JP2008533087A5 - - Google Patents
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- JP2008533087A5 JP2008533087A5 JP2008501279A JP2008501279A JP2008533087A5 JP 2008533087 A5 JP2008533087 A5 JP 2008533087A5 JP 2008501279 A JP2008501279 A JP 2008501279A JP 2008501279 A JP2008501279 A JP 2008501279A JP 2008533087 A5 JP2008533087 A5 JP 2008533087A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- pyrazol
- quinazolin
- amine
- dimethyl
- 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 21
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 15
- LZNOABFJNNIWJV-UHFFFAOYSA-N 2-(1h-pyrazol-5-yl)quinazoline Chemical class N1C=CC(C=2N=C3C=CC=CC3=CN=2)=N1 LZNOABFJNNIWJV-UHFFFAOYSA-N 0.000 claims 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 12
- 125000000623 heterocyclic group Chemical group 0.000 claims 12
- 125000003342 alkenyl group Chemical group 0.000 claims 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims 11
- -1 cyano, nitro, amino, methylenedioxy, phenyl Chemical group 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 10
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 9
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims 9
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 9
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 9
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000004103 aminoalkyl group Chemical group 0.000 claims 8
- 208000035475 disorder Diseases 0.000 claims 8
- 125000001188 haloalkyl group Chemical group 0.000 claims 8
- 125000001475 halogen functional group Chemical group 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 8
- 125000003282 alkyl amino group Chemical group 0.000 claims 7
- 201000010099 disease Diseases 0.000 claims 7
- 125000004438 haloalkoxy group Chemical group 0.000 claims 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 7
- 125000002837 carbocyclic group Chemical group 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 102000004257 Potassium Channel Human genes 0.000 claims 5
- 125000002950 monocyclic group Chemical group 0.000 claims 5
- 125000002757 morpholinyl group Chemical group 0.000 claims 5
- 108020001213 potassium channel Proteins 0.000 claims 5
- 125000001424 substituent group Chemical group 0.000 claims 5
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 4
- 230000000694 effects Effects 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000001624 naphthyl group Chemical group 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 125000003386 piperidinyl group Chemical group 0.000 claims 3
- 125000003367 polycyclic group Chemical group 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 3
- 208000023504 respiratory system disease Diseases 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 208000019901 Anxiety disease Diseases 0.000 claims 2
- 206010010904 Convulsion Diseases 0.000 claims 2
- 208000010228 Erectile Dysfunction Diseases 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 208000002193 Pain Diseases 0.000 claims 2
- 206010046543 Urinary incontinence Diseases 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 230000036506 anxiety Effects 0.000 claims 2
- 206010015037 epilepsy Diseases 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000002541 furyl group Chemical group 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 208000020016 psychiatric disease Diseases 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 201000000980 schizophrenia Diseases 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- LUMKJCXWGTXDCT-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-4-piperidin-1-ylquinazoline Chemical compound N1=C(C)C=C(C)N1C1=NC(N2CCCCC2)=C(C=CC=C2)C2=N1 LUMKJCXWGTXDCT-UHFFFAOYSA-N 0.000 claims 1
- IATRPJHLBLVBDI-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n,n-diethylquinazolin-4-amine Chemical compound N=1C2=CC=CC=C2C(N(CC)CC)=NC=1N1N=C(C)C=C1C IATRPJHLBLVBDI-UHFFFAOYSA-N 0.000 claims 1
- LNHADOZOBGZFKT-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(1,2,3,4-tetrahydronaphthalen-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2C3=CC=CC=C3CCC2)=C(C=CC=C2)C2=N1 LNHADOZOBGZFKT-UHFFFAOYSA-N 0.000 claims 1
- YGXYZTCBQCGBNE-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(1h-indol-7-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=3NC=CC=3C=CC=2)=C(C=CC=C2)C2=N1 YGXYZTCBQCGBNE-UHFFFAOYSA-N 0.000 claims 1
- PWWHIMGVYIKMCS-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(2-methylphenyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C(=CC=CC=2)C)=C(C=CC=C2)C2=N1 PWWHIMGVYIKMCS-UHFFFAOYSA-N 0.000 claims 1
- BKQMFIBJLHPXCS-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(2-pyrrolidin-1-ylethyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NCCN2CCCC2)=C(C=CC=C2)C2=N1 BKQMFIBJLHPXCS-UHFFFAOYSA-N 0.000 claims 1
- GOZZRZJXLZRECQ-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(3-methoxyphenyl)quinazolin-4-amine Chemical compound COC1=CC=CC(NC=2C3=CC=CC=C3N=C(N=2)N2C(=CC(C)=N2)C)=C1 GOZZRZJXLZRECQ-UHFFFAOYSA-N 0.000 claims 1
- FTZNQMOFFXWZHS-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(3-methylphenyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=C(C)C=CC=2)=C(C=CC=C2)C2=N1 FTZNQMOFFXWZHS-UHFFFAOYSA-N 0.000 claims 1
- UIEWRXCGQHKNHE-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(4-iodophenyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC(I)=CC=2)=C(C=CC=C2)C2=N1 UIEWRXCGQHKNHE-UHFFFAOYSA-N 0.000 claims 1
- PTBCYBGNJFQOBW-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(4-methylcyclohexyl)quinazolin-4-amine Chemical compound C1CC(C)CCC1NC1=NC(N2C(=CC(C)=N2)C)=NC2=CC=CC=C12 PTBCYBGNJFQOBW-UHFFFAOYSA-N 0.000 claims 1
- SYZRMPMKRDRKNP-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(4-methylphenyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC(C)=CC=2)=C(C=CC=C2)C2=N1 SYZRMPMKRDRKNP-UHFFFAOYSA-N 0.000 claims 1
- POUCPZAQSUGANK-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(4-morpholin-4-ylphenyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC(=CC=2)N2CCOCC2)=C(C=CC=C2)C2=N1 POUCPZAQSUGANK-UHFFFAOYSA-N 0.000 claims 1
- KJHCUZKDFBIUMP-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(4-phenylphenyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC(=CC=2)C=2C=CC=CC=2)=C(C=CC=C2)C2=N1 KJHCUZKDFBIUMP-UHFFFAOYSA-N 0.000 claims 1
- GLNRXTYBCPVBGP-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(furan-2-ylmethyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NCC=2OC=CC=2)=C(C=CC=C2)C2=N1 GLNRXTYBCPVBGP-UHFFFAOYSA-N 0.000 claims 1
- UQZOFDWFOMNJHI-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(oxan-4-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CCOCC2)=C(C=CC=C2)C2=N1 UQZOFDWFOMNJHI-UHFFFAOYSA-N 0.000 claims 1
- JQQXFPDPXCINPK-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-(thiophen-2-ylmethyl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NCC=2SC=CC=2)=C(C=CC=C2)C2=N1 JQQXFPDPXCINPK-UHFFFAOYSA-N 0.000 claims 1
- RGODJLANPPMVSR-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-[3-(trifluoromethyl)phenyl]quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=C(C=CC=2)C(F)(F)F)=C(C=CC=C2)C2=N1 RGODJLANPPMVSR-UHFFFAOYSA-N 0.000 claims 1
- FBLLMHHCBDVLOE-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-[4-(trifluoromethyl)phenyl]quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC(=CC=2)C(F)(F)F)=C(C=CC=C2)C2=N1 FBLLMHHCBDVLOE-UHFFFAOYSA-N 0.000 claims 1
- OFUSEDFMYBGKBL-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-ethylquinazolin-4-amine Chemical compound N=1C2=CC=CC=C2C(NCC)=NC=1N1N=C(C)C=C1C OFUSEDFMYBGKBL-UHFFFAOYSA-N 0.000 claims 1
- KHCBXUXAEDEPHQ-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-naphthalen-2-ylquinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=C3C=CC=CC3=CC=2)=C(C=CC=C2)C2=N1 KHCBXUXAEDEPHQ-UHFFFAOYSA-N 0.000 claims 1
- SWCVPLSWABSUIW-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-pentan-3-ylquinazolin-4-amine Chemical compound N=1C2=CC=CC=C2C(NC(CC)CC)=NC=1N1N=C(C)C=C1C SWCVPLSWABSUIW-UHFFFAOYSA-N 0.000 claims 1
- GLWUGSGVMNPFLG-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-phenylquinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC=CC=2)=C(C=CC=C2)C2=N1 GLWUGSGVMNPFLG-UHFFFAOYSA-N 0.000 claims 1
- HUKYQZQUKBYDEP-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-piperidin-4-ylquinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CCNCC2)=C(C=CC=C2)C2=N1 HUKYQZQUKBYDEP-UHFFFAOYSA-N 0.000 claims 1
- PZXBCNSEPUEPHG-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-propylquinazolin-4-amine Chemical compound N=1C2=CC=CC=C2C(NCCC)=NC=1N1N=C(C)C=C1C PZXBCNSEPUEPHG-UHFFFAOYSA-N 0.000 claims 1
- UEKJCEWDFGCVIO-UHFFFAOYSA-N 2-(3,5-dimethylpyrazol-1-yl)-n-pyridin-2-ylquinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2N=CC=CC=2)=C(C=CC=C2)C2=N1 UEKJCEWDFGCVIO-UHFFFAOYSA-N 0.000 claims 1
- RSNZNAOHQQKYBI-UHFFFAOYSA-N 2-[3,5-di(propan-2-yl)pyrazol-1-yl]-n-(4-methylcyclohexyl)quinazolin-4-amine Chemical compound N1=C(C(C)C)C=C(C(C)C)N1C1=NC(NC2CCC(C)CC2)=C(C=CC=C2)C2=N1 RSNZNAOHQQKYBI-UHFFFAOYSA-N 0.000 claims 1
- 201000004384 Alopecia Diseases 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 206010002383 Angina Pectoris Diseases 0.000 claims 1
- 206010003225 Arteriospasm coronary Diseases 0.000 claims 1
- 206010003591 Ataxia Diseases 0.000 claims 1
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims 1
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims 1
- 208000020925 Bipolar disease Diseases 0.000 claims 1
- 206010048994 Bladder spasm Diseases 0.000 claims 1
- 201000006474 Brain Ischemia Diseases 0.000 claims 1
- 206010008120 Cerebral ischaemia Diseases 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- 201000003883 Cystic fibrosis Diseases 0.000 claims 1
- 206010012289 Dementia Diseases 0.000 claims 1
- 206010012735 Diarrhoea Diseases 0.000 claims 1
- 208000005171 Dysmenorrhea Diseases 0.000 claims 1
- 206010013935 Dysmenorrhoea Diseases 0.000 claims 1
- 208000018522 Gastrointestinal disease Diseases 0.000 claims 1
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- 206010062016 Immunosuppression Diseases 0.000 claims 1
- 206010022562 Intermittent claudication Diseases 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 241001465754 Metazoa Species 0.000 claims 1
- 208000019695 Migraine disease Diseases 0.000 claims 1
- 208000019022 Mood disease Diseases 0.000 claims 1
- 208000008238 Muscle Spasticity Diseases 0.000 claims 1
- 206010068871 Myotonic dystrophy Diseases 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000018737 Parkinson disease Diseases 0.000 claims 1
- 208000005107 Premature Birth Diseases 0.000 claims 1
- 206010036590 Premature baby Diseases 0.000 claims 1
- 208000003782 Raynaud disease Diseases 0.000 claims 1
- 208000012322 Raynaud phenomenon Diseases 0.000 claims 1
- 208000036071 Rhinorrhea Diseases 0.000 claims 1
- 206010039101 Rhinorrhoea Diseases 0.000 claims 1
- 208000021386 Sjogren Syndrome Diseases 0.000 claims 1
- 208000030886 Traumatic Brain injury Diseases 0.000 claims 1
- 206010047163 Vasospasm Diseases 0.000 claims 1
- 230000006578 abscission Effects 0.000 claims 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 1
- 231100000360 alopecia Toxicity 0.000 claims 1
- 206010003119 arrhythmia Diseases 0.000 claims 1
- 230000006793 arrhythmia Effects 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims 1
- 230000033228 biological regulation Effects 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 206010008118 cerebral infarction Diseases 0.000 claims 1
- 208000029078 coronary artery disease Diseases 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 206010013781 dry mouth Diseases 0.000 claims 1
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims 1
- 201000008980 hyperinsulinism Diseases 0.000 claims 1
- 230000001506 immunosuppresive effect Effects 0.000 claims 1
- 201000001881 impotence Diseases 0.000 claims 1
- 208000035231 inattentive type attention deficit hyperactivity disease Diseases 0.000 claims 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims 1
- 230000006698 induction Effects 0.000 claims 1
- 208000021156 intermittent vascular claudication Diseases 0.000 claims 1
- 208000002551 irritable bowel syndrome Diseases 0.000 claims 1
- 208000028867 ischemia Diseases 0.000 claims 1
- 208000017169 kidney disease Diseases 0.000 claims 1
- 206010027175 memory impairment Diseases 0.000 claims 1
- 206010027599 migraine Diseases 0.000 claims 1
- 230000000116 mitigating effect Effects 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 208000031225 myocardial ischemia Diseases 0.000 claims 1
- SMYSNYASGKZITB-UHFFFAOYSA-N n-(1,3-benzodioxol-5-yl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=C3OCOC3=CC=2)=C(C=CC=C2)C2=N1 SMYSNYASGKZITB-UHFFFAOYSA-N 0.000 claims 1
- GVWVXUCTNPBDOS-UHFFFAOYSA-N n-(2,3-dihydro-1h-inden-2-yl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CC3=CC=CC=C3C2)=C(C=CC=C2)C2=N1 GVWVXUCTNPBDOS-UHFFFAOYSA-N 0.000 claims 1
- XRENJEYJRMYBJG-UHFFFAOYSA-N n-(2-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C(=CC=CC=2)Cl)=C(C=CC=C2)C2=N1 XRENJEYJRMYBJG-UHFFFAOYSA-N 0.000 claims 1
- DMXDSQCPDWYXEG-UHFFFAOYSA-N n-(3,4-dichlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=C(Cl)C(Cl)=CC=2)=C(C=CC=C2)C2=N1 DMXDSQCPDWYXEG-UHFFFAOYSA-N 0.000 claims 1
- GSGGDGRMJIJMCL-UHFFFAOYSA-N n-(3-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=C(Cl)C=CC=2)=C(C=CC=C2)C2=N1 GSGGDGRMJIJMCL-UHFFFAOYSA-N 0.000 claims 1
- ITFQWXZRHMHPKI-UHFFFAOYSA-N n-(4-bromophenyl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC(Br)=CC=2)=C(C=CC=C2)C2=N1 ITFQWXZRHMHPKI-UHFFFAOYSA-N 0.000 claims 1
- RUYWKBFOCUBMAM-UHFFFAOYSA-N n-(4-chlorophenyl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=CC(Cl)=CC=2)=C(C=CC=C2)C2=N1 RUYWKBFOCUBMAM-UHFFFAOYSA-N 0.000 claims 1
- PXBQVKMTASSKGZ-UHFFFAOYSA-N n-(4-tert-butylcyclohexyl)-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CCC(CC2)C(C)(C)C)=C(C=CC=C2)C2=N1 PXBQVKMTASSKGZ-UHFFFAOYSA-N 0.000 claims 1
- LVPJYSLBTVOBHB-UHFFFAOYSA-N n-[(3,4-difluorophenyl)methyl]-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NCC=2C=C(F)C(F)=CC=2)=C(C=CC=C2)C2=N1 LVPJYSLBTVOBHB-UHFFFAOYSA-N 0.000 claims 1
- GHSYVHJFWCWZMZ-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NCC=2C=CC(Cl)=CC=2)=C(C=CC=C2)C2=N1 GHSYVHJFWCWZMZ-UHFFFAOYSA-N 0.000 claims 1
- LADYYLFFMKHLJJ-UHFFFAOYSA-N n-[3,5-bis(trifluoromethyl)phenyl]-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC=2C=C(C=C(C=2)C(F)(F)F)C(F)(F)F)=C(C=CC=C2)C2=N1 LADYYLFFMKHLJJ-UHFFFAOYSA-N 0.000 claims 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1
- PULDFTZDWXGLNN-UHFFFAOYSA-N n-benzyl-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NCC=2C=CC=CC=2)=C(C=CC=C2)C2=N1 PULDFTZDWXGLNN-UHFFFAOYSA-N 0.000 claims 1
- QHKVGLNFNULLIU-UHFFFAOYSA-N n-butyl-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N=1C2=CC=CC=C2C(NCCCC)=NC=1N1N=C(C)C=C1C QHKVGLNFNULLIU-UHFFFAOYSA-N 0.000 claims 1
- OJUFPACNUKNWJK-UHFFFAOYSA-N n-cycloheptyl-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CCCCCC2)=C(C=CC=C2)C2=N1 OJUFPACNUKNWJK-UHFFFAOYSA-N 0.000 claims 1
- WUFKOMSQZCSKNK-UHFFFAOYSA-N n-cyclohexyl-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CCCCC2)=C(C=CC=C2)C2=N1 WUFKOMSQZCSKNK-UHFFFAOYSA-N 0.000 claims 1
- XWPPYAGCVFNLFU-UHFFFAOYSA-N n-cyclohexyl-2-(3-methylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=CN1C1=NC(NC2CCCCC2)=C(C=CC=C2)C2=N1 XWPPYAGCVFNLFU-UHFFFAOYSA-N 0.000 claims 1
- TWLTUFCLTQFHHS-UHFFFAOYSA-N n-cyclohexyl-2-[3,5-di(propan-2-yl)pyrazol-1-yl]quinazolin-4-amine Chemical compound N1=C(C(C)C)C=C(C(C)C)N1C1=NC(NC2CCCCC2)=C(C=CC=C2)C2=N1 TWLTUFCLTQFHHS-UHFFFAOYSA-N 0.000 claims 1
- CVPOZEGTLACCOF-UHFFFAOYSA-N n-cyclohexyl-2-pyrazol-1-ylquinazolin-4-amine Chemical compound C1CCCCC1NC1=NC(N2N=CC=C2)=NC2=CC=CC=C12 CVPOZEGTLACCOF-UHFFFAOYSA-N 0.000 claims 1
- NCNJDONJFVRFNJ-UHFFFAOYSA-N n-cyclooctyl-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CCCCCCC2)=C(C=CC=C2)C2=N1 NCNJDONJFVRFNJ-UHFFFAOYSA-N 0.000 claims 1
- DKJFZUFVQZQPRB-UHFFFAOYSA-N n-cyclopentyl-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CCCC2)=C(C=CC=C2)C2=N1 DKJFZUFVQZQPRB-UHFFFAOYSA-N 0.000 claims 1
- ZBJUURWCGAROLY-UHFFFAOYSA-N n-cyclopropyl-2-(3,5-dimethylpyrazol-1-yl)quinazolin-4-amine Chemical compound N1=C(C)C=C(C)N1C1=NC(NC2CC2)=C(C=CC=C2)C2=N1 ZBJUURWCGAROLY-UHFFFAOYSA-N 0.000 claims 1
- 201000003631 narcolepsy Diseases 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 208000030761 polycystic kidney disease Diseases 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 239000000651 prodrug Substances 0.000 claims 1
- 229940002612 prodrug Drugs 0.000 claims 1
- 230000000069 prophylactic effect Effects 0.000 claims 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims 1
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| DKPA200500366 | 2005-03-14 | ||
| PCT/EP2006/060643 WO2006097441A1 (en) | 2005-03-14 | 2006-03-13 | Potassium channel modulating agents and their medical use |
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| JP2008533087A JP2008533087A (ja) | 2008-08-21 |
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| NZ (1) | NZ556248A (OSRAM) |
| WO (1) | WO2006097441A1 (OSRAM) |
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| US7132439B2 (en) | 2002-05-13 | 2006-11-07 | Icagen, Inc. | Bis-benzimidazoles and related compounds as potassium channel modulators |
| AU2007217099A1 (en) | 2006-02-17 | 2007-08-30 | Janssen Pharmaceutica N.V. | Pyrazolylquinazolinones as potassium channel openers |
| JP2010502674A (ja) * | 2006-09-07 | 2010-01-28 | ノイロサーチ アクティーゼルスカブ | カリウムチャンネル調節剤として有用なピリジニル−ピリミジン誘導体 |
| AU2007304195A1 (en) | 2006-10-03 | 2008-04-10 | Neurosearch A/S | Indazolyl derivatives useful as potassium channel modulating agents |
| EP2114916A2 (en) * | 2007-02-02 | 2009-11-11 | NeuroSearch A/S | Pyridinyl-pyrazole derivatives and their use as potassium channel modulators |
| EP2142547A1 (en) * | 2007-03-28 | 2010-01-13 | NeuroSearch A/S | Purinyl derivatives and their use as potassium channel modulators |
| EP2203436A1 (en) | 2007-09-17 | 2010-07-07 | Neurosearch A/S | Pyrazine derivatives and their use as potassium channel modulators |
| CN102177154A (zh) * | 2008-09-02 | 2011-09-07 | 神经研究公司 | 吡唑基-嘧啶衍生物及其作为钾通道调节剂的应用 |
| KR101123292B1 (ko) * | 2008-09-26 | 2012-03-19 | 주식회사 엘지생명과학 | 몬테루카스트 나트륨염의 제조방법 |
| US20110237607A1 (en) * | 2008-09-26 | 2011-09-29 | Neurosearch A/S | Substituted purinyl-pyrazol derivatives and their use as potassium channel modulators |
| WO2010034707A1 (en) * | 2008-09-26 | 2010-04-01 | Neurosearch A/S | Substituted purinyl-pyrazol derivatives and their use as potassium channel modulators |
| EP3575288B1 (en) | 2009-09-03 | 2021-10-27 | Bristol-Myers Squibb Company | Quinazolines as potassium ion channel inhibitors |
| JP6223443B2 (ja) | 2012-06-26 | 2017-11-01 | サニオナ・エイピイエス | フェニルトリアゾール誘導体及びｇａｂａａ受容体複合体を調節するための該フェニルトリアゾール誘導体の使用 |
| US9242966B2 (en) | 2013-03-11 | 2016-01-26 | Bristol-Myers Squibb Company | Phthalazines as potassium ion channel inhibitors |
| JP2016516691A (ja) * | 2013-03-11 | 2016-06-09 | ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ | カリウムイオンチャネル阻害剤としてのイソキノリン |
| CA2969839A1 (en) * | 2014-12-05 | 2016-06-09 | Subramaniam Ananthan | Heterocyclic compounds as biogenic amine transport modulators |
| WO2016090299A1 (en) | 2014-12-05 | 2016-06-09 | Subramaniam Ananthan | Novel quinazolines as biogenic amine transport modulators |
| BR112018006873A2 (pt) * | 2015-10-05 | 2018-11-06 | The Trustees Of Columbia University In The City Of New York | ativadores do fluxo autofágico e fosfolipase d e depuração de agregados de proteína incluindo tau e tratamento de proteinopatias |
| US10774064B2 (en) | 2016-06-02 | 2020-09-15 | Cadent Therapeutics, Inc. | Potassium channel modulators |
| HRP20220079T1 (hr) | 2017-01-23 | 2022-04-15 | Cadent Therapeutics, Inc. | Modulatori kalijevih kanala |
| JP7457505B2 (ja) | 2017-05-10 | 2024-03-28 | ユニバーシティー オブ ロチェスター | 神経精神障害を処置する方法 |
| FR3066761B1 (fr) * | 2017-05-23 | 2020-10-30 | Centre Nat Rech Scient | Nouveaux composes inhibiteurs des canaux ioniques |
| CA3116339A1 (en) | 2018-10-22 | 2020-04-30 | Cadent Therapeutics, Inc. | Crystalline forms of potassium channel modulators |
| WO2024191106A1 (ko) * | 2023-03-13 | 2024-09-19 | 주식회사 미토이뮨테라퓨틱스 | 뇌전증 예방 또는 치료용 약학적 조성물 |
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|---|---|---|---|---|
| US3340260A (en) * | 1962-12-03 | 1967-09-05 | Ciba Geigy Corp | 4-amino-pyrimidines |
| IL88507A (en) | 1987-12-03 | 1993-02-21 | Smithkline Beckman Intercredit | 2,4-diaminoquinazolines, process for their preparation and pharmaceutical compositions comprising them |
| PT100905A (pt) | 1991-09-30 | 1994-02-28 | Eisai Co Ltd | Compostos heterociclicos azotados biciclicos contendo aneis de benzeno, ciclo-hexano ou piridina e de pirimidina, piridina ou imidazol substituidos e composicoes farmaceuticas que os contem |
| JP2657760B2 (ja) | 1992-07-15 | 1997-09-24 | 小野薬品工業株式会社 | ４−アミノキナゾリン誘導体およびそれを含有する医薬品 |
| US5539895A (en) * | 1994-05-12 | 1996-07-23 | International Business Machines Corporation | Hierarchical computer cache system |
| US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
| AU2002250394A1 (en) | 2001-03-23 | 2002-10-08 | Bayer Corporation | Rho-kinase inhibitors |
| WO2004065392A1 (en) * | 2003-01-24 | 2004-08-05 | Smithkline Beecham Corporation | Condensed pyridines and pyrimidines and their use as alk-5 receptor ligands |
| CL2004000409A1 (es) | 2003-03-03 | 2005-01-07 | Vertex Pharma | Compuestos derivados de 2-(cilo sustituido)-1-(amino u oxi sustituido)-quinazolina, inhibidores de canales ionicos de sodio y calcio dependientes de voltaje; composicion farmaceutica; y uso del compuesto en el tratamiento de dolor agudo, cronico, neu |
| EP1742634B1 (en) * | 2004-04-13 | 2010-10-27 | ICAgen, Inc. | Polycyclic pyrimidines as potassium ion channel modulators |
| JP2008526734A (ja) | 2004-12-31 | 2008-07-24 | エスケー ケミカルズ カンパニー リミテッド | 糖尿及び肥満治療予防に有効なキナゾリン誘導体 |
| US20090036475A1 (en) | 2005-03-22 | 2009-02-05 | Neurosearch A/S | Pyrazolyl-Pyrimidines as Potassium Channel Modulating Agents and Their Medical Use |
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- 2006-03-13 MX MX2007010991A patent/MX2007010991A/es active IP Right Grant
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- 2006-03-13 EP EP06725016.7A patent/EP1861388B1/en active Active
- 2006-03-13 AU AU2006224605A patent/AU2006224605B2/en not_active Ceased
- 2006-03-13 NZ NZ556248A patent/NZ556248A/en not_active IP Right Cessation
- 2006-03-13 JP JP2008501279A patent/JP4966958B2/ja not_active Expired - Fee Related
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