JP2006503033A5 - - Google Patents
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- Publication number
- JP2006503033A5 JP2006503033A5 JP2004536098A JP2004536098A JP2006503033A5 JP 2006503033 A5 JP2006503033 A5 JP 2006503033A5 JP 2004536098 A JP2004536098 A JP 2004536098A JP 2004536098 A JP2004536098 A JP 2004536098A JP 2006503033 A5 JP2006503033 A5 JP 2006503033A5
- Authority
- JP
- Japan
- Prior art keywords
- dihydro
- benzimidazol
- anilino
- cyclohexylmethyl
- amino
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 27
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 25
- -1 sulfonylamino, amino Chemical group 0.000 claims 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 17
- 125000002252 acyl group Chemical group 0.000 claims 16
- 125000003545 alkoxy group Chemical group 0.000 claims 16
- 150000001875 compounds Chemical class 0.000 claims 16
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 16
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 15
- 125000004414 alkyl thio group Chemical group 0.000 claims 12
- 229910052736 halogen Inorganic materials 0.000 claims 12
- 150000002367 halogens Chemical class 0.000 claims 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 12
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 11
- 150000002825 nitriles Chemical class 0.000 claims 11
- 125000003386 piperidinyl group Chemical group 0.000 claims 10
- 125000004442 acylamino group Chemical group 0.000 claims 9
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 9
- SOWBFZRMHSNYGE-UHFFFAOYSA-N oxamic acid Chemical compound NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 claims 9
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 claims 9
- 125000004076 pyridyl group Chemical group 0.000 claims 9
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 7
- 125000004423 acyloxy group Chemical group 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 7
- 125000001072 heteroaryl group Chemical group 0.000 claims 7
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 239000001257 hydrogen Substances 0.000 claims 7
- 125000002757 morpholinyl group Chemical group 0.000 claims 7
- 125000004193 piperazinyl group Chemical group 0.000 claims 7
- 125000003373 pyrazinyl group Chemical group 0.000 claims 7
- 125000002098 pyridazinyl group Chemical group 0.000 claims 7
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 7
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims 7
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 230000001154 acute effect Effects 0.000 claims 6
- 125000004104 aryloxy group Chemical group 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 6
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims 5
- 239000002253 acid Substances 0.000 claims 5
- 125000003282 alkyl amino group Chemical group 0.000 claims 5
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims 5
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims 5
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 5
- 125000001422 pyrrolinyl group Chemical group 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 4
- 208000002193 Pain Diseases 0.000 claims 4
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims 4
- 208000011341 adult acute respiratory distress syndrome Diseases 0.000 claims 4
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims 4
- 125000003342 alkenyl group Chemical group 0.000 claims 4
- 125000000304 alkynyl group Chemical group 0.000 claims 4
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 4
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims 4
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims 4
- 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 4
- 125000004276 dioxalanyl group Chemical group 0.000 claims 4
- 201000010099 disease Diseases 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- 125000002883 imidazolyl group Chemical group 0.000 claims 4
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 4
- 125000001041 indolyl group Chemical group 0.000 claims 4
- 125000000842 isoxazolyl group Chemical group 0.000 claims 4
- 125000001624 naphthyl group Chemical group 0.000 claims 4
- 125000002971 oxazolyl group Chemical group 0.000 claims 4
- 125000003226 pyrazolyl group Chemical group 0.000 claims 4
- 125000000168 pyrrolyl group Chemical group 0.000 claims 4
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 4
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 4
- 208000011580 syndromic disease Diseases 0.000 claims 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 4
- 125000003831 tetrazolyl group Chemical group 0.000 claims 4
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 125000004069 aziridinyl group Chemical group 0.000 claims 3
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 3
- 125000002541 furyl group Chemical group 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 3
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims 3
- 125000000335 thiazolyl group Chemical group 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- OHZVAMGTHJQJRP-UHFFFAOYSA-N 6-anilino-3-(cyclohexylmethyl)-5-(4-methylpiperazin-1-yl)-1h-benzimidazol-2-one Chemical compound C1CN(C)CCN1C(C(=C1)NC=2C=CC=CC=2)=CC2=C1NC(=O)N2CC1CCCCC1 OHZVAMGTHJQJRP-UHFFFAOYSA-N 0.000 claims 2
- CDHZEXCQSDIULJ-OAQYLSRUSA-N 6-anilino-3-(cyclohexylmethyl)-5-[(2r)-2-(methoxymethyl)pyrrolidin-1-yl]-1h-benzimidazol-2-one Chemical compound COC[C@H]1CCCN1C(C(=C1)NC=2C=CC=CC=2)=CC2=C1NC(=O)N2CC1CCCCC1 CDHZEXCQSDIULJ-OAQYLSRUSA-N 0.000 claims 2
- IMYMPIIYMNMYJD-UHFFFAOYSA-N 6-anilino-3-phenyl-1h-benzimidazol-2-one Chemical compound C=1C=C2N(C=3C=CC=CC=3)C(=O)NC2=CC=1NC1=CC=CC=C1 IMYMPIIYMNMYJD-UHFFFAOYSA-N 0.000 claims 2
- BUOVXGXUGSOFGZ-UHFFFAOYSA-N 6-anilino-5-(4-benzylpiperazin-1-yl)-3-(cyclohexylmethyl)-1h-benzimidazol-2-one Chemical compound C1CN(CC=2C=CC=CC=2)CCN1C=1C=C2N(CC3CCCCC3)C(=O)NC2=CC=1NC1=CC=CC=C1 BUOVXGXUGSOFGZ-UHFFFAOYSA-N 0.000 claims 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 201000001320 Atherosclerosis Diseases 0.000 claims 2
- 206010007559 Cardiac failure congestive Diseases 0.000 claims 2
- 208000000094 Chronic Pain Diseases 0.000 claims 2
- 206010009900 Colitis ulcerative Diseases 0.000 claims 2
- 208000011231 Crohn disease Diseases 0.000 claims 2
- 206010012442 Dermatitis contact Diseases 0.000 claims 2
- 206010018366 Glomerulonephritis acute Diseases 0.000 claims 2
- 208000035895 Guillain-Barré syndrome Diseases 0.000 claims 2
- 206010019280 Heart failures Diseases 0.000 claims 2
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 2
- 201000009906 Meningitis Diseases 0.000 claims 2
- 206010049567 Miller Fisher syndrome Diseases 0.000 claims 2
- 206010051606 Necrotising colitis Diseases 0.000 claims 2
- 201000004681 Psoriasis Diseases 0.000 claims 2
- 206010063837 Reperfusion injury Diseases 0.000 claims 2
- 206010040047 Sepsis Diseases 0.000 claims 2
- 206010040070 Septic Shock Diseases 0.000 claims 2
- 208000006011 Stroke Diseases 0.000 claims 2
- 206010044248 Toxic shock syndrome Diseases 0.000 claims 2
- 231100000650 Toxic shock syndrome Toxicity 0.000 claims 2
- 206010048873 Traumatic arthritis Diseases 0.000 claims 2
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 2
- 201000006704 Ulcerative Colitis Diseases 0.000 claims 2
- 208000027418 Wounds and injury Diseases 0.000 claims 2
- 150000007513 acids Chemical class 0.000 claims 2
- 231100000851 acute glomerulonephritis Toxicity 0.000 claims 2
- 208000005298 acute pain Diseases 0.000 claims 2
- 239000003146 anticoagulant agent Substances 0.000 claims 2
- 150000001543 aryl boronic acids Chemical class 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- 208000019664 bone resorption disease Diseases 0.000 claims 2
- 208000015114 central nervous system disease Diseases 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- 208000010247 contact dermatitis Diseases 0.000 claims 2
- 238000007887 coronary angioplasty Methods 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 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 2
- 206010012601 diabetes mellitus Diseases 0.000 claims 2
- 210000003714 granulocyte Anatomy 0.000 claims 2
- 238000001631 haemodialysis Methods 0.000 claims 2
- 230000000322 hemodialysis Effects 0.000 claims 2
- 230000002757 inflammatory effect Effects 0.000 claims 2
- 208000014674 injury Diseases 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- XMSZANIMCDLNKA-UHFFFAOYSA-N methyl hypofluorite Chemical compound COF XMSZANIMCDLNKA-UHFFFAOYSA-N 0.000 claims 2
- 201000006417 multiple sclerosis Diseases 0.000 claims 2
- 208000010125 myocardial infarction Diseases 0.000 claims 2
- 208000004995 necrotizing enterocolitis Diseases 0.000 claims 2
- 201000008482 osteoarthritis Diseases 0.000 claims 2
- 201000006195 perinatal necrotizing enterocolitis Diseases 0.000 claims 2
- 208000037803 restenosis Diseases 0.000 claims 2
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 2
- 208000017520 skin disease Diseases 0.000 claims 2
- 201000000596 systemic lupus erythematosus Diseases 0.000 claims 2
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- 230000002537 thrombolytic effect Effects 0.000 claims 2
- 238000002054 transplantation Methods 0.000 claims 2
- 230000008733 trauma Effects 0.000 claims 2
- 208000035408 type 1 diabetes mellitus 1 Diseases 0.000 claims 2
- SLVDKURCOZKCMZ-OAQYLSRUSA-N (2r)-1-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]pyrrolidine-2-carboxamide Chemical compound NC(=O)[C@H]1CCCN1C(C(=C1)NC=2C=CC=CC=2)=CC2=C1NC(=O)N2CC1CCCCC1 SLVDKURCOZKCMZ-OAQYLSRUSA-N 0.000 claims 1
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims 1
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 claims 1
- 125000006705 (C5-C7) cycloalkyl group Chemical group 0.000 claims 1
- UKRCBKWWONLCEW-UHFFFAOYSA-N 1-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]-n,n-diethylpiperidine-3-carboxamide Chemical compound C1C(C(=O)N(CC)CC)CCCN1C(C(=C1)NC=2C=CC=CC=2)=CC2=C1NC(=O)N2CC1CCCCC1 UKRCBKWWONLCEW-UHFFFAOYSA-N 0.000 claims 1
- PKTWRUXQFULFIY-UHFFFAOYSA-N 1-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]pyrrole-2-carbonitrile Chemical compound C1=CC=C(C#N)N1C=1C=C2N(CC3CCCCC3)C(=O)NC2=CC=1NC1=CC=CC=C1 PKTWRUXQFULFIY-UHFFFAOYSA-N 0.000 claims 1
- PZMSXOGDCFTNTO-UHFFFAOYSA-N 2-(5-anilino-2-oxo-3h-benzimidazol-1-yl)acetonitrile Chemical compound C=1C=C2N(CC#N)C(=O)NC2=CC=1NC1=CC=CC=C1 PZMSXOGDCFTNTO-UHFFFAOYSA-N 0.000 claims 1
- JPKITMLZTXBACT-UHFFFAOYSA-N 2-[4-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]piperazin-1-yl]-n-propan-2-ylacetamide Chemical compound C1CN(CC(=O)NC(C)C)CCN1C(C(=C1)NC=2C=CC=CC=2)=CC2=C1NC(=O)N2CC1CCCCC1 JPKITMLZTXBACT-UHFFFAOYSA-N 0.000 claims 1
- JKNVRJIMHDSEPB-UHFFFAOYSA-N 3-(1-amino-2-methylpropan-2-yl)-6-phenoxy-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(C(C)(CN)C)C2=CC=C1OC1=CC=CC=C1 JKNVRJIMHDSEPB-UHFFFAOYSA-N 0.000 claims 1
- GBCKIYOEOYUTHP-UHFFFAOYSA-N 3-(1-amino-2-methylpropan-2-yl)-6-phenylsulfanyl-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(C(C)(CN)C)C2=CC=C1SC1=CC=CC=C1 GBCKIYOEOYUTHP-UHFFFAOYSA-N 0.000 claims 1
- NPAJELYNMTZOAX-UHFFFAOYSA-N 3-(2-amino-2-methylpropyl)-6-phenoxy-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CC(C)(N)C)C2=CC=C1OC1=CC=CC=C1 NPAJELYNMTZOAX-UHFFFAOYSA-N 0.000 claims 1
- WKCNTSLDZLPBDR-UHFFFAOYSA-N 3-(2-amino-2-methylpropyl)-6-phenylsulfanyl-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CC(C)(N)C)C2=CC=C1SC1=CC=CC=C1 WKCNTSLDZLPBDR-UHFFFAOYSA-N 0.000 claims 1
- YQEXNJOKBHTRKD-UHFFFAOYSA-N 3-(2-aminoethyl)-6-phenoxy-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CCN)C2=CC=C1OC1=CC=CC=C1 YQEXNJOKBHTRKD-UHFFFAOYSA-N 0.000 claims 1
- MTRGADFZIZCVFZ-UHFFFAOYSA-N 3-(2-aminoethyl)-6-phenylsulfanyl-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CCN)C2=CC=C1SC1=CC=CC=C1 MTRGADFZIZCVFZ-UHFFFAOYSA-N 0.000 claims 1
- GZLWKZOTGVUAPE-UHFFFAOYSA-N 3-(3-morpholin-4-ylpropyl)-1h-benzimidazol-2-one Chemical compound O=C1NC2=CC=CC=C2N1CCCN1CCOCC1 GZLWKZOTGVUAPE-UHFFFAOYSA-N 0.000 claims 1
- JDKNAANKLRZFGN-UHFFFAOYSA-N 3-(5-anilino-2-oxo-3h-benzimidazol-1-yl)propanenitrile Chemical compound C=1C=C2N(CCC#N)C(=O)NC2=CC=1NC1=CC=CC=C1 JDKNAANKLRZFGN-UHFFFAOYSA-N 0.000 claims 1
- UJPMROIABHMCFU-UHFFFAOYSA-N 3-(cyclohexylmethyl)-5-[2-(dimethylamino)ethyl-methylamino]-6-(2-methylanilino)-1h-benzimidazol-2-one Chemical compound O=C1NC=2C=C(NC=3C(=CC=CC=3)C)C(N(C)CCN(C)C)=CC=2N1CC1CCCCC1 UJPMROIABHMCFU-UHFFFAOYSA-N 0.000 claims 1
- PWYCWPXBNIRCOY-UHFFFAOYSA-N 3-(cyclohexylmethyl)-5-[3-(dimethylamino)propyl-methylamino]-6-(2-methylanilino)-1h-benzimidazol-2-one Chemical compound O=C1NC=2C=C(NC=3C(=CC=CC=3)C)C(N(C)CCCN(C)C)=CC=2N1CC1CCCCC1 PWYCWPXBNIRCOY-UHFFFAOYSA-N 0.000 claims 1
- OXAPWQMWCQHKMT-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2,4-difluoroanilino)-1h-benzimidazol-2-one Chemical compound FC1=CC(F)=CC=C1NC1=CC=C(N(CC2CCCCC2)C(=O)N2)C2=C1 OXAPWQMWCQHKMT-UHFFFAOYSA-N 0.000 claims 1
- UICDKTQWZWZFPX-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2,4-difluoroanilino)-5-[2-(dimethylamino)ethoxy]-1h-benzimidazol-2-one Chemical compound O=C1NC=2C=C(NC=3C(=CC(F)=CC=3)F)C(OCCN(C)C)=CC=2N1CC1CCCCC1 UICDKTQWZWZFPX-UHFFFAOYSA-N 0.000 claims 1
- LVTLZGUHAMLQQJ-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2,4-difluoroanilino)-5-[2-(dimethylamino)ethylsulfanyl]-1h-benzimidazol-2-one Chemical compound O=C1NC=2C=C(NC=3C(=CC(F)=CC=3)F)C(SCCN(C)C)=CC=2N1CC1CCCCC1 LVTLZGUHAMLQQJ-UHFFFAOYSA-N 0.000 claims 1
- HJPBUDSTYFDXGG-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2-fluoroanilino)-1h-benzimidazol-2-one Chemical compound FC1=CC=CC=C1NC1=CC=C(N(CC2CCCCC2)C(=O)N2)C2=C1 HJPBUDSTYFDXGG-UHFFFAOYSA-N 0.000 claims 1
- WDJAXOKEGNQZBA-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2-fluoroanilino)-5-piperazin-1-yl-1h-benzimidazol-2-one Chemical compound FC1=CC=CC=C1NC(C(=C1)N2CCNCC2)=CC2=C1N(CC1CCCCC1)C(=O)N2 WDJAXOKEGNQZBA-UHFFFAOYSA-N 0.000 claims 1
- KXRHJSGUPVRUAR-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2-methoxyanilino)-1h-benzimidazol-2-one Chemical compound COC1=CC=CC=C1NC1=CC=C(N(CC2CCCCC2)C(=O)N2)C2=C1 KXRHJSGUPVRUAR-UHFFFAOYSA-N 0.000 claims 1
- BULVVOAMLWUBIW-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2-methylanilino)-1h-benzimidazol-2-one Chemical compound CC1=CC=CC=C1NC1=CC=C(N(CC2CCCCC2)C(=O)N2)C2=C1 BULVVOAMLWUBIW-UHFFFAOYSA-N 0.000 claims 1
- QQYBXGCMNFIXND-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(2-methylanilino)-5-(4-methylpiperazin-1-yl)-1h-benzimidazol-2-one Chemical compound C1CN(C)CCN1C(C(=C1)NC=2C(=CC=CC=2)C)=CC2=C1NC(=O)N2CC1CCCCC1 QQYBXGCMNFIXND-UHFFFAOYSA-N 0.000 claims 1
- JHBMKMXVDCROIO-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(3,4-difluoroanilino)-1h-benzimidazol-2-one Chemical compound C1=C(F)C(F)=CC=C1NC1=CC=C(N(CC2CCCCC2)C(=O)N2)C2=C1 JHBMKMXVDCROIO-UHFFFAOYSA-N 0.000 claims 1
- MFZGRCSBCGFAOB-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(3,5-dichloroanilino)-1h-benzimidazol-2-one Chemical compound ClC1=CC(Cl)=CC(NC=2C=C3NC(=O)N(CC4CCCCC4)C3=CC=2)=C1 MFZGRCSBCGFAOB-UHFFFAOYSA-N 0.000 claims 1
- IPCRBKBYFVHWDU-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(3-fluoroanilino)-1h-benzimidazol-2-one Chemical compound FC1=CC=CC(NC=2C=C3NC(=O)N(CC4CCCCC4)C3=CC=2)=C1 IPCRBKBYFVHWDU-UHFFFAOYSA-N 0.000 claims 1
- IXKMLQFAOZNLOW-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(4-fluoroanilino)-1h-benzimidazol-2-one Chemical compound C1=CC(F)=CC=C1NC1=CC=C(N(CC2CCCCC2)C(=O)N2)C2=C1 IXKMLQFAOZNLOW-UHFFFAOYSA-N 0.000 claims 1
- DQRGKGAHWCBAGG-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-(4-methylanilino)-1h-benzimidazol-2-one Chemical compound C1=CC(C)=CC=C1NC1=CC=C(N(CC2CCCCC2)C(=O)N2)C2=C1 DQRGKGAHWCBAGG-UHFFFAOYSA-N 0.000 claims 1
- VNHGPYLTBKZKIH-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-[3-(trifluoromethyl)anilino]-1h-benzimidazol-2-one Chemical compound FC(F)(F)C1=CC=CC(NC=2C=C3NC(=O)N(CC4CCCCC4)C3=CC=2)=C1 VNHGPYLTBKZKIH-UHFFFAOYSA-N 0.000 claims 1
- RJKYWJUTUYFGPK-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-phenoxy-1h-benzimidazol-2-one Chemical compound C=1C=C2N(CC3CCCCC3)C(=O)NC2=CC=1OC1=CC=CC=C1 RJKYWJUTUYFGPK-UHFFFAOYSA-N 0.000 claims 1
- UGKWUWKAPSRZKE-UHFFFAOYSA-N 3-(cyclohexylmethyl)-6-phenylsulfanyl-1h-benzimidazol-2-one Chemical compound C=1C=C2N(CC3CCCCC3)C(=O)NC2=CC=1SC1=CC=CC=C1 UGKWUWKAPSRZKE-UHFFFAOYSA-N 0.000 claims 1
- WHTCLKOZAGPLJV-UHFFFAOYSA-N 3-[4-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]piperazin-1-yl]pyrazine-2-carbonitrile Chemical compound C1CN(C=2C(=NC=CN=2)C#N)CCN1C=1C=C2N(CC3CCCCC3)C(=O)NC2=CC=1NC1=CC=CC=C1 WHTCLKOZAGPLJV-UHFFFAOYSA-N 0.000 claims 1
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- LWYSQOCAPNWUFW-UHFFFAOYSA-N 3-[[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]-methylamino]propanenitrile Chemical compound O=C1NC=2C=C(NC=3C=CC=CC=3)C(N(CCC#N)C)=CC=2N1CC1CCCCC1 LWYSQOCAPNWUFW-UHFFFAOYSA-N 0.000 claims 1
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- UBFGHBMCONTASQ-UHFFFAOYSA-N 6-anilino-3-[3-(1h-imidazol-5-yl)propyl]-1h-benzimidazol-2-one Chemical compound C=1C=C2N(CCCC=3N=CNC=3)C(=O)NC2=CC=1NC1=CC=CC=C1 UBFGHBMCONTASQ-UHFFFAOYSA-N 0.000 claims 1
- ZGRUIMOHJQWWKU-UHFFFAOYSA-N 6-anilino-3-[3-(4-methylpiperazin-1-yl)propyl]-1h-benzimidazol-2-one Chemical compound C1CN(C)CCN1CCCN1C(=O)NC2=CC(NC=3C=CC=CC=3)=CC=C21 ZGRUIMOHJQWWKU-UHFFFAOYSA-N 0.000 claims 1
- DNIVZQCKRZQNMV-UHFFFAOYSA-N 6-anilino-3-[3-(dimethylamino)propyl]-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CCCN(C)C)C2=CC=C1NC1=CC=CC=C1 DNIVZQCKRZQNMV-UHFFFAOYSA-N 0.000 claims 1
- LKLGQXBJMJEELQ-UHFFFAOYSA-N 6-anilino-3-[[2-(trifluoromethyl)phenyl]methyl]-1h-benzimidazol-2-one Chemical compound FC(F)(F)C1=CC=CC=C1CN1C(=O)NC2=CC(NC=3C=CC=CC=3)=CC=C21 LKLGQXBJMJEELQ-UHFFFAOYSA-N 0.000 claims 1
- RDLHROHHQQRREX-UHFFFAOYSA-N 6-anilino-3-[[3-(trifluoromethyl)phenyl]methyl]-1h-benzimidazol-2-one Chemical compound FC(F)(F)C1=CC=CC(CN2C(NC3=CC(NC=4C=CC=CC=4)=CC=C32)=O)=C1 RDLHROHHQQRREX-UHFFFAOYSA-N 0.000 claims 1
- VCAPHPCCDHJXLO-UHFFFAOYSA-N 6-anilino-3-[[4-(dimethylamino)phenyl]methyl]-1h-benzimidazol-2-one Chemical compound C1=CC(N(C)C)=CC=C1CN1C(=O)NC2=CC(NC=3C=CC=CC=3)=CC=C21 VCAPHPCCDHJXLO-UHFFFAOYSA-N 0.000 claims 1
- GFWUWVCQBZZKBF-UHFFFAOYSA-N 6-anilino-3-[[4-(trifluoromethyl)phenyl]methyl]-1h-benzimidazol-2-one Chemical compound C1=CC(C(F)(F)F)=CC=C1CN1C(=O)NC2=CC(NC=3C=CC=CC=3)=CC=C21 GFWUWVCQBZZKBF-UHFFFAOYSA-N 0.000 claims 1
- GRGXSMLVXPKASV-UHFFFAOYSA-N 6-anilino-3-[[4-[2-(dimethylamino)ethoxy]phenyl]methyl]-1h-benzimidazol-2-one Chemical compound C1=CC(OCCN(C)C)=CC=C1CN1C(=O)NC2=CC(NC=3C=CC=CC=3)=CC=C21 GRGXSMLVXPKASV-UHFFFAOYSA-N 0.000 claims 1
- FGTZEMSXGFZIKW-UHFFFAOYSA-N 6-anilino-3-benzyl-1h-benzimidazol-2-one Chemical compound C=1C=C2N(CC=3C=CC=CC=3)C(=O)NC2=CC=1NC1=CC=CC=C1 FGTZEMSXGFZIKW-UHFFFAOYSA-N 0.000 claims 1
- RUVWNABBHAMHMT-UHFFFAOYSA-N 6-anilino-3-butyl-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CCCC)C2=CC=C1NC1=CC=CC=C1 RUVWNABBHAMHMT-UHFFFAOYSA-N 0.000 claims 1
- MNFFOJYNTBBZEF-UHFFFAOYSA-N 6-anilino-3-cyclopentyl-1h-benzimidazol-2-one Chemical compound C=1C=C2N(C3CCCC3)C(=O)NC2=CC=1NC1=CC=CC=C1 MNFFOJYNTBBZEF-UHFFFAOYSA-N 0.000 claims 1
- BKRCFSKLVVBRHO-UHFFFAOYSA-N 6-anilino-3-hexyl-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CCCCCC)C2=CC=C1NC1=CC=CC=C1 BKRCFSKLVVBRHO-UHFFFAOYSA-N 0.000 claims 1
- HTKMMCNALQIGBR-UHFFFAOYSA-N 6-anilino-3-pentyl-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(CCCCC)C2=CC=C1NC1=CC=CC=C1 HTKMMCNALQIGBR-UHFFFAOYSA-N 0.000 claims 1
- OQNBOVHKDJKCNN-UHFFFAOYSA-N 6-anilino-3-phenacyl-1h-benzimidazol-2-one Chemical compound C=1C=CC=CC=1C(=O)CN(C(NC1=C2)=O)C1=CC=C2NC1=CC=CC=C1 OQNBOVHKDJKCNN-UHFFFAOYSA-N 0.000 claims 1
- ARKKKPAZFLJRTQ-UHFFFAOYSA-N 6-anilino-3-tert-butyl-1h-benzimidazol-2-one Chemical compound C1=C2NC(=O)N(C(C)(C)C)C2=CC=C1NC1=CC=CC=C1 ARKKKPAZFLJRTQ-UHFFFAOYSA-N 0.000 claims 1
- WWZJOGVORXARTG-UHFFFAOYSA-N 6-anilino-5-(4-benzyl-1,4-diazepan-1-yl)-3-(cyclohexylmethyl)-1h-benzimidazol-2-one Chemical compound C1CCN(CC=2C=CC=CC=2)CCN1C=1C=C2N(CC3CCCCC3)C(=O)NC2=CC=1NC1=CC=CC=C1 WWZJOGVORXARTG-UHFFFAOYSA-N 0.000 claims 1
- DVZCBGLTZKSJFF-UHFFFAOYSA-N 6-anilino-5-[bis(2-methoxyethyl)amino]-3-(cyclohexylmethyl)-1h-benzimidazol-2-one Chemical compound O=C1NC=2C=C(NC=3C=CC=CC=3)C(N(CCOC)CCOC)=CC=2N1CC1CCCCC1 DVZCBGLTZKSJFF-UHFFFAOYSA-N 0.000 claims 1
- LBDIDYGHBUMFHA-UHFFFAOYSA-N 6-anilino-5-[butyl(propyl)amino]-3-(cyclohexylmethyl)-1h-benzimidazol-2-one Chemical compound O=C1NC=2C=C(NC=3C=CC=CC=3)C(N(CCC)CCCC)=CC=2N1CC1CCCCC1 LBDIDYGHBUMFHA-UHFFFAOYSA-N 0.000 claims 1
- SANCYSIIASBAPV-UHFFFAOYSA-N 6-phenoxy-3-(piperidin-4-ylmethyl)-1h-benzimidazol-2-one Chemical compound C=1C=C2N(CC3CCNCC3)C(=O)NC2=CC=1OC1=CC=CC=C1 SANCYSIIASBAPV-UHFFFAOYSA-N 0.000 claims 1
- MQTSEYJNZAOEKM-UHFFFAOYSA-N 6-phenoxy-3-piperidin-4-yl-1h-benzimidazol-2-one Chemical compound C=1C=C2N(C3CCNCC3)C(=O)NC2=CC=1OC1=CC=CC=C1 MQTSEYJNZAOEKM-UHFFFAOYSA-N 0.000 claims 1
- LNHNLSJJGMVWHV-UHFFFAOYSA-N 6-phenylsulfanyl-3-(piperidin-4-ylmethyl)-1h-benzimidazol-2-one Chemical compound C=1C=C2N(CC3CCNCC3)C(=O)NC2=CC=1SC1=CC=CC=C1 LNHNLSJJGMVWHV-UHFFFAOYSA-N 0.000 claims 1
- AYIUPNGQLKISLS-UHFFFAOYSA-N 6-phenylsulfanyl-3-piperidin-4-yl-1h-benzimidazol-2-one Chemical compound C=1C=C2N(C3CCNCC3)C(=O)NC2=CC=1SC1=CC=CC=C1 AYIUPNGQLKISLS-UHFFFAOYSA-N 0.000 claims 1
- IBULLIFRDJTEEU-UHFFFAOYSA-N 8-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one Chemical compound C1CN(C=2C(=CC=3NC(=O)N(CC4CCCCC4)C=3C=2)NC=2C=CC=CC=2)CCC11C(=O)NCN1C1=CC=CC=C1 IBULLIFRDJTEEU-UHFFFAOYSA-N 0.000 claims 1
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- 208000011623 Obstructive Lung disease Diseases 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 150000001879 copper Chemical class 0.000 claims 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- LXWUPBYKNNRHPI-UHFFFAOYSA-N ethyl 3-[[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]-(furan-2-ylmethyl)amino]propanoate Chemical compound C=1C=2N(CC3CCCCC3)C(=O)NC=2C=C(NC=2C=CC=CC=2)C=1N(CCC(=O)OCC)CC1=CC=CO1 LXWUPBYKNNRHPI-UHFFFAOYSA-N 0.000 claims 1
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- PSCAJBGOBLZMPC-UHFFFAOYSA-N n-[1-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]pyrrolidin-3-yl]-n-methylacetamide Chemical compound C1C(N(C)C(C)=O)CCN1C(C(=C1)NC=2C=CC=CC=2)=CC2=C1NC(=O)N2CC1CCCCC1 PSCAJBGOBLZMPC-UHFFFAOYSA-N 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 1
- RFIOZSIHFNEKFF-UHFFFAOYSA-M piperazine-1-carboxylate Chemical compound [O-]C(=O)N1CCNCC1 RFIOZSIHFNEKFF-UHFFFAOYSA-M 0.000 claims 1
- SRJOCJYGOFTFLH-UHFFFAOYSA-M piperidine-4-carboxylate Chemical compound [O-]C(=O)C1CCNCC1 SRJOCJYGOFTFLH-UHFFFAOYSA-M 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- YGKXBTHPZDUVAA-UHFFFAOYSA-N tert-butyl 4-[6-anilino-3-(cyclohexylmethyl)-2-oxo-1h-benzimidazol-5-yl]-1,4-diazepane-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCCN1C(C(=C1)NC=2C=CC=CC=2)=CC2=C1NC(=O)N2CC1CCCCC1 YGKXBTHPZDUVAA-UHFFFAOYSA-N 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41042002P | 2002-09-13 | 2002-09-13 | |
| PCT/US2003/027692 WO2004024699A1 (en) | 2002-09-13 | 2003-09-04 | Benzimidazolones and their use as cytokine inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006503033A JP2006503033A (ja) | 2006-01-26 |
| JP2006503033A5 true JP2006503033A5 (enExample) | 2006-10-19 |
| JP4551765B2 JP4551765B2 (ja) | 2010-09-29 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004536098A Expired - Lifetime JP4551765B2 (ja) | 2002-09-13 | 2003-09-04 | ベンズイミダゾロン及びサイトカイン抑制剤としてのそれらの使用 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7115644B2 (enExample) |
| EP (1) | EP1539708B1 (enExample) |
| JP (1) | JP4551765B2 (enExample) |
| AT (1) | ATE382039T1 (enExample) |
| AU (1) | AU2003265924A1 (enExample) |
| CA (1) | CA2498754C (enExample) |
| DE (1) | DE60318320T2 (enExample) |
| ES (1) | ES2297265T3 (enExample) |
| WO (1) | WO2004024699A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005023761A2 (en) * | 2003-09-11 | 2005-03-17 | Kemia, Inc. | Cytokine inhibitors |
| WO2007015877A2 (en) * | 2005-07-20 | 2007-02-08 | Kalypsys, Inc. | Inhibitors of p38 kinase and methods of treating inflammatory disorders |
| WO2011021678A1 (ja) * | 2009-08-21 | 2011-02-24 | 武田薬品工業株式会社 | 縮合複素環化合物 |
| BR112014030940B1 (pt) * | 2012-06-11 | 2022-09-06 | UCB Biopharma SRL | Benzimidazóis que modulam tnf-alfa e composição farmacêutica compreendendo os mesmos |
| US8901304B1 (en) | 2013-11-05 | 2014-12-02 | King Fahd University Of Petroleum And Minerals | Benzo[D]imidazole derivatives of piperidine and piperazine |
| US20190060286A1 (en) | 2016-02-29 | 2019-02-28 | University Of Florida Research Foundation, Incorpo | Chemotherapeutic Methods |
| CN109563051B (zh) * | 2016-08-22 | 2024-06-11 | 南京明德新药研发有限公司 | 作为pde4抑制剂的并环类化合物 |
| BR112020006677A2 (pt) | 2017-10-05 | 2020-10-06 | Fulcrum Therapeutics, Inc. | uso de inibidores p38 para reduzir a expressão de dux4 |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| GB201820165D0 (en) * | 2018-12-11 | 2019-01-23 | Ucb Biopharma Sprl | Therapeutic agents |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW203049B (enExample) * | 1990-04-13 | 1993-04-01 | Yamanouchi Pharma Co Ltd | |
| US5281714A (en) | 1990-08-16 | 1994-01-25 | American Home Products Corporation | N,N',N'-trisubstituted-5-bisaminomethylene-1,3-dioxane-4,6-dione inhibitors of acyl-CoA: cholesterol-acyl transferase |
| US5200422A (en) | 1990-09-24 | 1993-04-06 | Neurosearch A/S | Benzimidazole derivatives, their preparation and use |
| TW284688B (enExample) | 1991-11-20 | 1996-09-01 | Takeda Pharm Industry Co Ltd | |
| DE4140540A1 (de) | 1991-12-09 | 1993-06-17 | Bayer Ag | Neue azaheterocyclylmethyl-chromane |
| US5354865A (en) | 1992-09-10 | 1994-10-11 | Abbott Laboratories | Phenylmethyl derivatives having lipoxygenase inhibitory activity |
| AU675484B2 (en) | 1993-03-24 | 1997-02-06 | Neurosearch A/S | Benzimidazole compounds, their use and preparation |
| US6300325B1 (en) * | 1997-01-23 | 2001-10-09 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
| GB9811427D0 (en) | 1998-05-29 | 1998-07-22 | Zeneca Ltd | Chemical compounds |
| EP1158985B1 (en) | 1999-01-13 | 2011-12-28 | Bayer HealthCare LLC | OMEGA-CARBOXY ARYL SUBSTITUTED DIPHENYL UREAS AS p38 KINASE INHIBITORS |
| EP1140840B1 (en) | 1999-01-13 | 2006-03-22 | Bayer Pharmaceuticals Corp. | -g(v)-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors |
| DE19907813A1 (de) | 1999-02-24 | 2000-08-31 | Boehringer Ingelheim Pharma | Substituierte bicyclische Heterocyclen, deren Herstellung und deren Verwendung als Arzneimittel |
| JP2000344757A (ja) | 1999-03-18 | 2000-12-12 | Clariant Internatl Ltd | チアジン−インジゴ化合物およびその新規中間体の製造方法 |
| IL147309A0 (en) | 1999-07-21 | 2002-08-14 | Fujisawa Pharmaceutical Co | Benzimidazolone derivatives and pharmaceutical compositions containg the same |
-
2003
- 2003-09-03 US US10/654,452 patent/US7115644B2/en not_active Expired - Lifetime
- 2003-09-04 JP JP2004536098A patent/JP4551765B2/ja not_active Expired - Lifetime
- 2003-09-04 AT AT03795649T patent/ATE382039T1/de active
- 2003-09-04 CA CA2498754A patent/CA2498754C/en not_active Expired - Lifetime
- 2003-09-04 AU AU2003265924A patent/AU2003265924A1/en not_active Abandoned
- 2003-09-04 EP EP03795649A patent/EP1539708B1/en not_active Expired - Lifetime
- 2003-09-04 ES ES03795649T patent/ES2297265T3/es not_active Expired - Lifetime
- 2003-09-04 WO PCT/US2003/027692 patent/WO2004024699A1/en not_active Ceased
- 2003-09-04 DE DE60318320T patent/DE60318320T2/de not_active Expired - Lifetime
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