JP2004524301A5 - - Google Patents
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- Publication number
- JP2004524301A5 JP2004524301A5 JP2002561468A JP2002561468A JP2004524301A5 JP 2004524301 A5 JP2004524301 A5 JP 2004524301A5 JP 2002561468 A JP2002561468 A JP 2002561468A JP 2002561468 A JP2002561468 A JP 2002561468A JP 2004524301 A5 JP2004524301 A5 JP 2004524301A5
- Authority
- JP
- Japan
- Prior art keywords
- lower alkyl
- optionally substituted
- amino
- carbonyl
- pyridin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 193
- 150000001875 compounds Chemical class 0.000 claims 59
- 125000001072 heteroaryl group Chemical group 0.000 claims 59
- 125000003107 substituted aryl group Chemical group 0.000 claims 44
- 229910052739 hydrogen Inorganic materials 0.000 claims 43
- 239000001257 hydrogen Substances 0.000 claims 42
- 125000000753 cycloalkyl group Chemical group 0.000 claims 39
- 125000003118 aryl group Chemical group 0.000 claims 36
- 150000002431 hydrogen Chemical class 0.000 claims 35
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 33
- 125000003342 alkenyl group Chemical group 0.000 claims 20
- 229910052736 halogen Inorganic materials 0.000 claims 18
- 150000002367 halogens Chemical class 0.000 claims 18
- 229910052760 oxygen Inorganic materials 0.000 claims 18
- 229910052717 sulfur Inorganic materials 0.000 claims 17
- 150000003839 salts Chemical class 0.000 claims 16
- -1 — CF 3 Chemical group 0.000 claims 14
- 125000000304 alkynyl group Chemical group 0.000 claims 13
- 208000023275 Autoimmune disease Diseases 0.000 claims 12
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 12
- 125000004104 aryloxy group Chemical group 0.000 claims 9
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 9
- 150000003857 carboxamides Chemical class 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 8
- 125000004938 5-pyridyl group Chemical group N1=CC=CC(=C1)* 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 7
- 206010020751 Hypersensitivity Diseases 0.000 claims 6
- 206010061218 Inflammation Diseases 0.000 claims 6
- 230000007815 allergy Effects 0.000 claims 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims 6
- 230000004054 inflammatory process Effects 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 208000026935 allergic disease Diseases 0.000 claims 5
- 239000003791 organic solvent mixture Substances 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 3
- GOIATKIVIBJITI-UHFFFAOYSA-N 1,3-dimethyl-n-[[3-(trifluoromethyl)phenyl]carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=CC(C(F)(F)F)=C1 GOIATKIVIBJITI-UHFFFAOYSA-N 0.000 claims 2
- GOCPUHUZDSFDKP-UHFFFAOYSA-N 2-[2-chloro-4-[(1,3-dimethylpyrazolo[3,4-b]pyridine-5-carbonyl)carbamoylamino]phenoxy]acetic acid Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(OCC(O)=O)C(Cl)=C1 GOCPUHUZDSFDKP-UHFFFAOYSA-N 0.000 claims 2
- 201000001320 Atherosclerosis Diseases 0.000 claims 2
- 208000011231 Crohn disease Diseases 0.000 claims 2
- 102000004127 Cytokines Human genes 0.000 claims 2
- 108090000695 Cytokines Proteins 0.000 claims 2
- 208000007342 Diabetic Nephropathies Diseases 0.000 claims 2
- 206010018364 Glomerulonephritis Diseases 0.000 claims 2
- 208000022559 Inflammatory bowel disease Diseases 0.000 claims 2
- 206010033645 Pancreatitis Diseases 0.000 claims 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 2
- 238000009825 accumulation Methods 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 230000003092 anti-cytokine Effects 0.000 claims 2
- 230000003110 anti-inflammatory effect Effects 0.000 claims 2
- 208000006673 asthma Diseases 0.000 claims 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- 208000033679 diabetic kidney disease Diseases 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 239000002955 immunomodulating agent Substances 0.000 claims 2
- 230000002584 immunomodulator Effects 0.000 claims 2
- 229940121354 immunomodulator Drugs 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 210000000265 leukocyte Anatomy 0.000 claims 2
- 210000004698 lymphocyte Anatomy 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 238000013508 migration Methods 0.000 claims 2
- 230000005012 migration Effects 0.000 claims 2
- 210000001616 monocyte Anatomy 0.000 claims 2
- 201000006417 multiple sclerosis Diseases 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 239000003960 organic solvent Substances 0.000 claims 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical group ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 208000005069 pulmonary fibrosis Diseases 0.000 claims 2
- 208000037803 restenosis Diseases 0.000 claims 2
- 206010039073 rheumatoid arthritis Diseases 0.000 claims 2
- 230000002194 synthesizing effect Effects 0.000 claims 2
- 238000002054 transplantation Methods 0.000 claims 2
- ZYVWCCQRGRSCIL-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[(3-phenoxyphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(OC=3C=CC=CC=3)C=CC=2)C=NC2=C1C(C)=NN2C ZYVWCCQRGRSCIL-UHFFFAOYSA-N 0.000 claims 1
- LVCKXOBXLBVIJH-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[(3-phenylphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C=CC=2)C=2C=CC=CC=2)C=NC2=C1C(C)=NN2C LVCKXOBXLBVIJH-UHFFFAOYSA-N 0.000 claims 1
- XXSGYDJPECEVTC-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[(3-propan-2-yloxyphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound CC(C)OC1=CC=CC(NC(=O)NC(=O)C=2C(=C3C(C)=NN(C)C3=NC=2)N2CCN(C)CC2)=C1 XXSGYDJPECEVTC-UHFFFAOYSA-N 0.000 claims 1
- FWBAGKSGLMHTPL-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[(3-propan-2-ylphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound CC(C)C1=CC=CC(NC(=O)NC(=O)C=2C(=C3C(C)=NN(C)C3=NC=2)N2CCN(C)CC2)=C1 FWBAGKSGLMHTPL-UHFFFAOYSA-N 0.000 claims 1
- HSKNPSOFQYRKGV-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[[3-(1,3-thiazol-2-yl)phenyl]carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C=CC=2)C=2SC=CN=2)C=NC2=C1C(C)=NN2C HSKNPSOFQYRKGV-UHFFFAOYSA-N 0.000 claims 1
- AUBBKQFYRYTBPJ-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[[3-(trifluoromethoxy)phenyl]carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(OC(F)(F)F)C=CC=2)C=NC2=C1C(C)=NN2C AUBBKQFYRYTBPJ-UHFFFAOYSA-N 0.000 claims 1
- NFVJESWZLANVHQ-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[[3-(trifluoromethyl)phenyl]carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C=CC=2)C(F)(F)F)C=NC2=C1C(C)=NN2C NFVJESWZLANVHQ-UHFFFAOYSA-N 0.000 claims 1
- WMWMGLNDMDCYRW-UHFFFAOYSA-N 1,3-dimethyl-4-(4-methylpiperazin-1-yl)-n-[[4-methyl-3-(trifluoromethyl)phenyl]carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C(C)=CC=2)C(F)(F)F)C=NC2=C1C(C)=NN2C WMWMGLNDMDCYRW-UHFFFAOYSA-N 0.000 claims 1
- TTYWXIHRYBDIOD-UHFFFAOYSA-N 1,3-dimethyl-n-[(3-phenoxyphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC(C=1)=CC=CC=1OC1=CC=CC=C1 TTYWXIHRYBDIOD-UHFFFAOYSA-N 0.000 claims 1
- KCHIAQACEMORFI-UHFFFAOYSA-N 1,3-dimethyl-n-[(3-phenylphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC(C=1)=CC=CC=1C1=CC=CC=C1 KCHIAQACEMORFI-UHFFFAOYSA-N 0.000 claims 1
- ZNDPCVMYGZAQKN-UHFFFAOYSA-N 1,3-dimethyl-n-[(3-propan-2-yloxyphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound CC(C)OC1=CC=CC(NC(=O)NC(=O)C=2C=C3C(C)=NN(C)C3=NC=2)=C1 ZNDPCVMYGZAQKN-UHFFFAOYSA-N 0.000 claims 1
- ADPNVYBUUNXTOP-UHFFFAOYSA-N 1,3-dimethyl-n-[[4-nitro-3-(trifluoromethyl)phenyl]carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C([N+]([O-])=O)C(C(F)(F)F)=C1 ADPNVYBUUNXTOP-UHFFFAOYSA-N 0.000 claims 1
- ZETPZBPPNBEEHT-UHFFFAOYSA-N 2-[4-[(1,3-dimethylpyrazolo[3,4-b]pyridine-5-carbonyl)carbamoylamino]-2-(trifluoromethyl)phenoxy]acetic acid Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(OCC(O)=O)C(C(F)(F)F)=C1 ZETPZBPPNBEEHT-UHFFFAOYSA-N 0.000 claims 1
- 125000006305 3-iodophenyl group Chemical group [H]C1=C([H])C(I)=C([H])C(*)=C1[H] 0.000 claims 1
- RVOTYWZKYZQTGL-UHFFFAOYSA-N 4-(4-aminopyridin-1-ium-1-yl)-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide;chloride Chemical compound [Cl-].C=1C=C(N)C=C[N+]=1C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 RVOTYWZKYZQTGL-UHFFFAOYSA-N 0.000 claims 1
- ZXTPSQAMQAMHBC-UHFFFAOYSA-N 4-(benzylamino)-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C=1C=CC=CC=1CNC1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 ZXTPSQAMQAMHBC-UHFFFAOYSA-N 0.000 claims 1
- QQVBRDBUWOGBNS-UHFFFAOYSA-N 4-(dimethylamino)-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=NC=2N(C)N=C(C)C=2C(N(C)C)=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 QQVBRDBUWOGBNS-UHFFFAOYSA-N 0.000 claims 1
- XESPAXAQASLWTF-UHFFFAOYSA-N 4-(dimethylamino)-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-3-methyl-[1,2]oxazolo[5,4-b]pyridine-5-carboxamide Chemical compound C1=NC=2ON=C(C)C=2C(N(C)C)=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 XESPAXAQASLWTF-UHFFFAOYSA-N 0.000 claims 1
- ASSHQRAAVBQYJP-UHFFFAOYSA-N 4-[(1,3-dimethylpyrazolo[3,4-b]pyridine-5-carbonyl)carbamoylamino]-2-propan-2-yloxybenzoic acid Chemical compound C1=C(C(O)=O)C(OC(C)C)=CC(NC(=O)NC(=O)C=2C=C3C(C)=NN(C)C3=NC=2)=C1 ASSHQRAAVBQYJP-UHFFFAOYSA-N 0.000 claims 1
- HDXSYFONCWNDKS-UHFFFAOYSA-N 4-[(1,3-dimethylpyrazolo[3,4-b]pyridine-5-carbonyl)carbamoylamino]benzoic acid Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(C(O)=O)C=C1 HDXSYFONCWNDKS-UHFFFAOYSA-N 0.000 claims 1
- OEDWDTMHBQBERN-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)amino]-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CC(N)CCC1NC1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 OEDWDTMHBQBERN-UHFFFAOYSA-N 0.000 claims 1
- UBPZDSAPJJBUFY-UHFFFAOYSA-N 4-[2-(dimethylamino)ethyl-methylamino]-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-3-methyl-[1,2]oxazolo[5,4-b]pyridine-5-carboxamide Chemical compound C1=NC=2ON=C(C)C=2C(N(C)CCN(C)C)=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 UBPZDSAPJJBUFY-UHFFFAOYSA-N 0.000 claims 1
- OILKJMSMFKCLQG-UHFFFAOYSA-N 4-[2-(dimethylamino)ethylamino]-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=NC=2N(C)N=C(C)C=2C(NCCN(C)C)=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 OILKJMSMFKCLQG-UHFFFAOYSA-N 0.000 claims 1
- VANKRQSZRCNTFJ-UHFFFAOYSA-N 4-[3-(dimethylamino)propylamino]-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=NC=2N(C)N=C(C)C=2C(NCCCN(C)C)=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 VANKRQSZRCNTFJ-UHFFFAOYSA-N 0.000 claims 1
- HXGOEYNWLRIYOM-UHFFFAOYSA-N 4-[3-(dimethylamino)pyrrolidin-1-yl]-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1C(N(C)C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C(F)=CC=2)C(F)(F)F)C=NC2=C1C(C)=NN2C HXGOEYNWLRIYOM-UHFFFAOYSA-N 0.000 claims 1
- IGPKCTCZMFQRNJ-UHFFFAOYSA-N 4-[[1,3-dimethyl-4-(4-methylpiperazin-1-yl)pyrazolo[3,4-b]pyridine-5-carbonyl]carbamoylamino]-2-propan-2-yloxybenzoic acid Chemical compound C1=C(C(O)=O)C(OC(C)C)=CC(NC(=O)NC(=O)C=2C(=C3C(C)=NN(C)C3=NC=2)N2CCN(C)CC2)=C1 IGPKCTCZMFQRNJ-UHFFFAOYSA-N 0.000 claims 1
- ZOABRVQTSNAFKK-UHFFFAOYSA-N 4-[bis(2-hydroxyethyl)amino]-n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound OCCN(CCO)C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 ZOABRVQTSNAFKK-UHFFFAOYSA-N 0.000 claims 1
- TUBGGADNUUTKBO-UHFFFAOYSA-N 4-chloro-1,3-dimethyl-n-[[4-(trifluoromethyl)phenyl]carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound ClC1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(C(F)(F)F)C=C1 TUBGGADNUUTKBO-UHFFFAOYSA-N 0.000 claims 1
- XWBLGFUXMDXSKY-UHFFFAOYSA-N 4-chloro-n-[(3,4-dichlorophenyl)carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound ClC1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(Cl)C(Cl)=C1 XWBLGFUXMDXSKY-UHFFFAOYSA-N 0.000 claims 1
- BBUDNVUFVDCAJR-UHFFFAOYSA-N 4-chloro-n-[(3-chlorophenyl)carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound ClC1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=CC(Cl)=C1 BBUDNVUFVDCAJR-UHFFFAOYSA-N 0.000 claims 1
- JTRDGMJZPGXEBS-UHFFFAOYSA-N 4-chloro-n-[(4-chlorophenyl)carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound ClC1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 JTRDGMJZPGXEBS-UHFFFAOYSA-N 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 1
- MFORNGKVWCJAME-UHFFFAOYSA-N 6-[2-(dimethylamino)ethyl-methylamino]-1,3-dimethyl-n-[(3-propan-2-yloxyphenyl)carbamoyl]pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound CC(C)OC1=CC=CC(NC(=O)NC(=O)C=2C(=NC=3N(C)N=C(C)C=3C=2)N(C)CCN(C)C)=C1 MFORNGKVWCJAME-UHFFFAOYSA-N 0.000 claims 1
- BFGXWJIJYOFDGT-UHFFFAOYSA-N C1=NC=2N(C)N=C(C)C=2C(N(C)CCN(C)C)=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 Chemical compound C1=NC=2N(C)N=C(C)C=2C(N(C)CCN(C)C)=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 BFGXWJIJYOFDGT-UHFFFAOYSA-N 0.000 claims 1
- JSDAVEDFYJULNR-UHFFFAOYSA-N C1CN(C=2C=CC=CC=2)CCN1C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 Chemical compound C1CN(C=2C=CC=CC=2)CCN1C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 JSDAVEDFYJULNR-UHFFFAOYSA-N 0.000 claims 1
- MUZSOYKQWPHFSF-UHFFFAOYSA-N C1CN(CC=2C=CC=CC=2)CCN1C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 Chemical compound C1CN(CC=2C=CC=CC=2)CCN1C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 MUZSOYKQWPHFSF-UHFFFAOYSA-N 0.000 claims 1
- KVHUXIFWKBBIDX-UHFFFAOYSA-N C=1C=C(F)C(C(F)(F)F)=CC=1NC(=O)NC(=O)C=1C=C2C(C)=NN(C)C2=NC=1N1CCOCC1 Chemical compound C=1C=C(F)C(C(F)(F)F)=CC=1NC(=O)NC(=O)C=1C=C2C(C)=NN(C)C2=NC=1N1CCOCC1 KVHUXIFWKBBIDX-UHFFFAOYSA-N 0.000 claims 1
- XRAGWIBZBRJKSQ-UHFFFAOYSA-N C=1C=C(F)C(C(F)(F)F)=CC=1NC(=O)NC(=O)C=1C=C2C(C)=NN(C)C2=NC=1OCC1=CC=CC=C1 Chemical compound C=1C=C(F)C(C(F)(F)F)=CC=1NC(=O)NC(=O)C=1C=C2C(C)=NN(C)C2=NC=1OCC1=CC=CC=C1 XRAGWIBZBRJKSQ-UHFFFAOYSA-N 0.000 claims 1
- CQLLPQXLRVJDFL-UHFFFAOYSA-N CC(C)OC1=NC=2N(C)N=C(C)C=2C=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 Chemical compound CC(C)OC1=NC=2N(C)N=C(C)C=2C=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 CQLLPQXLRVJDFL-UHFFFAOYSA-N 0.000 claims 1
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- SBUYYHRQYFVKDB-UHFFFAOYSA-N CN1CC(C(CC1)C1=NNC2=NC=C(C=C21)C(=O)NC(=O)NC2=CC(=C(C=C2)F)C(F)(F)F)C Chemical compound CN1CC(C(CC1)C1=NNC2=NC=C(C=C21)C(=O)NC(=O)NC2=CC(=C(C=C2)F)C(F)(F)F)C SBUYYHRQYFVKDB-UHFFFAOYSA-N 0.000 claims 1
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- UUBPUQQUTVTYNV-UHFFFAOYSA-N n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1-methyl-4-(4-methylpiperazin-1-yl)-3-phenylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C(F)=CC=2)C(F)(F)F)C=NC2=C1C(C=1C=CC=CC=1)=NN2C UUBPUQQUTVTYNV-UHFFFAOYSA-N 0.000 claims 1
- WXHDSTCUAPVBPP-UHFFFAOYSA-N n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-1-methylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C=1N=C2N(C)N=CC2=CC=1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 WXHDSTCUAPVBPP-UHFFFAOYSA-N 0.000 claims 1
- ZCAKXARKDWASCE-UHFFFAOYSA-N n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-3-methyl-1-phenylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C12=NC=C(C(=O)NC(=O)NC=3C=C(C(F)=CC=3)C(F)(F)F)C=C2C(C)=NN1C1=CC=CC=C1 ZCAKXARKDWASCE-UHFFFAOYSA-N 0.000 claims 1
- BZEQYSDHDBRTEO-UHFFFAOYSA-N n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-3-methyl-4-morpholin-4-yl-[1,2]oxazolo[5,4-b]pyridine-5-carboxamide Chemical compound C1COCCN1C1=C2C(C)=NOC2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 BZEQYSDHDBRTEO-UHFFFAOYSA-N 0.000 claims 1
- NMUWENQCJRQTNB-UHFFFAOYSA-N n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-4-(4-methylpiperazin-1-yl)-1,3-diphenylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C(F)=CC=2)C(F)(F)F)C=NC2=C1C(C=1C=CC=CC=1)=NN2C1=CC=CC=C1 NMUWENQCJRQTNB-UHFFFAOYSA-N 0.000 claims 1
- BMNAPGFYTMRGNJ-UHFFFAOYSA-N n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-4-[4-(2-hydroxyethyl)piperazin-1-yl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(CCO)CCN1C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 BMNAPGFYTMRGNJ-UHFFFAOYSA-N 0.000 claims 1
- JIERCNPPZQAMNG-UHFFFAOYSA-N n-[[4-fluoro-3-(trifluoromethyl)phenyl]carbamoyl]-6-methoxy-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound COC1=NC=2N(C)N=C(C)C=2C=C1C(=O)NC(=O)NC1=CC=C(F)C(C(F)(F)F)=C1 JIERCNPPZQAMNG-UHFFFAOYSA-N 0.000 claims 1
- IHXWJCUXLRUNHW-UHFFFAOYSA-N n-[[4-hydroxy-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethyl-4-(4-methylpiperazin-1-yl)pyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1CN(C)CCN1C1=C(C(=O)NC(=O)NC=2C=C(C(O)=CC=2)C(F)(F)F)C=NC2=C1C(C)=NN2C IHXWJCUXLRUNHW-UHFFFAOYSA-N 0.000 claims 1
- ZYFZTXNBKJWHQE-UHFFFAOYSA-N n-[[4-hydroxy-3-(trifluoromethyl)phenyl]carbamoyl]-1,3-dimethylpyrazolo[3,4-b]pyridine-5-carboxamide Chemical compound C1=C2C(C)=NN(C)C2=NC=C1C(=O)NC(=O)NC1=CC=C(O)C(C(F)(F)F)=C1 ZYFZTXNBKJWHQE-UHFFFAOYSA-N 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 1
- UVQHNYBTGPTABN-UHFFFAOYSA-N propan-2-yl 2-chloro-5-[[1,3-dimethyl-4-(4-methylpiperazin-1-yl)pyrazolo[3,4-b]pyridine-5-carbonyl]carbamoylamino]benzoate Chemical compound C1=C(Cl)C(C(=O)OC(C)C)=CC(NC(=O)NC(=O)C=2C(=C3C(C)=NN(C)C3=NC=2)N2CCN(C)CC2)=C1 UVQHNYBTGPTABN-UHFFFAOYSA-N 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
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| PCT/US2002/003016 WO2002060900A2 (en) | 2001-01-31 | 2002-01-30 | Antagonists of mcp-1 function and methods of use thereof |
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| US6962926B2 (en) * | 2001-01-31 | 2005-11-08 | Telik, Inc. | Antagonist of MCP-1 function, and compositions and methods of use thereof |
| DE10153259A1 (de) | 2001-10-31 | 2003-05-22 | Osram Opto Semiconductors Gmbh | Optoelektronisches Bauelement |
| EP1478358B1 (en) | 2002-02-11 | 2013-07-03 | Bayer HealthCare LLC | Sorafenib tosylate for the treatment of diseases characterized by abnormal angiogenesis |
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| RU2008127501A (ru) | 2006-01-13 | 2010-02-20 | Вайет (Us) | Сульфонилзамещенные 1н-индолы в качастве лигандов 5-гидрокситриптаминовых рецепторов |
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| US20100074886A1 (en) * | 2006-10-05 | 2010-03-25 | Anuk Das | Ccr2 antagonists for treatment of fibrosis |
| US8278345B2 (en) | 2006-11-09 | 2012-10-02 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
| SI2091948T1 (sl) | 2006-11-30 | 2012-07-31 | Probiodrug Ag | Novi inhibitorji glutaminil ciklaze |
| EA200901140A1 (ru) | 2007-03-01 | 2010-04-30 | Пробиодруг Аг | Новое применение ингибиторов глутаминилциклазы |
| EP2142514B1 (en) | 2007-04-18 | 2014-12-24 | Probiodrug AG | Thiourea derivatives as glutaminyl cyclase inhibitors |
| US7709215B2 (en) | 2007-06-01 | 2010-05-04 | Cytonics Corporation | Method for diagnosing and treating acute joint injury |
| JP5588339B2 (ja) * | 2007-06-25 | 2014-09-10 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規化学化合物 |
| CA2700691A1 (en) * | 2007-10-01 | 2009-04-09 | F. Hoffmann-La Roche Ag | New biaryl derivatives |
| EP2249646A4 (en) * | 2008-02-06 | 2013-09-25 | Glaxo Group Ltd | PDE4 muscarinic Antagonist-DOPPELPHARMACOPHOREN |
| UY31636A1 (es) * | 2008-02-06 | 2009-08-03 | Farmacoforos duales-antagonistas muscarinicos de pde4 | |
| TW201000476A (en) | 2008-02-06 | 2010-01-01 | Glaxo Group Ltd | Dual pharmacophores-PDE4-muscarinic antagonistics |
| WO2009100170A1 (en) * | 2008-02-06 | 2009-08-13 | Glaxo Group Limited | Dual pharmacophores - pde4-muscarinic antagonistics |
| AR070564A1 (es) * | 2008-02-06 | 2010-04-21 | Glaxo Group Ltd | Derivados de 1h-pirazolo[3,4-b]piridin-5-ilo,inhibidores de fosfodiesterasas pde4 y antagonistas de receptores muscarinicos de acetilcolina(machr), utiles en el tratamiento y/o profilaxis de enfermedades respiratorias y alergicas,y composiciones farmaceuticas que los comprenden |
| CN102695546B (zh) | 2009-09-11 | 2014-09-10 | 前体生物药物股份公司 | 作为谷氨酰胺酰环化酶抑制剂的杂环衍生物 |
| WO2011076744A1 (en) | 2009-12-21 | 2011-06-30 | Novartis Ag | Disubstituted heteroaryl-fused pyridines |
| WO2011107530A2 (en) | 2010-03-03 | 2011-09-09 | Probiodrug Ag | Novel inhibitors |
| SG183229A1 (en) | 2010-03-10 | 2012-09-27 | Probiodrug Ag | Heterocyclic inhibitors of glutaminyl cyclase (qc, ec 2.3.2.5) |
| EP2560953B1 (en) | 2010-04-21 | 2016-01-06 | Probiodrug AG | Inhibitors of glutaminyl cyclase |
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| CN108558876B (zh) * | 2018-05-28 | 2020-08-04 | 中南大学 | 吡唑[3,4-b]并吡啶类衍生物及其制备方法和应用 |
| CN112830897B (zh) * | 2019-11-22 | 2022-09-09 | 石家庄以岭药业股份有限公司 | 含脲基苯并咪唑类衍生物及其制备方法和应用 |
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- 2002-01-30 BR BR0206839-7A patent/BR0206839A/pt not_active IP Right Cessation
- 2002-01-30 KR KR10-2003-7010170A patent/KR20030079976A/ko not_active Ceased
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- 2002-01-30 CA CA002432997A patent/CA2432997A1/en not_active Abandoned
- 2002-01-30 WO PCT/US2002/003016 patent/WO2002060900A2/en not_active Ceased
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