ES2742442T3 - Compuestos inhibidores - Google Patents
Compuestos inhibidores Download PDFInfo
- Publication number
- ES2742442T3 ES2742442T3 ES17192253T ES17192253T ES2742442T3 ES 2742442 T3 ES2742442 T3 ES 2742442T3 ES 17192253 T ES17192253 T ES 17192253T ES 17192253 T ES17192253 T ES 17192253T ES 2742442 T3 ES2742442 T3 ES 2742442T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- methyl
- methoxy
- pyrimidin
- phenyl
- 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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- 150000001875 compounds Chemical class 0.000 title claims abstract description 182
- 239000003112 inhibitor Substances 0.000 title description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 538
- -1 trifluoromethoxy, cyano, nitro, hydroxy, amino, carboxy, carbamoyl Chemical group 0.000 claims abstract description 221
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 178
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 168
- 239000001257 hydrogen Substances 0.000 claims abstract description 132
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 132
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 116
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 112
- 125000001424 substituent group Chemical group 0.000 claims abstract description 102
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 101
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 72
- 125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 70
- 150000003839 salts Chemical class 0.000 claims abstract description 69
- 125000003118 aryl group Chemical group 0.000 claims abstract description 65
- 239000012453 solvate Substances 0.000 claims abstract description 59
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 55
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 46
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims abstract description 42
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 42
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 42
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 42
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 39
- 125000005843 halogen group Chemical group 0.000 claims abstract description 35
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 26
- 125000005647 linker group Chemical group 0.000 claims abstract description 22
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 20
- 206010028980 Neoplasm Diseases 0.000 claims abstract description 19
- 238000011282 treatment Methods 0.000 claims abstract description 19
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims abstract description 18
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract description 18
- 201000011510 cancer Diseases 0.000 claims abstract description 16
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims abstract description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 12
- 239000011593 sulfur Chemical group 0.000 claims abstract description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 11
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 11
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims abstract description 9
- 239000001301 oxygen Chemical group 0.000 claims abstract description 9
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000001589 carboacyl group Chemical group 0.000 claims abstract description 7
- 125000002950 monocyclic group Chemical group 0.000 claims abstract description 7
- 125000004404 heteroalkyl group Chemical group 0.000 claims abstract description 6
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 6
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims abstract description 6
- 125000003709 fluoroalkyl group Chemical group 0.000 claims abstract description 5
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 4
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 4
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims abstract description 4
- 125000003367 polycyclic group Chemical group 0.000 claims abstract description 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims abstract description 3
- 210000004556 brain Anatomy 0.000 claims abstract description 3
- 210000000481 breast Anatomy 0.000 claims abstract description 3
- 210000001072 colon Anatomy 0.000 claims abstract description 3
- 210000004185 liver Anatomy 0.000 claims abstract description 3
- 210000000496 pancreas Anatomy 0.000 claims abstract description 3
- 208000003174 Brain Neoplasms Diseases 0.000 claims abstract 2
- 208000026310 Breast neoplasm Diseases 0.000 claims abstract 2
- 206010033128 Ovarian cancer Diseases 0.000 claims abstract 2
- 206010061535 Ovarian neoplasm Diseases 0.000 claims abstract 2
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims abstract 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims abstract 2
- 208000000453 Skin Neoplasms Diseases 0.000 claims abstract 2
- 208000029742 colonic neoplasm Diseases 0.000 claims abstract 2
- 208000014018 liver neoplasm Diseases 0.000 claims abstract 2
- 208000020816 lung neoplasm Diseases 0.000 claims abstract 2
- 210000002307 prostate Anatomy 0.000 claims abstract 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 60
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 34
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 25
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 13
- 239000000460 chlorine Substances 0.000 claims description 12
- 239000008194 pharmaceutical composition Substances 0.000 claims description 9
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 8
- TWFXSDGKDLLPFZ-UHFFFAOYSA-N pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound N1=C(N=CC2=C1C(=NC=C2)N)N TWFXSDGKDLLPFZ-UHFFFAOYSA-N 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- VNFGDCQZPRUFQD-UHFFFAOYSA-N pyrido[3,4-d]pyrimidin-2-amine Chemical compound C1=CN=CC2=NC(N)=NC=C21 VNFGDCQZPRUFQD-UHFFFAOYSA-N 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000002246 antineoplastic agent Substances 0.000 claims description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 4
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 4
- CDOLQNUQAVYWSO-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[(5-pyridin-3-ylisoquinolin-3-yl)amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C=3C=NC=CC=3)C=CC=C2C=N1 CDOLQNUQAVYWSO-UHFFFAOYSA-N 0.000 claims description 2
- AXUBLMKYJQFBSV-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[(5-pyrimidin-5-ylisoquinolin-3-yl)amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C=3C=NC=NC=3)C=CC=C2C=N1 AXUBLMKYJQFBSV-UHFFFAOYSA-N 0.000 claims description 2
- MDGZHKQHZCXJPC-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-(1-methylpyrazol-3-yl)isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C3=NN(C)C=C3)C=CC=C2C=N1 MDGZHKQHZCXJPC-UHFFFAOYSA-N 0.000 claims description 2
- MWMDRWOZUKCWOR-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-(1-methylpyrazol-4-yl)isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C3=CN(C)N=C3)C=CC=C2C=N1 MWMDRWOZUKCWOR-UHFFFAOYSA-N 0.000 claims description 2
- KNSSMLHMVQKSBT-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-(1-piperidin-4-ylpyrazol-4-yl)isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C3=CN(N=C3)C3CCNCC3)C=CC=C2C=N1 KNSSMLHMVQKSBT-UHFFFAOYSA-N 0.000 claims description 2
- CVCXKRQKUXTNCP-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-(1-propan-2-ylpyrazol-4-yl)isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C3=CN(N=C3)C(C)C)C=CC=C2C=N1 CVCXKRQKUXTNCP-UHFFFAOYSA-N 0.000 claims description 2
- XFDJSKUKGCTUDF-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-(2-methylpyrazol-3-yl)isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C=3N(N=CC=3)C)C=CC=C2C=N1 XFDJSKUKGCTUDF-UHFFFAOYSA-N 0.000 claims description 2
- LJSHPLPKDCEPTG-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-(3-methylimidazol-4-yl)isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C=3N(C=NC=3)C)C=CC=C2C=N1 LJSHPLPKDCEPTG-UHFFFAOYSA-N 0.000 claims description 2
- YHXOZAUTEWFRER-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-[1-(1-methylpiperidin-4-yl)pyrazol-4-yl]isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=CC2=C(C3=CN(N=C3)C3CCN(C)CC3)C=CC=C2C=N1 YHXOZAUTEWFRER-UHFFFAOYSA-N 0.000 claims description 2
- OOWQQNLKTLHXPR-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[5-[1-(2-methoxyethyl)pyrazol-4-yl]isoquinolin-3-yl]amino]phenyl]methanone Chemical compound C1=NN(CCOC)C=C1C(C1=C2)=CC=CC1=CN=C2NC1=CC=C(C(=O)N2CC(C2)OC)C=C1OC OOWQQNLKTLHXPR-UHFFFAOYSA-N 0.000 claims description 2
- JNOICPXAHVQUIV-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[8-(1-methylpyrazol-4-yl)pyrido[3,4-d]pyrimidin-2-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=NC=C(C=CN=C2C3=CN(C)N=C3)C2=N1 JNOICPXAHVQUIV-UHFFFAOYSA-N 0.000 claims description 2
- DYMJWMGOGCSIJA-UHFFFAOYSA-N (3-methoxyazetidin-1-yl)-[3-methoxy-4-[[8-[(2-methoxy-2-methylpropyl)amino]pyrido[3,4-d]pyrimidin-2-yl]amino]phenyl]methanone Chemical compound C1C(OC)CN1C(=O)C(C=C1OC)=CC=C1NC1=NC=C(C=CN=C2NCC(C)(C)OC)C2=N1 DYMJWMGOGCSIJA-UHFFFAOYSA-N 0.000 claims description 2
- LYHLZMPYIRFEBP-UHFFFAOYSA-N 1-[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]azetidine-3-carbonitrile Chemical compound COC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2N1CC(C#N)C1 LYHLZMPYIRFEBP-UHFFFAOYSA-N 0.000 claims description 2
- KUNMZXUUNAOQPD-UHFFFAOYSA-N 1-[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]piperidine-4-carbonitrile Chemical compound COC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2N1CCC(C#N)CC1 KUNMZXUUNAOQPD-UHFFFAOYSA-N 0.000 claims description 2
- ZEXFDYKYEXLWHS-UHFFFAOYSA-N 1-[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]pyrrolidin-3-ol Chemical compound COC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2N1CCC(O)C1 ZEXFDYKYEXLWHS-UHFFFAOYSA-N 0.000 claims description 2
- OFRMASLPWOMYHN-UHFFFAOYSA-N 1-[3-methoxy-4-[[6-(2-propan-2-ylsulfonylanilino)-7H-purin-2-yl]amino]phenyl]piperidin-4-ol Chemical group COc1cc(ccc1Nc1nc(Nc2ccccc2S(=O)(=O)C(C)C)c2[nH]cnc2n1)N1CCC(O)CC1 OFRMASLPWOMYHN-UHFFFAOYSA-N 0.000 claims description 2
- NKLGUNXXPRNDHH-UHFFFAOYSA-N 1-[[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]amino]-2-methylpropan-2-ol Chemical compound C=1C=C(NC=2N=C3C(NCC(C)(C)O)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 NKLGUNXXPRNDHH-UHFFFAOYSA-N 0.000 claims description 2
- CYTRCVJXFAZABO-UHFFFAOYSA-N 1-[[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]amino]propan-2-ol Chemical compound C=1C=C(NC=2N=C3C(NCC(C)O)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 CYTRCVJXFAZABO-UHFFFAOYSA-N 0.000 claims description 2
- 125000004484 1-methylpiperidin-4-yl group Chemical group CN1CCC(CC1)* 0.000 claims description 2
- WXBAASKSGKSOSZ-UHFFFAOYSA-N 2-[4-[3-methoxy-4-[[8-(oxan-4-ylamino)pyrido[3,4-d]pyrimidin-2-yl]amino]phenyl]pyrazol-1-yl]ethanol Chemical compound COC1=CC(C2=CN(CCO)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2NC1CCOCC1 WXBAASKSGKSOSZ-UHFFFAOYSA-N 0.000 claims description 2
- MPEMZDUAUZJMOJ-UHFFFAOYSA-N 2-[[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]amino]-2-methylpropan-1-ol Chemical compound C=1C=C(NC=2N=C3C(NC(C)(C)CO)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 MPEMZDUAUZJMOJ-UHFFFAOYSA-N 0.000 claims description 2
- YDMASSGDTTWIMX-UHFFFAOYSA-N 2-[[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]amino]ethanol Chemical compound C=1C=C(NC=2N=C3C(NCCO)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 YDMASSGDTTWIMX-UHFFFAOYSA-N 0.000 claims description 2
- JKJBMSVBYHQRIO-UHFFFAOYSA-N 2-[[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]amino]propan-1-ol Chemical compound C=1C=C(NC=2N=C3C(NC(C)CO)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 JKJBMSVBYHQRIO-UHFFFAOYSA-N 0.000 claims description 2
- VMNKAAXTWKTQBZ-UHFFFAOYSA-N 2-[[2-[2-methoxy-4-(1-methylpyrazol-4-yl)anilino]pyrido[3,4-d]pyrimidin-8-yl]amino]propane-1,3-diol Chemical compound C=1C=C(NC=2N=C3C(NC(CO)CO)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 VMNKAAXTWKTQBZ-UHFFFAOYSA-N 0.000 claims description 2
- XVWBYYWZQXVZLG-UHFFFAOYSA-N 2-n-[2-(difluoromethoxy)-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(2-methoxy-2-methylpropyl)-6-methylpyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound N1=C2C(NCC(C)(C)OC)=NC(C)=CC2=CN=C1NC(C(=C1)OC(F)F)=CC=C1C=1C=NN(C)C=1 XVWBYYWZQXVZLG-UHFFFAOYSA-N 0.000 claims description 2
- MBMGZVRAAURXAC-UHFFFAOYSA-N 2-n-[2-(difluoromethoxy)-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(2-methoxy-2-methylpropyl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound N1=C2C(NCC(C)(C)OC)=NC=CC2=CN=C1NC(C(=C1)OC(F)F)=CC=C1C=1C=NN(C)C=1 MBMGZVRAAURXAC-UHFFFAOYSA-N 0.000 claims description 2
- XVMCFRTZSZRUTA-UHFFFAOYSA-N 2-n-[2-(difluoromethoxy)-4-fluorophenyl]-8-n-(2-methoxy-2-methylpropyl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound N1=C2C(NCC(C)(C)OC)=NC=CC2=CN=C1NC1=CC=C(F)C=C1OC(F)F XVMCFRTZSZRUTA-UHFFFAOYSA-N 0.000 claims description 2
- XEQUNIUZQRDLMG-UHFFFAOYSA-N 2-n-[2-ethoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(oxan-4-yl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound CCOC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2NC1CCOCC1 XEQUNIUZQRDLMG-UHFFFAOYSA-N 0.000 claims description 2
- QUIQOCPVVLSGIC-UHFFFAOYSA-N 2-n-[2-ethoxy-4-(4-methyl-1,2,4-triazol-3-yl)phenyl]-8-n-(2-methoxy-2-methylpropyl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound C=1C=C(NC=2N=C3C(NCC(C)(C)OC)=NC=CC3=CN=2)C(OCC)=CC=1C1=NN=CN1C QUIQOCPVVLSGIC-UHFFFAOYSA-N 0.000 claims description 2
- RXLSCAACZFVGJF-UHFFFAOYSA-N 2-n-[2-ethoxy-4-(4-methyl-1,2,4-triazol-3-yl)phenyl]-8-n-[(3-methyloxolan-3-yl)methyl]pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound CCOC1=CC(C=2N(C=NN=2)C)=CC=C1NC(N=C12)=NC=C1C=CN=C2NCC1(C)CCOC1 RXLSCAACZFVGJF-UHFFFAOYSA-N 0.000 claims description 2
- GONPDSQILJJULJ-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n,8-n-dimethylpyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound C=1C=C(NC=2N=C3C(N(C)C)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 GONPDSQILJJULJ-UHFFFAOYSA-N 0.000 claims description 2
- CNYJTBHMNLHACD-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(1-methylpiperidin-4-yl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound COC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2NC1CCN(C)CC1 CNYJTBHMNLHACD-UHFFFAOYSA-N 0.000 claims description 2
- YHFRXIUIHKRDLF-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(2,2,2-trifluoroethyl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound C=1C=C(NC=2N=C3C(NCC(F)(F)F)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 YHFRXIUIHKRDLF-UHFFFAOYSA-N 0.000 claims description 2
- QZZFLPGPIFLIDL-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(2-methylpropyl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound C=1C=C(NC=2N=C3C(NCC(C)C)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 QZZFLPGPIFLIDL-UHFFFAOYSA-N 0.000 claims description 2
- RNQJDYAGBGETGI-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(3-methylbutyl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound C=1C=C(NC=2N=C3C(NCCC(C)C)=NC=CC3=CN=2)C(OC)=CC=1C=1C=NN(C)C=1 RNQJDYAGBGETGI-UHFFFAOYSA-N 0.000 claims description 2
- MJPOKEITVYMJIC-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(oxan-4-yl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound COC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2NC1CCOCC1 MJPOKEITVYMJIC-UHFFFAOYSA-N 0.000 claims description 2
- ZUXWJMBALSCMPR-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(oxetan-2-ylmethyl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound COC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2NCC1CCO1 ZUXWJMBALSCMPR-UHFFFAOYSA-N 0.000 claims description 2
- SATXVBGBRZGLLQ-UHFFFAOYSA-N 2-n-[2-methoxy-4-(1-methylpyrazol-4-yl)phenyl]-8-n-(oxetan-3-yl)pyrido[3,4-d]pyrimidine-2,8-diamine Chemical compound COC1=CC(C2=CN(C)N=C2)=CC=C1NC(N=C12)=NC=C1C=CN=C2NC1COC1 SATXVBGBRZGLLQ-UHFFFAOYSA-N 0.000 claims description 2
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- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
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Classifications
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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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
- C07D471/04—Ortho-condensed systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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- A—HUMAN NECESSITIES
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- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
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- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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| EP2268647B1 (en) | 2008-03-21 | 2017-01-25 | The General Hospital Corporation | Compounds and compositions for the detection and treatment of alzheimer's disease and related disorders |
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| GB201216018D0 (en) | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Pharmacologically active compounds |
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| RU2718876C2 (ru) * | 2013-08-23 | 2020-04-15 | Ньюфарма, Инк. | Некоторые химические соединения, композиции и способы |
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| JP6616934B2 (ja) * | 2014-05-22 | 2019-12-04 | 株式会社 資生堂 | レナリドミドの光学分割方法 |
| US10947201B2 (en) | 2015-02-17 | 2021-03-16 | Neupharma, Inc. | Certain chemical entities, compositions, and methods |
| US11208696B2 (en) | 2015-04-17 | 2021-12-28 | Netherlands Translational Research Center B.V. | Prognostic biomarkers for TTK inhibitor chemotherapy |
| RU2695337C2 (ru) * | 2015-05-29 | 2019-07-23 | Тейдзин Фарма Лимитед | ПРОИЗВОДНОЕ ПИРИДО[3,4-d]ПИРИМИДИНА И ЕГО ФАРМАЦЕВТИЧЕСКИ ПРИЕМЛЕМАЯ СОЛЬ |
| WO2017012559A1 (zh) * | 2015-07-21 | 2017-01-26 | 广州再极医药科技有限公司 | 稠环嘧啶类化合物、中间体、其制备方法、组合物和应用 |
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| CN109996800B (zh) | 2016-11-28 | 2021-11-19 | 帝人制药株式会社 | 吡啶并[3,4-d]嘧啶衍生物或其溶剂合物的晶体 |
| SI3546458T1 (sl) | 2016-11-28 | 2021-03-31 | Teijin Pharma Limited | Derivati ((piridin-2-il)-amino)pirido(3,4-d)pirimidina in ((piridazin-3-il)amino)pirido(3,4-d)pirimidina kot zaviralci CDK4/6 za zdravljenje npr. revmatoidnega artritisa, arterioskleroze, pljučne fibroze, možganske kapi ali raka |
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| EP3701304B1 (en) | 2017-10-26 | 2022-05-04 | CommScope Connectivity Belgium BVBA | Telecommunications system |
| GB201809458D0 (en) * | 2018-06-08 | 2018-07-25 | Crt Pioneer Fund Lp | Salt form |
| GB201809460D0 (en) * | 2018-06-08 | 2018-07-25 | Crt Pioneer Fund Lp | Salt form |
| CA3156777A1 (en) | 2019-10-30 | 2021-05-06 | Fusheng ZHOU | Substituted heterocyclic fused cyclic compound, preparation method therefor and pharmaceutical use thereof |
| KR102396930B1 (ko) * | 2020-01-15 | 2022-05-12 | 한국과학기술연구원 | 피리도[3,4-d]피리미딘 유도체 및 이를 포함하는 치료용 약학 조성물 |
| EP4090663A1 (en) * | 2020-01-15 | 2022-11-23 | Blueprint Medicines Corporation | Map4k1 inhibitors |
| WO2022002118A1 (zh) * | 2020-07-01 | 2022-01-06 | 四川海思科制药有限公司 | 一种并环杂环衍生物及其在医药上的应用 |
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| US20230303564A1 (en) * | 2020-08-17 | 2023-09-28 | Medshine Discovery Inc. | Pyrimidine ring compound |
| JP2023549540A (ja) | 2020-11-18 | 2023-11-27 | デシフェラ・ファーマシューティカルズ,エルエルシー | Gcn2およびperkキナーゼ阻害剤およびその使用方法 |
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