AU2007260216A1 - Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them - Google Patents
Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them Download PDFInfo
- Publication number
- AU2007260216A1 AU2007260216A1 AU2007260216A AU2007260216A AU2007260216A1 AU 2007260216 A1 AU2007260216 A1 AU 2007260216A1 AU 2007260216 A AU2007260216 A AU 2007260216A AU 2007260216 A AU2007260216 A AU 2007260216A AU 2007260216 A1 AU2007260216 A1 AU 2007260216A1
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- Australia
- Prior art keywords
- group
- alkyl
- phenyl
- preferably consisting
- heterocycloalkyl
- 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.)
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- 238000002360 preparation method Methods 0.000 title claims description 135
- 150000003839 salts Chemical class 0.000 title claims description 22
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 14
- MJEPPEQNLZSPAP-UHFFFAOYSA-N 1h-pyrazolo[4,3-b]pyridin-3-amine Chemical class C1=CN=C2C(N)=NNC2=C1 MJEPPEQNLZSPAP-UHFFFAOYSA-N 0.000 title description 8
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 250
- 229910052739 hydrogen Inorganic materials 0.000 claims description 229
- 150000001875 compounds Chemical class 0.000 claims description 215
- 239000001257 hydrogen Substances 0.000 claims description 202
- 239000004202 carbamide Substances 0.000 claims description 186
- -1 hydroxy, amino Chemical group 0.000 claims description 168
- 150000002431 hydrogen Chemical class 0.000 claims description 141
- 238000006243 chemical reaction Methods 0.000 claims description 120
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 109
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 107
- 229910052736 halogen Inorganic materials 0.000 claims description 89
- 150000002367 halogens Chemical class 0.000 claims description 89
- 238000000034 method Methods 0.000 claims description 83
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 80
- 201000010099 disease Diseases 0.000 claims description 79
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 63
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 59
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 57
- 229910052757 nitrogen Inorganic materials 0.000 claims description 51
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 48
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 46
- 125000003118 aryl group Chemical group 0.000 claims description 37
- 206010028980 Neoplasm Diseases 0.000 claims description 36
- 239000002253 acid Substances 0.000 claims description 36
- 238000011282 treatment Methods 0.000 claims description 31
- 230000033115 angiogenesis Effects 0.000 claims description 30
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 30
- 229910052760 oxygen Inorganic materials 0.000 claims description 30
- 239000001301 oxygen Substances 0.000 claims description 30
- 125000001072 heteroaryl group Chemical group 0.000 claims description 28
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 28
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 26
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 26
- 150000001412 amines Chemical class 0.000 claims description 24
- 239000000460 chlorine Substances 0.000 claims description 24
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 24
- 230000006444 vascular growth Effects 0.000 claims description 24
- 230000009467 reduction Effects 0.000 claims description 23
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 22
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 18
- 206010030113 Oedema Diseases 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 229910052801 chlorine Inorganic materials 0.000 claims description 14
- 125000004939 6-pyridyl group Chemical group N1=CC=CC=C1* 0.000 claims description 13
- 238000005859 coupling reaction Methods 0.000 claims description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
- 125000006239 protecting group Chemical group 0.000 claims description 11
- 229910052701 rubidium Inorganic materials 0.000 claims description 11
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 10
- 125000005549 heteroarylene group Chemical group 0.000 claims description 10
- 150000002429 hydrazines Chemical class 0.000 claims description 10
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- 230000036573 scar formation Effects 0.000 claims description 10
- 239000001117 sulphuric acid Substances 0.000 claims description 10
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- 206010027476 Metastases Diseases 0.000 claims description 9
- 201000004681 Psoriasis Diseases 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 9
- 230000001419 dependent effect Effects 0.000 claims description 9
- 239000012948 isocyanate Substances 0.000 claims description 9
- 150000002513 isocyanates Chemical class 0.000 claims description 9
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical compound ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 claims description 9
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 8
- 239000005864 Sulphur Substances 0.000 claims description 8
- 125000000732 arylene group 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
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 206010012442 Dermatitis contact Diseases 0.000 claims description 7
- 102100025027 E3 ubiquitin-protein ligase TRIM69 Human genes 0.000 claims description 7
- 101000830203 Homo sapiens E3 ubiquitin-protein ligase TRIM69 Proteins 0.000 claims description 7
- 206010021143 Hypoxia Diseases 0.000 claims description 7
- 206010053613 Type IV hypersensitivity reaction Diseases 0.000 claims description 7
- 206010064930 age-related macular degeneration Diseases 0.000 claims description 7
- 208000006673 asthma Diseases 0.000 claims description 7
- 208000010247 contact dermatitis Diseases 0.000 claims description 7
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- 201000006417 multiple sclerosis Diseases 0.000 claims description 7
- 208000002815 pulmonary hypertension Diseases 0.000 claims description 7
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- 230000005951 type IV hypersensitivity Effects 0.000 claims description 7
- 208000027930 type IV hypersensitivity disease Diseases 0.000 claims description 7
- 208000003174 Brain Neoplasms Diseases 0.000 claims description 6
- 208000017442 Retinal disease Diseases 0.000 claims description 6
- 206010038923 Retinopathy Diseases 0.000 claims description 6
- 206010052779 Transplant rejections Diseases 0.000 claims description 6
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- 208000029078 coronary artery disease Diseases 0.000 claims description 6
- 230000007954 hypoxia Effects 0.000 claims description 6
- 208000030613 peripheral artery disease Diseases 0.000 claims description 6
- 230000002062 proliferating effect Effects 0.000 claims description 6
- 230000029663 wound healing Effects 0.000 claims description 6
- 125000006584 (C3-C10) heterocycloalkyl group Chemical group 0.000 claims description 5
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims description 5
- 206010003445 Ascites Diseases 0.000 claims description 5
- 206010061692 Benign muscle neoplasm Diseases 0.000 claims description 5
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims description 5
- 206010048962 Brain oedema Diseases 0.000 claims description 5
- 201000009273 Endometriosis Diseases 0.000 claims description 5
- 208000019693 Lung disease Diseases 0.000 claims description 5
- 206010025415 Macular oedema Diseases 0.000 claims description 5
- 201000004458 Myoma Diseases 0.000 claims description 5
- 150000001204 N-oxides Chemical class 0.000 claims description 5
- 101100258315 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) crc-1 gene Proteins 0.000 claims description 5
- 206010055870 Postmenopausal haemorrhage Diseases 0.000 claims description 5
- 206010037423 Pulmonary oedema Diseases 0.000 claims description 5
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims description 5
- 208000006011 Stroke Diseases 0.000 claims description 5
- 208000011341 adult acute respiratory distress syndrome Diseases 0.000 claims description 5
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 230000001684 chronic effect Effects 0.000 claims description 5
- 210000004087 cornea Anatomy 0.000 claims description 5
- 125000006588 heterocycloalkylene group Chemical group 0.000 claims description 5
- 201000010230 macular retinal edema Diseases 0.000 claims description 5
- 210000005036 nerve Anatomy 0.000 claims description 5
- 201000011461 pre-eclampsia Diseases 0.000 claims description 5
- 230000008929 regeneration Effects 0.000 claims description 5
- 238000011069 regeneration method Methods 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 208000006386 Bone Resorption Diseases 0.000 claims description 4
- 206010033266 Ovarian Hyperstimulation Syndrome Diseases 0.000 claims description 4
- 230000024279 bone resorption Effects 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 230000009615 deamination Effects 0.000 claims description 4
- 238000006481 deamination reaction Methods 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 3
- FQEIBEOBXKJAMZ-UHFFFAOYSA-N [3-(trifluoromethyl)phenyl]urea Chemical compound NC(=O)NC1=CC=CC(C(F)(F)F)=C1 FQEIBEOBXKJAMZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 3
- QBEWEBNLZYGINF-UHFFFAOYSA-N 1-[4-(1-methyl-6-propan-2-ylpyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound C=12C=NN(C)C2=NC(C(C)C)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C(F)(F)F)=C1 QBEWEBNLZYGINF-UHFFFAOYSA-N 0.000 claims description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 54
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 5
- ZJEVYKHEGWJGLW-UHFFFAOYSA-N [4-(trifluoromethyl)pyridin-2-yl]urea Chemical compound NC(=O)NC1=CC(C(F)(F)F)=CC=N1 ZJEVYKHEGWJGLW-UHFFFAOYSA-N 0.000 claims 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
- KKSQNQFHTYAYMO-UHFFFAOYSA-N 1-(2-fluoro-5-methylphenyl)-3-[4-[1-methyl-6-(methylsulfonylmethyl)pyrazolo[3,4-b]pyridin-4-yl]phenyl]urea Chemical compound CC1=CC=C(F)C(NC(=O)NC=2C=CC(=CC=2)C=2C=3C=NN(C)C=3N=C(CS(C)(=O)=O)C=2)=C1 KKSQNQFHTYAYMO-UHFFFAOYSA-N 0.000 claims 1
- YBYWJWSXJXWZGJ-UHFFFAOYSA-N 1-(2-fluoro-5-methylphenyl)-3-[4-[1-methyl-6-(piperidin-1-ylmethyl)pyrazolo[3,4-b]pyridin-4-yl]phenyl]urea Chemical compound CC1=CC=C(F)C(NC(=O)NC=2C=CC(=CC=2)C=2C=3C=NN(C)C=3N=C(CN3CCCCC3)C=2)=C1 YBYWJWSXJXWZGJ-UHFFFAOYSA-N 0.000 claims 1
- NHXXPINLNYZVMB-UHFFFAOYSA-N 1-(2-fluoro-5-methylphenyl)-3-[4-[1-methyl-6-[(4-methylpiperazin-1-yl)methyl]pyrazolo[3,4-b]pyridin-4-yl]phenyl]urea Chemical compound C1CN(C)CCN1CC1=CC(C=2C=CC(NC(=O)NC=3C(=CC=C(C)C=3)F)=CC=2)=C(C=NN2C)C2=N1 NHXXPINLNYZVMB-UHFFFAOYSA-N 0.000 claims 1
- NIAAGVAFAREREG-UHFFFAOYSA-N 1-[2-fluoro-5-(trifluoromethyl)phenyl]-3-[4-(1-methylpyrazolo[3,4-b]pyridin-4-yl)phenyl]urea Chemical compound C1=CN=C2N(C)N=CC2=C1C(C=C1)=CC=C1NC(=O)NC1=CC(C(F)(F)F)=CC=C1F NIAAGVAFAREREG-UHFFFAOYSA-N 0.000 claims 1
- XTKQSZLRPSAAHE-UHFFFAOYSA-N 1-[3-methyl-4-[(4-methylpiperazin-1-yl)methyl]phenyl]-3-[4-(1-methylpyrazolo[3,4-b]pyridin-4-yl)phenyl]urea Chemical compound C1CN(C)CCN1CC(C(=C1)C)=CC=C1NC(=O)NC1=CC=C(C=2C=3C=NN(C)C=3N=CC=2)C=C1 XTKQSZLRPSAAHE-UHFFFAOYSA-N 0.000 claims 1
- VCBBDYQEYOVQBP-UHFFFAOYSA-N 1-[4-(1-methylpyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-phenylurea Chemical compound C1=CN=C2N(C)N=CC2=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CC=C1 VCBBDYQEYOVQBP-UHFFFAOYSA-N 0.000 claims 1
- GCOCXYJUJVARQQ-UHFFFAOYSA-N 1-[4-(1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound FC(F)(F)C1=CC=CC(NC(=O)NC=2C=CC(=CC=2)C=2C=3C=NNC=3N=CC=2)=C1 GCOCXYJUJVARQQ-UHFFFAOYSA-N 0.000 claims 1
- UBXWQHJFLDNFNR-UHFFFAOYSA-N 1-[4-(6-cyclobutyl-1-methylpyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound N1=C2N(C)N=CC2=C(C=2C=CC(NC(=O)NC=3C=C(C=CC=3)C(F)(F)F)=CC=2)C=C1C1CCC1 UBXWQHJFLDNFNR-UHFFFAOYSA-N 0.000 claims 1
- HRJAFLDQXNTASV-UHFFFAOYSA-N 1-[4-(6-cyclopropyl-1-methylpyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound N1=C2N(C)N=CC2=C(C=2C=CC(NC(=O)NC=3C=C(C=CC=3)C(F)(F)F)=CC=2)C=C1C1CC1 HRJAFLDQXNTASV-UHFFFAOYSA-N 0.000 claims 1
- GHUZFSHGCIUHOO-UHFFFAOYSA-N 1-[4-(6-methyl-1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound C=12C=NNC2=NC(C)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C(F)(F)F)=C1 GHUZFSHGCIUHOO-UHFFFAOYSA-N 0.000 claims 1
- QHWBHEYMIKAPRK-UHFFFAOYSA-N 1-[4-(6-propan-2-yl-1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound C=12C=NNC2=NC(C(C)C)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C(F)(F)F)=C1 QHWBHEYMIKAPRK-UHFFFAOYSA-N 0.000 claims 1
- FDNGYLCQEAECIB-UHFFFAOYSA-N 1-[4-(6-tert-butyl-1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-(2-methylphenyl)urea Chemical compound CC1=CC=CC=C1NC(=O)NC1=CC=C(C=2C=3C=NNC=3N=C(C=2)C(C)(C)C)C=C1 FDNGYLCQEAECIB-UHFFFAOYSA-N 0.000 claims 1
- XGTVOKJZLRYVCR-UHFFFAOYSA-N 1-[4-(6-tert-butyl-1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-(3-ethylphenyl)urea Chemical compound CCC1=CC=CC(NC(=O)NC=2C=CC(=CC=2)C=2C=3C=NNC=3N=C(C=2)C(C)(C)C)=C1 XGTVOKJZLRYVCR-UHFFFAOYSA-N 0.000 claims 1
- HZTHQFPFMMNUOX-UHFFFAOYSA-N 1-[4-(6-tert-butyl-1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-(3-fluorophenyl)urea Chemical compound C=12C=NNC2=NC(C(C)(C)C)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(F)=C1 HZTHQFPFMMNUOX-UHFFFAOYSA-N 0.000 claims 1
- NKLXPIJJUOHMQD-UHFFFAOYSA-N 1-[4-(6-tert-butyl-1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-(3-methylphenyl)urea Chemical compound CC1=CC=CC(NC(=O)NC=2C=CC(=CC=2)C=2C=3C=NNC=3N=C(C=2)C(C)(C)C)=C1 NKLXPIJJUOHMQD-UHFFFAOYSA-N 0.000 claims 1
- QKEUOHYHRLHRGG-UHFFFAOYSA-N 1-[4-(6-tert-butyl-1h-pyrazolo[3,4-b]pyridin-4-yl)phenyl]-3-(4-fluorophenyl)urea Chemical compound C=12C=NNC2=NC(C(C)(C)C)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC=C(F)C=C1 QKEUOHYHRLHRGG-UHFFFAOYSA-N 0.000 claims 1
- UIQMRYGYZRPKLJ-UHFFFAOYSA-N 1-[4-[1-(3-morpholin-4-ylpropyl)-6-propan-2-ylpyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound C=12C=NN(CCCN3CCOCC3)C2=NC(C(C)C)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C(F)(F)F)=C1 UIQMRYGYZRPKLJ-UHFFFAOYSA-N 0.000 claims 1
- BSNZWVMUAACBRR-UHFFFAOYSA-N 1-[4-[1-methyl-6-(methylsulfonylmethyl)pyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound C1=C(CS(C)(=O)=O)N=C2N(C)N=CC2=C1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C(F)(F)F)=C1 BSNZWVMUAACBRR-UHFFFAOYSA-N 0.000 claims 1
- YLNZXNLODMUZAZ-UHFFFAOYSA-N 1-[4-[1-methyl-6-(piperidin-1-ylmethyl)pyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound N1=C2N(C)N=CC2=C(C=2C=CC(NC(=O)NC=3C=C(C=CC=3)C(F)(F)F)=CC=2)C=C1CN1CCCCC1 YLNZXNLODMUZAZ-UHFFFAOYSA-N 0.000 claims 1
- RAFVVENBFDAWAI-UHFFFAOYSA-N 1-[4-[1-methyl-6-[(4-methylpiperazin-1-yl)methyl]pyrazolo[3,4-b]pyridin-4-yl]phenyl]-1-[3-(trifluoromethyl)phenyl]urea Chemical compound C1CN(C)CCN1CC1=CC(C=2C=CC(=CC=2)N(C(N)=O)C=2C=C(C=CC=2)C(F)(F)F)=C(C=NN2C)C2=N1 RAFVVENBFDAWAI-UHFFFAOYSA-N 0.000 claims 1
- QXBQIOODDHYQPM-UHFFFAOYSA-N 1-[4-[1-methyl-6-[(4-methylpiperazin-1-yl)methyl]pyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-[4-(trifluoromethyl)pyridin-2-yl]urea Chemical compound C1CN(C)CCN1CC1=CC(C=2C=CC(NC(=O)NC=3N=CC=C(C=3)C(F)(F)F)=CC=2)=C(C=NN2C)C2=N1 QXBQIOODDHYQPM-UHFFFAOYSA-N 0.000 claims 1
- ANZNZKXMKQPXJC-UHFFFAOYSA-N 1-[4-[6-(methoxymethyl)-1-methylpyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound C=12C=NN(C)C2=NC(COC)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC=CC(C(F)(F)F)=C1 ANZNZKXMKQPXJC-UHFFFAOYSA-N 0.000 claims 1
- VCRHZIXCSHTRAA-UHFFFAOYSA-N 1-[4-[6-(methoxymethyl)-1-methylpyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-[4-(trifluoromethyl)pyridin-2-yl]urea Chemical compound C=12C=NN(C)C2=NC(COC)=CC=1C(C=C1)=CC=C1NC(=O)NC1=CC(C(F)(F)F)=CC=N1 VCRHZIXCSHTRAA-UHFFFAOYSA-N 0.000 claims 1
- QFRZTVAXGJBUJA-UHFFFAOYSA-N 1-[4-[6-[(2,6-dimethylmorpholin-4-yl)methyl]-1-methylpyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-(2-fluoro-5-methylphenyl)urea Chemical compound C1C(C)OC(C)CN1CC1=CC(C=2C=CC(NC(=O)NC=3C(=CC=C(C)C=3)F)=CC=2)=C(C=NN2C)C2=N1 QFRZTVAXGJBUJA-UHFFFAOYSA-N 0.000 claims 1
- BFMIVRGLXXLCDL-UHFFFAOYSA-N 1-[4-[6-[(2,6-dimethylmorpholin-4-yl)methyl]-1-methylpyrazolo[3,4-b]pyridin-4-yl]phenyl]-3-[3-(trifluoromethyl)phenyl]urea Chemical compound C1C(C)OC(C)CN1CC1=CC(C=2C=CC(NC(=O)NC=3C=C(C=CC=3)C(F)(F)F)=CC=2)=C(C=NN2C)C2=N1 BFMIVRGLXXLCDL-UHFFFAOYSA-N 0.000 claims 1
- ASLNKSWEZAKAIT-UHFFFAOYSA-N 2-[2,2-dimethyl-3-[1-methyl-4-[4-[[3-(trifluoromethyl)phenyl]carbamoylamino]phenyl]pyrazolo[3,4-b]pyridin-6-yl]cyclobutyl]-n,n-dimethylacetamide Chemical compound CC1(C)C(CC(=O)N(C)C)CC1C1=CC(C=2C=CC(NC(=O)NC=3C=C(C=CC=3)C(F)(F)F)=CC=2)=C(C=NN2C)C2=N1 ASLNKSWEZAKAIT-UHFFFAOYSA-N 0.000 claims 1
- ASTAZOPDKJAWKA-UHFFFAOYSA-N 4-(6-methyl-1H-pyrazolo[3,4-b]pyridin-4-yl)aniline Chemical compound C=12C=NNC2=NC(C)=CC=1C1=CC=C(N)C=C1 ASTAZOPDKJAWKA-UHFFFAOYSA-N 0.000 claims 1
- 101100341170 Caenorhabditis elegans irg-7 gene Proteins 0.000 claims 1
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Classifications
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Transplantation (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
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- Biomedical Technology (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06090109.7 | 2006-06-13 | ||
| EP06090109A EP1867648A1 (en) | 2006-06-13 | 2006-06-13 | Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them. |
| EP07090020.4 | 2007-02-15 | ||
| EP07090020 | 2007-02-15 | ||
| PCT/EP2007/005432 WO2007144204A1 (en) | 2006-06-13 | 2007-06-12 | Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2007260216A1 true AU2007260216A1 (en) | 2007-12-21 |
Family
ID=38445661
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2007260216A Abandoned AU2007260216A1 (en) | 2006-06-13 | 2007-06-12 | Substituted aminopyrazolopyridines and salts thereof, their preparations and pharmaceutical compositions comprising them |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US7846928B2 (enExample) |
| EP (1) | EP2061790B1 (enExample) |
| JP (1) | JP5475442B2 (enExample) |
| KR (1) | KR20090018212A (enExample) |
| AR (1) | AR061346A1 (enExample) |
| AU (1) | AU2007260216A1 (enExample) |
| BR (1) | BRPI0711961A2 (enExample) |
| CA (1) | CA2654789C (enExample) |
| CL (1) | CL2007001711A1 (enExample) |
| CR (1) | CR10505A (enExample) |
| EA (1) | EA200802407A1 (enExample) |
| EC (1) | ECSP088963A (enExample) |
| ES (1) | ES2515117T3 (enExample) |
| GT (1) | GT200800285A (enExample) |
| IL (1) | IL195813A0 (enExample) |
| MX (1) | MX2008015955A (enExample) |
| NO (1) | NO20090171L (enExample) |
| PE (1) | PE20080205A1 (enExample) |
| TW (1) | TW200815438A (enExample) |
| UY (1) | UY30409A1 (enExample) |
| WO (1) | WO2007144204A1 (enExample) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20061119A1 (es) * | 2005-01-19 | 2006-11-27 | Aventis Pharma Sa | PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie |
| CN101903384A (zh) | 2007-11-02 | 2010-12-01 | 沃泰克斯药物股份有限公司 | 作为蛋白激酶Cθ抑制剂的[1H-吡唑并[3,4-B]吡啶-4-基]-苯基或-吡啶-2-基衍生物 |
| MX2010011920A (es) * | 2008-05-05 | 2010-11-26 | Amgen Inc | Compuestos de urea como moduladores de gamma secretasa. |
| EP2671891A3 (en) | 2008-06-27 | 2014-03-05 | Amgen Inc. | Ang-2 inhibition to treat multiple sclerosis |
| JP5689069B2 (ja) | 2008-11-20 | 2015-03-25 | ジェネンテック， インコーポレイテッド | ピラゾロピリジンｐｉ３ｋ阻害剤化合物及び使用方法 |
| US8846673B2 (en) | 2009-08-11 | 2014-09-30 | Bristol-Myers Squibb Company | Azaindazoles as kinase inhibitors and use thereof |
| JP2013515032A (ja) | 2009-12-21 | 2013-05-02 | ノバルティス アーゲー | 二置換ヘテロアリール縮合ピリジン類 |
| US9663511B2 (en) | 2012-03-26 | 2017-05-30 | Arroyo BioSciences, LLC | Sphingosine 1-phosphate receptor antagonists |
| WO2013188848A2 (en) * | 2012-06-15 | 2013-12-19 | The Regents Of The University Of California | Antiviral compounds and methods of use |
| US11059817B2 (en) | 2015-09-23 | 2021-07-13 | The Regents Of The University Of California | Potent antiviral pyrazolopyridine compounds |
| JOP20190024A1 (ar) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
| KR102717600B1 (ko) | 2017-10-06 | 2024-10-15 | 포르마 세라퓨틱스 인크. | 유비퀴틴 특이적 펩티다제 30의 억제 |
| KR102526964B1 (ko) | 2018-02-26 | 2023-04-28 | 길리애드 사이언시즈, 인코포레이티드 | Hbv 복제 억제제로서의 치환된 피롤리진 화합물 |
| CN112513036B (zh) | 2018-05-17 | 2024-05-24 | 福马治疗有限公司 | 用作泛素特异性肽酶30抑制剂的稠合双环化合物 |
| ES2945834T3 (es) | 2018-10-05 | 2023-07-07 | Forma Therapeutics Inc | Pirrolinas fusionadas que actúan como inhibidores de la proteasa 30 específica de ubiquitina (USP30) |
| TW202136238A (zh) * | 2020-01-06 | 2021-10-01 | 大陸商廣東東陽光藥業有限公司 | RORγt抑制劑及其製備方法和用途 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6670364B2 (en) * | 2001-01-31 | 2003-12-30 | Telik, Inc. | Antagonists of MCP-1 function and methods of use thereof |
| PL1638941T3 (pl) | 2003-05-22 | 2010-11-30 | Abbvie Bahamas Ltd | Indazolowe, benzizoksazolowe i benzizotiazolowe inhibitory kinaz |
| WO2005063756A1 (en) * | 2003-12-22 | 2005-07-14 | Sb Pharmco Puerto Rico Inc | Crf receptor antagonists and methods relating thereto |
| FR2876691B1 (fr) * | 2004-10-18 | 2006-12-29 | Sanofi Aventis Sa | Derives de pyridine, leur preparation, leur application en therapeutique |
| CA2585934C (en) * | 2004-10-29 | 2013-09-10 | Abbott Laboratories | Novel pyrazolopyridine urea kinase inhibitors |
| PE20061119A1 (es) * | 2005-01-19 | 2006-11-27 | Aventis Pharma Sa | PIRAZOLO PIRIDINAS SUSTITUIDAS COMO INHIBIDORES DE CINASAS FAK, KDR Y Tie |
| EP1683796A1 (en) * | 2005-01-24 | 2006-07-26 | Schering Aktiengesellschaft | Pyrazolopyridines, their preparation and their medical use |
| RS50821B (sr) | 2005-06-27 | 2010-08-31 | Sanofi-Aventis | Derivati pirazolopiridina kao inhibitori beta-adrenergičnog receptora kinaze 1 |
-
2007
- 2007-06-11 TW TW096121006A patent/TW200815438A/zh unknown
- 2007-06-12 ES ES07764753.5T patent/ES2515117T3/es active Active
- 2007-06-12 AR ARP070102552A patent/AR061346A1/es unknown
- 2007-06-12 CL CL2007001711A patent/CL2007001711A1/es unknown
- 2007-06-12 BR BRPI0711961-5A patent/BRPI0711961A2/pt not_active IP Right Cessation
- 2007-06-12 EA EA200802407A patent/EA200802407A1/ru unknown
- 2007-06-12 EP EP07764753.5A patent/EP2061790B1/en active Active
- 2007-06-12 CA CA2654789A patent/CA2654789C/en not_active Expired - Fee Related
- 2007-06-12 JP JP2009514716A patent/JP5475442B2/ja not_active Expired - Fee Related
- 2007-06-12 WO PCT/EP2007/005432 patent/WO2007144204A1/en not_active Ceased
- 2007-06-12 KR KR1020097000562A patent/KR20090018212A/ko not_active Withdrawn
- 2007-06-12 MX MX2008015955A patent/MX2008015955A/es not_active Application Discontinuation
- 2007-06-12 US US11/761,672 patent/US7846928B2/en not_active Expired - Fee Related
- 2007-06-12 UY UY30409A patent/UY30409A1/es not_active Application Discontinuation
- 2007-06-12 PE PE2007000741A patent/PE20080205A1/es not_active Application Discontinuation
- 2007-06-12 AU AU2007260216A patent/AU2007260216A1/en not_active Abandoned
-
2008
- 2008-12-09 IL IL195813A patent/IL195813A0/en unknown
- 2008-12-12 CR CR10505A patent/CR10505A/es not_active Application Discontinuation
- 2008-12-12 GT GT200800285A patent/GT200800285A/es unknown
- 2008-12-12 EC EC2008008963A patent/ECSP088963A/es unknown
-
2009
- 2009-01-12 NO NO20090171A patent/NO20090171L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP2061790A1 (en) | 2009-05-27 |
| JP2009539914A (ja) | 2009-11-19 |
| IL195813A0 (en) | 2009-09-22 |
| UY30409A1 (es) | 2008-01-31 |
| ES2515117T3 (es) | 2014-10-29 |
| CA2654789C (en) | 2014-08-05 |
| CA2654789A1 (en) | 2007-12-21 |
| JP5475442B2 (ja) | 2014-04-16 |
| MX2008015955A (es) | 2009-01-09 |
| AR061346A1 (es) | 2008-08-20 |
| KR20090018212A (ko) | 2009-02-19 |
| US7846928B2 (en) | 2010-12-07 |
| WO2007144204A1 (en) | 2007-12-21 |
| EP2061790B1 (en) | 2014-08-13 |
| GT200800285A (es) | 2009-03-09 |
| EA200802407A1 (ru) | 2009-06-30 |
| CR10505A (es) | 2009-03-20 |
| US20080058326A1 (en) | 2008-03-06 |
| TW200815438A (en) | 2008-04-01 |
| CL2007001711A1 (es) | 2008-01-04 |
| NO20090171L (no) | 2009-03-12 |
| PE20080205A1 (es) | 2008-06-01 |
| BRPI0711961A2 (pt) | 2012-01-17 |
| ECSP088963A (es) | 2009-01-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1 | Application lapsed section 142(2)(a) - no request for examination in relevant period |