CN102452988B - 一种喹唑啉衍生物及其制备方法 - Google Patents
一种喹唑啉衍生物及其制备方法 Download PDFInfo
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- CN102452988B CN102452988B CN201010521382.4A CN201010521382A CN102452988B CN 102452988 B CN102452988 B CN 102452988B CN 201010521382 A CN201010521382 A CN 201010521382A CN 102452988 B CN102452988 B CN 102452988B
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- 0 CN*c(c1c2nccc1)ccc2O Chemical compound CN*c(c1c2nccc1)ccc2O 0.000 description 6
- NHOLYIFIMXMDOW-ZHACJKMWSA-N C/C(/NC)=C1/C=CC=NC1C1N=CC=CC1 Chemical compound C/C(/NC)=C1/C=CC=NC1C1N=CC=CC1 NHOLYIFIMXMDOW-ZHACJKMWSA-N 0.000 description 1
- LVDNGVMRJNCNSY-JKHKTYJBSA-N C/C=C\C(/C(/N)=C(\C1=C)/N=CC=C1NC)=C Chemical compound C/C=C\C(/C(/N)=C(\C1=C)/N=CC=C1NC)=C LVDNGVMRJNCNSY-JKHKTYJBSA-N 0.000 description 1
- ZUDJJEFMKJDRSE-ALCCZGGFSA-N C/C=C\C(C(C1NCC=CC1=C)NC)=C Chemical compound C/C=C\C(C(C1NCC=CC1=C)NC)=C ZUDJJEFMKJDRSE-ALCCZGGFSA-N 0.000 description 1
- YLCWIFQLZYLURX-UHFFFAOYSA-N NC1=C2C=CC=NC2C2N=CC=CC2=C1 Chemical compound NC1=C2C=CC=NC2C2N=CC=CC2=C1 YLCWIFQLZYLURX-UHFFFAOYSA-N 0.000 description 1
- YUSGCLPSBBEIKG-UHFFFAOYSA-N NCc(cc1)cnc1-c1ccccn1 Chemical compound NCc(cc1)cnc1-c1ccccn1 YUSGCLPSBBEIKG-UHFFFAOYSA-N 0.000 description 1
- YDEUKNRKEYICTH-UHFFFAOYSA-N Nc(c1c2nccc1)ccc2O Chemical compound Nc(c1c2nccc1)ccc2O YDEUKNRKEYICTH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
- C07F15/0053—Ruthenium compounds without a metal-carbon linkage
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic Table
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201010521382.4A CN102452988B (zh) | 2010-10-27 | 2010-10-27 | 一种喹唑啉衍生物及其制备方法 |
| EP11835642.7A EP2634178B1 (en) | 2010-10-27 | 2011-10-27 | Quinazoline derivative and quinazoline complex protein kinase inhibitor for inhibiting multiplication of tumor cells and preparation method thereof |
| JP2013535272A JP5837079B2 (ja) | 2010-10-27 | 2011-10-27 | キナゾリン錯体、ならびにキナゾリン錯体の調製方法 |
| US13/882,100 US9233995B2 (en) | 2010-10-27 | 2011-10-27 | Quinazoline derivatives and quinazoline complex protein kinase inhibitor for inhibiting multiplication of tumor cells and preparation method thereof |
| PCT/CN2011/081453 WO2012055369A1 (zh) | 2010-10-27 | 2011-10-27 | 一种抑制肿瘤细胞增殖的喹唑啉衍生物、喹唑啉配合物蛋白激酶抑制剂及它们的制备方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201010521382.4A CN102452988B (zh) | 2010-10-27 | 2010-10-27 | 一种喹唑啉衍生物及其制备方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102452988A CN102452988A (zh) | 2012-05-16 |
| CN102452988B true CN102452988B (zh) | 2016-01-27 |
Family
ID=45993179
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201010521382.4A Expired - Fee Related CN102452988B (zh) | 2010-10-27 | 2010-10-27 | 一种喹唑啉衍生物及其制备方法 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US9233995B2 (enExample) |
| EP (1) | EP2634178B1 (enExample) |
| JP (1) | JP5837079B2 (enExample) |
| CN (1) | CN102452988B (enExample) |
| WO (1) | WO2012055369A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR092289A1 (es) | 2011-11-14 | 2015-04-15 | Sunshine Lake Pharma Co Ltd | Derivados de aminoquinazolina y sus sales y metodos de uso |
| JP2017512776A (ja) * | 2014-03-15 | 2017-05-25 | ウェイク フォレスト ユニバーシティ | 貴金属求電子体で修飾された官能化チロシンキナーゼ阻害剤およびそれと関連した方法 |
| EP2924045A1 (en) * | 2014-03-25 | 2015-09-30 | Medizinische Universität Wien | New agents for the treatment of cancer |
| CN106188147B (zh) * | 2015-05-08 | 2021-08-20 | 中国科学院化学研究所 | 含喹唑啉类配体的Pt配合物及其制备方法和应用 |
| CN105153047A (zh) * | 2015-08-25 | 2015-12-16 | 佛山市赛维斯医药科技有限公司 | 含新型苯并喹唑啉和邻位氟结构的酪氨酸激酶抑制剂及用途 |
| CN105153046A (zh) * | 2015-08-25 | 2015-12-16 | 佛山市赛维斯医药科技有限公司 | 双卤素取代的乙氧基苯并喹唑啉类酪氨酸激酶抑制剂及用途 |
| CN114524853B (zh) * | 2022-02-28 | 2023-12-12 | 南京师范大学 | 一种全反式维甲酸-芳基金属配合物、制备方法及应用 |
| CN116217550B (zh) * | 2022-12-26 | 2024-12-27 | 上海前瞻创新研究院有限公司 | 一种咪唑三联吡啶钌配合物溶解氧检测探针及其制备方法与应用 |
| CN119569738B (zh) * | 2024-12-09 | 2026-05-08 | 太原学院 | 一种喹唑啉小分子化合物及其制备方法与应用 |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001068652A1 (en) * | 2000-03-17 | 2001-09-20 | Novo Nordisk A/S | Condensed imidazoles as histamine h3 receptor ligands |
| WO2005097134A2 (en) * | 2004-03-31 | 2005-10-20 | The Scripps Research Institute | Quinazoline based protein kinase inhibitors |
| CN1724521A (zh) * | 2005-07-14 | 2006-01-25 | 沈阳中海生物技术开发有限公司 | 新的喹唑啉类衍生物、含有其的药物组合物以及它们的用途 |
| CN1882567A (zh) * | 2003-09-16 | 2006-12-20 | 阿斯利康(瑞典)有限公司 | 用作酪氨酸激酶抑制剂的喹唑啉衍生物 |
| CN101367793A (zh) * | 2008-09-26 | 2009-02-18 | 中国科学院广州生物医药与健康研究院 | 一种具有抗肿瘤活性的氨基喹唑啉衍生物及其盐类 |
| US20090111772A1 (en) * | 2007-09-10 | 2009-04-30 | Xiong Cai | Formulation of quinazoline based egfr inhibitors containing a zinc binding moiety |
| CN101431894A (zh) * | 2006-01-17 | 2009-05-13 | 陈国庆 | 螺环化合物和应用方法 |
| CN101535279A (zh) * | 2006-09-11 | 2009-09-16 | 柯瑞斯公司 | 含锌结合基的喹唑啉基egfr抑制剂 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ536114A (en) * | 2002-03-30 | 2007-11-30 | Boehringer Ingelheim Pharma | 4-(N-phenylamino)-quinazolines / quinolines as tyrosine kinase inhibitors |
| WO2005026150A1 (en) | 2003-09-16 | 2005-03-24 | Astrazeneca Ab | Quinazoline derivatives as tyrosine kinase inhibitors |
| US20100234371A1 (en) | 2005-08-22 | 2010-09-16 | Frank Himmelsbach | Bicyclic heterocycles, pharmaceutical compositions containing these compounds, the use thereof and processes for the preparation thereof |
| ES2526718T3 (es) | 2007-09-10 | 2015-01-14 | Curis, Inc. | Inhibidores de EGFR basados en sales de tartrato o complejos de quinazolina que contienen un resto que se une al cinc |
-
2010
- 2010-10-27 CN CN201010521382.4A patent/CN102452988B/zh not_active Expired - Fee Related
-
2011
- 2011-10-27 JP JP2013535272A patent/JP5837079B2/ja not_active Expired - Fee Related
- 2011-10-27 WO PCT/CN2011/081453 patent/WO2012055369A1/zh not_active Ceased
- 2011-10-27 EP EP11835642.7A patent/EP2634178B1/en not_active Not-in-force
- 2011-10-27 US US13/882,100 patent/US9233995B2/en not_active Expired - Fee Related
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001068652A1 (en) * | 2000-03-17 | 2001-09-20 | Novo Nordisk A/S | Condensed imidazoles as histamine h3 receptor ligands |
| CN1882567A (zh) * | 2003-09-16 | 2006-12-20 | 阿斯利康(瑞典)有限公司 | 用作酪氨酸激酶抑制剂的喹唑啉衍生物 |
| WO2005097134A2 (en) * | 2004-03-31 | 2005-10-20 | The Scripps Research Institute | Quinazoline based protein kinase inhibitors |
| CN1724521A (zh) * | 2005-07-14 | 2006-01-25 | 沈阳中海生物技术开发有限公司 | 新的喹唑啉类衍生物、含有其的药物组合物以及它们的用途 |
| CN101431894A (zh) * | 2006-01-17 | 2009-05-13 | 陈国庆 | 螺环化合物和应用方法 |
| CN101535279A (zh) * | 2006-09-11 | 2009-09-16 | 柯瑞斯公司 | 含锌结合基的喹唑啉基egfr抑制剂 |
| US20090111772A1 (en) * | 2007-09-10 | 2009-04-30 | Xiong Cai | Formulation of quinazoline based egfr inhibitors containing a zinc binding moiety |
| CN101367793A (zh) * | 2008-09-26 | 2009-02-18 | 中国科学院广州生物医药与健康研究院 | 一种具有抗肿瘤活性的氨基喹唑啉衍生物及其盐类 |
Non-Patent Citations (5)
| Title |
|---|
| Andrew J. Barker等.Studies leading to the identification of ZD1839 (IressaTM): An orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer.《Bioorganic & Medicinal Chemistry Letters》.2001,第11卷(第14期), * |
| Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy) -N-hydroxyheptanamide (CUDC-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer;Xiong Cai等;《Journal of Medicinal Chemistry》;20100209;第53卷(第5期);第2002页流程1和流程2,第2005页流程6 * |
| New trends for metal complexes with anticancer activity;Pieter CA Bruijnincx等;《Current Opinion in Chemical Biology》;20080125;第12卷(第2期);第197-206页 * |
| Studies leading to the identification of ZD1839 (IressaTM): An orally active, selective epidermal growth factor receptor tyrosine kinase inhibitor targeted to the treatment of cancer;Andrew J. Barker等;《Bioorganic & Medicinal Chemistry Letters》;20010723;第11卷(第14期);第1912页流程2,第1913-1914页表1-3 * |
| 新型8-氨基喹啉-蛋氨酸衍生物合钌金属药物的合成和细胞毒性及其与DNA相互作用研究;干宁等;《中国药学杂志》;20071008;第42卷(第19期);第1509页右栏图1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| US20130225811A1 (en) | 2013-08-29 |
| EP2634178A4 (en) | 2013-09-04 |
| EP2634178B1 (en) | 2016-08-24 |
| WO2012055369A1 (zh) | 2012-05-03 |
| EP2634178A1 (en) | 2013-09-04 |
| JP2013542210A (ja) | 2013-11-21 |
| JP5837079B2 (ja) | 2015-12-24 |
| US9233995B2 (en) | 2016-01-12 |
| CN102452988A (zh) | 2012-05-16 |
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Granted publication date: 20160127 |