JPS59184165A - ５−アルキル−２−（４−フルオロフエニル）−ピリミジン - Google Patents
５−アルキル−２−（４−フルオロフエニル）−ピリミジンInfo
- Publication number
- JPS59184165A JPS59184165A JP5669283A JP5669283A JPS59184165A JP S59184165 A JPS59184165 A JP S59184165A JP 5669283 A JP5669283 A JP 5669283A JP 5669283 A JP5669283 A JP 5669283A JP S59184165 A JPS59184165 A JP S59184165A
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- formula
- fluorophenyl
- pyrimidine
- alkyl
- 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
Links
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 abstract description 22
- 238000006243 chemical reaction Methods 0.000 abstract description 6
- 239000000463 material Substances 0.000 abstract description 5
- CTXAFVNTZWVKNC-UHFFFAOYSA-N 2-(4-fluorophenyl)-5-propylpyrimidine Chemical compound N1=CC(CCC)=CN=C1C1=CC=C(F)C=C1 CTXAFVNTZWVKNC-UHFFFAOYSA-N 0.000 abstract description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 3
- 239000002904 solvent Substances 0.000 abstract description 3
- AEKVBBNGWBBYLL-UHFFFAOYSA-N 4-fluorobenzonitrile Chemical compound FC1=CC=C(C#N)C=C1 AEKVBBNGWBBYLL-UHFFFAOYSA-N 0.000 abstract description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical class C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract description 2
- -1 amidine hydrochloride Chemical class 0.000 abstract description 2
- 239000007789 gas Substances 0.000 abstract description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 239000000126 substance Substances 0.000 abstract description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000006482 condensation reaction Methods 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004988 Nematic liquid crystal Substances 0.000 description 3
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- LNEMDIUSUQPKIP-UHFFFAOYSA-N 2-phenyl-1,3-dioxane Chemical compound O1CCCOC1C1=CC=CC=C1 LNEMDIUSUQPKIP-UHFFFAOYSA-N 0.000 description 1
- JQDATBKJKUWNGA-UHFFFAOYSA-N 4-fluorobenzenecarboximidamide;hydrochloride Chemical compound Cl.NC(=N)C1=CC=C(F)C=C1 JQDATBKJKUWNGA-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- VJCWGXGMXAVKJU-UHFFFAOYSA-N cyclohexyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC1CCCCC1 VJCWGXGMXAVKJU-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
- OPYYWWIJPHKUDZ-UHFFFAOYSA-N phenyl cyclohexanecarboxylate Chemical compound C1CCCCC1C(=O)OC1=CC=CC=C1 OPYYWWIJPHKUDZ-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
Landscapes
- Liquid Crystal Substances (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5669283A JPS59184165A (ja) | 1983-03-31 | 1983-03-31 | ５−アルキル−２−（４−フルオロフエニル）−ピリミジン |
| US06/593,434 US4581155A (en) | 1983-03-31 | 1984-03-26 | Halogenopyrimidine derivatives |
| EP84103419A EP0123907B1 (en) | 1983-03-31 | 1984-03-28 | Fluoropyrimidine derivatives |
| DE8484103419T DE3479120D1 (en) | 1983-03-31 | 1984-03-28 | Fluoropyrimidine derivatives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5669283A JPS59184165A (ja) | 1983-03-31 | 1983-03-31 | ５−アルキル−２−（４−フルオロフエニル）−ピリミジン |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59184165A true JPS59184165A (ja) | 1984-10-19 |
| JPS6228136B2 JPS6228136B2 (enrdf_load_stackoverflow) | 1987-06-18 |
Family
ID=13034497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5669283A Granted JPS59184165A (ja) | 1983-03-31 | 1983-03-31 | ５−アルキル−２−（４−フルオロフエニル）−ピリミジン |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59184165A (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4640795A (en) * | 1986-03-21 | 1987-02-03 | Chisso Corporation | 5-alkyl-2-(3,4-difluorophenyl)pyrimidine and nematic liquid crystal composition containing same |
| JP2000080367A (ja) * | 1990-04-13 | 2000-03-21 | Merck Patent Gmbh | 液晶媒体 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5283477A (en) * | 1976-01-01 | 1977-07-12 | Hoffmann La Roche | Phenyl pyrimidine |
-
1983
- 1983-03-31 JP JP5669283A patent/JPS59184165A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5283477A (en) * | 1976-01-01 | 1977-07-12 | Hoffmann La Roche | Phenyl pyrimidine |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4640795A (en) * | 1986-03-21 | 1987-02-03 | Chisso Corporation | 5-alkyl-2-(3,4-difluorophenyl)pyrimidine and nematic liquid crystal composition containing same |
| JP2000080367A (ja) * | 1990-04-13 | 2000-03-21 | Merck Patent Gmbh | 液晶媒体 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6228136B2 (enrdf_load_stackoverflow) | 1987-06-18 |
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