JP2015523387A5 - - Google Patents
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- Publication number
- JP2015523387A5 JP2015523387A5 JP2015523172A JP2015523172A JP2015523387A5 JP 2015523387 A5 JP2015523387 A5 JP 2015523387A5 JP 2015523172 A JP2015523172 A JP 2015523172A JP 2015523172 A JP2015523172 A JP 2015523172A JP 2015523387 A5 JP2015523387 A5 JP 2015523387A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrazol
- ylmethyl
- phenoxy
- yloxy
- pyridin
- 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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- -1 = O Chemical group 0.000 claims 33
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 24
- 125000000623 heterocyclic group Chemical group 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 12
- 150000003839 salts Chemical class 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000001475 halogen functional group Chemical group 0.000 claims 5
- 125000005647 linker group Chemical group 0.000 claims 4
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 230000001404 mediated effect Effects 0.000 claims 2
- IFVFOBKPWWNHFY-UHFFFAOYSA-N (1-hydroxycyclopropyl)-[4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]quinolin-2-yl]methyl]piperazin-1-yl]methanone Chemical compound C1CN(CC=2N=C3C=CC(OC=4C=CC(=CC=4)C=4NN=CC=4)=CC3=CC=2)CCN1C(=O)C1(O)CC1 IFVFOBKPWWNHFY-UHFFFAOYSA-N 0.000 claims 1
- ZCHQIMVQVKLHBO-GOTSBHOMSA-N (1s,2s)-2-[methyl-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]amino]cyclohexan-1-ol Chemical compound CN([C@@H]1[C@H](CCCC1)O)CC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 ZCHQIMVQVKLHBO-GOTSBHOMSA-N 0.000 claims 1
- QQBNHIPXAMSXDB-OALUTQOASA-N (1s,5s)-3-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]-8-oxa-3-azabicyclo[3.2.1]octane Chemical compound C([C@@]1(CC[C@@](C2)(O1)[H])[H])N2CC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 QQBNHIPXAMSXDB-OALUTQOASA-N 0.000 claims 1
- VQSPDJXKRNSSRK-SFHVURJKSA-N (2s)-2-hydroxy-1-[4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]quinolin-2-yl]methyl]piperazin-1-yl]propan-1-one Chemical compound C1CN(C(=O)[C@@H](O)C)CCN1CC1=CC=C(C=C(OC=2C=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 VQSPDJXKRNSSRK-SFHVURJKSA-N 0.000 claims 1
- PZILIWJLCPPYMG-VWLOTQADSA-N (2s)-2-phenyl-2-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methylamino]acetamide Chemical compound N([C@H](C(=O)N)C=1C=CC=CC=1)CC(N=C1C=C2)=CC=C1C=C2OC(N=C1)=CC=C1C1=CC=NN1 PZILIWJLCPPYMG-VWLOTQADSA-N 0.000 claims 1
- HSTMOISBVYSKBD-INIZCTEOSA-N (2s)-n-ethyl-1-methoxy-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]propan-2-amine Chemical compound C=1C=C2NC(CN(CC)[C@@H](C)COC)=NC2=CC=1OC(C=C1)=CC=C1C1=CC=NN1 HSTMOISBVYSKBD-INIZCTEOSA-N 0.000 claims 1
- MCBRYUMNYSUPNR-IYBDPMFKSA-N (2s,6r)-2,6-dimethyl-4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]morpholine Chemical compound C1[C@@H](C)O[C@@H](C)CN1CC1=NC2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2N1 MCBRYUMNYSUPNR-IYBDPMFKSA-N 0.000 claims 1
- CFMJYWFFWOMPKU-IRXDYDNUSA-N (2s,6s)-2,6-dimethyl-4-[[6-[[4-(1h-pyrazol-5-yl)phenyl]methyl]-1h-benzimidazol-2-yl]methyl]morpholine Chemical compound C1[C@H](C)O[C@@H](C)CN1CC(NC1=C2)=NC1=CC=C2CC1=CC=C(C=2NN=CC=2)C=C1 CFMJYWFFWOMPKU-IRXDYDNUSA-N 0.000 claims 1
- WIKGOYCAOBBNTN-INIZCTEOSA-N (3r)-1-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methyl]pyrrolidine-3-carbonitrile Chemical compound C1[C@H](C#N)CCN1CC1=CC=C(C=C(OC=2N=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 WIKGOYCAOBBNTN-INIZCTEOSA-N 0.000 claims 1
- NLICEIZLJIPMOZ-MRXNPFEDSA-N (3r)-n-methyl-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]oxolan-3-amine Chemical compound CN([C@H]1COCC1)CC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 NLICEIZLJIPMOZ-MRXNPFEDSA-N 0.000 claims 1
- DMCBYAJTPSLYRF-HNNXBMFYSA-N (3s)-1-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]pyrrolidin-3-ol Chemical compound C1[C@@H](O)CCN1CC(NC1=C2)=NC1=CC=C2OC1=CC=C(C=2NN=CC=2)C=C1 DMCBYAJTPSLYRF-HNNXBMFYSA-N 0.000 claims 1
- CBXSVYDQRXUHOZ-SFHVURJKSA-N (3s)-1-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methyl]pyrrolidin-3-ol Chemical compound C1[C@@H](O)CCN1CC1=CC=C(C=C(OC=2N=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 CBXSVYDQRXUHOZ-SFHVURJKSA-N 0.000 claims 1
- QHOWKGIBWNFMGZ-FQEVSTJZSA-N (3s)-3-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methylamino]pyrrolidin-2-one Chemical compound O=C1NCC[C@@H]1NCC1=CC=C(C=C(OC=2N=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 QHOWKGIBWNFMGZ-FQEVSTJZSA-N 0.000 claims 1
- DDNDGMWWIBXYCG-SANMLTNESA-N (3s)-3-hydroxy-1-[1-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxynaphthalen-2-yl]methyl]piperidin-4-yl]pyrrolidin-2-one Chemical compound O=C1[C@@H](O)CCN1C1CCN(CC=2C=C3C=CC(OC=4N=CC(=CC=4)C=4NN=CC=4)=CC3=CC=2)CC1 DDNDGMWWIBXYCG-SANMLTNESA-N 0.000 claims 1
- GTJLDVVTURSXGH-HNNXBMFYSA-N (3s)-3-methyl-4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]morpholine Chemical compound C[C@H]1COCCN1CC1=NC2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2N1 GTJLDVVTURSXGH-HNNXBMFYSA-N 0.000 claims 1
- AEKZLAYERXIEPV-HNNXBMFYSA-N (3s)-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]oxolan-3-amine Chemical compound N=1C2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2NC=1CN[C@H]1CCOC1 AEKZLAYERXIEPV-HNNXBMFYSA-N 0.000 claims 1
- NLICEIZLJIPMOZ-INIZCTEOSA-N (3s)-n-methyl-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]oxolan-3-amine Chemical compound CN([C@@H]1COCC1)CC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 NLICEIZLJIPMOZ-INIZCTEOSA-N 0.000 claims 1
- VHPMVZBCNHLNDN-HOTGVXAUSA-N (3s,5s)-3,5-dimethyl-4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]morpholine Chemical compound C[C@H]1COC[C@H](C)N1CC1=NC2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2N1 VHPMVZBCNHLNDN-HOTGVXAUSA-N 0.000 claims 1
- LSTZAADQVYMEGP-GOSISDBHSA-N (5r)-5-[[6-[4-(1h-pyrazol-5-yl)phenoxy]imidazo[1,2-a]pyridin-2-yl]methoxy]piperidin-2-one Chemical compound C1NC(=O)CC[C@H]1OCC1=CN(C=C(OC=2C=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 LSTZAADQVYMEGP-GOSISDBHSA-N 0.000 claims 1
- GICNMVGQMHRWML-IBGZPJMESA-N (5s)-5-[6-[4-(1h-pyrazol-5-yl)phenoxy]quinolin-2-yl]oxypiperidin-2-one Chemical compound C1NC(=O)CC[C@@H]1OC1=CC=C(C=C(OC=2C=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 GICNMVGQMHRWML-IBGZPJMESA-N 0.000 claims 1
- ZPECYVOUACBRAL-INIZCTEOSA-N (5s)-5-[[5-[4-(1h-pyrazol-5-yl)phenoxy]indazol-2-yl]methyl]pyrrolidin-2-one Chemical compound N1C(=O)CC[C@H]1CN1N=C2C=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC2=C1 ZPECYVOUACBRAL-INIZCTEOSA-N 0.000 claims 1
- LWIVKWCGQULCQD-HNNXBMFYSA-N (5s)-5-[[5-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyindazol-1-yl]methyl]pyrrolidin-2-one Chemical compound N1C(=O)CC[C@H]1CN1C2=CC=C(OC=3N=CC(=CC=3)C=3NN=CC=3)C=C2C=N1 LWIVKWCGQULCQD-HNNXBMFYSA-N 0.000 claims 1
- GHKGGIKBGMUWIS-KRWDZBQOSA-N (5s)-5-[[6-[4-(1h-pyrazol-5-yl)phenoxy]isoquinolin-1-yl]oxymethyl]pyrrolidin-2-one Chemical compound N1C(=O)CC[C@H]1COC1=NC=CC2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C12 GHKGGIKBGMUWIS-KRWDZBQOSA-N 0.000 claims 1
- 125000005960 1,4-diazepanyl group Chemical group 0.000 claims 1
- 125000005962 1,4-oxazepanyl group Chemical group 0.000 claims 1
- WDXWPPAHOUXELJ-UHFFFAOYSA-N 1-(1,4-dioxan-2-yl)-n-methyl-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]methanamine Chemical compound N=1C2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2NC=1CN(C)CC1COCCO1 WDXWPPAHOUXELJ-UHFFFAOYSA-N 0.000 claims 1
- DZAOREJXYFNBJA-UHFFFAOYSA-N 1-(oxan-4-yl)-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]methanamine Chemical compound C1COCCC1CNCC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 DZAOREJXYFNBJA-UHFFFAOYSA-N 0.000 claims 1
- FVKPKLGUBVWBLT-UHFFFAOYSA-N 1-(oxolan-2-yl)-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]methanamine Chemical compound C1CCOC1CNCC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 FVKPKLGUBVWBLT-UHFFFAOYSA-N 0.000 claims 1
- QPVIYPPRTZGLTH-LBAQZLPGSA-N 1-[(1s)-5-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methyl]-2,5-diazabicyclo[2.2.1]heptan-2-yl]ethanone Chemical compound C([C@](N(C1)C(C)=O)(C2)[H])C1N2CC(N=C1C=C2)=CC=C1C=C2OC(N=C1)=CC=C1C=1C=CNN=1 QPVIYPPRTZGLTH-LBAQZLPGSA-N 0.000 claims 1
- FVKPKLGUBVWBLT-GOSISDBHSA-N 1-[(2r)-oxolan-2-yl]-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]methanamine Chemical compound C([C@@H]1OCCC1)NCC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 FVKPKLGUBVWBLT-GOSISDBHSA-N 0.000 claims 1
- FVKPKLGUBVWBLT-SFHVURJKSA-N 1-[(2s)-oxolan-2-yl]-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]methanamine Chemical compound C([C@H]1OCCC1)NCC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 FVKPKLGUBVWBLT-SFHVURJKSA-N 0.000 claims 1
- YJQOQHAGGJOSAV-NRFANRHFSA-N 1-[(3s)-3-(hydroxymethyl)-4-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methyl]piperazin-1-yl]ethanone Chemical compound OC[C@@H]1CN(C(=O)C)CCN1CC1=CC=C(C=C(OC=2N=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 YJQOQHAGGJOSAV-NRFANRHFSA-N 0.000 claims 1
- SDNRQYIHEQYIAQ-UHFFFAOYSA-N 1-[1-[2-[5-[4-(1h-pyrazol-5-yl)phenoxy]indazol-1-yl]ethyl]piperidin-4-yl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1CCN(CCN2C3=CC=C(OC=4C=CC(=CC=4)C=4NN=CC=4)C=C3C=N2)CC1 SDNRQYIHEQYIAQ-UHFFFAOYSA-N 0.000 claims 1
- KTVJPFLVEAFOBJ-UHFFFAOYSA-N 1-[1-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-2,3-dihydro-1-benzofuran-2-yl]methyl]piperidin-4-yl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1CCN(CC2OC3=CC(OC=4C=CC(=CC=4)C=4NN=CC=4)=CC=C3C2)CC1 KTVJPFLVEAFOBJ-UHFFFAOYSA-N 0.000 claims 1
- IFPGAJVLPUNQML-UHFFFAOYSA-N 1-[1-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxy-2,3-dihydro-1-benzofuran-2-yl]methyl]piperidin-4-yl]pyrrolidin-2-one Chemical compound O=C1CCCN1C1CCN(CC2OC3=CC(OC=4N=CC(=CC=4)C=4NN=CC=4)=CC=C3C2)CC1 IFPGAJVLPUNQML-UHFFFAOYSA-N 0.000 claims 1
- AQVYQCGFNDJTDQ-UHFFFAOYSA-N 1-[2-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methyl]-1,3,3a,4,6,6a-hexahydropyrrolo[3,4-c]pyrrol-5-yl]ethanone Chemical compound C1C2CN(C(=O)C)CC2CN1CC(N=C1C=C2)=CC=C1C=C2OC(N=C1)=CC=C1C1=CC=NN1 AQVYQCGFNDJTDQ-UHFFFAOYSA-N 0.000 claims 1
- FYFQGZWOBIQLKI-UHFFFAOYSA-N 1-[3-[[methyl-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methyl]amino]methyl]azetidin-1-yl]ethanone Chemical compound C=1C=C2C=C(OC=3N=CC(=CC=3)C=3NN=CC=3)C=CC2=NC=1CN(C)CC1CN(C(C)=O)C1 FYFQGZWOBIQLKI-UHFFFAOYSA-N 0.000 claims 1
- ZIKUPLGQIWYEJB-UHFFFAOYSA-N 1-[4-[2-[5-[4-(1h-pyrazol-5-yl)phenoxy]indazol-1-yl]ethyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CCN1C2=CC=C(OC=3C=CC(=CC=3)C=3NN=CC=3)C=C2C=N1 ZIKUPLGQIWYEJB-UHFFFAOYSA-N 0.000 claims 1
- GOQUUIMJQZQXCY-UHFFFAOYSA-N 1-[4-[2-[5-[4-(1h-pyrazol-5-yl)phenoxy]indazol-2-yl]ethyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CCN1N=C2C=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC2=C1 GOQUUIMJQZQXCY-UHFFFAOYSA-N 0.000 claims 1
- DODRESGUWBQESN-UHFFFAOYSA-N 1-[4-[2-[5-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyindazol-1-yl]ethyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CCN1C2=CC=C(OC=3N=CC(=CC=3)C=3NN=CC=3)C=C2C=N1 DODRESGUWBQESN-UHFFFAOYSA-N 0.000 claims 1
- HNCQIANMHNFLCL-UHFFFAOYSA-N 1-[4-[2-[5-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyindol-1-yl]ethyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CCN1C2=CC=C(OC=3N=CC(=CC=3)C=3NN=CC=3)C=C2C=C1 HNCQIANMHNFLCL-UHFFFAOYSA-N 0.000 claims 1
- RCTXHOZAIVHGFY-UHFFFAOYSA-N 1-[4-[2-[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxy-1-benzofuran-3-yl]ethyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CCC1=COC2=CC(OC=3N=CC(=CC=3)C=3NN=CC=3)=CC=C12 RCTXHOZAIVHGFY-UHFFFAOYSA-N 0.000 claims 1
- AKQQLRQDMZSMFD-UHFFFAOYSA-N 1-[4-[2-[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxy-2,3-dihydro-1-benzofuran-3-yl]ethyl]-1,4-diazepan-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCCN1CCC1C2=CC=C(OC=3N=CC(=CC=3)C=3NN=CC=3)C=C2OC1 AKQQLRQDMZSMFD-UHFFFAOYSA-N 0.000 claims 1
- RRFUTHNPFJQDMH-UHFFFAOYSA-N 1-[4-[2-[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxy-2,3-dihydro-1-benzofuran-3-yl]ethyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CCC1C2=CC=C(OC=3N=CC(=CC=3)C=3NN=CC=3)C=C2OC1 RRFUTHNPFJQDMH-UHFFFAOYSA-N 0.000 claims 1
- WSAAKOOUCHELIF-UHFFFAOYSA-N 1-[4-[3-[5-[4-(1h-pyrazol-5-yl)phenoxy]indazol-2-yl]propyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CCCN1N=C2C=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC2=C1 WSAAKOOUCHELIF-UHFFFAOYSA-N 0.000 claims 1
- DWNTUXDWDNLLIM-UHFFFAOYSA-N 1-[4-[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1C1=CC=C(C=C(OC=2N=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 DWNTUXDWDNLLIM-UHFFFAOYSA-N 0.000 claims 1
- IZCIVWZHDWJIBQ-UHFFFAOYSA-N 1-[4-[[5-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxy-1h-indol-2-yl]methyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CC1=CC2=CC(OC=3N=CC(=CC=3)C=3NN=CC=3)=CC=C2N1 IZCIVWZHDWJIBQ-UHFFFAOYSA-N 0.000 claims 1
- GYSHNLMYPVECDD-UHFFFAOYSA-N 1-[4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]quinolin-2-yl]methyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CC1=CC=C(C=C(OC=2C=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 GYSHNLMYPVECDD-UHFFFAOYSA-N 0.000 claims 1
- UJZIDMOAVRUZRG-UHFFFAOYSA-N 1-[4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]quinolin-2-yl]methyl]piperazin-1-yl]propan-1-one Chemical compound C1CN(C(=O)CC)CCN1CC1=CC=C(C=C(OC=2C=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 UJZIDMOAVRUZRG-UHFFFAOYSA-N 0.000 claims 1
- XBBJVLRSZZVPDG-UHFFFAOYSA-N 1-[4-[[6-[4-(1h-pyrazol-5-yl)phenoxy]quinoxalin-2-yl]methyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CC1=CN=C(C=C(OC=2C=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 XBBJVLRSZZVPDG-UHFFFAOYSA-N 0.000 claims 1
- OCELLLYRRBLAMV-UHFFFAOYSA-N 1-[4-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxy-1-benzofuran-3-yl]methyl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1CC1=COC2=CC(OC=3N=CC(=CC=3)C=3NN=CC=3)=CC=C12 OCELLLYRRBLAMV-UHFFFAOYSA-N 0.000 claims 1
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- VZOSALFYAXVAPX-UHFFFAOYSA-N n-methyl-1-(oxolan-3-yl)-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]methanamine Chemical compound N=1C2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2NC=1CN(C)CC1CCOC1 VZOSALFYAXVAPX-UHFFFAOYSA-N 0.000 claims 1
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- NQEDXMFIEOOFND-IBGZPJMESA-N n-methyl-1-[(2s)-oxolan-2-yl]-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]methanamine Chemical class N=1C2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2NC=1CN(C)C[C@@H]1CCCO1 NQEDXMFIEOOFND-IBGZPJMESA-N 0.000 claims 1
- JBXGMBUMJFGUEK-UHFFFAOYSA-N n-methyl-1-[2-[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxy-1-benzofuran-3-yl]ethyl]piperidine-4-carboxamide Chemical compound C1CC(C(=O)NC)CCN1CCC1=COC2=CC(OC=3N=CC(=CC=3)C=3NN=CC=3)=CC=C12 JBXGMBUMJFGUEK-UHFFFAOYSA-N 0.000 claims 1
- GMHGSKAFBBCBPG-UHFFFAOYSA-N n-methyl-1-[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methanamine Chemical compound C1=CC2=NC(CNC)=CC=C2C=C1OC(N=C1)=CC=C1C1=CC=NN1 GMHGSKAFBBCBPG-UHFFFAOYSA-N 0.000 claims 1
- CVSQXIMBBJFSPS-UHFFFAOYSA-N n-methyl-1-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-2,3-dihydro-1-benzofuran-2-yl]methyl]piperidine-4-carboxamide Chemical compound C1CC(C(=O)NC)CCN1CC1OC2=CC(OC=3C=CC(=CC=3)C=3NN=CC=3)=CC=C2C1 CVSQXIMBBJFSPS-UHFFFAOYSA-N 0.000 claims 1
- SEOXJTRNMQSPFQ-UHFFFAOYSA-N n-methyl-n-[1-[[6-[5-(1h-pyrazol-5-yl)pyridin-2-yl]oxyquinolin-2-yl]methyl]piperidin-4-yl]acetamide Chemical compound C1CC(N(C)C(C)=O)CCN1CC1=CC=C(C=C(OC=2N=CC(=CC=2)C=2NN=CC=2)C=C2)C2=N1 SEOXJTRNMQSPFQ-UHFFFAOYSA-N 0.000 claims 1
- CRJOFMIHOFVOGJ-UHFFFAOYSA-N n-methyl-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]cyclopentanamine Chemical compound C1CCCC1N(C)CC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 CRJOFMIHOFVOGJ-UHFFFAOYSA-N 0.000 claims 1
- LZIHOFZRBZYAMN-UHFFFAOYSA-N n-methyl-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]cyclopropanamine Chemical compound C1CC1N(C)CC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 LZIHOFZRBZYAMN-UHFFFAOYSA-N 0.000 claims 1
- CFJNOQHDULUVAH-UHFFFAOYSA-N n-methyl-n-[[6-[4-(1h-pyrazol-5-yl)phenoxy]-1h-benzimidazol-2-yl]methyl]oxan-4-amine Chemical compound C1COCCC1N(C)CC(NC1=CC=2)=NC1=CC=2OC(C=C1)=CC=C1C1=CC=NN1 CFJNOQHDULUVAH-UHFFFAOYSA-N 0.000 claims 1
- 125000000160 oxazolidinyl group Chemical group 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 229940080818 propionamide Drugs 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 1
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| PCT/US2013/050624 WO2014014874A1 (en) | 2012-07-17 | 2013-07-16 | Pyrazole derivatives which inhibit leukotriene production |
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| NZ628587A (en) | 2012-03-06 | 2016-07-29 | Boehringer Ingelheim Int | Benzodioxanes in combination with other actives for inhibiting leukotriene production |
| US9403830B2 (en) | 2012-07-17 | 2016-08-02 | Boehringer Ingelheim International Gmbh | Inhibitors of leukotriene production |
| JP2016523982A (ja) * | 2013-07-15 | 2016-08-12 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ロイコトリエン生成の阻害剤 |
| JP6353899B2 (ja) * | 2013-07-15 | 2018-07-04 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | ロイコトリエン生成の阻害剤 |
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| WO2018050825A1 (de) | 2016-09-19 | 2018-03-22 | Bayer Cropscience Aktiengesellschaft | Pyrazolo[1,5-a]pyridin- derivative und ihre verwendung als schädlingsbekämpfungsmittel |
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| CN110229091B (zh) * | 2019-06-21 | 2022-11-22 | 天津科技大学 | 具有白三烯a4水解酶抑制作用的1，5-二取代吲哚衍生物及应用 |
| CA3164134A1 (en) | 2019-12-06 | 2021-06-10 | Vertex Pharmaceuticals Incorporated | Substituted tetrahydrofurans as modulators of sodium channels |
| CN113045551B (zh) * | 2019-12-27 | 2024-07-09 | 广东东阳光药业股份有限公司 | 一种作为甲状腺激素β受体激动剂的化合物及其用途 |
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| EP2734516B1 (en) * | 2011-07-19 | 2015-06-17 | Boehringer Ingelheim International GmbH | Arylpyrazole ethers as inhibitors of leukotriene a4 hydrolase |
| TW201350474A (zh) | 2012-03-06 | 2013-12-16 | Boehringer Ingelheim Int | 白三烯素生成之苯并二噁烷抑制劑 |
| NZ628587A (en) | 2012-03-06 | 2016-07-29 | Boehringer Ingelheim Int | Benzodioxanes in combination with other actives for inhibiting leukotriene production |
| US9403830B2 (en) | 2012-07-17 | 2016-08-02 | Boehringer Ingelheim International Gmbh | Inhibitors of leukotriene production |
-
2013
- 2013-07-16 US US13/942,988 patent/US9403830B2/en active Active
- 2013-07-16 WO PCT/US2013/050624 patent/WO2014014874A1/en not_active Ceased
- 2013-07-16 AR ARP130102537 patent/AR091786A1/es unknown
- 2013-07-16 TW TW102125428A patent/TW201416354A/zh unknown
- 2013-07-16 EP EP13740484.4A patent/EP2885285B1/en active Active
- 2013-07-16 JP JP2015523172A patent/JP6256467B2/ja active Active
- 2013-07-17 UY UY0001034917A patent/UY34917A/es unknown
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