JP2001139549A5 - - Google Patents
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- Publication number
- JP2001139549A5 JP2001139549A5 JP1999324451A JP32445199A JP2001139549A5 JP 2001139549 A5 JP2001139549 A5 JP 2001139549A5 JP 1999324451 A JP1999324451 A JP 1999324451A JP 32445199 A JP32445199 A JP 32445199A JP 2001139549 A5 JP2001139549 A5 JP 2001139549A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- alkyl group
- hydrogen atom
- added
- aryl group
- 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.)
- Granted
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 8
- 125000003118 aryl group Chemical group 0.000 description 6
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- UCGAMTHGINQRCK-UHFFFAOYSA-N 2,3-diphenyl-6-pyridin-3-ylpyridine Chemical compound C1=CC=CC=C1C1=CC=C(C=2C=NC=CC=2)N=C1C1=CC=CC=C1 UCGAMTHGINQRCK-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- -1 dimethylaminophenyl group Chemical group 0.000 description 2
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine hydrate Chemical compound O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- GZPHSAQLYPIAIN-UHFFFAOYSA-N 3-pyridinecarbonitrile Chemical compound N#CC1=CC=CN=C1 GZPHSAQLYPIAIN-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32445199A JP4603646B2 (ja) | 1999-11-15 | 1999-11-15 | 新規なジピリジル誘導体 |
| AU79633/00A AU7963300A (en) | 1999-11-15 | 2000-10-30 | Novel bipyridyl derivatives |
| PCT/JP2000/007628 WO2001036387A1 (en) | 1999-11-15 | 2000-10-30 | Novel bipyridyl derivatives |
| US10/130,068 US6603007B1 (en) | 1999-11-15 | 2000-10-30 | Bipyridyl derivatives |
| CNB008157065A CN1177822C (zh) | 1999-11-15 | 2000-10-30 | 二吡啶基衍生物 |
| EP00970206A EP1231207A4 (en) | 1999-11-15 | 2000-10-30 | NEW BIPYRIDYL DERIVATIVES |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32445199A JP4603646B2 (ja) | 1999-11-15 | 1999-11-15 | 新規なジピリジル誘導体 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010173177A Division JP5235947B2 (ja) | 2010-07-30 | 2010-07-30 | 新規なジピリジル誘導体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001139549A JP2001139549A (ja) | 2001-05-22 |
| JP2001139549A5 true JP2001139549A5 (https=) | 2006-12-28 |
| JP4603646B2 JP4603646B2 (ja) | 2010-12-22 |
Family
ID=18165968
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP32445199A Expired - Fee Related JP4603646B2 (ja) | 1999-11-15 | 1999-11-15 | 新規なジピリジル誘導体 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6603007B1 (https=) |
| EP (1) | EP1231207A4 (https=) |
| JP (1) | JP4603646B2 (https=) |
| CN (1) | CN1177822C (https=) |
| AU (1) | AU7963300A (https=) |
| WO (1) | WO2001036387A1 (https=) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1492784A4 (en) * | 2002-03-28 | 2006-03-29 | Merck & Co Inc | SUBSTITUTED 2,3-DIPHENYLPYRIDINES |
| US7087106B2 (en) * | 2003-02-20 | 2006-08-08 | University Of Florida | Materials and methods for inhibiting fouling of surfaces exposed to aquatic environments |
| JP2005029517A (ja) | 2003-07-07 | 2005-02-03 | Sankio Chemical Co Ltd | 新規ビピリジン誘導体 |
| KR101058103B1 (ko) * | 2008-04-15 | 2011-08-24 | 삼성모바일디스플레이주식회사 | 바이피리딘계 화합물 및 이를 포함한 유기막을 구비한 유기발광 소자 |
| TWI490215B (zh) * | 2008-05-16 | 2015-07-01 | Semiconductor Energy Lab | 有機化合物，苯並唑衍生物，以及使用苯並唑衍生物之發光元件，發光裝置，和電子裝置 |
| US9105852B2 (en) | 2012-02-17 | 2015-08-11 | Semiconductor Energy Laboratory Co., Ltd. | Bipyridine compound, light-emitting element material, organic semiconductor material, light-emitting element, display module, lighting module, light-emitting device, lighting device, display device and electronic device |
| TWI633100B (zh) | 2013-07-19 | 2018-08-21 | 半導體能源研究所股份有限公司 | 有機化合物、發光元件、顯示器模組、照明模組、發光裝置、顯示裝置、照明設備及電子裝置 |
| EP2915811A1 (en) * | 2014-03-04 | 2015-09-09 | Centre Régional de Lutte contre le Cancer - Centre François Baclesse | MCL-1 modulating compounds for cancer treatment |
| CN114350062B (zh) * | 2021-12-08 | 2023-05-02 | 界首市天鸿新材料股份有限公司 | 高刚性低屈服聚丙烯扭结膜及其制备方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1268194A (en) * | 1968-03-18 | 1972-03-22 | Ici Ltd | Pyridine derivatives and their manufacture |
| NZ212525A (en) * | 1985-06-24 | 1989-02-24 | Dfc New Zealand Ltd Formerly D | Nitrogen-containing heterocyclic compounds, and pharmaceutical compositions containing such |
| JP2583062B2 (ja) * | 1987-06-23 | 1997-02-19 | 和光純薬工業株式会社 | 複素環化合物の製造法 |
| WO1992002513A1 (en) * | 1990-08-06 | 1992-02-20 | Fujisawa Pharmaceutical Co., Ltd. | Heterocyclic compounds |
| US5932737A (en) * | 1994-12-02 | 1999-08-03 | Fujisawa Pharmaceutical Co., Ltd. | Peptide compounds for treatment of no-mediated diseases |
| CZ296163B6 (cs) * | 1996-05-20 | 2006-01-11 | Karboxyamidy chinolinu jako inhibitory TNF a inhibitory PDE-IV | |
| ATE309218T1 (de) | 1997-05-22 | 2005-11-15 | Daiichi Suntory Pharma Co Ltd | Herstellungsverfahren und trennverfahren für 2', 4'-dipyridylderivate und herstellverfahren für benzoxazepinderivate und deren salze |
| GB2328686B (en) | 1997-08-25 | 2001-09-26 | Sankio Chemical Co Ltd | Method for producing arylamine |
| CA2324251A1 (en) * | 1998-04-23 | 1999-11-04 | Novartis Ag | Certain heteroaryl substituted thiol inhibitors of endothelin-converting enzyme |
| JP2000247956A (ja) * | 1999-02-26 | 2000-09-12 | Japan Energy Corp | 三環系フェニルピリジン誘導体およびそれを含有する液晶組成物 |
| JP4603648B2 (ja) * | 1999-11-30 | 2010-12-22 | 富士フイルムファインケミカルズ株式会社 | ピリジン誘導体の製造方法 |
-
1999
- 1999-11-15 JP JP32445199A patent/JP4603646B2/ja not_active Expired - Fee Related
-
2000
- 2000-10-30 EP EP00970206A patent/EP1231207A4/en not_active Withdrawn
- 2000-10-30 WO PCT/JP2000/007628 patent/WO2001036387A1/ja not_active Ceased
- 2000-10-30 US US10/130,068 patent/US6603007B1/en not_active Expired - Fee Related
- 2000-10-30 AU AU79633/00A patent/AU7963300A/en not_active Abandoned
- 2000-10-30 CN CNB008157065A patent/CN1177822C/zh not_active Expired - Fee Related
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