CN101594870A - 4-氨基喹唑啉衍生物及其使用方法 - Google Patents
4-氨基喹唑啉衍生物及其使用方法 Download PDFInfo
- Publication number
- CN101594870A CN101594870A CNA2007800393013A CN200780039301A CN101594870A CN 101594870 A CN101594870 A CN 101594870A CN A2007800393013 A CNA2007800393013 A CN A2007800393013A CN 200780039301 A CN200780039301 A CN 200780039301A CN 101594870 A CN101594870 A CN 101594870A
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- cancer
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- chemical compound
- compound
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83950306P | 2006-08-22 | 2006-08-22 | |
| US60/839,503 | 2006-08-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101594870A true CN101594870A (zh) | 2009-12-02 |
Family
ID=39107412
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNA2007800393013A Pending CN101594870A (zh) | 2006-08-22 | 2007-08-22 | 4-氨基喹唑啉衍生物及其使用方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US20080051422A1 (enExample) |
| EP (1) | EP2054063A4 (enExample) |
| JP (1) | JP2010501572A (enExample) |
| KR (1) | KR20090042994A (enExample) |
| CN (1) | CN101594870A (enExample) |
| AU (1) | AU2007288204A1 (enExample) |
| CA (1) | CA2661223A1 (enExample) |
| MX (1) | MX2009001814A (enExample) |
| WO (1) | WO2008024439A2 (enExample) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102321076A (zh) * | 2011-07-07 | 2012-01-18 | 中国科学技术大学 | 拉帕替尼中间体及其类似物的制备方法 |
| CN102659764A (zh) * | 2012-04-16 | 2012-09-12 | 中国科学院广州生物医药与健康研究院 | 酪氨酸激酶不可逆抑制剂及其制备方法和用途 |
| CN102911164A (zh) * | 2012-11-07 | 2013-02-06 | 江苏金桥盐化集团利海化工有限公司 | 一种拉帕替尼关键中间体的制备方法 |
| CN103923070A (zh) * | 2013-01-14 | 2014-07-16 | 意大利合成制造有限公司 | 利用新中间体制备拉帕替尼及其盐的有效方法 |
| CN104513231A (zh) * | 2015-01-09 | 2015-04-15 | 安润医药科技(苏州)有限公司 | 拉帕替尼及其中间体的合成方法 |
| CN107827877A (zh) * | 2017-11-21 | 2018-03-23 | 陕西师范大学 | 二烷基氨基喹唑啉类化合物及其在制备抗肿瘤药物中的应用 |
| CN108187055A (zh) * | 2018-03-06 | 2018-06-22 | 北京大学 | 一种具有协同增效作用的抗癌组合物 |
| CN108285421A (zh) * | 2018-01-26 | 2018-07-17 | 黑龙江鑫创生物科技开发有限公司 | 一种微通道反应器合成拉帕替尼中间体的方法 |
| CN108690001A (zh) * | 2018-06-26 | 2018-10-23 | 苏州市贝克生物科技有限公司 | 拉帕替尼类似物的合成 |
| CN109414440A (zh) * | 2016-07-01 | 2019-03-01 | 亚狮康私人有限公司 | 用于治疗癌症的维持疗法 |
| CN111868039A (zh) * | 2017-09-26 | 2020-10-30 | 加利福尼亚大学董事会 | 用于治疗癌症的组合物和方法 |
| US12545686B2 (en) | 2021-09-23 | 2026-02-10 | Katmai Pharmaceuticals, Inc. | Polymorphic forms of (s)-n-(3-bromo-2-fluorophenyl)-7-((4-methylpiperazin-1-yl)methyl)-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-amine as EGFR inhibitors |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110053964A1 (en) * | 2006-08-22 | 2011-03-03 | Roger Tung | 4-aminoquinazoline derivatives and methods of use thereof |
| EP2054063A4 (en) * | 2006-08-22 | 2010-10-27 | Concert Pharmaceuticals Inc | 4-AMINOCHINAZOLINE DERIVATIVES AND METHOD FOR THEIR USE |
| JP5580592B2 (ja) * | 2006-09-11 | 2014-08-27 | キュリス,インコーポレイテッド | 亜鉛結合部分を含むキナゾリン系egfrインヒビター |
| US7547781B2 (en) | 2006-09-11 | 2009-06-16 | Curis, Inc. | Quinazoline based EGFR inhibitors containing a zinc binding moiety |
| US8119616B2 (en) | 2007-09-10 | 2012-02-21 | Curis, Inc. | Formulation of quinazoline based EGFR inhibitors containing a zinc binding moiety |
| US20090215802A1 (en) * | 2007-09-13 | 2009-08-27 | Protia, Llc | Deuterium-enriched lapatinib |
| JP5562865B2 (ja) | 2007-12-17 | 2014-07-30 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Trpv1のイミダゾロ−、オキサゾロ−、及びチアゾロピリミジン・モジュレーター |
| WO2009121042A1 (en) * | 2008-03-28 | 2009-10-01 | Concert Pharmaceuticals, Inc. | Quinazoline derivatives and methods of treatment |
| US8252805B2 (en) | 2008-05-07 | 2012-08-28 | Teva Pharmaceutical Industries Ltd. | Forms of lapatinib ditosylate and processes for preparation thereof |
| WO2010027848A2 (en) * | 2008-08-26 | 2010-03-11 | Teva Pharmaceutical Industries Ltd. | Forms of lapatinib compounds and processes for the preparation thereof |
| EP2328414B1 (en) * | 2008-08-29 | 2013-12-11 | Concert Pharmaceuticals Inc. | Substituted triazolo-pyridazine derivatives |
| WO2010027448A1 (en) * | 2008-09-02 | 2010-03-11 | Actimis Pharmaceuticals Inc. | Isotopically enriched pyrimidin-5-yl acetic acid derivatives as crth2 antagonists |
| WO2010028015A2 (en) * | 2008-09-03 | 2010-03-11 | Auspex Pharmaceuticals, Inc | 2-oxo-1,2-dihydro-quinoline modulators of immune function |
| CN101735200B (zh) * | 2008-11-17 | 2013-01-02 | 岑均达 | 喹唑啉类化合物 |
| US20110053968A1 (en) | 2009-06-09 | 2011-03-03 | Auspex Pharmaceuticals, Inc. | Aminopyrimidine inhibitors of tyrosine kinase |
| US8916574B2 (en) | 2009-09-28 | 2014-12-23 | Qilu Pharmaceutical Co., Ltd. | 4-(substituted anilino)-quinazoline derivatives useful as tyrosine kinase inhibitors |
| US20110195066A1 (en) * | 2010-02-05 | 2011-08-11 | Auspex Pharmaceuticals, Inc. | Quinoline inhibitors of tyrosine kinase |
| UY33226A (es) * | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina deuterada como inhibidores de la cdk4/6 |
| CN102453025B (zh) * | 2010-10-18 | 2014-08-13 | 齐鲁制药有限公司 | 拉帕替尼中间体晶型及其制备方法 |
| WO2012082337A2 (en) * | 2010-12-17 | 2012-06-21 | Glaxo Wellcome Manufacturing Pte Ltd | Combination |
| CZ2012712A3 (cs) | 2012-10-17 | 2014-04-30 | Zentiva, K.S. | Nový způsob výroby klíčového intermediátu výroby lapatinibu |
| US9024023B2 (en) | 2013-01-14 | 2015-05-05 | F.I.S.—Fabbrica Italiana Sintetici S.p.A. | Efficient process for the preparation of lapatinib and salts thereof by means of new intermediates |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6221335B1 (en) * | 1994-03-25 | 2001-04-24 | Isotechnika, Inc. | Method of using deuterated calcium channel blockers |
| JP4386967B2 (ja) * | 1996-07-13 | 2009-12-16 | グラクソ、グループ、リミテッド | プロテインチロシンキナーゼ阻害剤としての縮合複素環式化合物 |
| US6225318B1 (en) * | 1996-10-17 | 2001-05-01 | Pfizer Inc | 4-aminoquinazolone derivatives |
| GB9800569D0 (en) | 1998-01-12 | 1998-03-11 | Glaxo Group Ltd | Heterocyclic compounds |
| US6440710B1 (en) * | 1998-12-10 | 2002-08-27 | The Scripps Research Institute | Antibody-catalyzed deuteration, tritiation, dedeuteration or detritiation of carbonyl compounds |
| EP1104760B1 (en) * | 1999-12-03 | 2003-03-12 | Pfizer Products Inc. | Sulfamoylheteroaryl pyrazole compounds as anti-inflammatory/analgesic agents |
| TW200413273A (en) * | 2002-11-15 | 2004-08-01 | Wako Pure Chem Ind Ltd | Heavy hydrogenation method of heterocyclic rings |
| JP2007501809A (ja) * | 2003-08-08 | 2007-02-01 | ユリシーズ・ファーマシューティカル・プロダクツ・インコーポレイテッド | 抗菌剤としてのハロゲン化キナゾリニルニトロフラン |
| EP1682123A1 (en) * | 2003-11-07 | 2006-07-26 | SmithKline Beecham (Cork) Limited | Cancer treatment method |
| EP1768963A4 (en) * | 2004-06-03 | 2009-06-10 | Smithkline Beecham Cork Ltd | CANCER TREATMENT METHOD |
| WO2005120512A2 (en) * | 2004-06-04 | 2005-12-22 | Smithkline Beecham (Cork) Limited | Cancer treatment method |
| WO2006002422A2 (en) * | 2004-06-24 | 2006-01-05 | Novartis Vaccines And Diagnostics Inc. | Compounds for immunopotentiation |
| CA2624179A1 (en) * | 2005-10-06 | 2007-04-12 | Auspex Pharmaceuticals, Inc. | Deuterated inhibitors of gastric h+, k+-atpase with enhanced therapeutic properties |
| US7750168B2 (en) * | 2006-02-10 | 2010-07-06 | Sigma-Aldrich Co. | Stabilized deuteroborane-tetrahydrofuran complex |
| US20110053964A1 (en) * | 2006-08-22 | 2011-03-03 | Roger Tung | 4-aminoquinazoline derivatives and methods of use thereof |
| EP2054063A4 (en) * | 2006-08-22 | 2010-10-27 | Concert Pharmaceuticals Inc | 4-AMINOCHINAZOLINE DERIVATIVES AND METHOD FOR THEIR USE |
| WO2008030382A1 (en) * | 2006-09-05 | 2008-03-13 | Schering Corporation | Pharmaceutical combinations for lipid management and in the treatment of atherosclerosis and hepatic steatosis |
| US20090215802A1 (en) * | 2007-09-13 | 2009-08-27 | Protia, Llc | Deuterium-enriched lapatinib |
| WO2010005585A2 (en) * | 2008-07-09 | 2010-01-14 | Concert Pharmaceuticals Inc. | 4-aminoquinazoline prodrugs |
-
2007
- 2007-08-22 EP EP07811504A patent/EP2054063A4/en not_active Withdrawn
- 2007-08-22 CA CA002661223A patent/CA2661223A1/en not_active Abandoned
- 2007-08-22 KR KR1020097005957A patent/KR20090042994A/ko not_active Ceased
- 2007-08-22 CN CNA2007800393013A patent/CN101594870A/zh active Pending
- 2007-08-22 US US11/895,174 patent/US20080051422A1/en not_active Abandoned
- 2007-08-22 AU AU2007288204A patent/AU2007288204A1/en not_active Abandoned
- 2007-08-22 MX MX2009001814A patent/MX2009001814A/es active IP Right Grant
- 2007-08-22 WO PCT/US2007/018655 patent/WO2008024439A2/en not_active Ceased
- 2007-08-22 JP JP2009525631A patent/JP2010501572A/ja active Pending
-
2010
- 2010-09-02 US US12/874,981 patent/US20110097320A1/en not_active Abandoned
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102321076B (zh) * | 2011-07-07 | 2013-08-21 | 中国科学技术大学 | 拉帕替尼中间体及其类似物的制备方法 |
| CN102321076A (zh) * | 2011-07-07 | 2012-01-18 | 中国科学技术大学 | 拉帕替尼中间体及其类似物的制备方法 |
| CN102659764A (zh) * | 2012-04-16 | 2012-09-12 | 中国科学院广州生物医药与健康研究院 | 酪氨酸激酶不可逆抑制剂及其制备方法和用途 |
| CN102911164A (zh) * | 2012-11-07 | 2013-02-06 | 江苏金桥盐化集团利海化工有限公司 | 一种拉帕替尼关键中间体的制备方法 |
| CN103923070A (zh) * | 2013-01-14 | 2014-07-16 | 意大利合成制造有限公司 | 利用新中间体制备拉帕替尼及其盐的有效方法 |
| CN104513231A (zh) * | 2015-01-09 | 2015-04-15 | 安润医药科技(苏州)有限公司 | 拉帕替尼及其中间体的合成方法 |
| CN109414440A (zh) * | 2016-07-01 | 2019-03-01 | 亚狮康私人有限公司 | 用于治疗癌症的维持疗法 |
| CN111868039A (zh) * | 2017-09-26 | 2020-10-30 | 加利福尼亚大学董事会 | 用于治疗癌症的组合物和方法 |
| CN107827877A (zh) * | 2017-11-21 | 2018-03-23 | 陕西师范大学 | 二烷基氨基喹唑啉类化合物及其在制备抗肿瘤药物中的应用 |
| CN108285421A (zh) * | 2018-01-26 | 2018-07-17 | 黑龙江鑫创生物科技开发有限公司 | 一种微通道反应器合成拉帕替尼中间体的方法 |
| CN108187055A (zh) * | 2018-03-06 | 2018-06-22 | 北京大学 | 一种具有协同增效作用的抗癌组合物 |
| CN108690001A (zh) * | 2018-06-26 | 2018-10-23 | 苏州市贝克生物科技有限公司 | 拉帕替尼类似物的合成 |
| US12545686B2 (en) | 2021-09-23 | 2026-02-10 | Katmai Pharmaceuticals, Inc. | Polymorphic forms of (s)-n-(3-bromo-2-fluorophenyl)-7-((4-methylpiperazin-1-yl)methyl)-7,8-dihydro-[1,4]dioxino[2,3-g]quinazolin-4-amine as EGFR inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2007288204A1 (en) | 2008-02-28 |
| JP2010501572A (ja) | 2010-01-21 |
| CA2661223A1 (en) | 2008-02-28 |
| KR20090042994A (ko) | 2009-05-04 |
| EP2054063A4 (en) | 2010-10-27 |
| WO2008024439A2 (en) | 2008-02-28 |
| MX2009001814A (es) | 2009-03-02 |
| US20080051422A1 (en) | 2008-02-28 |
| EP2054063A2 (en) | 2009-05-06 |
| WO2008024439A3 (en) | 2009-02-26 |
| US20110097320A1 (en) | 2011-04-28 |
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Legal Events
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| C06 | Publication | ||
| PB01 | Publication | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Open date: 20091202 |