JP6507855B2 - キナゾリン化合物、その製造方法、およびその用途 - Google Patents
キナゾリン化合物、その製造方法、およびその用途 Download PDFInfo
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- JP6507855B2 JP6507855B2 JP2015109152A JP2015109152A JP6507855B2 JP 6507855 B2 JP6507855 B2 JP 6507855B2 JP 2015109152 A JP2015109152 A JP 2015109152A JP 2015109152 A JP2015109152 A JP 2015109152A JP 6507855 B2 JP6507855 B2 JP 6507855B2
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- Prior art keywords
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- pyrimidyl
- carbon atoms
- phenyl
- pyridyl
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- -1 Quinazoline compound Chemical class 0.000 title claims description 461
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 87
- 125000004432 carbon atom Chemical group C* 0.000 claims description 78
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 77
- 150000001875 compounds Chemical class 0.000 claims description 69
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 57
- 239000000463 material Substances 0.000 claims description 54
- 125000001424 substituent group Chemical group 0.000 claims description 51
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 45
- 125000004076 pyridyl group Chemical group 0.000 claims description 44
- 229910052731 fluorine Inorganic materials 0.000 claims description 41
- 125000000217 alkyl group Chemical group 0.000 claims description 40
- 125000001153 fluoro group Chemical group F* 0.000 claims description 39
- 125000004185 ester group Chemical group 0.000 claims description 37
- 125000003545 alkoxy group Chemical group 0.000 claims description 33
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 29
- 125000001624 naphthyl group Chemical group 0.000 claims description 29
- 125000006267 biphenyl group Chemical group 0.000 claims description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 24
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 23
- 125000005561 phenanthryl group Chemical group 0.000 claims description 19
- 238000002347 injection Methods 0.000 claims description 17
- 239000007924 injection Substances 0.000 claims description 17
- 125000003118 aryl group Chemical group 0.000 claims description 16
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 14
- 239000003054 catalyst Substances 0.000 claims description 14
- 125000001725 pyrenyl group Chemical group 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 238000007363 ring formation reaction Methods 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
- 125000000747 amidyl group Chemical group [H][N-]* 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 229910052805 deuterium Inorganic materials 0.000 claims description 3
- 125000004431 deuterium atom Chemical group 0.000 claims description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
- 125000002560 nitrile group Chemical group 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 125000003368 amide group Chemical group 0.000 claims description 2
- 125000005620 boronic acid group Chemical group 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000003246 quinazolines Chemical class 0.000 claims 1
- 239000010410 layer Substances 0.000 description 60
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 20
- 125000005493 quinolyl group Chemical group 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 235000010290 biphenyl Nutrition 0.000 description 15
- 239000004305 biphenyl Chemical group 0.000 description 15
- 239000007787 solid Substances 0.000 description 15
- 239000000758 substrate Substances 0.000 description 15
- 239000010408 film Substances 0.000 description 13
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 12
- 230000005525 hole transport Effects 0.000 description 12
- 239000000203 mixture Substances 0.000 description 12
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000002585 base Substances 0.000 description 8
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 8
- 229910052763 palladium Inorganic materials 0.000 description 8
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 8
- 125000006268 biphenyl-3-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])C(*)=C([H])C([H])=C1[H] 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 125000005956 isoquinolyl group Chemical group 0.000 description 6
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 6
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 6
- 238000005160 1H NMR spectroscopy Methods 0.000 description 5
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 5
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 5
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 229910052749 magnesium Inorganic materials 0.000 description 5
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 5
- 238000001771 vacuum deposition Methods 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 239000002019 doping agent Substances 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 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 4
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 4
- 230000006798 recombination Effects 0.000 description 4
- 238000005215 recombination Methods 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- 239000010409 thin film Substances 0.000 description 4
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 3
- YNQAOTPJELKSLS-UHFFFAOYSA-N 1-(2-phenylphenyl)isoquinoline Chemical group C1(=NC=CC2=CC=CC=C12)C1=C(C=CC=C1)C1=CC=CC=C1 YNQAOTPJELKSLS-UHFFFAOYSA-N 0.000 description 3
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-UHFFFAOYSA-N 0.000 description 3
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 3
- 239000005695 Ammonium acetate Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- AURDOXRTEWRZAH-UHFFFAOYSA-N ClC=1C=C2C(=NC(=NC2=CC1)C=1C=C(C=C(C1)C1=CC=C(C=C1)C1=NC=CC=C1)C1=CC=C(C=C1)C1=NC=CC=C1)C1=CC=CC=C1 Chemical compound ClC=1C=C2C(=NC(=NC2=CC1)C=1C=C(C=C(C1)C1=CC=C(C=C1)C1=NC=CC=C1)C1=CC=C(C=C1)C1=NC=CC=C1)C1=CC=CC=C1 AURDOXRTEWRZAH-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 229940043376 ammonium acetate Drugs 0.000 description 3
- 235000019257 ammonium acetate Nutrition 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052733 gallium Inorganic materials 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 229910052738 indium Inorganic materials 0.000 description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 229910052741 iridium Inorganic materials 0.000 description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 3
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical compound C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 3
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 239000011775 sodium fluoride Substances 0.000 description 3
- 235000013024 sodium fluoride Nutrition 0.000 description 3
- 238000000859 sublimation Methods 0.000 description 3
- 230000008022 sublimation Effects 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 3
- 235000019798 tripotassium phosphate Nutrition 0.000 description 3
- 238000007738 vacuum evaporation Methods 0.000 description 3
- UGOMMVLRQDMAQQ-UHFFFAOYSA-N xphos Chemical group CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 UGOMMVLRQDMAQQ-UHFFFAOYSA-N 0.000 description 3
- BANFGGCAQWUIAJ-UHFFFAOYSA-N (4-pyridin-2-ylphenyl)boronic acid Chemical compound C1=CC(B(O)O)=CC=C1C1=CC=CC=N1 BANFGGCAQWUIAJ-UHFFFAOYSA-N 0.000 description 2
- QFMZQPDHXULLKC-UHFFFAOYSA-N 1,2-bis(diphenylphosphino)ethane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCP(C=1C=CC=CC=1)C1=CC=CC=C1 QFMZQPDHXULLKC-UHFFFAOYSA-N 0.000 description 2
- LVEYOSJUKRVCCF-UHFFFAOYSA-N 1,3-bis(diphenylphosphino)propane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCCP(C=1C=CC=CC=1)C1=CC=CC=C1 LVEYOSJUKRVCCF-UHFFFAOYSA-N 0.000 description 2
- UHXOHPVVEHBKKT-UHFFFAOYSA-N 1-(2,2-diphenylethenyl)-4-[4-(2,2-diphenylethenyl)phenyl]benzene Chemical compound C=1C=C(C=2C=CC(C=C(C=3C=CC=CC=3)C=3C=CC=CC=3)=CC=2)C=CC=1C=C(C=1C=CC=CC=1)C1=CC=CC=C1 UHXOHPVVEHBKKT-UHFFFAOYSA-N 0.000 description 2
- XUNKEUNEDNWXFV-UHFFFAOYSA-N 1-(2-phenylphenyl)anthracene Chemical group C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC2=CC3=CC=CC=C3C=C12 XUNKEUNEDNWXFV-UHFFFAOYSA-N 0.000 description 2
- MXVLMYZRJAHEIS-UHFFFAOYSA-N 1-(2-phenylphenyl)naphthalene Chemical group C1=CC=CC=C1C1=CC=CC=C1C1=CC=CC2=CC=CC=C12 MXVLMYZRJAHEIS-UHFFFAOYSA-N 0.000 description 2
- IPROLCYNCVIXLY-UHFFFAOYSA-N 2-(3,5-dibromophenyl)-4-phenylquinazoline Chemical compound BrC=1C=C(C=C(C=1)Br)C1=NC2=CC=CC=C2C(=N1)C1=CC=CC=C1 IPROLCYNCVIXLY-UHFFFAOYSA-N 0.000 description 2
- ZGNCKIDXVHSMJL-UHFFFAOYSA-N 2-methylquinoline-8-carboxylic acid Chemical compound C1=CC=C(C(O)=O)C2=NC(C)=CC=C21 ZGNCKIDXVHSMJL-UHFFFAOYSA-N 0.000 description 2
- OBAJPWYDYFEBTF-UHFFFAOYSA-N 2-tert-butyl-9,10-dinaphthalen-2-ylanthracene Chemical compound C1=CC=CC2=CC(C3=C4C=CC=CC4=C(C=4C=C5C=CC=CC5=CC=4)C4=CC=C(C=C43)C(C)(C)C)=CC=C21 OBAJPWYDYFEBTF-UHFFFAOYSA-N 0.000 description 2
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- 150000003852 triazoles Chemical class 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 1
- WTVXIBRMWGUIMI-UHFFFAOYSA-N trifluoro($l^{1}-oxidanylsulfonyl)methane Chemical group [O]S(=O)(=O)C(F)(F)F WTVXIBRMWGUIMI-UHFFFAOYSA-N 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- KAAYGTMPJQOOGY-UHFFFAOYSA-N tris(2,5-dimethylphenyl)phosphane Chemical compound CC1=CC=C(C)C(P(C=2C(=CC=C(C)C=2)C)C=2C(=CC=C(C)C=2)C)=C1 KAAYGTMPJQOOGY-UHFFFAOYSA-N 0.000 description 1
- DLQYXUGCCKQSRJ-UHFFFAOYSA-N tris(furan-2-yl)phosphane Chemical compound C1=COC(P(C=2OC=CC=2)C=2OC=CC=2)=C1 DLQYXUGCCKQSRJ-UHFFFAOYSA-N 0.000 description 1
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- CXNIUSPIQKWYAI-UHFFFAOYSA-N xantphos Chemical compound C=12OC3=C(P(C=4C=CC=CC=4)C=4C=CC=CC=4)C=CC=C3C(C)(C)C2=CC=CC=1P(C=1C=CC=CC=1)C1=CC=CC=C1 CXNIUSPIQKWYAI-UHFFFAOYSA-N 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- NVCBVYYESHBQKS-UHFFFAOYSA-L zinc;2-carboxyquinolin-8-olate Chemical compound [Zn+2].C1=C(C([O-])=O)N=C2C(O)=CC=CC2=C1.C1=C(C([O-])=O)N=C2C(O)=CC=CC2=C1 NVCBVYYESHBQKS-UHFFFAOYSA-L 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Description
Ar1は、炭素数6〜12の芳香族炭化水素基(メチル基、メトキシ基、ピリジル基、ピリミジル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキル基で置換されていてもよい)を表す。
Ar2およびAr3は、各々独立に、水素原子、メチル基、メトキシ基、フッ素原子、または炭素数6〜12の芳香族炭化水素基(メチル基、メトキシ基、ピリジル基、ピリミジル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキル基で置換されていてもよい)を表す。
Ar4およびAr5は、各々独立に、フェニル基、ピリジル基、ピリミジル基、炭素数6〜18の芳香族炭化水素基で置換されたピリミジル基、またはベンゼン環および/またはピリジン環が2〜6つ連結および/または縮環した6員環のみからなる芳香族基{これらの基は、メチル基、メトキシ基、フッ素原子、ピリミジル基(当該ピリミジル基は、メチル基、炭素数2〜10のアルキル基、および炭素数6〜18の芳香族炭化水素基からなる群より選ばれる置換基を少なくとも一つ有していてもよい)、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキルで置換されていてもよい}を表す。
R1およびR2は、各々独立に、水素原子、メチル基、メトキシ基、フェニル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキル基を表す。
また、式中の各水素原子は各々独立に重水素原子であってもよい。)
実験例−2(実施例)
実験例−3(実施例)
実験例−4(実施例)
アルゴン気流下、6−クロロ−4−フェニル−2−[4,4’’−ビス(2−ピリジル)−1,1’:3’,1’’−テルフェニル−5’−イル]キナゾリン(A−1) 1.41g(2.26mmol)、フェニルボロン酸 331mg(2.72mmol)、酢酸パラジウム 10.1mg(0.0452mmol)、及び2−ジシクロヘキシルホスフィノ−2’,4’,6’−トリイソプロピルビフェニル 43.1mg(0.0904mmol)をTHF 45mLに加え、さらに3M−炭酸カリウム水溶液 1.5mLを添加し、5.5時間加熱還流した。室温まで冷却後、水を加えて析出した固体を濾取し、水、メタノール、およびヘキサンで洗浄した。得られた固体をトルエン 100mLで再結晶することで、目的の4,6−ジフェニル−2−[4,4’’−ビス(2−ピリジル)−1,1’:3’,1’’−テルフェニル−5’−イル]キナゾリン(A−2)の白色固体(収量1.21g、収率81%)を得た。
試験例−1(実施例)
有機電界発光素子の作製および評価を以下の様にして行った。基板には、2mm幅の酸化インジウム−スズ(ITO)膜がストライプ状にパターンされたITO透明電極付きガラス基板を用いた。この基板をイソプロピルアルコールで洗浄した後、酸素プラズマ洗浄にて表面処理を行った。洗浄後の基板に、真空蒸着法で各層の真空蒸着を行い、断面図を図1に示すような、発光面積4mm2の有機電界発光素子を作製した。
試験例−1の電子輸送層5の4−フェニル−2−[4,4’’−ビス(2−ピリジル)−1,1’:3’,1’’−テルフェニル−5’−イル]キナゾリン(A−3)に変えて、実験例−4で得られた4,6−ジフェニル−2−[4,4’’−ビス(2−ピリジル)−1,1’:3’,1’’−テルフェニル−5’−イル]キナゾリン(A−2)を用いた以外は、試験例−1と同様にして有機電界発光素子を作製し、試験例−1と同様に評価した。作製した素子の測定値は、543cd/m2、5.43cd/Aであった。
試験例−1の電子輸送層5における4−フェニル−2−[4,4’’−ビス(2−ピリジル)−1,1’:3’,1’’−テルフェニル−5’−イル]キナゾリン(A−3)に変えて、特許番号WO2008129912に記載の2,4−ジフェニル−6−[4,4’’−ジ(2−ピリジル)−1,1’:3’,1’’−テルフェニル−5’−イル]−1,3,5−トリアジン(下記式で表される)を真空蒸着した有機電界発光素子を、試験例−1と同様に作製、測定した。作製した素子の測定値は、456cd/m2、4.56cd/Aであった。
試験例−1の電子輸送層5における4−フェニル−2−[4,4’’−ビス(2−ピリジル)−1,1’:3’,1’’−テルフェニル−5’−イル]キナゾリン(A−3)に変えて、特許番号WO2006104118に含まれる2,4−ジフェニルキナゾリン(下記式で表される)を真空蒸着した有機電界発光素子を、試験例−1と同様に作製、測定した。作製した素子の測定値は、130cd/m2、1.30cd/Aであった。
2.正孔注入層
3.正孔輸送層
4.発光層
5.電子輸送層
6.陰極層
Claims (19)
- 一般式(1)で示されるキナゾリン化合物。
Ar1は、炭素数6〜12の芳香族炭化水素基(メチル基、メトキシ基、ピリジル基、ピリミジル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキル基で置換されていてもよい)を表す。
Ar2およびAr3は、各々独立に、水素原子、メチル基、メトキシ基、フッ素原子、または炭素数6〜12の芳香族炭化水素基(メチル基、メトキシ基、ピリジル基、ピリミジル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキル基で置換されていてもよい)を表す。
Ar4およびAr5は、各々独立に、フェニル基、ピリジル基、ピリミジル基、炭素数6〜18の芳香族炭化水素基で置換されたピリミジル基、またはベンゼン環および/またはピリジン環が2〜6つ連結および/または縮環した6員環のみからなる芳香族基{これらの基は、メチル基、メトキシ基、フッ素原子、ピリミジル基(当該ピリミジル基は、メチル基、炭素数2〜10のアルキル基、および炭素数6〜18の芳香族炭化水素基からなる群より選ばれる置換基を少なくとも一つ有していてもよい)、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキルで置換されていてもよい)を表す。
R1およびR2は、各々独立に、水素原子、メチル基、メトキシ基、フェニル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキル基を表す。
また、式中の各水素原子は各々独立に重水素原子であってもよい。) - Ar4およびAr5が、各々独立に、フェニル基、ピリジル基、ピリミジル基、炭素数6〜18の芳香族炭化水素基で置換されたピリミジル基、またはベンゼン環および/またはピリジン環が2〜6つ連結および/または縮環した6員環のみからなる芳香族基{これらの基は、メチル基、メトキシ基、炭素数2〜10のアルキル基、炭素数2〜10のアルコキシ基、フッ素原子、またはピリミジル基(当該ピリミジル基は、メチル基、フェニル基、ビフェニル基、ナフチル基、アントラシル基、フェナントリル基、およびピレニル基からなる群より選ばれる置換基を少なくとも一つ有していてもよい)で置換されていてもよい}である請求項1に記載のキナゾリン化合物。
- Ar4およびAr5が、各々独立に、フェニル基、ピリジル基、ピリミジル基、炭素数6〜18の芳香族炭化水素基で置換されたピリミジル基、またはベンゼン環および/またはピリジン環が2〜5つ連結および/または縮環した6員環のみからなる芳香族基{これらの基は、メチル基、メトキシ基、炭素数2〜10のアルキル基、炭素数2〜10のアルコキシ基、フッ素原子、またはピリミジル基(当該ピリミジル基は、メチル基、フェニル基、ビフェニル基、ナフチル基、アントラシル基、フェナントリル基、およびピレニル基からなる群より選ばれる置換基を少なくとも一つ有していてもよい)で置換されていてもよい}であるである請求項1又は2に記載のキナゾリン化合物。
- Ar4およびAr5が、各々独立に、フェニル基、ピリジル基、ピリミジル基、炭素数6〜18の芳香族炭化水素基で置換されたピリミジル基、またはベンゼン環および/またはピリジン環が2〜4つ連結および/または縮環した6員環のみからなる芳香族基{これらの基は、メチル基、メトキシ基、炭素数2〜10のアルキル基、炭素数2〜10のアルコキシ基、フッ素原子、またはピリミジル基(当該ピリミジル基は、メチル基、フェニル基、ビフェニル基、ナフチル基、アントラシル基、フェナントリル基、およびピレニル基からなる群より選ばれる置換基を少なくとも一つ有していてもよい)で置換されていてもよい}である請求項1〜3のいずれか一項に記載のキナゾリン化合物。
- Ar1が炭素数6〜12の芳香族炭化水素基(メチル基、メトキシ基、炭素数2〜10のアルキル基、炭素数2〜10のアルコキシ基、ピリジル基、ピリミジル基、またはフッ素原子で置換されていてもよい)である請求項1〜4のいずれか一項に記載のキナゾリン化合物。
- Ar1がフェニル基、ナフチル基、またはビフェニル基(これらの基は、メチル基、メトキシ基、ピリジル基、ピリミジル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基もしくはエステルアルキル基で置換されていてもよい)である請求項1〜4のいずれか一項に記載のキナゾリン化合物。
- Ar1がフェニル基、ナフチル基、またはビフェニル基である請求項1〜6のいずれか一項に記載のキナゾリン化合物。
- Ar1がフェニル基である請求項1〜7のいずれか一項に記載のキナゾリン化合物。
- R1およびR2が、水素原子である請求項1〜8のいずれか一項に記載のキナゾリン化合物。
- Ar2およびAr3が、各々独立に、水素原子、メチル基、メトキシ基、フッ素原子、または炭素数6〜12の芳香族炭化水素基(メチル基、メトキシ基、炭素数2〜10のアルキル基、炭素数2〜10のアルコキシ基、ピリジル基、ピリミジル基、またはフッ素原子で置換されていてもよい)である請求項1〜9のいずれか一項に記載のキナゾリン化合物。
- Ar2およびAr3が、各々独立にフェニル基、ナフチル基、もしくはビフェニル基(これらの置換基は、メチル基、メトキシ基、ピリジル基、ピリミジル基、フッ素原子、または炭素数2〜10のアルキル基、アルコキシ基、アルコキシアルキル基、エステル基、もしくはエステルアルキル基で置換されていてもよい)、水素原子、メチル基、メトキシ基、またはフッ素原子である請求項1〜9のいずれか一項に記載のキナゾリン化合物。
- Ar2およびAr3が、各々独立に、水素原子、フェニル基、ナフチル基、またはビフェニル基である請求項1〜9のいずれか一項に記載のキナゾリン化合物。
- Ar2およびAr3が、各々独立に、水素原子もしくはフェニル基である請求項1〜12のいずれか一項に記載のキナゾリン化合物。
- 金属触媒の存在下、または金属触媒および塩基の存在下、一般式(2)で表される化合物と一般式(3)で表される化合物と一般式(4)で表される化合物を1段階または2段階でカップリング反応させることを特徴とする、請求項1に記載のキナゾリン化合物の製造方法。
- 一般式(2)で示されるキナゾリン化合物。
- 触媒の存在下、酸の存在下、塩基の存在下、触媒および酸の存在下、または触媒及び塩基の存在下であって、窒素源の存在下または非存在下に、一般式(5)で表される化合物と一般式(6)で表される化合物を環化反応させることを特徴とする、請求項15に記載の一般式(2)で表されるキナゾリン化合物の製造方法。
- 請求項1〜13に記載のキナゾリン化合物を含む有機電界発光素子用材料。
- 請求項1〜13に記載のキナゾリン化合物を含む発光層ホスト材料、電子注入材料または電子輸送材料。
- 請求項1〜13に記載のキナゾリン化合物を含む電子注入材料または電子輸送材料。
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