PH12015501058B1 - Pyrimidine-2,4-diamine derivatives for treatment of cancer - Google Patents
Pyrimidine-2,4-diamine derivatives for treatment of cancer Download PDFInfo
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- PH12015501058B1 PH12015501058B1 PH12015501058A PH12015501058A PH12015501058B1 PH 12015501058 B1 PH12015501058 B1 PH 12015501058B1 PH 12015501058 A PH12015501058 A PH 12015501058A PH 12015501058 A PH12015501058 A PH 12015501058A PH 12015501058 B1 PH12015501058 B1 PH 12015501058B1
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- YAAWASYJIRZXSZ-UHFFFAOYSA-N pyrimidine-2,4-diamine Chemical class NC1=CC=NC(N)=N1 YAAWASYJIRZXSZ-UHFFFAOYSA-N 0.000 title claims description 9
- 206010028980 Neoplasm Diseases 0.000 title abstract description 48
- 201000011510 cancer Diseases 0.000 title abstract description 40
- 238000011282 treatment Methods 0.000 title abstract description 26
- 150000001875 compounds Chemical class 0.000 claims abstract description 198
- 150000003839 salts Chemical class 0.000 claims abstract description 29
- 125000001424 substituent group Chemical group 0.000 claims description 307
- 125000001072 heteroaryl group Chemical group 0.000 claims description 174
- -1 benzothiophen-3-yl Chemical group 0.000 claims description 141
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 125
- 229910052739 hydrogen Inorganic materials 0.000 claims description 120
- 239000001257 hydrogen Substances 0.000 claims description 115
- 125000003118 aryl group Chemical group 0.000 claims description 113
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 91
- 125000000217 alkyl group Chemical group 0.000 claims description 70
- 229910052736 halogen Inorganic materials 0.000 claims description 54
- 150000002367 halogens Chemical class 0.000 claims description 54
- 125000004429 atom Chemical group 0.000 claims description 43
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 40
- 229910052799 carbon Inorganic materials 0.000 claims description 15
- 125000000814 indol-3-yl group Chemical group [H]C1=C([H])C([H])=C2N([H])C([H])=C([*])C2=C1[H] 0.000 claims description 10
- 125000004531 indol-5-yl group Chemical group [H]N1C([H])=C([H])C2=C([H])C(*)=C([H])C([H])=C12 0.000 claims description 10
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 7
- 125000004552 isoquinolin-4-yl group Chemical group C1=NC=C(C2=CC=CC=C12)* 0.000 claims description 7
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 6
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 5
- 125000004512 1,2,3-thiadiazol-4-yl group Chemical group S1N=NC(=C1)* 0.000 claims description 4
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000004532 benzofuran-3-yl group Chemical group O1C=C(C2=C1C=CC=C2)* 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- 229940124530 sulfonamide Drugs 0.000 claims 4
- FOADOKMOPCNTEM-UHFFFAOYSA-N 4-n-[2-(4-chlorophenyl)ethyl]-6-(2,3-dichlorophenyl)pyrimidine-2,4-diamine Chemical compound C=1C(C=2C(=C(Cl)C=CC=2)Cl)=NC(N)=NC=1NCCC1=CC=C(Cl)C=C1 FOADOKMOPCNTEM-UHFFFAOYSA-N 0.000 claims 1
- WQWJWKFDPCLWSN-UHFFFAOYSA-N 6-(2,3-dimethylphenyl)-4-n-(2-phenylethyl)pyrimidine-2,4-diamine Chemical compound CC1=CC=CC(C=2N=C(N)N=C(NCCC=3C=CC=CC=3)C=2)=C1C WQWJWKFDPCLWSN-UHFFFAOYSA-N 0.000 claims 1
- NKFLEFWUYAUDJV-UHFFFAOYSA-N pyridine-3-sulfonamide Chemical compound NS(=O)(=O)C1=CC=CN=C1 NKFLEFWUYAUDJV-UHFFFAOYSA-N 0.000 claims 1
- 102100039792 Oxidized purine nucleoside triphosphate hydrolase Human genes 0.000 abstract description 19
- 230000005764 inhibitory process Effects 0.000 abstract description 5
- 230000008901 benefit Effects 0.000 abstract description 4
- 201000010099 disease Diseases 0.000 abstract description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 3
- 101000744394 Homo sapiens Oxidized purine nucleoside triphosphate hydrolase Proteins 0.000 abstract description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 142
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 102
- 125000004093 cyano group Chemical group *C#N 0.000 description 95
- 239000000203 mixture Substances 0.000 description 86
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 63
- 239000000047 product Substances 0.000 description 51
- 235000019439 ethyl acetate Nutrition 0.000 description 50
- 238000005481 NMR spectroscopy Methods 0.000 description 40
- 239000011541 reaction mixture Substances 0.000 description 40
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 39
- 239000007787 solid Substances 0.000 description 39
- 125000004122 cyclic group Chemical group 0.000 description 36
- 238000006243 chemical reaction Methods 0.000 description 35
- 125000005842 heteroatom Chemical group 0.000 description 33
- JPZOAVGMSDSWSW-UHFFFAOYSA-N 4,6-dichloropyrimidin-2-amine Chemical compound NC1=NC(Cl)=CC(Cl)=N1 JPZOAVGMSDSWSW-UHFFFAOYSA-N 0.000 description 32
- 238000000034 method Methods 0.000 description 32
- 229910052757 nitrogen Inorganic materials 0.000 description 32
- 239000000243 solution Substances 0.000 description 31
- 239000002904 solvent Substances 0.000 description 31
- 125000004433 nitrogen atom Chemical group N* 0.000 description 28
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 27
- 239000002585 base Substances 0.000 description 27
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 27
- YMWUJEATGCHHMB-UHFFFAOYSA-N dichloromethane Natural products ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 24
- 239000012043 crude product Substances 0.000 description 23
- 150000002431 hydrogen Chemical class 0.000 description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 22
- 239000012044 organic layer Substances 0.000 description 22
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 21
- 125000004432 carbon atom Chemical group C* 0.000 description 21
- 229910052760 oxygen Inorganic materials 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- 238000004440 column chromatography Methods 0.000 description 20
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 20
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 19
- 239000012267 brine Substances 0.000 description 19
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 19
- 125000002619 bicyclic group Chemical group 0.000 description 18
- 210000004027 cell Anatomy 0.000 description 18
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium on carbon Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 16
- 229910052717 sulfur Inorganic materials 0.000 description 16
- 238000007792 addition Methods 0.000 description 15
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 14
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 14
- 230000000694 effects Effects 0.000 description 14
- 125000001041 indolyl group Chemical group 0.000 description 14
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 13
- 229920006395 saturated elastomer Polymers 0.000 description 13
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- 125000002950 monocyclic group Chemical group 0.000 description 12
- 125000006574 non-aromatic ring group Chemical group 0.000 description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 12
- 238000002953 preparative HPLC Methods 0.000 description 12
- 230000002829 reductive effect Effects 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 11
- 239000007858 starting material Substances 0.000 description 11
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 10
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 10
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- 239000008194 pharmaceutical composition Substances 0.000 description 10
- 125000004434 sulfur atom Chemical group 0.000 description 10
- 125000002947 alkylene group Chemical group 0.000 description 9
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 9
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 9
- 125000004193 piperazinyl group Chemical group 0.000 description 9
- 125000003386 piperidinyl group Chemical group 0.000 description 9
- 125000004076 pyridyl group Chemical group 0.000 description 9
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- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 9
- 206010025323 Lymphomas Diseases 0.000 description 8
- 208000009956 adenocarcinoma Diseases 0.000 description 8
- 239000002671 adjuvant Substances 0.000 description 8
- 125000001246 bromo group Chemical group Br* 0.000 description 8
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- 239000010410 layer Substances 0.000 description 8
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 8
- 125000001624 naphthyl group Chemical group 0.000 description 8
- 230000000144 pharmacologic effect Effects 0.000 description 8
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- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 8
- 229940124597 therapeutic agent Drugs 0.000 description 8
- 238000004587 chromatography analysis Methods 0.000 description 7
- 238000004128 high performance liquid chromatography Methods 0.000 description 7
- 125000002757 morpholinyl group Chemical group 0.000 description 7
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 7
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- 125000000714 pyrimidinyl group Chemical group 0.000 description 7
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
- FIPBRZXDWSODDX-UHFFFAOYSA-N 4-chloro-6-phenylpyrimidin-2-amine Chemical compound NC1=NC(Cl)=CC(C=2C=CC=CC=2)=N1 FIPBRZXDWSODDX-UHFFFAOYSA-N 0.000 description 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
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- CXWJDRREGHIEMH-UHFFFAOYSA-N 6-chloro-4-n-methylpyrimidine-2,4-diamine Chemical compound CNC1=CC(Cl)=NC(N)=N1 CXWJDRREGHIEMH-UHFFFAOYSA-N 0.000 description 4
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Classifications
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| PCT/SE2013/051387 WO2014084778A1 (en) | 2012-11-27 | 2013-11-26 | Pyrimidine-2,4-diamine derivatives for treatment of cancer |
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| BR112015011497B1 (pt) * | 2012-11-27 | 2023-01-10 | Thomas Helledays Stiftelse För Medicinsk Forskning | Composto, e, formulação farmacêutica |
| WO2015172747A1 (en) * | 2014-05-16 | 2015-11-19 | Zhaoyin Wang | Spirocyclic molecules as mth1 inhibitors |
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