPKHFHSA-N 0.000 claims 1
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| EP1577306A1 (de) | 2004-03-17 | 2005-09-21 | Boehringer Ingelheim Pharma GmbH & Co.KG | Neue Benzoxazinonderivate als langwirksame Betamimetika zur Behandlung von Atemwegserkrankungen |
| WO2005092841A1 (en) | 2004-03-23 | 2005-10-06 | Pfizer Limited | Compounds having beta-agonist activity |
| EP1789394A1 (de) | 2004-05-13 | 2007-05-30 | Boehringer Ingelheim International Gmbh | Hydroxy-substituierte benzkondensierte heterozyklen als betaagonisten zur behandlung von atemwegserkrankungen |
| EP1595873A1 (de) | 2004-05-13 | 2005-11-16 | Boehringer Ingelheim Pharma GmbH & Co.KG | Substituierte Cycloalkylderivate zur Behandlung von Atemswegerkrankungen |
| DE102004024453A1 (de) | 2004-05-14 | 2006-01-05 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue langwirksame Bronchodilatoren zur Behandlung von Atemwegserkrankungen |
| CN1984876A (zh) | 2004-06-03 | 2007-06-20 | 施万制药 | 二胺类β2肾上腺素能受体激动剂 |
| EP1778638A1 (en) | 2004-07-21 | 2007-05-02 | Theravance, Inc. | Diaryl ether beta2 adrenergic receptor agonists |
| JP2008510015A (ja) | 2004-08-16 | 2008-04-03 | セラヴァンス， インコーポレーテッド | β２アドレナリン作用性レセプターアゴニスト活性およびムスカリン性レセプターアンタゴニスト活性を有する化合物 |
| WO2006023457A1 (en) | 2004-08-16 | 2006-03-02 | Theravance, Inc. | COMPOUNDS HAVING β2 ADRENERGIC RECEPTOR AGONIST AND MUSCARINIC RECEPTOR ANTAGONIST ACTIVITY |
| EP1786762A2 (en) | 2004-09-10 | 2007-05-23 | Theravance, Inc. | Amidine substituted aryl aniline compounds |
| GB0426164D0 (en) | 2004-11-29 | 2004-12-29 | Novartis Ag | Organic compounds |
| CN101137625A (zh) | 2005-01-11 | 2008-03-05 | 葛兰素集团有限公司 | β2肾上腺素能激动剂的肉桂酸盐 |
| GB0511066D0 (en) | 2005-05-31 | 2005-07-06 | Novartis Ag | Organic compounds |
| AU2006271356A1 (en) | 2005-07-18 | 2007-01-25 | Pfizer Limited | Process for the preparation of sulfonamide derivatives |
| TW200738658A (en) * | 2005-08-09 | 2007-10-16 | Astrazeneca Ab | Novel compounds |
| TW200740781A (en) | 2005-08-29 | 2007-11-01 | Astrazeneca Ab | Novel compounds |
| TW200738659A (en) * | 2005-08-29 | 2007-10-16 | Astrazeneca Ab | Novel compounds |
| TW200745084A (en) | 2006-03-08 | 2007-12-16 | Astrazeneca Ab | Novel compounds |
| US20090029958A1 (en) * | 2006-03-08 | 2009-01-29 | Lilian Alcaraz | Phenethanolamine derivatives as beta2 adrenoreceptor agonists |
| TW200745067A (en) | 2006-03-14 | 2007-12-16 | Astrazeneca Ab | Novel compounds |
| WO2008041914A1 (en) | 2006-10-06 | 2008-04-10 | Astrazeneca Ab | 5-(2-AMINO-L-HYDROXYETHYL)-8-HYDROXY-2-OXOQUINOLINE DERIVATIVES AND OTHER COMPOUNDS AS β2 -ADRENERGIC AGONISTS |
| US20100056508A1 (en) | 2006-12-20 | 2010-03-04 | Astrazeneca Ab | Amine derivatives and their use in beta-2-adrenoreceptor mediated diseases |
| TW200833670A (en) | 2006-12-20 | 2008-08-16 | Astrazeneca Ab | Novel compounds 569 |
| GB0702456D0 (en) * | 2007-02-08 | 2007-03-21 | Astrazeneca Ab | New combination |
| GB0702458D0 (en) | 2007-02-08 | 2007-03-21 | Astrazeneca Ab | Salts 668 |
| GB0702457D0 (en) | 2007-02-08 | 2007-03-21 | Astrazeneca Ab | New combination 666 |
| GB0702459D0 (en) | 2007-02-08 | 2007-03-21 | Astrazeneca Ab | Salts 669 |
| GB0703999D0 (en) | 2007-03-01 | 2007-04-11 | Astrazeneca Ab | New combination 667 |
| GB0704000D0 (en) | 2007-03-01 | 2007-04-11 | Astrazeneca Ab | Salts 670 |
| WO2009037503A2 (en) | 2007-09-18 | 2009-03-26 | Astrazeneca Ab | New combination - 012 for the treatment of respiratory diseases |
-
2007
- 2007-03-02 TW TW096107171A patent/TW200745067A/zh unknown
- 2007-03-12 AU AU2007225471A patent/AU2007225471A1/en not_active Abandoned
- 2007-03-12 CA CA002644014A patent/CA2644014A1/en not_active Abandoned
- 2007-03-12 JP JP2009500323A patent/JP2009530272A/ja not_active Withdrawn
- 2007-03-12 US US12/282,634 patent/US7951954B2/en not_active Expired - Fee Related
- 2007-03-12 BR BRPI0709589-9A patent/BRPI0709589A2/pt not_active IP Right Cessation
- 2007-03-12 KR KR1020087024962A patent/KR20080103104A/ko not_active Withdrawn
- 2007-03-12 RU RU2008136553/04A patent/RU2008136553A/ru not_active Application Discontinuation
- 2007-03-12 WO PCT/SE2007/000233 patent/WO2007106016A1/en not_active Ceased
- 2007-03-12 EP EP07716051A patent/EP1996566A1/en not_active Withdrawn
- 2007-03-14 AR ARP070101043A patent/AR059842A1/es unknown
- 2007-03-14 UY UY30206A patent/UY30206A1/es unknown
-
2008
- 2008-08-18 IL IL193530A patent/IL193530A0/en unknown
- 2008-09-15 EC EC2008008741A patent/ECSP088741A/es unknown
- 2008-10-13 NO NO20084278A patent/NO20084278L/no not_active Application Discontinuation
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