JP2005213239A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005213239A5 JP2005213239A5 JP2004025806A JP2004025806A JP2005213239A5 JP 2005213239 A5 JP2005213239 A5 JP 2005213239A5 JP 2004025806 A JP2004025806 A JP 2004025806A JP 2004025806 A JP2004025806 A JP 2004025806A JP 2005213239 A5 JP2005213239 A5 JP 2005213239A5
- Authority
- JP
- Japan
- Prior art keywords
- ion
- bonded
- general formula
- ions
- compound represented
- 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
- -1 acrolein compound Chemical class 0.000 claims description 22
- 125000004429 atom Chemical group 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 3
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical class C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N acrylaldehyde Natural products C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 description 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 description 1
- XHLHPRDBBAGVEG-UHFFFAOYSA-N 1-tetralone Chemical compound C1=CC=C2C(=O)CCCC2=C1 XHLHPRDBBAGVEG-UHFFFAOYSA-N 0.000 description 1
- OPOJRMTZHYUKLY-UHFFFAOYSA-N 1h-1,3,5-triazin-2-one Chemical compound O=C1N=CN=CN1 OPOJRMTZHYUKLY-UHFFFAOYSA-N 0.000 description 1
- DNCYBUMDUBHIJZ-UHFFFAOYSA-N 1h-pyrimidin-6-one Chemical compound O=C1C=CN=CN1 DNCYBUMDUBHIJZ-UHFFFAOYSA-N 0.000 description 1
- SIJBDWPVNAYVGY-UHFFFAOYSA-N 2,2-dimethyl-1,3-dioxolane Chemical compound CC1(C)OCCO1 SIJBDWPVNAYVGY-UHFFFAOYSA-N 0.000 description 1
- YROIEQHEBPTQKR-UHFFFAOYSA-N 2h-1,2,4-thiadiazine Chemical compound N1SC=CN=C1 YROIEQHEBPTQKR-UHFFFAOYSA-N 0.000 description 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical group C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 229940097043 glucuronic acid Drugs 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical compound C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Chemical compound [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229940085991 phosphate ion Drugs 0.000 description 1
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004025806A JP4700916B2 (ja) | 2004-02-02 | 2004-02-02 | ピリジン誘導体の製造方法 |
| US11/046,743 US7723522B2 (en) | 2004-02-02 | 2005-02-01 | Pyridine derivative production method |
| DE602005007639T DE602005007639D1 (de) | 2004-02-02 | 2005-02-01 | Herstellung von pyridin-derivaten unter verwendung von pyrimidinium derivaten als zwischenprodukte |
| EP05002053A EP1559711B1 (en) | 2004-02-02 | 2005-02-01 | Preparation of pyridine derivatives using pyrimidinium derivatives as intermediates |
| CN200510006703.6A CN1680325B (zh) | 2004-02-02 | 2005-02-02 | 吡啶衍生物的生产方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004025806A JP4700916B2 (ja) | 2004-02-02 | 2004-02-02 | ピリジン誘導体の製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005213239A JP2005213239A (ja) | 2005-08-11 |
| JP2005213239A5 true JP2005213239A5 (enExample) | 2007-03-15 |
| JP4700916B2 JP4700916B2 (ja) | 2011-06-15 |
Family
ID=34650891
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004025806A Expired - Lifetime JP4700916B2 (ja) | 2004-02-02 | 2004-02-02 | ピリジン誘導体の製造方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US7723522B2 (enExample) |
| EP (1) | EP1559711B1 (enExample) |
| JP (1) | JP4700916B2 (enExample) |
| CN (1) | CN1680325B (enExample) |
| DE (1) | DE602005007639D1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008093392A1 (ja) | 2007-01-29 | 2008-08-07 | Fujifilm Finechemicals Co., Ltd. | ２，３'－ビピリジル－６'－オンの製造方法 |
| JP2009286756A (ja) | 2008-05-30 | 2009-12-10 | Fujifilm Finechemicals Co Ltd | トリアゾール誘導体またはその塩 |
| US8741491B2 (en) | 2011-06-17 | 2014-06-03 | Fluidic, Inc. | Ionic liquid containing sulfonate ions |
| CN102977007B (zh) * | 2012-12-24 | 2014-11-05 | 湖南大学 | 一种合成3-芳基吡啶衍生物的方法 |
| CN109810052B (zh) * | 2017-11-20 | 2020-06-23 | 新发药业有限公司 | 一种高选择性的阿帕替尼的简便制备方法 |
| US11424484B2 (en) | 2019-01-24 | 2022-08-23 | Octet Scientific, Inc. | Zinc battery electrolyte additive |
| MX2023004714A (es) * | 2020-10-23 | 2023-07-24 | Vertellus Holdings Llc | Métodos para fabricar derivados de ácido nicotínico. |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1178658C (zh) * | 1998-04-24 | 2004-12-08 | 麦克公司 | 合成环加氧酶-2抑制剂的方法 |
| JP3032980B1 (ja) | 1999-06-14 | 2000-04-17 | 三協化学株式会社 | ２―ピリジルピリジン誘導体の製造方法 |
| US6124474A (en) * | 1999-12-21 | 2000-09-26 | Abbott Laboratories | Synthesis of chiral 2-azetidinemethanol compounds |
| JP2001261653A (ja) | 2000-03-17 | 2001-09-26 | Sankio Chemical Co Ltd | ピリジン誘導体の合成法 |
-
2004
- 2004-02-02 JP JP2004025806A patent/JP4700916B2/ja not_active Expired - Lifetime
-
2005
- 2005-02-01 DE DE602005007639T patent/DE602005007639D1/de not_active Expired - Lifetime
- 2005-02-01 US US11/046,743 patent/US7723522B2/en active Active
- 2005-02-01 EP EP05002053A patent/EP1559711B1/en not_active Expired - Lifetime
- 2005-02-02 CN CN200510006703.6A patent/CN1680325B/zh not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| McConnell et al. | Luminescent properties of ruthenium (II) complexes with sterically expansive ligands bound to DNA defects | |
| JP2009523146A5 (enExample) | ||
| Barboza et al. | Structural correlations between luminescent properties and excited state internal proton transfer in some Zinc (II) N, N′-Bis (salicylidenes) | |
| JP2012054542A5 (ja) | トリアゾール誘導体および複素環化合物 | |
| JP2010525122A5 (enExample) | ||
| JP2010510976A5 (enExample) | ||
| WO2004020430A3 (fr) | Derives de dioxane-2-alkylcarbamates, leur preparation et leur application en therapeutique | |
| JP2005213239A5 (enExample) | ||
| HUP0002931A2 (hu) | Eljárás peszticid hatású pirazolszármazékok és intermedierjeik előállítására, és az új kiindulási anyagok és intermedierek | |
| JP2003503505A5 (enExample) | ||
| CN103951694A (zh) | 吖啶或苯并吖啶衍生物及其合成方法 | |
| JP2013137963A5 (enExample) | ||
| Nguyen et al. | Investigation of isomerism in anthracene-isothiouronium salts and application of these salts for anion sensing | |
| Kim et al. | Negative solovatochromism of azo dyes derived from (dialkylamino) thiazole dimers | |
| JPH029854A (ja) | ３‐アミノ‐アクリロニトリルの製法 | |
| CA2540370A1 (en) | Novel thioxylose compounds, preparation method thereof, pharmaceutical compositions containing same and use thereof in therapeutics | |
| Baumane et al. | Synthesis, structure, and electrochemical characteristics of 4-aryl-2-carbamoylmethylthio-5-ethoxycarbonyl-1, 4-dihydropyridine-3-carboxylic acid nitriles | |
| JP2006176509A5 (enExample) | ||
| CA2558191A1 (en) | Composition containing benzamidine derivative and method for stabilizing benzamidine derivative | |
| JP2014214127A5 (enExample) | ||
| TWI599568B (zh) | 具碳烯結構的鉑錯合物及使用其的有機發光二極體 | |
| JP2005225819A (ja) | ピロール環を有するアゾール化合物およびその製造方法 | |
| JP2009542767A5 (ja) | 芳香族アザ複素環、その製造方法及びこの材料の有機エレクトロニクス中での使用ならびに有機エレクトロニクス構成要素 | |
| WO2005021561A1 (ja) | 円偏光発光性を有する新規光学活性希土類錯体 | |
| JP6434530B2 (ja) | 有機アミン塩及びその製造方法、並びに、アゾ色素の製造方法 |