TWI478923B - 喹唑啉酮化合物及其用途 - Google Patents
喹唑啉酮化合物及其用途 Download PDFInfo
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- TWI478923B TWI478923B TW099135360A TW99135360A TWI478923B TW I478923 B TWI478923 B TW I478923B TW 099135360 A TW099135360 A TW 099135360A TW 99135360 A TW99135360 A TW 99135360A TW I478923 B TWI478923 B TW I478923B
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- Prior art keywords
- methyl
- alkyl
- amino
- pyrazolo
- hydroxyphenyl
- Prior art date
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- -1 Quinazolinone compound Chemical class 0.000 title claims description 91
- 125000000217 alkyl group Chemical group 0.000 claims description 332
- 150000001875 compounds Chemical class 0.000 claims description 196
- QMNUDYFKZYBWQX-UHFFFAOYSA-N 1H-quinazolin-4-one Chemical compound C1=CC=C2C(=O)N=CNC2=C1 QMNUDYFKZYBWQX-UHFFFAOYSA-N 0.000 claims description 112
- 229910052739 hydrogen Inorganic materials 0.000 claims description 74
- 239000001257 hydrogen Substances 0.000 claims description 66
- 229910020008 S(O) Inorganic materials 0.000 claims description 63
- 125000003545 alkoxy group Chemical group 0.000 claims description 54
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 50
- 125000003118 aryl group Chemical group 0.000 claims description 42
- 125000005843 halogen group Chemical group 0.000 claims description 38
- 125000000623 heterocyclic group Chemical group 0.000 claims description 35
- 238000011282 treatment Methods 0.000 claims description 31
- 229910052757 nitrogen Inorganic materials 0.000 claims description 30
- 229910052760 oxygen Inorganic materials 0.000 claims description 29
- 125000001072 heteroaryl group Chemical group 0.000 claims description 28
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 28
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 24
- 125000004452 carbocyclyl group Chemical group 0.000 claims description 22
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 22
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 21
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 21
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- 208000006673 asthma Diseases 0.000 claims description 19
- 125000005842 heteroatom Chemical group 0.000 claims description 19
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
- 239000003814 drug Substances 0.000 claims description 17
- 229920006395 saturated elastomer Polymers 0.000 claims description 16
- 239000001301 oxygen Substances 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 150000002431 hydrogen Chemical class 0.000 claims description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 13
- 150000001412 amines Chemical class 0.000 claims description 11
- 150000002367 halogens Chemical class 0.000 claims description 11
- 125000001424 substituent group Chemical group 0.000 claims description 11
- 125000002837 carbocyclic group Chemical group 0.000 claims description 10
- 230000005764 inhibitory process Effects 0.000 claims description 10
- ONUHRYKLJYSRMY-UHFFFAOYSA-N hex-5-yn-1-amine Chemical compound NCCCCC#C ONUHRYKLJYSRMY-UHFFFAOYSA-N 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 208000024891 symptom Diseases 0.000 claims description 7
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 claims description 6
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 6
- 239000000969 carrier Substances 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 6
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical group O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 claims description 6
- HNXGLVMROGNHHV-UHFFFAOYSA-N 3-(4-amino-1H-pyrazol-5-yl)phenol Chemical compound NC1=CNN=C1C1=CC(O)=CC=C1 HNXGLVMROGNHHV-UHFFFAOYSA-N 0.000 claims description 5
- 206010061430 Arthritis allergic Diseases 0.000 claims description 5
- 206010061218 Inflammation Diseases 0.000 claims description 5
- 206010027476 Metastases Diseases 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 230000004054 inflammatory process Effects 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 230000009401 metastasis Effects 0.000 claims description 5
- 206010039073 rheumatoid arthritis Diseases 0.000 claims description 5
- 206010006458 Bronchitis chronic Diseases 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 206010009900 Colitis ulcerative Diseases 0.000 claims description 4
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 claims description 4
- 206010039085 Rhinitis allergic Diseases 0.000 claims description 4
- 201000006704 Ulcerative Colitis Diseases 0.000 claims description 4
- 201000010105 allergic rhinitis Diseases 0.000 claims description 4
- 201000008937 atopic dermatitis Diseases 0.000 claims description 4
- 206010006451 bronchitis Diseases 0.000 claims description 4
- 208000007451 chronic bronchitis Diseases 0.000 claims description 4
- 230000002401 inhibitory effect Effects 0.000 claims description 4
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims description 4
- 239000003149 muscarinic antagonist Substances 0.000 claims description 4
- 230000002265 prevention Effects 0.000 claims description 4
- 150000003431 steroids Chemical class 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000000474 3-butynyl group Chemical group [H]C#CC([H])([H])C([H])([H])* 0.000 claims description 3
- 206010006187 Breast cancer Diseases 0.000 claims description 3
- 208000026310 Breast neoplasm Diseases 0.000 claims description 3
- 206010009944 Colon cancer Diseases 0.000 claims description 3
- 208000001333 Colorectal Neoplasms Diseases 0.000 claims description 3
- 201000003883 Cystic fibrosis Diseases 0.000 claims description 3
- 206010012434 Dermatitis allergic Diseases 0.000 claims description 3
- 206010012442 Dermatitis contact Diseases 0.000 claims description 3
- 206010014561 Emphysema Diseases 0.000 claims description 3
- 201000009794 Idiopathic Pulmonary Fibrosis Diseases 0.000 claims description 3
- 206010023232 Joint swelling Diseases 0.000 claims description 3
- 206010033645 Pancreatitis Diseases 0.000 claims description 3
- 206010036790 Productive cough Diseases 0.000 claims description 3
- 206010039491 Sarcoma Diseases 0.000 claims description 3
- 206010041067 Small cell lung cancer Diseases 0.000 claims description 3
- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 3
- 239000003443 antiviral agent Substances 0.000 claims description 3
- 208000010668 atopic eczema Diseases 0.000 claims description 3
- 208000010247 contact dermatitis Diseases 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 229910001873 dinitrogen Inorganic materials 0.000 claims description 3
- 229960000289 fluticasone propionate Drugs 0.000 claims description 3
- WMWTYOKRWGGJOA-CENSZEJFSA-N fluticasone propionate Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@]1(F)[C@@H]2[C@@H]2C[C@@H](C)[C@@](C(=O)SCF)(OC(=O)CC)[C@@]2(C)C[C@@H]1O WMWTYOKRWGGJOA-CENSZEJFSA-N 0.000 claims description 3
- 206010017758 gastric cancer Diseases 0.000 claims description 3
- 230000012010 growth Effects 0.000 claims description 3
- 208000036971 interstitial lung disease 2 Diseases 0.000 claims description 3
- 201000001441 melanoma Diseases 0.000 claims description 3
- 125000002950 monocyclic group Chemical group 0.000 claims description 3
- 201000008482 osteoarthritis Diseases 0.000 claims description 3
- 201000009890 sinusitis Diseases 0.000 claims description 3
- 208000000587 small cell lung carcinoma Diseases 0.000 claims description 3
- 208000024794 sputum Diseases 0.000 claims description 3
- 210000003802 sputum Anatomy 0.000 claims description 3
- 201000011549 stomach cancer Diseases 0.000 claims description 3
- 229960000278 theophylline Drugs 0.000 claims description 3
- 229940075420 xanthine Drugs 0.000 claims description 3
- XWTYSIMOBUGWOL-UHFFFAOYSA-N (+-)-Terbutaline Chemical group CC(C)(C)NCC(O)C1=CC(O)=CC(O)=C1 XWTYSIMOBUGWOL-UHFFFAOYSA-N 0.000 claims description 2
- XJGAJHPRETZYHH-UHFFFAOYSA-N 2-[[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-5-ethynyl-3-[[4-(trifluoromethyl)phenyl]methyl]quinazolin-4-one Chemical compound N1=C(C=2C=C(O)C=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=C(C(F)(F)F)C=C1 XJGAJHPRETZYHH-UHFFFAOYSA-N 0.000 claims description 2
- ALEMKYQPUYKWDY-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(3-chlorophenyl)methyl]-5-ethynylquinazolin-4-one Chemical compound N1=C(C=2C=CC(O)=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=CC(Cl)=C1 ALEMKYQPUYKWDY-UHFFFAOYSA-N 0.000 claims description 2
- XBXWIWWWJFNCCA-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-5-ethynyl-3-[(2-fluoro-4-methoxyphenyl)methyl]quinazolin-4-one Chemical compound FC1=CC(OC)=CC=C1CN1C(=O)C2=C(C#C)C=CC=C2N=C1CN1C2=NC=NC(N)=C2C(C=2C=CC(O)=CC=2)=N1 XBXWIWWWJFNCCA-UHFFFAOYSA-N 0.000 claims description 2
- SLSFBDKQYOLPNC-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-5-ethynyl-3-[(4-methoxyphenyl)methyl]quinazolin-4-one Chemical compound C1=CC(OC)=CC=C1CN1C(=O)C2=C(C#C)C=CC=C2N=C1CN1C2=NC=NC(N)=C2C(C=2C=CC(O)=CC=2)=N1 SLSFBDKQYOLPNC-UHFFFAOYSA-N 0.000 claims description 2
- MRMCLXSJPGYHCS-UHFFFAOYSA-N 4-(4-amino-1H-pyrazol-5-yl)phenol Chemical compound NC=1C(=NNC=1)C1=CC=C(C=C1)O MRMCLXSJPGYHCS-UHFFFAOYSA-N 0.000 claims description 2
- KUVIULQEHSCUHY-XYWKZLDCSA-N Beclometasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(Cl)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)COC(=O)CC)(OC(=O)CC)[C@@]1(C)C[C@@H]2O KUVIULQEHSCUHY-XYWKZLDCSA-N 0.000 claims description 2
- VOVIALXJUBGFJZ-KWVAZRHASA-N Budesonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@H]3OC(CCC)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O VOVIALXJUBGFJZ-KWVAZRHASA-N 0.000 claims description 2
- BRSSMNMTNKVBGA-UHFFFAOYSA-N CC(C)NCCCCC#CC1=C2C(=CC=C1)N=C(N(C2=O)CC3=CC=CC=C3Cl)CN4C5=NC=NC(=C5C(=N4)C6=CC(=CC=C6)O)N Chemical compound CC(C)NCCCCC#CC1=C2C(=CC=C1)N=C(N(C2=O)CC3=CC=CC=C3Cl)CN4C5=NC=NC(=C5C(=N4)C6=CC(=CC=C6)O)N BRSSMNMTNKVBGA-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- 102000014150 Interferons Human genes 0.000 claims description 2
- 108010050904 Interferons Proteins 0.000 claims description 2
- GIIZNNXWQWCKIB-UHFFFAOYSA-N Serevent Chemical compound C1=C(O)C(CO)=CC(C(O)CNCCCCCCOCCCCC=2C=CC=CC=2)=C1 GIIZNNXWQWCKIB-UHFFFAOYSA-N 0.000 claims description 2
- NDAUXUAQIAJITI-UHFFFAOYSA-N albuterol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C(CO)=C1 NDAUXUAQIAJITI-UHFFFAOYSA-N 0.000 claims description 2
- 229950000210 beclometasone dipropionate Drugs 0.000 claims description 2
- 229960004436 budesonide Drugs 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229960001469 fluticasone furoate Drugs 0.000 claims description 2
- XTULMSXFIHGYFS-VLSRWLAYSA-N fluticasone furoate Chemical compound O([C@]1([C@@]2(C)C[C@H](O)[C@]3(F)[C@@]4(C)C=CC(=O)C=C4[C@@H](F)C[C@H]3[C@@H]2C[C@H]1C)C(=O)SCF)C(=O)C1=CC=CO1 XTULMSXFIHGYFS-VLSRWLAYSA-N 0.000 claims description 2
- 229960002848 formoterol Drugs 0.000 claims description 2
- BPZSYCZIITTYBL-UHFFFAOYSA-N formoterol Chemical compound C1=CC(OC)=CC=C1CC(C)NCC(O)C1=CC=C(O)C(NC=O)=C1 BPZSYCZIITTYBL-UHFFFAOYSA-N 0.000 claims description 2
- 229960004078 indacaterol Drugs 0.000 claims description 2
- QZZUEBNBZAPZLX-QFIPXVFZSA-N indacaterol Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2[C@@H](O)CNC1CC(C=C(C(=C2)CC)CC)=C2C1 QZZUEBNBZAPZLX-QFIPXVFZSA-N 0.000 claims description 2
- 229940079322 interferon Drugs 0.000 claims description 2
- OEXHQOGQTVQTAT-JRNQLAHRSA-N ipratropium Chemical group O([C@H]1C[C@H]2CC[C@@H](C1)[N@@+]2(C)C(C)C)C(=O)C(CO)C1=CC=CC=C1 OEXHQOGQTVQTAT-JRNQLAHRSA-N 0.000 claims description 2
- 229960001888 ipratropium Drugs 0.000 claims description 2
- 210000001503 joint Anatomy 0.000 claims description 2
- 239000002829 mitogen activated protein kinase inhibitor Substances 0.000 claims description 2
- 108010068338 p38 Mitogen-Activated Protein Kinases Proteins 0.000 claims description 2
- 125000003367 polycyclic group Chemical group 0.000 claims description 2
- 229960002052 salbutamol Drugs 0.000 claims description 2
- 229960004017 salmeterol Drugs 0.000 claims description 2
- 229960000195 terbutaline Drugs 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 206010039083 rhinitis Diseases 0.000 claims 4
- 206010003246 arthritis Diseases 0.000 claims 2
- 208000035250 cutaneous malignant susceptibility to 1 melanoma Diseases 0.000 claims 2
- 208000001848 dysentery Diseases 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 230000004614 tumor growth Effects 0.000 claims 2
- XHNPZUAUPCCLTH-UHFFFAOYSA-N 2-[[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-5-[3-[2-(2-methoxyethoxy)ethoxy]prop-1-ynyl]quinazolin-4-one Chemical compound C=1C=CC=C(Cl)C=1CN1C(=O)C=2C(C#CCOCCOCCOC)=CC=CC=2N=C1CN(C1=NC=NC(N)=C11)N=C1C1=CC=CC(O)=C1 XHNPZUAUPCCLTH-UHFFFAOYSA-N 0.000 claims 1
- ZTVJMMUPVCALPD-UHFFFAOYSA-N 2-[[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(4-chlorophenyl)methyl]-5-ethynylquinazolin-4-one Chemical compound N1=C(C=2C=C(O)C=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=C(Cl)C=C1 ZTVJMMUPVCALPD-UHFFFAOYSA-N 0.000 claims 1
- KXTXIKMQFXXVEO-UHFFFAOYSA-N 2-[[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-5-ethynyl-3-[(2-fluorophenyl)methyl]quinazolin-4-one Chemical compound N1=C(C=2C=C(O)C=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=CC=C1F KXTXIKMQFXXVEO-UHFFFAOYSA-N 0.000 claims 1
- YSQFSEVNOOJNRC-UHFFFAOYSA-N 2-[[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-5-ethynyl-3-[(3-methoxyphenyl)methyl]quinazolin-4-one Chemical compound COC1=CC=CC(CN2C(C3=C(C#C)C=CC=C3N=C2CN2C3=NC=NC(N)=C3C(C=3C=C(O)C=CC=3)=N2)=O)=C1 YSQFSEVNOOJNRC-UHFFFAOYSA-N 0.000 claims 1
- HUYJOCXOVRKEIW-UHFFFAOYSA-N 2-[[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-5-ethynyl-3-[(3-methylsulfonylphenyl)methyl]quinazolin-4-one Chemical compound CS(=O)(=O)C1=CC=CC(CN2C(C3=C(C#C)C=CC=C3N=C2CN2C3=NC=NC(N)=C3C(C=3C=C(O)C=CC=3)=N2)=O)=C1 HUYJOCXOVRKEIW-UHFFFAOYSA-N 0.000 claims 1
- MVSVRQJROSZUBJ-UHFFFAOYSA-N 2-[[4-amino-3-(3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-5-ethynyl-3-[[3-(trifluoromethyl)phenyl]methyl]quinazolin-4-one Chemical compound N1=C(C=2C=C(O)C=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=CC(C(F)(F)F)=C1 MVSVRQJROSZUBJ-UHFFFAOYSA-N 0.000 claims 1
- RTLSICZZXIACFX-UHFFFAOYSA-N 2-[[4-amino-3-(4-fluoro-3-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-5-ethynylquinazolin-4-one Chemical compound N1=C(C=2C=C(O)C(F)=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=CC=C1Cl RTLSICZZXIACFX-UHFFFAOYSA-N 0.000 claims 1
- FDUASEWUQUUQIV-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-5-(3-cyclopentylprop-1-ynyl)quinazolin-4-one Chemical compound N1=C(C=2C=CC(O)=CC=2)C=2C(N)=NC=NC=2N1CC(N(C(=O)C1=2)CC=3C(=CC=CC=3)Cl)=NC1=CC=CC=2C#CCC1CCCC1 FDUASEWUQUUQIV-UHFFFAOYSA-N 0.000 claims 1
- DFYDLTALGVPURS-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-5-(5-hydroxypent-1-ynyl)quinazolin-4-one Chemical compound N1=C(C=2C=CC(O)=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#CCCCO)=C2C(=O)N1CC1=CC=CC=C1Cl DFYDLTALGVPURS-UHFFFAOYSA-N 0.000 claims 1
- VNIUXACFQIIIKG-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-5-[6-[4-(dimethylamino)piperidin-1-yl]-6-oxohex-1-ynyl]quinazolin-4-one Chemical compound C1CC(N(C)C)CCN1C(=O)CCCC#CC1=CC=CC2=C1C(=O)N(CC=1C(=CC=CC=1)Cl)C(CN1C3=NC=NC(N)=C3C(C=3C=CC(O)=CC=3)=N1)=N2 VNIUXACFQIIIKG-UHFFFAOYSA-N 0.000 claims 1
- DENSYDWNLNJEQR-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-chlorophenyl)methyl]-5-ethynylquinazolin-4-one Chemical compound N1=C(C=2C=CC(O)=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=CC=C1Cl DENSYDWNLNJEQR-UHFFFAOYSA-N 0.000 claims 1
- DQQLMDLGTUARHB-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(2-fluoro-3-methoxyphenyl)methyl]-5-(6-morpholin-4-yl-6-oxohex-1-ynyl)quinazolin-4-one Chemical compound COC1=CC=CC(CN2C(C3=C(C#CCCCC(=O)N4CCOCC4)C=CC=C3N=C2CN2C3=NC=NC(N)=C3C(C=3C=CC(O)=CC=3)=N2)=O)=C1F DQQLMDLGTUARHB-UHFFFAOYSA-N 0.000 claims 1
- ZMQNQPZQOPWFCX-UHFFFAOYSA-N 2-[[4-amino-3-(4-hydroxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]methyl]-3-[(4-chloro-2-fluorophenyl)methyl]-5-ethynylquinazolin-4-one Chemical compound N1=C(C=2C=CC(O)=CC=2)C=2C(N)=NC=NC=2N1CC1=NC2=CC=CC(C#C)=C2C(=O)N1CC1=CC=C(Cl)C=C1F ZMQNQPZQOPWFCX-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
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Priority Applications (39)
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|---|---|---|---|
| AU2010309832A AU2010309832B2 (en) | 2009-10-19 | 2010-10-19 | Compounds |
| NZ599162A NZ599162A (en) | 2009-10-19 | 2010-10-19 | Compounds having Phosphoinositide 3-kinase Inhibitor Activity |
| UY0001033337A UY33337A (es) | 2010-10-18 | 2011-04-15 | DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS |
| PL11787742T PL2630149T3 (pl) | 2010-10-18 | 2011-10-18 | Pochodne chinazolin-4(3H)-onu stosowane jako inhibitory kinazy PI3 |
| BR112013009395A BR112013009395A2 (pt) | 2010-10-18 | 2011-10-18 | derivados de quinazolin-4 (3h)-ona usados como inibidores da pi3 cinase |
| PT117877423T PT2630149E (pt) | 2010-10-18 | 2011-10-18 | Derivados de quinazolin-4(3h)-ona utilizados como inibidores de pi3-cinase |
| MX2013004298A MX346336B (es) | 2010-10-18 | 2011-10-18 | Derivados de quinazolin-4 (3h)-ona utilizados como inhibidores de pi3 cinasa. |
| AU2011317334A AU2011317334B2 (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4(3H)-one derivatives used as PI3 kinase inhibitors |
| CA2811171A CA2811171A1 (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4 (3h) -one derivatives used as pi3 kinase inhibitors |
| PCT/GB2011/052015 WO2012052753A1 (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4 (3h) -one derivatives used as pi3 kinase inhibitors |
| RS20150206A RS53898B1 (sr) | 2010-10-18 | 2011-10-18 | Derivati kvinazolin-4(3h)-ona korišćeni kao inhibitori pi3 kinaze |
| KR1020137011430A KR101857000B1 (ko) | 2010-10-18 | 2011-10-18 | Ｐｉ3 키나아제 저해제로 사용되는 퀴나졸린-4(3ｈ)-온 유도체 |
| MEP-2015-43A ME02064B (me) | 2009-10-19 | 2011-10-18 | Derivati kvinazolin-4(3h)-ona korisceni kao inhibitori pi3 kinaze |
| EP11787742.3A EP2630149B1 (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4(3h)-one derivatives used as pi3 kinase inhibitors |
| JP2013533289A JP5422783B2 (ja) | 2010-10-18 | 2011-10-18 | Ｐｉ３キナーゼ阻害剤として使用するキナゾリン−４（３ｈ）−オン誘導体 |
| UAA201303201A UA109667C2 (xx) | 2010-10-18 | 2011-10-18 | Похідні хіназолін-4(3h)-ону, що використовуються як інгібітори pi3-кінази |
| SI201130442T SI2630149T1 (sl) | 2010-10-18 | 2011-10-18 | Derivati kinazolin-4(3H)-ona uporabljeni kot inhibitorji PI3 kinaze |
| DK11787742T DK2630149T3 (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4 (3H) -one derivatives, USED AS PI 3-kinase inhibitors |
| PH1/2013/500648A PH12013500648A1 (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4 (3h) -one derivatives used as pi3 kinase inhibitors |
| PE2013000869A PE20131464A1 (es) | 2010-10-18 | 2011-10-18 | Derivados de quinazolin-4 (3h)-ona utilizados como inhibidores de pi3 cinasa |
| ES11787742.3T ES2533570T3 (es) | 2010-10-18 | 2011-10-18 | Derivados de quinazolin-4(3H)-ona, que se usan como agentes inhibidores de las PI3 cinasas |
| EA201390579A EA026946B1 (ru) | 2010-10-18 | 2011-10-18 | Производные хиназолин-4(3h)-она, используемые как ингибиторы pi3-киназы |
| NZ609147A NZ609147A (en) | 2009-10-19 | 2011-10-18 | Quinazolin-4 (3h) -one derivatives used as pi3 kinase inhibitors |
| HRP20150318TT HRP20150318T1 (xx) | 2010-10-18 | 2011-10-18 | Derivati kinazolin-4(3h)-ona koji se upotrebljavaju kao inhibitori pi3 kinaze |
| HK13111905.6A HK1184461B (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4 (3h) -one derivatives used as pi3 kinase inhibitors |
| SG2013017470A SG188958A1 (en) | 2010-10-18 | 2011-10-18 | Quinazolin-4 (3h) -one derivatives used as pi3 kinase inhibitors |
| IL225212A IL225212A (en) | 2010-10-18 | 2013-03-14 | 6 - (2 - ((4-Amino-3- (3-Hydroxyphenyl) - h1- pyrazolo [d-3,4] pyrimidin-1-yl) methyl) -3- (2-chlorobenzyl) -4-oxo- 3,4-Dehydroquinazoline-5-yl) - n, n-bis (2-methoxyethyl) hex-5-inamide, Pharmaceutical preparations containing it and uses |
| GT201300097A GT201300097A (es) | 2010-10-18 | 2013-04-11 | Derivados de quinazolin-4 (3h)-ona utilizados como inhibidores de p13 cinasa |
| NI201300035A NI201300035A (es) | 2009-10-19 | 2013-04-16 | Derivados de quinazolin - 4 (3h) - ona utilizados como inhibidores de pi3 cinasa |
| CL2013001057A CL2013001057A1 (es) | 2010-10-18 | 2013-04-17 | Un compuesto 6-(2-((4-amino-3-(3-hidroxifenil)-1h-pirazolo[3,4-d]pirimidin-1-il)metil)-3-(2-clorobencil)-4-oxo-3,4-dihidroquinazolin-5-il)-n,n-bis(2-metoxietil)hex-5-inamida, inhibidores de pi3 cinasa; compuesto intermediario; composicion farmaceutica, util para tratar o prevenir epoc, rinitis, artritis reumatoidea y carcinomas. |
| US13/865,379 US9340545B2 (en) | 2010-10-18 | 2013-04-18 | Quinazolin-4 (3H)—one derivatives used as P13 kinase inhibitors |
| CO13106722A CO6690816A2 (es) | 2010-10-18 | 2013-04-26 | Derivados de quinazolin-4(3h)-ona utilizados como inhibidores de pi3 cinasa |
| ECSP13012612 ECSP13012612A (es) | 2010-10-18 | 2013-05-08 | Derivados de quinazolin-4-(3h)-ona utilizados como inhibidores de p13 cinasa |
| ZA2013/03614A ZA201303614B (en) | 2010-10-18 | 2013-05-17 | Quinazolin-4(3h)-one derivatives used as p13 kinase inhibitors |
| CR20130233A CR20130233A (es) | 2010-10-18 | 2013-05-20 | Derivados que quinazolin-4 (3h)-ona utilizados como inhibidores de pi3 cinaza |
| SM201500076T SMT201500076B (it) | 2010-10-18 | 2015-03-23 | Derivati di chinazolin-4(3H)-one utilizzati come inibitori della PI3 chinasi |
| CY20151100287T CY1116315T1 (el) | 2010-10-18 | 2015-03-23 | Παραγωγα κιναζολιν-4(3η)-ονης που χρησιμοποιουνται ως αναστολεις κινασης ρι3 |
| US15/092,707 US9637494B2 (en) | 2010-10-18 | 2016-04-07 | Quinazolin-4 (3H)-one derivatives used as P13 kinase inhibitors |
| US15/474,059 US10028959B2 (en) | 2010-10-18 | 2017-03-30 | Quinazolin-4 (3H)-one derivatives used as P13 kinase inhibitors |
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| UY33337A (es) | 2010-10-18 | 2011-10-31 | Respivert Ltd | DERIVADOS SUSTITUIDOS DE 1H-PIRAZOL[ 3,4-d]PIRIMIDINA COMO INHIBIDORES DE LAS FOSFOINOSITIDA 3-QUINASAS |
| EA029473B1 (ru) | 2011-12-15 | 2018-03-30 | Новартис Аг | Применение ингибиторов pi3k для лечения острой и церебральной малярии |
| TWI617561B (zh) | 2012-03-13 | 2018-03-11 | 瑞斯比維特有限公司 | 呈晶體型式之新穎化合物，包含其之醫藥組成物，製備該化合物之方法及包括該組成物之吸入裝置 |
| US8940742B2 (en) | 2012-04-10 | 2015-01-27 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| CN104870017B (zh) | 2012-11-08 | 2020-08-14 | 理森制药股份公司 | 含有PDE4抑制剂和PI3δ或双重PI3δ-γ激酶抑制剂的药物组合物 |
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| AR095353A1 (es) | 2013-03-15 | 2015-10-07 | Respivert Ltd | Compuesto |
| CN105431157A (zh) | 2013-06-14 | 2016-03-23 | 普赛奥克苏斯治疗公司 | 用于b型腺病毒的给药方案及制剂 |
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| PH12016500582B1 (en) | 2013-10-04 | 2023-06-30 | Infinity Pharmaceuticals Inc | Heterocyclic compounds and uses thereof |
| GB201320729D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
| GB201320732D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Methods of chemical synthesis |
| JP6701088B2 (ja) | 2014-03-19 | 2020-05-27 | インフィニティー ファーマシューティカルズ， インコーポレイテッド | Ｐｉ３ｋ−ガンマ媒介障害の治療で使用するための複素環式化合物 |
| GB201510197D0 (en) | 2014-06-12 | 2015-07-29 | Psioxus Therapeutics Ltd | Method of treating ovarian cancer |
| PE20170640A1 (es) | 2014-07-04 | 2017-05-26 | Lupin Ltd | Derivados de quinolizinona como inhibidores de pi3k |
| WO2016054491A1 (en) | 2014-10-03 | 2016-04-07 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
| AU2016322552B2 (en) | 2015-09-14 | 2021-03-25 | Infinity Pharmaceuticals, Inc. | Solid forms of isoquinolinone derivatives, process of making, compositions comprising, and methods of using the same |
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| WO2022017371A1 (zh) * | 2020-07-21 | 2022-01-27 | 中国医药研究开发中心有限公司 | 具有磷脂酰肌醇3-激酶δ和γ的双重抑制剂活性的杂环化合物及其医药用途 |
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