CA2728046A1 - S1p1 receptor agonists and use thereof - Google Patents
S1p1 receptor agonists and use thereof Download PDFInfo
- Publication number
- CA2728046A1 CA2728046A1 CA2728046A CA2728046A CA2728046A1 CA 2728046 A1 CA2728046 A1 CA 2728046A1 CA 2728046 A CA2728046 A CA 2728046A CA 2728046 A CA2728046 A CA 2728046A CA 2728046 A1 CA2728046 A1 CA 2728046A1
- Authority
- CA
- Canada
- Prior art keywords
- fluoro
- phenyl
- thiazolo
- phenylcyclopropyl
- 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.)
- Abandoned
Links
- 102000011011 Sphingosine 1-phosphate receptors Human genes 0.000 title claims abstract description 11
- 108050001083 Sphingosine 1-phosphate receptors Proteins 0.000 title claims abstract description 11
- 229940044601 receptor agonist Drugs 0.000 title abstract description 6
- 239000000018 receptor agonist Substances 0.000 title abstract description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 187
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 16
- 201000010099 disease Diseases 0.000 claims abstract description 10
- -1 monosubstituted amino Chemical group 0.000 claims description 314
- 201000006417 multiple sclerosis Diseases 0.000 claims description 181
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 103
- 229910052731 fluorine Inorganic materials 0.000 claims description 69
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 64
- 229920006395 saturated elastomer Polymers 0.000 claims description 64
- 229910052801 chlorine Inorganic materials 0.000 claims description 62
- 238000000034 method Methods 0.000 claims description 62
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 44
- 229910052739 hydrogen Inorganic materials 0.000 claims description 42
- 125000001153 fluoro group Chemical group F* 0.000 claims description 40
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 34
- 239000003814 drug Substances 0.000 claims description 32
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 29
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 27
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 26
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 24
- 229910052799 carbon Inorganic materials 0.000 claims description 23
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims description 21
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 19
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
- GFZWHAAOIVMHOI-UHFFFAOYSA-N azetidine-3-carboxylic acid Chemical compound OC(=O)C1CNC1 GFZWHAAOIVMHOI-UHFFFAOYSA-N 0.000 claims description 15
- 150000003839 salts Chemical class 0.000 claims description 15
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 13
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 13
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 11
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 10
- 125000002837 carbocyclic group Chemical group 0.000 claims description 10
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 10
- 125000004476 heterocycloamino group Chemical group 0.000 claims description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 10
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 230000001404 mediated effect Effects 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 7
- 125000001072 heteroaryl group Chemical group 0.000 claims description 7
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 7
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 7
- 125000004442 acylamino group Chemical group 0.000 claims description 6
- HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 5
- NQOYFWVJUAMDSC-UHFFFAOYSA-N 1-[[2-methyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound CC1=CC(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)=CC=C1CN1CC(C(O)=O)C1 NQOYFWVJUAMDSC-UHFFFAOYSA-N 0.000 claims description 5
- KCMALGDZUKTGJR-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 KCMALGDZUKTGJR-UHFFFAOYSA-N 0.000 claims description 5
- RSJXHKBDHLDTJG-UHFFFAOYSA-N 1-[[3-methyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C=1C=C(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)C(C)=CC=1CN1CC(C(O)=O)C1 RSJXHKBDHLDTJG-UHFFFAOYSA-N 0.000 claims description 5
- OSOQQWGQWAAXRR-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]cyclobutane-1,1-dicarboxylic acid Chemical compound C1C(C(=O)O)(C(O)=O)CC1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 OSOQQWGQWAAXRR-UHFFFAOYSA-N 0.000 claims description 5
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 5
- IXHZVOWTEVMNQD-UHFFFAOYSA-N 1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]cyclopropan-1-amine Chemical compound C=1C=C(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)C(F)=CC=1C1(N)CC1 IXHZVOWTEVMNQD-UHFFFAOYSA-N 0.000 claims description 4
- OIQUGXZGFRNXRR-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-(1-phenylcyclohexyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CCCCC3)C=3C=CC=CC=3)N=C2S1 OIQUGXZGFRNXRR-UHFFFAOYSA-N 0.000 claims description 4
- LWFNPYNEZMTEHO-UHFFFAOYSA-N 2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]propan-2-amine Chemical compound FC1=CC(C(C)(N)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 LWFNPYNEZMTEHO-UHFFFAOYSA-N 0.000 claims description 4
- NZOPMUNLWDQQBS-UHFFFAOYSA-N 2-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]propane-1,3-diol Chemical compound FC1=CC(CC(CO)CO)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 NZOPMUNLWDQQBS-UHFFFAOYSA-N 0.000 claims description 4
- RSJARRDGCGLARB-UHFFFAOYSA-N [3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methanol Chemical compound FC1=CC(CO)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 RSJARRDGCGLARB-UHFFFAOYSA-N 0.000 claims description 4
- 125000002431 aminoalkoxy group Chemical group 0.000 claims description 4
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 4
- 125000004475 heteroaralkyl group Chemical group 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- OHDAURMSEHMPFJ-IBGZPJMESA-N (1s)-2,2,2-trifluoro-1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethanol Chemical compound FC1=CC([C@H](O)C(F)(F)F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 OHDAURMSEHMPFJ-IBGZPJMESA-N 0.000 claims description 3
- JJMNOHMYOCDTNE-UHFFFAOYSA-N 1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethanol Chemical compound FC1=CC(C(O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 JJMNOHMYOCDTNE-UHFFFAOYSA-N 0.000 claims description 3
- DGRKENUAODQPTI-UHFFFAOYSA-N 1-[[3-amino-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C=1C=C(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)C(N)=CC=1CN1CC(C(O)=O)C1 DGRKENUAODQPTI-UHFFFAOYSA-N 0.000 claims description 3
- OIIKLYFYHWVBBT-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-(1-phenylcyclopent-3-en-1-yl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC=CC3)C=3C=CC=CC=3)N=C2S1 OIIKLYFYHWVBBT-UHFFFAOYSA-N 0.000 claims description 3
- XOISWOAQHPFMSU-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-(1-phenylcyclopentyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CCCC3)C=3C=CC=CC=3)N=C2S1 XOISWOAQHPFMSU-UHFFFAOYSA-N 0.000 claims description 3
- SJRVYCQTDNRXSQ-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidin-3-ol Chemical compound C1C(O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 SJRVYCQTDNRXSQ-UHFFFAOYSA-N 0.000 claims description 3
- QFXSDFZFPKZDSK-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-(2-phenyloxetan-2-yl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(OCC3)C=3C=CC=CC=3)N=C2S1 QFXSDFZFPKZDSK-UHFFFAOYSA-N 0.000 claims description 3
- WYDTUIYHKYBKDQ-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-[1-(4-fluorophenyl)cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC(F)=CC=3)N=C2S1 WYDTUIYHKYBKDQ-UHFFFAOYSA-N 0.000 claims description 3
- UMQXIFJBTRLNCD-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-[1-(4-hydroxyphenyl)cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC(O)=CC=3)N=C2S1 UMQXIFJBTRLNCD-UHFFFAOYSA-N 0.000 claims description 3
- ASUCRXBDHDVRQF-UHFFFAOYSA-N 2-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzoyl]amino]acetic acid Chemical compound FC1=CC(C(=O)NCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 ASUCRXBDHDVRQF-UHFFFAOYSA-N 0.000 claims description 3
- FQYFGWGKFYQDOL-UHFFFAOYSA-N 3-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]propanoic acid Chemical compound FC1=CC(CCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 FQYFGWGKFYQDOL-UHFFFAOYSA-N 0.000 claims description 3
- LQFBUKSMYSXBTE-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzoyl]amino]propanoic acid Chemical compound FC1=CC(C(=O)NCCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 LQFBUKSMYSXBTE-UHFFFAOYSA-N 0.000 claims description 3
- CPZNHEBXQUGQPL-UHFFFAOYSA-N 4-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzoyl]amino]butanoic acid Chemical compound FC1=CC(C(=O)NCCCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 CPZNHEBXQUGQPL-UHFFFAOYSA-N 0.000 claims description 3
- CFJDEAYMRZMDGQ-IYARVYRRSA-N C1[C@@H](C(=O)O)C[C@@H]1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 Chemical compound C1[C@@H](C(=O)O)C[C@@H]1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 CFJDEAYMRZMDGQ-IYARVYRRSA-N 0.000 claims description 3
- CFJDEAYMRZMDGQ-HDICACEKSA-N C1[C@H](C(=O)O)C[C@@H]1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 Chemical compound C1[C@H](C(=O)O)C[C@@H]1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 CFJDEAYMRZMDGQ-HDICACEKSA-N 0.000 claims description 3
- BSFNCTKLBHOCNB-UHFFFAOYSA-N [2-amino-4-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]-2-(hydroxymethyl)butyl] dihydrogen phosphate Chemical compound FC1=CC(CCC(CO)(N)COP(O)(O)=O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 BSFNCTKLBHOCNB-UHFFFAOYSA-N 0.000 claims description 3
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 3
- 125000004531 indol-5-yl group Chemical group [H]N1C([H])=C([H])C2=C([H])C(*)=C([H])C([H])=C12 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- KVSCIJUANFKDHN-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-(1-phenylcyclobutyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CCC3)C=3C=CC=CC=3)N=C2S1 KVSCIJUANFKDHN-UHFFFAOYSA-N 0.000 claims description 2
- XQLGIFYJCJXYBJ-UHFFFAOYSA-N 1-[[3-fluoro-4-[5-[1-(2-fluorophenyl)cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C(=CC=CC=3)F)N=C2S1 XQLGIFYJCJXYBJ-UHFFFAOYSA-N 0.000 claims description 2
- QILOXDHVYSGPRP-UHFFFAOYSA-N 1-[[3-fluoro-4-[6-(1-phenylcyclopropyl)-[1,3]thiazolo[4,5-c]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CN=C(C3(CC3)C=3C=CC=CC=3)C=C2S1 QILOXDHVYSGPRP-UHFFFAOYSA-N 0.000 claims description 2
- SINCOKVLJHSFIM-INIZCTEOSA-N 1-[[4-[5-[1-[(1s)-3,3-difluorocyclopentyl]cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]-3-fluorophenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)[C@@H]3CC(F)(F)CC3)N=C2S1 SINCOKVLJHSFIM-INIZCTEOSA-N 0.000 claims description 2
- ZKOGVNKSMKCWIJ-UHFFFAOYSA-N 2-[4-[(3,3-difluoroazetidin-1-yl)methyl]-2-fluorophenyl]-5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridine Chemical compound C=1C=C(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)C(F)=CC=1CN1CC(F)(F)C1 ZKOGVNKSMKCWIJ-UHFFFAOYSA-N 0.000 claims description 2
- YBBIQAQUTJCVHA-UHFFFAOYSA-N 3-[2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]propan-2-ylamino]propanoic acid Chemical compound FC1=CC(C(C)(NCCC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 YBBIQAQUTJCVHA-UHFFFAOYSA-N 0.000 claims description 2
- LAXZWYOIVOOUDB-UHFFFAOYSA-N 3-[[1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]cyclopropyl]amino]propanoic acid Chemical compound C=1C=C(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)C(F)=CC=1C1(NCCC(=O)O)CC1 LAXZWYOIVOOUDB-UHFFFAOYSA-N 0.000 claims description 2
- 125000004539 5-benzimidazolyl group Chemical group N1=CNC2=C1C=CC(=C2)* 0.000 claims description 2
- CIFFBENAZAIHLL-UHFFFAOYSA-N [2,6-dimethyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methanol Chemical compound CC1=C(CO)C(C)=CC(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)=C1 CIFFBENAZAIHLL-UHFFFAOYSA-N 0.000 claims description 2
- DLKFRHULCKAHOW-UHFFFAOYSA-N [2-methyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methanol Chemical compound C1=C(CO)C(C)=CC(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)=C1 DLKFRHULCKAHOW-UHFFFAOYSA-N 0.000 claims description 2
- VTWSHDBNPHFDGO-VWLOTQADSA-N (2s)-2-amino-4-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]-2-methylbutanoic acid Chemical compound FC1=CC(CC[C@@](N)(C)C(O)=O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 VTWSHDBNPHFDGO-VWLOTQADSA-N 0.000 claims 2
- HIVYIHLBVHGTEB-UHFFFAOYSA-N 2-[4-(azetidin-1-ylmethyl)-2-fluorophenyl]-5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridine Chemical compound C=1C=C(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)C(F)=CC=1CN1CCC1 HIVYIHLBVHGTEB-UHFFFAOYSA-N 0.000 claims 2
- UWAASNKMOLMYQX-UHFFFAOYSA-N 3-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]anilino]cyclobutane-1-carboxylic acid Chemical compound C1C(C(=O)O)CC1NC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 UWAASNKMOLMYQX-UHFFFAOYSA-N 0.000 claims 2
- HPLPYWLCVPJOBA-CQSZACIVSA-N (1r)-1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethanamine Chemical compound FC1=CC([C@H](N)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 HPLPYWLCVPJOBA-CQSZACIVSA-N 0.000 claims 1
- HPLPYWLCVPJOBA-AWEZNQCLSA-N (1s)-1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethanamine Chemical compound FC1=CC([C@@H](N)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 HPLPYWLCVPJOBA-AWEZNQCLSA-N 0.000 claims 1
- ICAUQGOTJWRMLA-OAQYLSRUSA-N (2r)-1-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-2-carboxylic acid Chemical compound OC(=O)[C@H]1CCN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 ICAUQGOTJWRMLA-OAQYLSRUSA-N 0.000 claims 1
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- ZQJUTZAZNIRVCT-INIZCTEOSA-N (3s)-3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methylamino]butanoic acid Chemical compound FC1=CC(CN[C@H](CC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 ZQJUTZAZNIRVCT-INIZCTEOSA-N 0.000 claims 1
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- RLARDFHOEZWBLI-UHFFFAOYSA-N 1-[[4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC1=CC=C(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)C=C1 RLARDFHOEZWBLI-UHFFFAOYSA-N 0.000 claims 1
- NJDMSHLMXQGQPH-UHFFFAOYSA-N 1-[[4-[5-[1-(3,3-difluorocyclobutyl)cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]-3-fluorophenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C3CC(F)(F)C3)N=C2S1 NJDMSHLMXQGQPH-UHFFFAOYSA-N 0.000 claims 1
- WNJZDTVKMZYSDS-UHFFFAOYSA-N 1-[[4-[5-[1-(4,4-difluorocyclohexyl)cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]-3-fluorophenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C3CCC(F)(F)CC3)N=C2S1 WNJZDTVKMZYSDS-UHFFFAOYSA-N 0.000 claims 1
- SINCOKVLJHSFIM-MRXNPFEDSA-N 1-[[4-[5-[1-[(1r)-3,3-difluorocyclopentyl]cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]-3-fluorophenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)[C@H]3CC(F)(F)CC3)N=C2S1 SINCOKVLJHSFIM-MRXNPFEDSA-N 0.000 claims 1
- HMZVKDYDGFUGHL-UHFFFAOYSA-N 2,2,2-trifluoro-n-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]acetamide Chemical compound FC1=CC(NC(=O)C(F)(F)F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 HMZVKDYDGFUGHL-UHFFFAOYSA-N 0.000 claims 1
- DCTBWKCMHAXEPQ-UHFFFAOYSA-N 2-(1h-indol-5-yl)-5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridine Chemical compound C1CC1(C=1N=C2SC(=NC2=CC=1)C=1C=C2C=CNC2=CC=1)C1=CC=CC=C1 DCTBWKCMHAXEPQ-UHFFFAOYSA-N 0.000 claims 1
- CEGSARAHLLYTNN-UHFFFAOYSA-N 2-(3h-benzimidazol-5-yl)-5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridine Chemical compound C1CC1(C=1N=C2SC(=NC2=CC=1)C=1C=C2N=CNC2=CC=1)C1=CC=CC=C1 CEGSARAHLLYTNN-UHFFFAOYSA-N 0.000 claims 1
- GTTMJUHHNGKUHO-UHFFFAOYSA-N 2-[1-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidin-3-yl]acetic acid Chemical compound C1C(CC(=O)O)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 GTTMJUHHNGKUHO-UHFFFAOYSA-N 0.000 claims 1
- ZZJXFUOCCZJZIB-UHFFFAOYSA-N 2-[2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethylamino]-2-oxoacetic acid Chemical compound FC1=CC(CCNC(=O)C(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 ZZJXFUOCCZJZIB-UHFFFAOYSA-N 0.000 claims 1
- VORCSLWLKKFQHC-UHFFFAOYSA-N 2-[2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethylamino]acetic acid Chemical compound FC1=CC(CCNCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 VORCSLWLKKFQHC-UHFFFAOYSA-N 0.000 claims 1
- SXWDUKRKCWUMIC-UHFFFAOYSA-N 2-[2-fluoro-4-[(3-fluoroazetidin-1-yl)methyl]phenyl]-5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridine Chemical compound C1C(F)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 SXWDUKRKCWUMIC-UHFFFAOYSA-N 0.000 claims 1
- CAEJYNFXMQCXEC-UHFFFAOYSA-N 2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]-n,n-dimethylethanamine Chemical compound FC1=CC(CCN(C)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 CAEJYNFXMQCXEC-UHFFFAOYSA-N 0.000 claims 1
- ZDARLJLQSUPMHM-UHFFFAOYSA-N 2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethanamine Chemical compound FC1=CC(CCN)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 ZDARLJLQSUPMHM-UHFFFAOYSA-N 0.000 claims 1
- AJPDBWBLDLBHFP-UHFFFAOYSA-N 2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethanol Chemical compound FC1=CC(CCO)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 AJPDBWBLDLBHFP-UHFFFAOYSA-N 0.000 claims 1
- SMRWUURWIUGKDT-UHFFFAOYSA-N 2-[4-(azetidin-1-ylmethyl)-3,5-dimethylphenyl]-5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridine Chemical compound CC1=CC(C=2SC3=NC(=CC=C3N=2)C2(CC2)C=2C=CC=CC=2)=CC(C)=C1CN1CCC1 SMRWUURWIUGKDT-UHFFFAOYSA-N 0.000 claims 1
- YEPAMKWOYZLGNG-UHFFFAOYSA-N 2-[5-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]-1,3-dihydroisoindol-2-yl]acetic acid Chemical compound C1=C2CN(CC(=O)O)CC2=CC=C1C(SC1=N2)=NC1=CC=C2C1(C=2C=CC=CC=2)CC1 YEPAMKWOYZLGNG-UHFFFAOYSA-N 0.000 claims 1
- WBCIJRRSDSFXLA-UHFFFAOYSA-N 2-[5-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]indol-1-yl]acetic acid Chemical compound C=1C=C2N(CC(=O)O)C=CC2=CC=1C(SC1=N2)=NC1=CC=C2C1(C=2C=CC=CC=2)CC1 WBCIJRRSDSFXLA-UHFFFAOYSA-N 0.000 claims 1
- YLQKFWVHNGZHGG-UHFFFAOYSA-N 2-[6-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]-3,4-dihydro-1h-isoquinolin-2-yl]acetic acid Chemical compound C=1C=C2CN(CC(=O)O)CCC2=CC=1C(SC1=N2)=NC1=CC=C2C1(C=2C=CC=CC=2)CC1 YLQKFWVHNGZHGG-UHFFFAOYSA-N 0.000 claims 1
- RMFNOJPTVRZKER-UHFFFAOYSA-N 2-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methoxy]acetic acid Chemical compound FC1=CC(COCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 RMFNOJPTVRZKER-UHFFFAOYSA-N 0.000 claims 1
- HUOCVQORDNRUEB-UHFFFAOYSA-N 2-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]pyrazole-3-carboxylic acid Chemical compound OC(=O)C1=CC=NN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 HUOCVQORDNRUEB-UHFFFAOYSA-N 0.000 claims 1
- REZUCMPLONFXFD-UHFFFAOYSA-N 2-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methylamino]-2-methylpropanoic acid Chemical compound FC1=CC(CNC(C)(C)C(O)=O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 REZUCMPLONFXFD-UHFFFAOYSA-N 0.000 claims 1
- VENLOUUVGMBXRA-UHFFFAOYSA-N 2-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methylamino]acetic acid Chemical compound FC1=CC(CNCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 VENLOUUVGMBXRA-UHFFFAOYSA-N 0.000 claims 1
- YUIKHXVWWXKXIN-UHFFFAOYSA-N 2-amino-2-[2-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethyl]propane-1,3-diol Chemical compound FC1=CC(CCC(CO)(CO)N)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 YUIKHXVWWXKXIN-UHFFFAOYSA-N 0.000 claims 1
- UFQKEEFNPMAHQH-UHFFFAOYSA-N 2-amino-3-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]propan-1-ol Chemical compound FC1=CC(CC(CO)N)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 UFQKEEFNPMAHQH-UHFFFAOYSA-N 0.000 claims 1
- KMCSQCGFOWMHTE-UHFFFAOYSA-N 2-amino-3-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]propanoic acid Chemical compound FC1=CC(CC(N)C(O)=O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 KMCSQCGFOWMHTE-UHFFFAOYSA-N 0.000 claims 1
- YSSZJWNEWXHKEG-UHFFFAOYSA-N 3-[1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethylamino]butanoic acid Chemical compound FC1=CC(C(C)NC(CC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 YSSZJWNEWXHKEG-UHFFFAOYSA-N 0.000 claims 1
- NMSLMMIQACOIGQ-UHFFFAOYSA-N 3-[1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethylamino]propanoic acid Chemical compound FC1=CC(C(NCCC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 NMSLMMIQACOIGQ-UHFFFAOYSA-N 0.000 claims 1
- OGKHLOKWFGATCA-UHFFFAOYSA-N 3-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]anilino]propanoic acid Chemical compound FC1=CC(NCCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 OGKHLOKWFGATCA-UHFFFAOYSA-N 0.000 claims 1
- MLRJRUKHPPYMSX-UHFFFAOYSA-N 3-[3-fluoro-n-methyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]anilino]propanoic acid Chemical compound FC1=CC(N(CCC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 MLRJRUKHPPYMSX-UHFFFAOYSA-N 0.000 claims 1
- JJKYWTRVADBCKT-UHFFFAOYSA-N 3-[4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]anilino]propanoic acid Chemical compound C1=CC(NCCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 JJKYWTRVADBCKT-UHFFFAOYSA-N 0.000 claims 1
- JAFPEQCJDDRMHW-UHFFFAOYSA-N 3-[5-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]-1,3-dihydroisoindol-2-yl]propanoic acid Chemical compound C1=C2CN(CCC(=O)O)CC2=CC=C1C(SC1=N2)=NC1=CC=C2C1(C=2C=CC=CC=2)CC1 JAFPEQCJDDRMHW-UHFFFAOYSA-N 0.000 claims 1
- KUPNRRBAHXLCPZ-UHFFFAOYSA-N 3-[5-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzimidazol-1-yl]propanoic acid Chemical compound C=1C=C2N(CCC(=O)O)C=NC2=CC=1C(SC1=N2)=NC1=CC=C2C1(C=2C=CC=CC=2)CC1 KUPNRRBAHXLCPZ-UHFFFAOYSA-N 0.000 claims 1
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- JPLZHBMBMUPCAN-UHFFFAOYSA-N 3-[6-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]-3,4-dihydro-1h-isoquinolin-2-yl]propanoic acid Chemical compound C=1C=C2CN(CCC(=O)O)CCC2=CC=1C(SC1=N2)=NC1=CC=C2C1(C=2C=CC=CC=2)CC1 JPLZHBMBMUPCAN-UHFFFAOYSA-N 0.000 claims 1
- BOUVVZYZJSJQLM-UHFFFAOYSA-N 3-[6-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzimidazol-1-yl]propanoic acid Chemical compound C1=C2N(CCC(=O)O)C=NC2=CC=C1C(SC1=N2)=NC1=CC=C2C1(C=2C=CC=CC=2)CC1 BOUVVZYZJSJQLM-UHFFFAOYSA-N 0.000 claims 1
- NMSLMMIQACOIGQ-MRXNPFEDSA-N 3-[[(1r)-1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethyl]amino]propanoic acid Chemical compound FC1=CC([C@H](NCCC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 NMSLMMIQACOIGQ-MRXNPFEDSA-N 0.000 claims 1
- NMSLMMIQACOIGQ-INIZCTEOSA-N 3-[[(1s)-1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethyl]amino]propanoic acid Chemical compound FC1=CC([C@@H](NCCC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 NMSLMMIQACOIGQ-INIZCTEOSA-N 0.000 claims 1
- OOBALZZYTSAKCV-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzoyl]-methylamino]propanoic acid Chemical compound FC1=CC(C(=O)N(CCC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 OOBALZZYTSAKCV-UHFFFAOYSA-N 0.000 claims 1
- POSXCHANUIGYIM-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzoyl]amino]-3-methylbutanoic acid Chemical compound FC1=CC(C(=O)NC(C)(CC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 POSXCHANUIGYIM-UHFFFAOYSA-N 0.000 claims 1
- NWNPYQKNBUPBID-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzoyl]amino]butanoic acid Chemical compound FC1=CC(C(=O)NC(CC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 NWNPYQKNBUPBID-UHFFFAOYSA-N 0.000 claims 1
- HNVBIOZWSOINAN-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]imidazole-4-carboxylic acid Chemical compound OC(=O)C1=CN=CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 HNVBIOZWSOINAN-UHFFFAOYSA-N 0.000 claims 1
- ZQJUTZAZNIRVCT-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methylamino]butanoic acid Chemical compound FC1=CC(CNC(CC(O)=O)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 ZQJUTZAZNIRVCT-UHFFFAOYSA-N 0.000 claims 1
- BJWDQTKPJXMMLJ-UHFFFAOYSA-N 3-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]sulfamoyl]propanoic acid Chemical compound FC1=CC(NS(=O)(=O)CCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 BJWDQTKPJXMMLJ-UHFFFAOYSA-N 0.000 claims 1
- CUZSURWZXLOBBS-UHFFFAOYSA-N 3-fluoro-1-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylic acid Chemical compound C1C(C(=O)O)(F)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 CUZSURWZXLOBBS-UHFFFAOYSA-N 0.000 claims 1
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- BLCXSRMPGZPVSR-UHFFFAOYSA-N 3-fluoro-n-(2-hydroxyethyl)-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzamide Chemical compound FC1=CC(C(=O)NCCO)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 BLCXSRMPGZPVSR-UHFFFAOYSA-N 0.000 claims 1
- IVKZRYKWMWLVFH-UHFFFAOYSA-N 3-fluoro-n-(2-hydroxyethyl)-n-methyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzamide Chemical compound FC1=CC(C(=O)N(CCO)C)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 IVKZRYKWMWLVFH-UHFFFAOYSA-N 0.000 claims 1
- JHYLQOKEUJNENW-UHFFFAOYSA-N 3-fluoro-n-(2-methoxyethyl)-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzamide Chemical compound FC1=CC(C(=O)NCCOC)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 JHYLQOKEUJNENW-UHFFFAOYSA-N 0.000 claims 1
- FSAIBDFYVQAJND-UHFFFAOYSA-N 3-fluoro-n-(2-methoxyethyl)-n-methyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]benzamide Chemical compound FC1=CC(C(=O)N(C)CCOC)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 FSAIBDFYVQAJND-UHFFFAOYSA-N 0.000 claims 1
- QWMWNHLXLLSOKR-UHFFFAOYSA-N 3-fluoro-n-methyl-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]aniline Chemical compound FC1=CC(NC)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 QWMWNHLXLLSOKR-UHFFFAOYSA-N 0.000 claims 1
- RNJUDXBXJHLETI-UHFFFAOYSA-N 4-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]anilino]-4-oxobutanoic acid Chemical compound FC1=CC(NC(=O)CCC(=O)O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 RNJUDXBXJHLETI-UHFFFAOYSA-N 0.000 claims 1
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- 239000000829 suppository Substances 0.000 description 3
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- 150000003624 transition metals Chemical class 0.000 description 3
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- KVQHZVCCVFVUPN-XYOKQWHBSA-N methyl (e)-3-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]prop-2-enoate Chemical compound FC1=CC(/C=C/C(=O)OC)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 KVQHZVCCVFVUPN-XYOKQWHBSA-N 0.000 description 2
- HNZZITTWMKDWLC-KRWDZBQOSA-N methyl 1-[(1s)-1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]ethyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1[C@@H](C)C(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 HNZZITTWMKDWLC-KRWDZBQOSA-N 0.000 description 2
- NYFQYNAAOOCLKO-DEOSSOPVSA-N methyl 1-[(1s)-1-[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]propyl]azetidine-3-carboxylate Chemical compound N1([C@@H](CC)C=2C=C(F)C(C=3SC4=NC(=CC=C4N=3)C3(CC3)C=3C=CC=CC=3)=CC=2)CC(C(=O)OC)C1 NYFQYNAAOOCLKO-DEOSSOPVSA-N 0.000 description 2
- SPWYTFODRYKQLD-UHFFFAOYSA-N methyl 1-[[3-amino-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1N)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 SPWYTFODRYKQLD-UHFFFAOYSA-N 0.000 description 2
- BFQLYEROZJLIAA-UHFFFAOYSA-N methyl 1-[[3-fluoro-4-[5-(1-phenylcyclopent-3-en-1-yl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC=CC3)C=3C=CC=CC=3)N=C2S1 BFQLYEROZJLIAA-UHFFFAOYSA-N 0.000 description 2
- YMYBSVNTTZZLAF-UHFFFAOYSA-N methyl 1-[[3-fluoro-4-[5-(1-phenylcyclopentyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CCCC3)C=3C=CC=CC=3)N=C2S1 YMYBSVNTTZZLAF-UHFFFAOYSA-N 0.000 description 2
- HHLVTKLAEICMJX-UHFFFAOYSA-N methyl 1-[[3-fluoro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 HHLVTKLAEICMJX-UHFFFAOYSA-N 0.000 description 2
- MERIQYJDQQNIFT-UHFFFAOYSA-N methyl 1-[[3-fluoro-4-[5-[1-(2-fluorophenyl)cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C(=CC=CC=3)F)N=C2S1 MERIQYJDQQNIFT-UHFFFAOYSA-N 0.000 description 2
- YAVSPJDHNOTNNG-UHFFFAOYSA-N methyl 1-[[3-fluoro-4-[5-[1-(4-fluorophenyl)cyclopropyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC(F)=CC=3)N=C2S1 YAVSPJDHNOTNNG-UHFFFAOYSA-N 0.000 description 2
- XTKDKYQZUQNXEA-UHFFFAOYSA-N methyl 1-[[3-fluoro-4-[5-[1-(4-fluorophenyl)ethenyl]-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1F)=CC=C1C1=NC2=CC=C(C(=C)C=3C=CC(F)=CC=3)N=C2S1 XTKDKYQZUQNXEA-UHFFFAOYSA-N 0.000 description 2
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- XGZKADDINVFAOE-UHFFFAOYSA-N methyl 1-[[3-nitro-4-[5-(1-phenylcyclopropyl)-[1,3]thiazolo[5,4-b]pyridin-2-yl]phenyl]methyl]azetidine-3-carboxylate Chemical compound C1C(C(=O)OC)CN1CC(C=C1[N+]([O-])=O)=CC=C1C1=NC2=CC=C(C3(CC3)C=3C=CC=CC=3)N=C2S1 XGZKADDINVFAOE-UHFFFAOYSA-N 0.000 description 2
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Landscapes
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| CA2728046A1 true CA2728046A1 (en) | 2009-12-23 |
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| TWI485153B (zh) * | 2010-01-13 | 2015-05-21 | Sanofi Aventis | 2,5,7-經取代唑并嘧啶衍生物 |
| TWI478929B (zh) * | 2010-01-13 | 2015-04-01 | Sanofi Aventis | 含2,5,7-經取代唑并嘧啶環之羧酸衍生物 |
| UY33178A (es) * | 2010-01-13 | 2011-08-31 | Sanofi Aventis | Derivados de ácido carboxílico heteroxíclicos que comprenden un anillo de oxazolopirimidina 2, 5, 7-sustituido |
| MY156476A (en) | 2010-01-14 | 2016-02-26 | Sanofi Sa | Heterocyclic carboxylic acid derivatives having a 2,5-substituted oxazolopyrimidine ring |
| AR079885A1 (es) | 2010-01-14 | 2012-02-29 | Sanofi Aventis | Derivados de oxazolo[5,4-d]pirimidina 2,5-sustituidos utiles para el tratamiento del sindrome del pie diabetico(dfs), composiciones farmaceuticas que los contienen y proceso para prepararlos. |
| PT2523962E (pt) * | 2010-01-14 | 2014-02-06 | Sanofi Sa | Derivados de ácidos carboxílicos com um anel oxazolopirimidina substituído em 2,5 |
| TW201206429A (en) * | 2010-07-08 | 2012-02-16 | Merck Serono Sa | Substituted oxadiazole derivatives |
| BR112013006016A2 (pt) | 2010-09-15 | 2016-06-07 | Hoffmann La Roche | compostos de azabenzotiazol, composições e métodos de uso |
| EP2688882B1 (en) * | 2011-03-25 | 2015-05-13 | Boehringer Ingelheim International GmbH | Pyrazole compounds as crth2 antagonists |
| US9321787B2 (en) | 2011-07-07 | 2016-04-26 | Sanofi | Carboxylic acid derivatives having an oxazolo[5,4-d]pyrimidine ring |
| US8580816B2 (en) * | 2011-07-07 | 2013-11-12 | Sanofi | Carboxylic acid derivatives having an oxazolo[5,4-b]pyridine ring |
| US8735402B2 (en) * | 2011-07-07 | 2014-05-27 | Sanofi | Cycloalkyloxycarboxylic acid derivatives |
| US8907093B2 (en) * | 2011-07-07 | 2014-12-09 | Sanofi | Carboxylic acid derivatives having an oxazolo[4,5-c]pyridine ring |
| WO2013158422A1 (en) | 2012-04-17 | 2013-10-24 | E. I. Du Pont De Nemours And Company | Heterocyclic compounds for controlling invertebrate pests |
| US9906186B2 (en) * | 2012-07-20 | 2018-02-27 | Mitsubishi Electric Corporation | Holding frame and solar cell module |
| JP2016509036A (ja) | 2013-02-20 | 2016-03-24 | バイエル・ファルマ・アクティエンゲゼルシャフト | Mknk1阻害剤としての置換イミダゾ[1,2−b]ピリダジン |
| NZ716822A (en) | 2013-08-21 | 2017-10-27 | Alios Biopharma Inc | Antiviral compounds |
| WO2016182850A1 (en) | 2015-05-08 | 2016-11-17 | Albany Molecular Research, Inc. | Methods and intermediates for the preparation of omacetaxine and cephalotaxine derivatives thereof |
| IL252151A0 (en) | 2017-05-07 | 2017-07-31 | Fainzilber Michael | Treatment of stress disorders |
| JP7252908B2 (ja) * | 2017-06-14 | 2023-04-05 | トレベナ・インコーポレイテッド | S1p1活性を調節するための化合物およびその使用法 |
| CN110256466A (zh) * | 2019-07-31 | 2019-09-20 | 昆山迪安医学检验实验室有限公司 | 一种噻唑[5,4-b]-吡啶基生物活性化合物的制备方法及其抗肿瘤活性的检测 |
| WO2021101854A1 (en) * | 2019-11-19 | 2021-05-27 | Trevena, Inc. | Compounds and methods of preparing compounds s1p1 modulators |
| CN115611793A (zh) * | 2021-07-14 | 2023-01-17 | 山东新华制药股份有限公司 | 硫代酰胺类化合物的合成方法 |
| CN116410213A (zh) * | 2023-02-21 | 2023-07-11 | 武汉大学 | 一种合成3-碳基-1-硼基环类化合物的方法 |
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| CA2424870A1 (en) | 2000-10-05 | 2003-04-04 | Takeda Chemical Industries, Ltd. | Agents for promoting the proliferation or differentiation of stem cells or neural progenitor cells |
| WO2002072549A1 (en) | 2001-03-12 | 2002-09-19 | Millennium Pharmaceuticals, Inc. | Functionalized heterocycles as modulators of chemokine receptor function and methods of use therefor |
| US7622479B2 (en) | 2001-11-26 | 2009-11-24 | Takeda Pharmaceutical Company Limited | Bicyclic derivative, its production and use |
| ATE441654T1 (de) | 2002-01-18 | 2009-09-15 | Merck & Co Inc | Edg-rezeptoragonisten |
| AU2004234067B2 (en) * | 2003-04-30 | 2008-02-28 | Novartis Ag | Aminopropanol derivatives as sphingosine-1-phosphate receptor modulators |
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| EP2939674A1 (en) | 2004-10-13 | 2015-11-04 | PTC Therapeutics, Inc. | Compounds for nonsense suppression, and methods for their use |
| US7919519B2 (en) * | 2005-11-23 | 2011-04-05 | Epix Pharmaceuticals Inc. | S1P receptor modulating compounds and use thereof |
| JP2009520688A (ja) * | 2005-11-23 | 2009-05-28 | エピックス デラウェア, インコーポレイテッド | S1p受容体調節化合物およびそれらの使用 |
| US20090182003A1 (en) | 2006-01-13 | 2009-07-16 | President And Fellows Of Harvard College | Methods and Compositions for Treatment Cell Proliferative Disorders |
| TW200806675A (en) | 2006-01-30 | 2008-02-01 | Array Biopharma Inc | Heterobicyclic thiophene compounds and methods of use |
| CN101379433B (zh) | 2006-02-08 | 2012-05-30 | 柯达图形通信有限责任公司 | 含有苯并*唑衍生物及其类似物作为敏化剂的紫外线敏感的平版印版前体 |
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| JP5571073B2 (ja) | 2014-08-13 |
| EP2306994B1 (en) | 2013-08-14 |
| WO2009154780A1 (en) | 2009-12-23 |
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| EEER | Examination request |
Effective date: 20140319 |
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| FZDE | Discontinued |
Effective date: 20160620 |