JP2018522815A5 - - Google Patents
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- Publication number
- JP2018522815A5 JP2018522815A5 JP2017556849A JP2017556849A JP2018522815A5 JP 2018522815 A5 JP2018522815 A5 JP 2018522815A5 JP 2017556849 A JP2017556849 A JP 2017556849A JP 2017556849 A JP2017556849 A JP 2017556849A JP 2018522815 A5 JP2018522815 A5 JP 2018522815A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- substituted
- aryl
- unsubstituted
- independently
- 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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- 125000003118 aryl group Chemical group 0.000 claims 33
- -1 -CF 3 Chemical group 0.000 claims 27
- 150000001875 compounds Chemical class 0.000 claims 24
- 125000001072 heteroaryl group Chemical group 0.000 claims 24
- 125000000217 alkyl group Chemical group 0.000 claims 17
- 125000004122 cyclic group Chemical group 0.000 claims 12
- 150000001408 amides Chemical class 0.000 claims 9
- 125000002252 acyl group Chemical group 0.000 claims 8
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000004414 alkyl thio group Chemical group 0.000 claims 8
- 229910052799 carbon Inorganic materials 0.000 claims 8
- 150000002148 esters Chemical class 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 8
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims 8
- 229940124530 sulfonamide Drugs 0.000 claims 8
- 150000003456 sulfonamides Chemical class 0.000 claims 8
- 125000003441 thioacyl group Chemical group 0.000 claims 8
- 125000005647 linker group Chemical group 0.000 claims 7
- OKQKDCXVLPGWPO-UHFFFAOYSA-N sulfanylidenephosphane Chemical compound S=P OKQKDCXVLPGWPO-UHFFFAOYSA-N 0.000 claims 7
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 6
- 150000001721 carbon Chemical group 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 5
- 229910052717 sulfur Inorganic materials 0.000 claims 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 4
- WSANLGASBHUYGD-UHFFFAOYSA-N sulfidophosphanium Chemical group S=[PH3] WSANLGASBHUYGD-UHFFFAOYSA-N 0.000 claims 4
- 125000000743 hydrocarbylene group Chemical group 0.000 claims 3
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 claims 3
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims 2
- 150000002500 ions Chemical class 0.000 claims 2
- 229910052698 phosphorus Inorganic materials 0.000 claims 2
- 239000011574 phosphorus Substances 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims 1
- DZBUGLKDJFMEHC-UHFFFAOYSA-O acridine;hydron Chemical compound C1=CC=CC2=CC3=CC=CC=C3[NH+]=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-O 0.000 claims 1
- 150000001299 aldehydes Chemical class 0.000 claims 1
- 150000001450 anions Chemical group 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000007942 carboxylates Chemical group 0.000 claims 1
- 150000001733 carboxylic acid esters Chemical class 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Chemical group SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 1
- DOUHZFSGSXMPIE-UHFFFAOYSA-N hydroxidooxidosulfur(.) Chemical group [O]SO DOUHZFSGSXMPIE-UHFFFAOYSA-N 0.000 claims 1
- 150000002466 imines Chemical class 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000000962 organic group Chemical group 0.000 claims 1
- 230000000737 periodic effect Effects 0.000 claims 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical group [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical group [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical group [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 1
- 150000003457 sulfones Chemical class 0.000 claims 1
- 150000003462 sulfoxides Chemical class 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1507340.6 | 2015-04-29 | ||
| GBGB1507340.6A GB201507340D0 (en) | 2015-04-29 | 2015-04-29 | Light emitting devices and compounds |
| PCT/GB2015/054171 WO2016174377A1 (en) | 2015-04-29 | 2015-12-29 | Light emitting devices and compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018522815A JP2018522815A (ja) | 2018-08-16 |
| JP2018522815A5 true JP2018522815A5 (https=) | 2019-02-14 |
| JP6861644B2 JP6861644B2 (ja) | 2021-04-21 |
Family
ID=53488882
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017556849A Active JP6861644B2 (ja) | 2015-04-29 | 2015-12-29 | 発光デバイス及び化合物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10593893B2 (https=) |
| EP (1) | EP3288956B1 (https=) |
| JP (1) | JP6861644B2 (https=) |
| KR (1) | KR102502081B1 (https=) |
| CN (1) | CN107810184A (https=) |
| GB (1) | GB201507340D0 (https=) |
| WO (1) | WO2016174377A1 (https=) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| GB201507340D0 (en) | 2015-04-29 | 2015-06-10 | Univ St Andrews | Light emitting devices and compounds |
| KR102509827B1 (ko) * | 2015-09-22 | 2023-03-15 | 덕산네오룩스 주식회사 | 유기전기소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
| KR102572294B1 (ko) * | 2015-09-25 | 2023-08-30 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
| JP6705148B2 (ja) * | 2015-10-15 | 2020-06-03 | コニカミノルタ株式会社 | π共役系化合物、有機エレクトロルミネッセンス素子材料、発光材料、発光性薄膜、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
| JP6838268B2 (ja) * | 2015-10-21 | 2021-03-03 | コニカミノルタ株式会社 | 光変換材料、光変換フィルム、及び発光素子 |
| CN106892857B (zh) | 2015-12-18 | 2020-02-18 | 昆山国显光电有限公司 | 热活化延迟荧光材料及其在有机电致发光器件中的应用 |
| CA3252823A1 (en) | 2016-06-13 | 2025-02-25 | Gilead Sciences, Inc. | Substituted tert-butyl-3-(2-chloro-phenyl)-3-hydroxyazetidine-1-carboxylate compounds |
| MX385718B (es) | 2016-06-13 | 2025-03-18 | Gilead Sciences Inc | Compuestos moduladores de fxr (nr1h4). |
| KR102182177B1 (ko) * | 2016-10-24 | 2020-11-24 | 주식회사 엘지화학 | 카바졸 유도체 및 이를 이용한 유기 발광 소자 |
| CN106831633B (zh) * | 2016-12-30 | 2019-05-28 | 上海天马有机发光显示技术有限公司 | 一种有机电致发光材料以及有机光电装置 |
| US11283027B1 (en) | 2017-03-03 | 2022-03-22 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| US10892425B1 (en) | 2017-03-03 | 2021-01-12 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| PT3600309T (pt) | 2017-03-28 | 2022-10-03 | Gilead Sciences Inc | Combinações terapêuticas para o tratamento de doenças hepáticas |
| US10547014B2 (en) | 2017-06-23 | 2020-01-28 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| WO2018237389A1 (en) * | 2017-06-23 | 2018-12-27 | Kyulux Inc. | Composition of matter for use in organic light-emitting diodes |
| US11069860B2 (en) | 2017-08-21 | 2021-07-20 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| CN107556292A (zh) * | 2017-09-22 | 2018-01-09 | 苏州大学 | 吖啶‑咔唑给体衍生物及其制备方法以及基于其的有机电致发光器件 |
| US11444250B2 (en) | 2017-12-05 | 2022-09-13 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| US10644249B2 (en) | 2017-12-22 | 2020-05-05 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| KR102512548B1 (ko) | 2017-12-22 | 2023-03-22 | 삼성디스플레이 주식회사 | 유기 전계 발광 소자 및 유기 전계 발광 소자용 함질소 화합물 |
| US11575088B2 (en) | 2017-12-22 | 2023-02-07 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| US11542260B2 (en) | 2018-01-31 | 2023-01-03 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| US11104669B2 (en) | 2018-02-02 | 2021-08-31 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| CN111868029A (zh) * | 2018-03-16 | 2020-10-30 | 日产化学株式会社 | 苯胺衍生物的制造方法 |
| US11608333B2 (en) | 2018-03-20 | 2023-03-21 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| US11498914B2 (en) | 2018-03-30 | 2022-11-15 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| US11778904B2 (en) | 2018-05-09 | 2023-10-03 | Kyulux, Inc. | Composition of matter for use in organic light-emitting diodes |
| EP3696167B1 (en) | 2018-07-27 | 2024-11-20 | Idemitsu Kosan Co.,Ltd. | Compound, material for organic electroluminescence element, organic electroluminescence element, and electronic device |
| CN109134347B (zh) * | 2018-09-19 | 2020-12-25 | 南京工业大学 | 一种具有tadf特性的双受体型多取代咔唑类化合物及其制备方法和应用 |
| EP3911647B1 (en) | 2019-01-15 | 2023-12-13 | Gilead Sciences, Inc. | Isoxazole compound as fxr agonist and pharmaceutical compositions comprising same |
| CA3233305A1 (en) | 2019-02-19 | 2020-08-27 | Gilead Sciences, Inc. | Solid forms of fxr agonists |
| AU2020407664A1 (en) | 2019-12-20 | 2022-08-18 | Tenaya Therapeutics, Inc. | Fluoroalkyl-oxadiazoles and uses thereof |
| US12052918B2 (en) * | 2020-06-24 | 2024-07-30 | The Regents Of The University Of Michigan | Organic electroluminescent device comprising two-dimensional emissive layer |
| AU2022270657A1 (en) | 2021-05-04 | 2023-11-16 | Tenaya Therapeutics, Inc. | 2-fluoroalkyl-1,3,4-oxadiazol-5-yl-thiazol, hdac6 inhibitors for use in the treatment of metabolic disease and hfpef |
| CN115568237B (zh) * | 2022-10-25 | 2026-03-24 | 中国科学院宁波材料技术与工程研究所 | 一种钙钛矿太阳能电池及其制备方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3368390B2 (ja) * | 1993-10-12 | 2003-01-20 | 株式会社リコー | 電界発光素子 |
| JP4810805B2 (ja) * | 2003-07-31 | 2011-11-09 | 三菱化学株式会社 | 有機化合物、電荷輸送材料、有機電界発光素子材料および有機電界発光素子 |
| DE102006048728A1 (de) | 2006-10-16 | 2008-04-17 | Merck Patent Gmbh | 3-Amino-imidazo{1,2-a]pyridinderivate |
| CA2708447C (en) | 2007-12-25 | 2016-05-10 | Kissei Pharmaceutical Co., Ltd. | Novel catechol derivative, pharmaceutical composition containing the same, use of the catechol derivative, and use of the pharmaceutical composition |
| EP2445905A1 (en) * | 2009-06-24 | 2012-05-02 | Georgia Tech Research Corporation | Polymerizable ambipolar hosts for phosphorescent guest emitters |
| WO2011156478A2 (en) * | 2010-06-08 | 2011-12-15 | The University Of North Carolina At Chapel Hill | Polymers with tunable band gaps for photonic and electronic applications |
| JP5883590B2 (ja) | 2010-08-06 | 2016-03-15 | キッセイ薬品工業株式会社 | 新規なカテコール誘導体、それを含有する医薬組成物およびそれらの用途 |
| US9142781B2 (en) | 2011-06-09 | 2015-09-22 | Novaled Ag | Compound for organic electronic device |
| WO2013183327A1 (ja) | 2012-06-07 | 2013-12-12 | 国立大学法人奈良先端科学技術大学院大学 | 縮合環構造を有する化合物の製造方法及び縮合環構造を有する化合物並びにこれを用いた有機発光素子 |
| US9512136B2 (en) * | 2012-11-26 | 2016-12-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
| JP6553022B2 (ja) | 2013-04-08 | 2019-07-31 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネッセント素子 |
| JP2015072889A (ja) * | 2013-05-02 | 2015-04-16 | 国立大学法人九州大学 | 発光素子 |
| EP3005433B1 (de) | 2013-06-06 | 2023-02-22 | Merck Patent GmbH | Organische elektrolumineszenzvorrichtung |
| WO2015022835A1 (ja) * | 2013-08-14 | 2015-02-19 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、照明装置、表示装置及び蛍光発光性化合物 |
| KR20170005853A (ko) * | 2014-05-14 | 2017-01-16 | 프레지던트 앤드 펠로우즈 오브 하바드 칼리지 | 유기 발광 다이오드 물질 |
| KR101706752B1 (ko) * | 2015-02-17 | 2017-02-27 | 서울대학교산학협력단 | 호스트, 인광 도펀트 및 형광 도펀트를 포함하는 유기발광소자 |
| GB201507340D0 (en) | 2015-04-29 | 2015-06-10 | Univ St Andrews | Light emitting devices and compounds |
-
2015
- 2015-04-29 GB GBGB1507340.6A patent/GB201507340D0/en not_active Ceased
- 2015-12-29 US US15/569,669 patent/US10593893B2/en active Active
- 2015-12-29 KR KR1020177034587A patent/KR102502081B1/ko active Active
- 2015-12-29 JP JP2017556849A patent/JP6861644B2/ja active Active
- 2015-12-29 EP EP15820241.6A patent/EP3288956B1/en active Active
- 2015-12-29 CN CN201580081262.8A patent/CN107810184A/zh active Pending
- 2015-12-29 WO PCT/GB2015/054171 patent/WO2016174377A1/en not_active Ceased
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