WO2003000254A1 - Fused cyclic compounds and medicinal use thereof - Google Patents
Fused cyclic compounds and medicinal use thereof Download PDFInfo
- Publication number
- WO2003000254A1 WO2003000254A1 PCT/JP2002/006405 JP0206405W WO03000254A1 WO 2003000254 A1 WO2003000254 A1 WO 2003000254A1 JP 0206405 W JP0206405 W JP 0206405W WO 03000254 A1 WO03000254 A1 WO 03000254A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- acid hydrochloride
- acid
- phenyl
- mouth
- Prior art date
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- 150000001923 cyclic compounds Chemical class 0.000 title abstract description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 320
- 150000003839 salts Chemical class 0.000 claims abstract description 123
- 208000005176 Hepatitis C Diseases 0.000 claims abstract description 93
- 241000711549 Hepacivirus C Species 0.000 claims abstract description 14
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 10
- -1 (3 Chemical group 0.000 claims description 751
- JWHOQZUREKYPBY-UHFFFAOYSA-N rubonic acid Natural products CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CC(=O)C34C)C2C1)C(=O)O JWHOQZUREKYPBY-UHFFFAOYSA-N 0.000 claims description 487
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 424
- 239000002253 acid Substances 0.000 claims description 335
- 125000001424 substituent group Chemical group 0.000 claims description 293
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 257
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 242
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 156
- 125000000623 heterocyclic group Chemical group 0.000 claims description 150
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 145
- 239000000446 fuel Substances 0.000 claims description 129
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 127
- 125000000217 alkyl group Chemical group 0.000 claims description 103
- 239000003814 drug Substances 0.000 claims description 91
- VDTQDVBTYFQIPB-UHFFFAOYSA-N 1-cyclohexylbenzimidazole-5-carboxylic acid Chemical compound C1=NC2=CC(C(=O)O)=CC=C2N1C1CCCCC1 VDTQDVBTYFQIPB-UHFFFAOYSA-N 0.000 claims description 90
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 78
- 238000000034 method Methods 0.000 claims description 77
- 229940124597 therapeutic agent Drugs 0.000 claims description 69
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 68
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 67
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 65
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 64
- ZRJYBKOKFGHSJQ-UHFFFAOYSA-N 1-cyclohexylbenzimidazole Chemical compound C1CCCCC1N1C2=CC=CC=C2N=C1 ZRJYBKOKFGHSJQ-UHFFFAOYSA-N 0.000 claims description 62
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 56
- 229910052757 nitrogen Inorganic materials 0.000 claims description 54
- 125000003118 aryl group Chemical group 0.000 claims description 51
- HNJBEVLQSNELDL-UHFFFAOYSA-N gamma-butyrolactam Natural products O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims description 47
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 47
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 46
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 44
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 44
- 125000005843 halogen group Chemical group 0.000 claims description 43
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 42
- 125000004434 sulfur atom Chemical group 0.000 claims description 42
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 41
- 125000003277 amino group Chemical group 0.000 claims description 40
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 40
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 37
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 36
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 36
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 35
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 34
- 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 33
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 33
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 32
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 31
- 125000004076 pyridyl group Chemical group 0.000 claims description 31
- FINXTJFVUXNTOQ-UHFFFAOYSA-N 2-hexyl-1h-benzimidazole Chemical compound C1=CC=C2NC(CCCCCC)=NC2=C1 FINXTJFVUXNTOQ-UHFFFAOYSA-N 0.000 claims description 30
- 239000003795 chemical substances by application Substances 0.000 claims description 30
- 125000005842 heteroatom Chemical group 0.000 claims description 30
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 29
- 125000001153 fluoro group Chemical group F* 0.000 claims description 29
- 229910052717 sulfur Inorganic materials 0.000 claims description 29
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 28
- 229910052731 fluorine Inorganic materials 0.000 claims description 28
- 241000700605 Viruses Species 0.000 claims description 26
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 26
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 23
- 108010050904 Interferons Proteins 0.000 claims description 23
- 102000014150 Interferons Human genes 0.000 claims description 23
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 23
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 23
- 229940079322 interferon Drugs 0.000 claims description 23
- VHCQVGQULWFQTM-UHFFFAOYSA-N Rubone Natural products COC1=CC(OC)=CC(O)=C1C(=O)C=CC1=CC(OC)=C(OC)C=C1OC VHCQVGQULWFQTM-UHFFFAOYSA-N 0.000 claims description 22
- 239000008194 pharmaceutical composition Substances 0.000 claims description 22
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 21
- 125000003545 alkoxy group Chemical group 0.000 claims description 20
- 229940079593 drug Drugs 0.000 claims description 20
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 20
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 19
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims description 17
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 17
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 16
- 208000006454 hepatitis Diseases 0.000 claims description 16
- HDOWRFHMPULYOA-UHFFFAOYSA-N piperidin-4-ol Chemical compound OC1CCNCC1 HDOWRFHMPULYOA-UHFFFAOYSA-N 0.000 claims description 16
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 16
- 125000002252 acyl group Chemical group 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 15
- WHZAEEFVNATXKX-UHFFFAOYSA-N 1-hexylbenzimidazole Chemical compound C1=CC=C2N(CCCCCC)C=NC2=C1 WHZAEEFVNATXKX-UHFFFAOYSA-N 0.000 claims description 14
- 229910052804 chromium Inorganic materials 0.000 claims description 14
- 239000011651 chromium Substances 0.000 claims description 14
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 14
- XUWHAWMETYGRKB-UHFFFAOYSA-N delta-valerolactam Natural products O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 claims description 14
- 231100000283 hepatitis Toxicity 0.000 claims description 14
- 239000003443 antiviral agent Substances 0.000 claims description 13
- 239000003937 drug carrier Substances 0.000 claims description 13
- 125000002541 furyl group Chemical group 0.000 claims description 13
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 13
- 229910052760 oxygen Inorganic materials 0.000 claims description 13
- 239000001301 oxygen Substances 0.000 claims description 13
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims description 12
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 12
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 11
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 11
- 239000002260 anti-inflammatory agent Substances 0.000 claims description 11
- 229940121363 anti-inflammatory agent Drugs 0.000 claims description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 11
- 125000005936 piperidyl group Chemical group 0.000 claims description 11
- 239000004480 active ingredient Substances 0.000 claims description 10
- 150000001721 carbon Chemical group 0.000 claims description 10
- 229960002944 cyclofenil Drugs 0.000 claims description 10
- 125000004494 ethyl ester group Chemical group 0.000 claims description 10
- KNEDIBQWCYGXCF-UHFFFAOYSA-N 1-cyclohexylbenzimidazole-5-carboxylic acid hydrochloride Chemical compound Cl.OC(=O)c1ccc2n(cnc2c1)C1CCCCC1 KNEDIBQWCYGXCF-UHFFFAOYSA-N 0.000 claims description 9
- COYPLDIXZODDDL-UHFFFAOYSA-N 3h-benzimidazole-5-carboxylic acid Chemical compound OC(=O)C1=CC=C2N=CNC2=C1 COYPLDIXZODDDL-UHFFFAOYSA-N 0.000 claims description 9
- 229940123066 Polymerase inhibitor Drugs 0.000 claims description 9
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 9
- 125000006479 2-pyridyl methyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims description 8
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 8
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 8
- FARSPAVQUKTXLF-UHFFFAOYSA-N 1h-benzimidazol-1-ium;chloride Chemical compound Cl.C1=CC=C2NC=NC2=C1 FARSPAVQUKTXLF-UHFFFAOYSA-N 0.000 claims description 7
- 125000004485 2-pyrrolidinyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])C1([H])* 0.000 claims description 7
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 7
- 125000005605 benzo group Chemical group 0.000 claims description 7
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 7
- 125000001207 fluorophenyl group Chemical group 0.000 claims description 7
- 230000000091 immunopotentiator Effects 0.000 claims description 7
- 150000004702 methyl esters Chemical class 0.000 claims description 7
- 239000005720 sucrose Substances 0.000 claims description 7
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 7
- 229930192474 thiophene Natural products 0.000 claims description 7
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 claims description 6
- HFHFGHLXUCOHLN-UHFFFAOYSA-N 2-fluorophenol Chemical compound OC1=CC=CC=C1F HFHFGHLXUCOHLN-UHFFFAOYSA-N 0.000 claims description 6
- DDMPIPCSFLSDEX-UHFFFAOYSA-N 3h-benzimidazole-5-carboxylic acid;hydrochloride Chemical compound Cl.OC(=O)C1=CC=C2N=CNC2=C1 DDMPIPCSFLSDEX-UHFFFAOYSA-N 0.000 claims description 6
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 claims description 6
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 claims description 6
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 6
- 239000004472 Lysine Substances 0.000 claims description 6
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052796 boron Inorganic materials 0.000 claims description 6
- 125000006244 carboxylic acid protecting group Chemical group 0.000 claims description 6
- 125000002950 monocyclic group Chemical group 0.000 claims description 6
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 229920002554 vinyl polymer Polymers 0.000 claims description 6
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 5
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 5
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 5
- CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 claims description 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
- 239000005973 Carvone Substances 0.000 claims description 5
- 241001024304 Mino Species 0.000 claims description 5
- 125000005236 alkanoylamino group Chemical group 0.000 claims description 5
- MYONAGGJKCJOBT-UHFFFAOYSA-N benzimidazol-2-one Chemical compound C1=CC=CC2=NC(=O)N=C21 MYONAGGJKCJOBT-UHFFFAOYSA-N 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 5
- 230000005494 condensation Effects 0.000 claims description 5
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims description 5
- 230000005764 inhibitory process Effects 0.000 claims description 5
- 235000020130 leben Nutrition 0.000 claims description 5
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 5
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 4
- RGNDOMTZQOEAFO-UHFFFAOYSA-N 1-piperidin-1-ylbenzimidazole Chemical compound C1CCCCN1N1C2=CC=CC=C2N=C1 RGNDOMTZQOEAFO-UHFFFAOYSA-N 0.000 claims description 4
- 125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 125000003047 N-acetyl group Chemical group 0.000 claims description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
- 239000004305 biphenyl Substances 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 150000003840 hydrochlorides Chemical class 0.000 claims description 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 4
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims description 3
- 125000006553 (C3-C8) cycloalkenyl group Chemical group 0.000 claims description 3
- GSFNQBFZFXUTBN-UHFFFAOYSA-N 2-chlorothiophene Chemical compound ClC1=CC=CS1 GSFNQBFZFXUTBN-UHFFFAOYSA-N 0.000 claims description 3
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 3
- 125000005977 3-phenylpropyloxy group Chemical group 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 241000233805 Phoenix Species 0.000 claims description 3
- 235000010290 biphenyl Nutrition 0.000 claims description 3
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims description 3
- 239000003623 enhancer Substances 0.000 claims description 3
- 230000002708 enhancing effect Effects 0.000 claims description 3
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims description 3
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N iso-butyl alcohol Natural products CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 3
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims description 3
- 239000001294 propane Substances 0.000 claims description 3
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 claims description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims description 2
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims description 2
- TULKODADVOEVTR-UHFFFAOYSA-N 3-hydroxy-n,n-dimethylbenzamide Chemical compound CN(C)C(=O)C1=CC=CC(O)=C1 TULKODADVOEVTR-UHFFFAOYSA-N 0.000 claims description 2
- KEINCPBIVGNTSZ-UHFFFAOYSA-N 4-methoxy-1h-benzimidazole Chemical compound COC1=CC=CC2=C1N=CN2 KEINCPBIVGNTSZ-UHFFFAOYSA-N 0.000 claims description 2
- CWDWFSXUQODZGW-UHFFFAOYSA-N 5-thiazolyl Chemical group [C]1=CN=CS1 CWDWFSXUQODZGW-UHFFFAOYSA-N 0.000 claims description 2
- LCGTWRLJTMHIQZ-UHFFFAOYSA-N 5H-dibenzo[b,f]azepine Chemical compound C1=CC2=CC=CC=C2NC2=CC=CC=C21 LCGTWRLJTMHIQZ-UHFFFAOYSA-N 0.000 claims description 2
- 241000709400 Ruba Species 0.000 claims description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-M Trifluoroacetate Chemical compound [O-]C(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-M 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 2
- CBCIHIVRDWLAME-UHFFFAOYSA-N hexanitrodiphenylamine Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O CBCIHIVRDWLAME-UHFFFAOYSA-N 0.000 claims description 2
- 239000012528 membrane Substances 0.000 claims description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 2
- XGYCWCIGCYGQFU-UHFFFAOYSA-N 1,2-thiazolidine 1,1-dioxide Chemical compound O=S1(=O)CCCN1 XGYCWCIGCYGQFU-UHFFFAOYSA-N 0.000 claims 2
- XQVUQRPTZAUIOS-UHFFFAOYSA-N 4-(3-bromophenoxy)phenol Chemical compound C1=CC(O)=CC=C1OC1=CC=CC(Br)=C1 XQVUQRPTZAUIOS-UHFFFAOYSA-N 0.000 claims 2
- LTEQMZWBSYACLV-UHFFFAOYSA-N Hexylbenzene Chemical compound CCCCCCC1=CC=CC=C1 LTEQMZWBSYACLV-UHFFFAOYSA-N 0.000 claims 2
- 229910000077 silane Inorganic materials 0.000 claims 2
- BBVIDBNAYOIXOE-UHFFFAOYSA-N 1,2,4-oxadiazole Chemical compound C=1N=CON=1 BBVIDBNAYOIXOE-UHFFFAOYSA-N 0.000 claims 1
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- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical group CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
- 125000006505 p-cyanobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C#N)C([H])([H])* 0.000 description 1
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- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
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- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
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- XGVXKJKTISMIOW-ZDUSSCGKSA-N simurosertib Chemical compound N1N=CC(C=2SC=3C(=O)NC(=NC=3C=2)[C@H]2N3CCC(CC3)C2)=C1C XGVXKJKTISMIOW-ZDUSSCGKSA-N 0.000 description 1
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- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
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- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical class CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 1
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- 239000003760 tallow Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- 125000005305 thiadiazolinyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- NZVYCXVTEHPMHE-ZSUJOUNUSA-N thymalfasin Chemical compound CC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O NZVYCXVTEHPMHE-ZSUJOUNUSA-N 0.000 description 1
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- 239000011135 tin Substances 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 description 1
- AISMNBXOJRHCIA-UHFFFAOYSA-N trimethylazanium;bromide Chemical compound Br.CN(C)C AISMNBXOJRHCIA-UHFFFAOYSA-N 0.000 description 1
- BYGOPQKDHGXNCD-UHFFFAOYSA-N tripotassium;iron(3+);hexacyanide Chemical compound [K+].[K+].[K+].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] BYGOPQKDHGXNCD-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
Definitions
- the present invention relates to a novel condensed ring compound useful as a therapeutic agent for hepatitis C, a pharmaceutically acceptable salt thereof, or a synthetic intermediate compound thereof.
- the present invention also relates to a novel use of a certain fused ring compound or a pharmaceutically acceptable salt thereof as a therapeutic agent for hepatitis C.
- anti-hepatitis C virus (HCV) action in particular, an anti-HCV action due to RNA-dependent RNA polymerase inhibitory activity, or a pharmaceutically acceptable fused ring compound effective for the prevention or treatment of hepatitis C.
- HCV anti-hepatitis C virus
- the present invention relates to a therapeutic agent for hepatitis C containing salt.
- C-type hepatitis virus HCV
- HCV C-type hepatitis virus
- HCV-infected patients can reach several degrees / 0 of the world population, and the infection is characterized by long-term chronicity.
- HCV is an enveloped RNA virus whose genome is a single-stranded plus-strand RNA and is classified into the genus Hepacivirus of the Flaviviridae family (from The International Committee on Taxonomy of Viruses of the International Union of Microbiological Societies).
- HBV hepatitis B virus
- HCV often shifts to persistent infection even when infected with an adult with a developed immune system, because it avoids the host's immune system for reasons that are not yet clear.
- liver cancer recurs due to inflammation that continues to occur in non-cancerous areas even if the cancer is removed by surgery It is known that there are many.
- HCV infection is involved in skin diseases such as chronic urticaria, lichen planus and cryoglopurinic purpura. (Joshikinkai, 111 (7), 1075-81, 2001).
- HCV hepatitis C
- symptomatic treatment that suppresses inflammation with anti-inflammatory drugs
- HCV is reduced to an extent that inflammation is not caused or HCV is reduced.
- interferon treatment is known as the only effective treatment for eliminating HCV.
- the number of people who can eliminate the virus by interferon is about 1 Z 3 in all patients, and it is known that the remaining people do not work at all or have only temporary effects. Therefore, there are great expectations for anti-HCV drugs that can be used instead of or in combination with interferon.
- Ribavirin (R-ibavirin: 1-] 3-D-ribofuranosyl 1 H-1, 2,4-triazole 1-carboxamide) has been marketed as a treatment for hepatitis C in combination with interferon. Although the effectiveness of interferon is enhanced, the effectiveness rate is still low, and further novel hepatitis C therapeutic agents are desired.
- the HCV gene encodes proteins such as serine protease, RNA helicase, and RNA-dependent RNA polymerase, and these proteins function as specific proteins essential for HCV growth.
- RNA-dependent RNA polymerase (hereinafter simply referred to as HCV polymerase) is an enzyme essential for virus growth.
- HCV polymerase RNA-dependent RNA polymerase
- For HCV gene replication with a positive-strand RNA gene first, positive-strand RNA is made into a saddle shape, complementary negative-strand RNA is synthesized, and then the negative-strand RNA is made into a saddle shape to amplify positive-strand RNA. It is thought that the procedure is to do.
- a site called NS 5 B in the protein precursor encoded by HCV has been shown to exhibit RNA-dependent RNA polymerase activity (EMB0 J., 15, 12-22, 1996). It is thought to play a central role in replication.
- inhibitors of HCV polymerase can be targets for the development of anti-HCV drugs, and the development is highly anticipated.
- effective HCV polymerase inhibitors have not yet been developed, and drugs that can treat hepatitis C are still insufficient.
- JP-A No. 2001-247550 WOO 1/47883, EP 1 1 6 2 1 96A1
- WO 0 2/04425 As therapeutic agents for hepatitis C having a benzimidazole skeleton, JP-A No. 2001-247550 (WOO 1/47883, EP 1 1 6 2 1 96A1) and WO 0 2/04425 are known.
- WO 9 7/36866 discloses the following compound D and the like, and describes the HCV helicase inhibitory activity of the compound.
- JP 2000-503017 WO 97/25316
- JP 10-505092 W 096/7646 are known.
- WO 97/25316 discloses the following compound A and the like, and the treatment of viral infection is described as its use.
- DNA viruses such as hepatitis B virus are listed as target viruses.
- the publication does not include the compounds disclosed in this specification, and there is no description about HCV, and there is no description suggesting it.
- JP 10-505092 discloses the following compound B, etc., and its use is described for the treatment of viral infection.
- herpes viruses and hepatitis B viruses which are DNA viruses, are described as target viruses.
- the gazette does not include the compounds disclosed in this specification, and relates to HCV. There is no description nor suggestion.
- Benzimidazole derivatives having antiviral activity are also described in JP-A-3_31264, US3644382 and US3778504.
- WO 9 8/3 707 2 discloses the use of benzimidazole derivatives as anti-human immunodeficiency virus (HIV) agents and anti-inflammatory agents as inhibitors of tumor necrosis factor (TNF) and cyclic AMP production.
- HBV human immunodeficiency virus
- TNF tumor necrosis factor
- WO 98Z0 53 27 describes the use of benzoimidazole derivatives as anti-HIV agents as reverse transcriptase inhibitors.
- J. Med. Chem. (13 (4), 697-704, 1970) describes the use of a benzimidazole derivative as an anti-influenza virus agent as a neuraminidase inhibitor.
- JP-A-8-50 1 3 1 8 US 58 1465 1
- JP-A-8-1 34073 US 5 56 3 14 3)
- the gazette discloses the following compound C as a catechol diether compound and describes its use as an anti-inflammatory agent.
- both publications do not contain the compound of the present invention, and the mechanism of action is that the former only describes phosphodiesterase IV and the latter only TNF. The description which suggests is not seen.
- Special Table 2000-1 5 9 749 discloses the following compound G and the like, and describes its therapeutic use for bronchitis, nephritis and the like.
- this publication does not contain the compound of the present invention, and only describes phosphodiesterase IV inhibition and blood glucose lowering activity, and there is no description relating to or suggesting anti-HCV action.
- US 6 2 1 1 1 77 discloses the following compound H, etc. The use for the agent is described. However, this publication does not contain the compound of the present invention, and there is no description relating to or suggesting anti-HCV action.
- WO 9 8Z50029, WO 9 8/500 30 and WO 98/50 031 describe benzoimidazole derivatives as anticancer agents having protein isopreyltransferase activity.
- WO 9 8Z50029, WO 9 8/500 30 and WO 98/50 031 describe benzoimidazole derivatives as anticancer agents having protein isopreyltransferase activity.
- WO 9 8Z50029, WO 9 8/500 30 and WO 98/50 031 describe benzoimidazole derivatives as anticancer agents having protein isopreyltransferase activity.
- WO 9 8Z50029, WO 9 8/500 30 and WO 98/50 031 describe benzoimidazole derivatives as anticancer agents having protein isopreyltransferase activity.
- JP-A-8-109 1 69 (EP 6945 3 5) describes the application of tachykun receptor antagonists to inflammatory diseases, and W096Z3 5 7 1 3 discloses osteoporosis as a growth hormone release promoter. Application to growth hormone-related diseases is described. However, there is no description regarding anti-HCV action in any of the publications, and there is no description suggesting it.
- WO 200 1/21 634 discloses the following compound I as a chemical library. However, this publication does not include the compound of the present invention, and although the antimicrobial activity of some compounds is described, there is no description regarding the anti-HCV action, and there is no description suggesting it.
- JP-A-53-14735 describes benzoimidazole derivatives as brighteners, but these do not include the compounds of the present invention.
- drugs with anti-HCV action are effective for the prevention and treatment of hepatitis C, especially anti-HCV drugs with RNA-dependent RNA polymerase inhibitory action of HCV. It has become clear that it can be a preventive and therapeutic agent for hepatitis C, and a preventive and therapeutic agent for diseases caused by hepatitis C.
- an object of the present invention is to provide a drug having an anti-HCV action, particularly a drug having an RNA-dependent RNA polymerase inhibitor effect.
- a therapeutic agent for hepatitis C comprising a condensed ring compound represented by the following general formula [I] or a pharmaceutically acceptable salt thereof as an active ingredient.
- the broken line is a single bond or a double bond.
- G 1 is C (one R 1 ) or a nitrogen atom
- G 2 is C (—R 2 ) or a nitrogen atom
- G 3 is C (one R 3 ) or a nitrogen atom
- G 4 is C (one R 4 ) or a nitrogen atom
- G 5 , G 6 , G 8 and G 9 are each independently a carbon atom or a nitrogen atom, and G 7 is substituted with C (one R 7 ), an oxygen atom, a sulfur atom, or R 8.
- RR 2 , R 3 and R 4 are each independently
- Group A a norogen atom, a hydroxyl group, a carboxyl group, an amino group, a C1-6 alkoxy group, a C 1-6 alkoxy C 1-6 alkoxy group, a C 1-6 anoloxycarbonyl group, and a C 1-6 alkyl Amino group.
- R al is an optionally substituted C1-6 alkyl group (as defined above), optionally substituted with 1 to 5 substituents selected from group B below C6-14 aryl C 1 -6 means an alkyl group or a dalucuronic acid residue.
- Group B halogen atom, cyano group, nitro group, C1-6 alkyl group, halogenated C1-6 alkyl group, C 1-6 alkanoyl group, one (CH 2 ) r — COOR bl , — (CH 2 ) r — CONR bl R b2 , one (CH 2 ) r — NR bl R b2 , one (CH 2 ) r one NR bl one COR b2 , one (CH 2 ) r — NHS 0 2 R bl , _ (CH 2 ) r — OR bl , one (CH 2 ) r — SR bl , ⁇ (CH 2 ) r — S 0 2 R bl and — (CH 2 ) r — S 0 2 NR bl R b2 .
- R bl and R b2 each independently represent a hydrogen atom or a CI-6 alkyl group, and r is 0 or an integer of 1 to 6.
- R a2 and R a3 are each independently a hydrogen atom, a C 1-6 alkoxy group or This means an optionally substituted CI-6 alkyl group (as defined above).
- R a4 means a hydrogen atom or a hydroxyl group.
- R a5 means a hydrogen atom, a C 1-6 alkanol group or a C 1-6 alkylsulfol group.
- R a6 means a hydrogen atom or an optionally substituted C 1-6 alkyl group (as defined above).
- R a7 means a hydroxyl group, an amino group, a C1-6 alkyl group or a C 1-6 alkylamino group.
- R a31 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above), or 1 to 5 substituents selected from the group B.
- C 6 -14 aryl represents a C1-6 alkyl group.
- a heterocyclic group comprising 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur atoms;
- 13 ⁇ 4 7 and 8 are a hydrogen atom or an optionally substituted C 1-6 alkyl group (as defined above),
- Group C a hydroxyl group, a C 1-6 alkyl group and a C 1-6 alkoxy group.
- heterocyclic group comprising 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur atoms;
- R 5 and R 6 are each independently
- R a8 means a hydrogen atom, a C 1-6 alkyl group, or a C 6-14 aryl C 1-6 alkyl group.
- R a9 means a hydrogen atom or a C 1-6 alkyl group.
- Ral () is an optionally substituted c ⁇ 6 alkyl group (as defined above), a C1-6 alkoxycarbonyl group or a C 1-6 alkanoylamino group, 1 is 0 or 1 Means an integer from 6 to 6.
- R al1 means a hydrogen atom or an optionally substituted C1-6 alkyl group (as defined above).
- Each Z is independently
- the heterocyclic group is selected from an oxygen atom, a nitrogen atom or a sulfur atom. Contains 4 heteroatoms.
- heterocyclic C1-6 alkyl group is a C1-6 alkyl substituted with the “heterocyclic group optionally substituted with 1 to 5 substituents selected from group D” as defined above. Means group.
- t independently represents 0 or an integer of 1 to 6.
- (2 '') may be substituted with 1 to 5 substituents selected from the group ⁇
- the heterocyclic group includes 1 to 4 heteroatoms selected from an oxygen atom, a nitrogen atom and a sulfur atom.
- Ral9 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above) or an optionally substituted 1 to 5 substituents selected from the group B C 6 -14 aryl group means C 1-6 alkyl group.
- R a27 and R a28 are each independently
- (6 ′ ′) a heterocyclic C 1-6 alkyl group which may be substituted with 1 to 5 substituents selected from the group B,
- heterocyclic C 1-6 alkyl group is C 1 substituted with “heterocyclic group optionally substituted with 1 to 5 substituents selected from group B” as defined above.
- -6 means an alkyl group.
- R a33 represents a hydrogen atom, a C 1-6 alkyl group, a hydroxyl group, or a C 1-6 alkoxy group.
- (6 ′ ′) a C6-14 aryl C1-6 alkyl group optionally substituted with 1 to 5 substituents selected from the group B;
- R is an amino group, a C-6 alkylamino group, or a heterocyclic group optionally substituted with 1 to 5 substituents selected from the group B, and p is an integer of 0 or 1 to 6 Means.
- R A22 and R A23 are each independently
- (6 ′ ′) may be substituted with 1 to 5 substituents selected from Group B , A telocyclic group,
- R a29 represents a hydrogen atom, a C 1-6 alkyl group or a C ⁇ 6 alkanol group
- (6 ′ ′) means a heterocyclic C 1-6 alkyl group which may be substituted with 1 to 5 substituents selected from Group ⁇ .
- R a29 is as defined above
- R a25 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above), or 1 to 1 substituents selected from the group B Or a heterocyclic group which may be substituted with 1 to 5 substituents selected from the group B.
- R a25 is as defined above, and q is 0, 1 or 2.
- R a26 is a hydrogen atom, an optionally substituted C1-6 alkyl group (as defined above), or 1 to 5 substituents selected from the group B.
- (q) a heterocyclic group containing 1 to 4 heteroatoms selected from oxygen, nitrogen and sulfur atoms; w is an integer from 1 to 3,
- n and n each independently represent 0 or an integer of 1 to 6.
- (3 ′ ′) a C6-14 aryl group that may be substituted with 1 to 5 substituents selected from the group ⁇ , a C 1-6 alkyl group,
- R b5 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above), or an optionally substituted 1 to 5 substituents selected from the group B C 6 A C-14 aryl group or a C6-14 aryl C1-6 alkyl group which may be substituted with 1 to 5 substituents selected from the group B;
- R al3 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above) or an optionally substituted 1 to 5 substituents selected from the group B C 6 -14 aryl represents a C 1-6 alkyl group.
- R a ′′ means a C6-14 aryl group which may be substituted with 1 to 5 substituents selected from the group B.
- R al5 and R al6 are each independently
- R b6 means a C1-6 alkyl group or a C6-14 end reel C1-6 alkyl group.
- R b7 represents a hydrogen atom, a C 1-6 alkyl group, a C 1-6 alkanoyl group, or a C 6-14 end reel C 1-6 alkyloxycarbonyl group.
- n ′, ring B ′, Z, and w are respectively synonymous with n, ring B, Z, and w, and may be the same as or different from ii, ring B, Z, and w, respectively.
- R al7 means a hydrogen atom or a C 1-6 alkyl group.
- the therapeutic agent for hepatitis C according to (1) which is a condensed ring selected from the group consisting of:
- the therapeutic agent for hepatitis C according to (5) which is a condensed ring selected from the group consisting of:
- the therapeutic agent for hepatitis C according to (6) comprising a condensed ring compound represented by the following general formula [I-1] or a pharmaceutically acceptable salt thereof as an active ingredient.
- the therapeutic agent for hepatitis C according to (6) comprising a condensed ring compound represented by the following general formula [I-12] or a pharmaceutically acceptable salt thereof as an active ingredient.
- the therapeutic agent for hepatitis C according to (6) comprising a fused ring compound represented by the following general formula [1-3] or a pharmaceutically acceptable salt thereof as an active ingredient.
- At least one of RRR 3 and R 4 is a carboxyl group, one COOR al , one CONR a2 R a3 , one S0 2 R a7 (R al , R a2 , R a3, and R a7 are (1) As described).
- the therapeutic agent for hepatitis C according to any one of (1) to (10).
- At least one of RR 2 , R 3 and R 4 is a carboxyl group, —COOR al , 1 CONR a2 R a3 or _S0 2 R a7 (R al , R a2 , R a3 and R a7 are ( 1) As described above.)
- the therapeutic agent for hepatitis C according to 1).
- R ⁇ RR 3 and R 4 are COOR al, C hepatitis therapeutic agent according to any one of R al is glucuronic acid residue (1) to (10).
- RRR 3 and one at least of R 4 is an oxygen atom, a heterocyclic group comprising one to four heteroatom selected from ChissoHara terminal and a sulfur atom (1) to ( 10. The therapeutic agent for hepatitis C according to any one of 1).
- At least one of the substituents that may be substituted by group A is a substituent substituted with a C1-6 alkoxy C1-6 alkoxy group, and any one of (1) to (17) A therapeutic agent for hepatitis C according to claim 1.
- Y is — (CH 2 ) m — CR al5 R a16 — (CH 2 ) n — (Each symbol is as described in (1).) (1) to (1 7 ) The therapeutic agent for hepatitis C according to any one of the above.
- At least one of Z is a heterocyclic group which may be substituted with 1 to 5 substituents selected from Group D;
- E ′ is an oxygen atom, a sulfur atom or N (—R a35 )
- E 2 is an oxygen atom, CH 2 or N (—R a35 )
- E 3 is an oxygen atom or a sulfur atom.
- R a35 is independently a hydrogen atom or a C1-6 alkyl group
- ⁇ is an integer of 1 to 3
- h and h ′ are the same or different and are an integer of 1 to 3, respectively.
- the therapeutic agent for hepatitis C according to any one of (1) to (19).
- At least one of Z is a heterocyclic group that may be substituted with 1 to 5 substituents selected from Group D; 2
- At least one of Group D is one (CH 2 ) T — C ONR A27 R A28 (where each symbol is as described in (1)), and at least one of R A27 and R A28
- the therapeutic agent for hepatitis C according to any one of (1) to (19), which is an I C1-6 alkoxy group.
- At least one of group D is _ (CH 2 ) T -NR A22 R A23 (each symbol is as defined in claim 1), and at least one of R A22 and R A23
- the therapeutic agent for hepatitis C according to any one of (1) to (19), wherein is an amino group or a C1-6 alkylamino group.
- At least one of Group D is a heterocyclic group containing 1 to 4 heteroatoms selected from oxygen, nitrogen, and sulfur atoms (1) to (19) A therapeutic agent for hepatitis C according to claim 1.
- a condensed ring selected from the group consisting of:
- Group A a halogen atom, a hydroxyl group, a carboxyl group, an amino group, a C1-6 alkanoloxy group, a C1-6 alkoxy C1-6 alkoxy group, a C1-6 alkoxycarbonyl group and a C1-6 alkylamino group.
- R al is an optionally substituted C 1-6 alkyl group (as defined above), It means a C6-14 aryl C1-6 alkynole group or a dalk carboxylic acid residue which may be substituted with 1 to 5 substituents selected from group B.
- Group B neuron atom, cyano group, nitro group, C1-6 alkyl group, halogenated C 1-6 alkyl group, C1-6 alkanoyl group, one (CH 2 ) r _COOR bl , one (CH 2 ) r -CONR bl R bz x one (CHJ r — NR bl R b2 ,-(CH 2 ) r -NR bl -COR b — (CH 2 ) r — NHS0 2 R bl , one (CH 2 ) r — OR bl , _ (CH 2 ) r _ SR bl ,-(CH 2 ) r and S 0 2 R bl and _ (CH 2 ) r — S 2 NR bl R b2 .
- R bl and R b2 each independently represent a hydrogen atom or a Cl-6 alkyl group, and r is 0 or an integer of 1 to 6.
- R a2 and R a3 each independently represent a hydrogen atom, a C 1-6 alkoxy group, or an optionally substituted C 1-6 alkyl group (as defined above).
- R a4 means a hydrogen atom or a hydroxyl group.
- R a5 means a hydrogen atom, a Cl_6 alkanol group or a C 1-6 alkylsulfonyl group.
- R a6 means a hydrogen atom or an optionally substituted C 1-6 alkyl group (as defined above).
- R a7 means a hydroxyl group, an amino group, a C 1-6 alkyl group, or a C-6 alkylamino group.
- R a31 is a hydrogen atom, an optionally substituted C1-6 alkyl group (as defined above) or an optionally substituted 1 to 5 substituents selected from the group B C 6- 14 aryl represents a C1-6 alkyl group.
- R 7 is a hydrogen atom or an optionally substituted C 1-6 alkyl group (as defined above),
- the ring Cy is
- Group C hydroxyl group, halogen atom, C 1-6 alkyl group and C 1-6 alkoxy group.
- R 5 'and R 6 are each independently
- the heterocyclic group includes 1 to 4 heteroatoms selected from an oxygen atom, a nitrogen atom and a sulfur atom.
- heterocyclic C 1-6 alkyl group is a C 1-substituted with a “heterocyclic group which may be substituted with 1 to 5 substituents selected from group D” as defined above. 6 means an alkyl group.
- t independently represents 0 or an integer of 1 to 6.
- the heterocyclic group includes 1 to 4 heteroatoms selected from an oxygen atom, a nitrogen atom and a sulfur atom.
- Ral9 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above) or an optionally substituted 1 to 5 substituents selected from the group B C 6 -14 aryl group means C1-6 alkyl group.
- R a27 and R a28 are each independently
- heterocyclic C 1-6 alkyl group is C1-substituted by the above-defined “heterocyclic group which may be substituted with 1 to 5 substituents selected from the group B”.
- 6 means an alkyl group.
- R a33 means a hydrogen atom, a C 1-6 alkyl group, a hydroxyl group, or a C 1-6 alkoxy group.
- R a21 is an amino group, a C 1-6 alkylamino group, or a heterocyclic group optionally substituted with 1 to 5 substituents selected from the group B, and p is 0 or 1 to 6 Means an integer.
- R a22 and R a23 are each independently
- (6) is a heterocyclic group which may be substituted with 1 to 5 substituents selected from the group ⁇ ,
- Ra 29 represents a hydrogen atom, a C1-6 alkyl group or a C1-6 alkanoyl group
- (6 ′) means a heterocyclic C 1-6 alkyl group which may be substituted with 1 to 5 substituents selected from Group B.
- R a29 is as defined above, R a25 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above), 1 to 5 substituents selected from the group B A C6-14 end reel group optionally substituted with a group or selected from the group B It means a heterocyclic group which may be substituted with 1 to 5 substituents.
- R a25 is as defined above, and q is 0, 1 or 2.
- R a26 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above), or an optionally substituted 1 to 5 substituents selected from the group B C 6 -Means a 14-aryl group or a heterocyclic group which may be substituted with 1 to 5 substituents selected from the group B.
- w is an integer from 1 to 3
- n and n each independently represent 0 or an integer of 1 to 6.
- R b5 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above), or an optionally substituted 1 to 5 substituents selected from the group B C 6 A C6-14 aryl group or a C1-6 alkyl group optionally substituted with 1 to 5 substituents selected from the group B;
- R al3 is a hydrogen atom, an optionally substituted C 1-6 alkyl group (as defined above) or an optionally substituted 1 to 5 substituents selected from the group B C 6 -14 end reel means C1-6 alkyl group.
- R al4 means a C6-14 aryl group which may be substituted with 1 to 5 substituents selected from the group B.
- R al5 and R al6 are each independently
- R b6 means a C1-6 alkyl group or a C6-14 aryl C1-6 alkyl group.
- R b7 represents a hydrogen atom, a C 1-6 alkyl group, a C 1-6 alkanol group, or a C 6-14 alkyl group, a C 1-6 alkyloxy group.
- n ′, ring B ′, Z, and w ′ have the same meaning as n, ring B, Z, and w, respectively, and may be the same as or different from n, ring B, Z, and w, respectively.
- R al7 means a hydrogen atom or a C 1-6 alkyl group.
- R ⁇ RR 3 and R 4 carboxyl group, One COOR al, One C_ ⁇ _NR a2 R a3, One S0 2 R a7 (R al, R a2, R a3 and R a7 are ( 29) As described. ),
- At least one of R ⁇ RR 3 and R 4 is a carboxyl group or one COOR al (where R al is as described in (29)).
- At least one of R ⁇ R 2 , R 3 and R 4 is one COOR al , and R al is a glucuronic acid residue (2 9) to (3 3) A fused ring compound or a pharmaceutically acceptable salt thereof.
- At least one of R ⁇ R 2 , R 3 and R 4 is a heterocyclic group containing 1 to 4 heteroatoms selected from oxygen atom, nitrogen atom and sulfur atom (2 9) to (3 3) or a pharmaceutically acceptable salt thereof.
- Ring Cy, F Cyclopentyl group, Cyclohexyl group, Cycloheptyl group, or Tetrahydrothiopyrael group Its acceptable salt.
- Y is one (CH 2) m -0- (CH 2) n -, one NHC0 2 _, one CONH- CHR a14 -, - (CH 2) m -NR a12 - (CH 2) n - s one C ON R al3 — (CH 2 ) n —, — O _ (CH 2 ) ra — CR a15 R a16 — (CH 2 ) n — or one (CH 2 ) n _ NR a12 — CHR a15 — (here And each symbol is as described in (29).)
- the fused ring compound or a pharmaceutically acceptable salt thereof according to any one of (29) to (46).
- Y is 1 (CH 2 ) m — 0 1 (CH 2 ) n — or 1 0_ (CH 2 ) m — CR al5 R a16 _ (CH 2 ) n — (where each symbol is (29) As described.)
- Y is one (CH 2 ) m — CR al5 R a16 — (CH 2 ) n ⁇ (Each symbol is as described in (29).) (29) to (46)
- R 2 is a carboxyl group
- RR 3 and R 4 are hydrogen atoms
- ring Cy is a cyclopentyl group, cyclohexyl group, or cycloheptyl group
- ring A ′ is a phenyl group
- At least one of Z is a heterocyclic C ⁇ 6 alkyl group which may be substituted with 1 to 5 substituents selected from Group D. (29) to (51) The fused ring compound or a pharmaceutically acceptable salt thereof.
- At least one of Z is a heterocyclic group which may be substituted with 1 to 5 substituents selected from Group D;
- E 1 is an oxygen atom, sulfur atom or N (—R a35 )
- E 2 is an oxygen atom, CH 2 or N (—R a35 )
- E 3 is an oxygen atom or sulfur atom.
- R a35 is independently a hydrogen atom or a C1-6 alkyl group
- f is an integer of 1 to 3
- h and h ′ are the same or different and are integers of 1 to 3, respectively.
- the fused ring compound or a pharmaceutically acceptable salt thereof according to any one of (29) to (51).
- At least one of Z is a heterocyclic group which may be substituted with 1 to 5 substituents selected from Group D;
- At least one of Group D is one (CH 2 ) t — CONR a27 R a28 (each symbol is as described in (29)), and at least one of R a27 and R a28 it is, C1- 6 fused ring compound or a pharmaceutically acceptable salt thereof according to any one of an alkoxy group (29) to (5 1).
- At least one of group D is one (CH 2 ) t — 0— (CH 2 ) P — COR 321 (each symbol is as described in (29)), and R a21 is an amino group
- At least one of group D is one (CH 2 ) t — NR a29 CO— R a24 (where each symbol is as described in (29)), and R a24 is an amino group or C1-6
- At least one of group D is one (CH 2 ) t — NR a22 R a23 (each symbol is as described in (29)), and at least one of R a22 and R a23 is The fused ring compound or a pharmaceutically acceptable salt thereof according to any one of (29) to (51), which is an amino group or a C1-6 alkylamino group.
- At least one of group D is a heterocyclic group containing 1 to 4 heteroatoms selected from oxygen atom, nitrogen atom and sulfur atom (29) any of (5 1) Or a pharmaceutically acceptable salt thereof.
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Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002423800A CA2423800A1 (en) | 2001-06-26 | 2002-06-26 | Fused cyclic compounds and medicinal use thereof |
IL15528402A IL155284A0 (en) | 2001-06-26 | 2002-06-26 | Fused ring compounds and pharmaceutical compositions containing the same |
AU2002346216A AU2002346216B2 (en) | 1999-12-27 | 2002-06-26 | Fused cyclic compounds and medicinal use thereof |
US10/344,997 US20040082635A1 (en) | 2001-06-26 | 2002-06-26 | Fused cyclic compounds and medicinal use thereof |
HU0301490A HUP0301490A2 (en) | 2002-06-26 | 2002-06-26 | Condensed cyclyc compounds and their pharmaceutical use |
KR10-2003-7002781A KR20030036735A (ko) | 2001-06-26 | 2002-06-26 | 축합환 화합물 및 그 의약 용도 |
MXPA03004936A MXPA03004936A (es) | 2001-06-26 | 2002-06-26 | Compuestos ciclicos fusionados y uso medicinal de los mismos. |
EP02743728A EP1400241A4 (en) | 2001-06-26 | 2002-06-26 | CONDENSED CYCLIC COMPOUNDS AND MEDICAL USES THEREOF |
SK347-2003A SK3472003A3 (en) | 2001-06-26 | 2002-06-26 | Fused cyclic compounds and medicinal use thereof |
BR0205684-4A BR0205684A (pt) | 2001-06-26 | 2002-06-26 | Compostos cìclicos fundidos e seu uso medicinal |
NO20030832A NO20030832L (no) | 2001-06-26 | 2003-02-21 | Kondenserte sykliske forbindelser og medisinsk anvendelse derav |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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JP2001193786 | 2001-06-26 | ||
JP2001-193786 | 2001-06-26 | ||
JP2001351537 | 2001-11-16 | ||
JP2001-351537 | 2001-11-16 |
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WO2003000254A1 true WO2003000254A1 (en) | 2003-01-03 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP2002/006405 WO2003000254A1 (en) | 1999-12-27 | 2002-06-26 | Fused cyclic compounds and medicinal use thereof |
Country Status (14)
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US (1) | US20040082635A1 (ja) |
EP (1) | EP1400241A4 (ja) |
KR (1) | KR20030036735A (ja) |
AR (1) | AR035543A1 (ja) |
BR (1) | BR0205684A (ja) |
CA (1) | CA2423800A1 (ja) |
IL (1) | IL155284A0 (ja) |
MX (1) | MXPA03004936A (ja) |
NO (1) | NO20030832L (ja) |
PE (1) | PE20030188A1 (ja) |
RU (1) | RU2003126233A (ja) |
SK (1) | SK3472003A3 (ja) |
TR (1) | TR200300544T1 (ja) |
WO (1) | WO2003000254A1 (ja) |
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EP1400241A1 (en) | 2004-03-24 |
AR035543A1 (es) | 2004-06-16 |
EP1400241A4 (en) | 2004-10-06 |
SK3472003A3 (en) | 2003-11-04 |
KR20030036735A (ko) | 2003-05-09 |
BR0205684A (pt) | 2003-06-17 |
IL155284A0 (en) | 2003-11-23 |
NO20030832D0 (no) | 2003-02-21 |
RU2003126233A (ru) | 2005-02-27 |
US20040082635A1 (en) | 2004-04-29 |
NO20030832L (no) | 2003-04-22 |
CA2423800A1 (en) | 2003-03-25 |
PE20030188A1 (es) | 2003-04-17 |
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