CA2661223A1 - 4-aminoquinazoline derivatives and methods of use thereof - Google Patents

4-aminoquinazoline derivatives and methods of use thereof Download PDF

Info

Publication number
CA2661223A1
CA2661223A1 CA002661223A CA2661223A CA2661223A1 CA 2661223 A1 CA2661223 A1 CA 2661223A1 CA 002661223 A CA002661223 A CA 002661223A CA 2661223 A CA2661223 A CA 2661223A CA 2661223 A1 CA2661223 A1 CA 2661223A1
Authority
CA
Canada
Prior art keywords
compound
cancer
subject
carcinoma
mmol
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.)
Abandoned
Application number
CA002661223A
Other languages
English (en)
French (fr)
Inventor
Roger Tung
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Concert Pharmaceuticals Inc
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of CA2661223A1 publication Critical patent/CA2661223A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/10Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/04Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Transplantation (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
CA002661223A 2006-08-22 2007-08-22 4-aminoquinazoline derivatives and methods of use thereof Abandoned CA2661223A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US83950306P 2006-08-22 2006-08-22
US60/839,503 2006-08-22
PCT/US2007/018655 WO2008024439A2 (en) 2006-08-22 2007-08-22 4-aminoquinazoline derivatives and methods of use thereof

Publications (1)

Publication Number Publication Date
CA2661223A1 true CA2661223A1 (en) 2008-02-28

Family

ID=39107412

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002661223A Abandoned CA2661223A1 (en) 2006-08-22 2007-08-22 4-aminoquinazoline derivatives and methods of use thereof

Country Status (9)

Country Link
US (2) US20080051422A1 (OSRAM)
EP (1) EP2054063A4 (OSRAM)
JP (1) JP2010501572A (OSRAM)
KR (1) KR20090042994A (OSRAM)
CN (1) CN101594870A (OSRAM)
AU (1) AU2007288204A1 (OSRAM)
CA (1) CA2661223A1 (OSRAM)
MX (1) MX2009001814A (OSRAM)
WO (1) WO2008024439A2 (OSRAM)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20090042994A (ko) * 2006-08-22 2009-05-04 콘서트 파마슈티컬즈, 인크. 4-아미노퀴나졸린 유도체 및 이의 사용방법
US20110053964A1 (en) * 2006-08-22 2011-03-03 Roger Tung 4-aminoquinazoline derivatives and methods of use thereof
US7547781B2 (en) 2006-09-11 2009-06-16 Curis, Inc. Quinazoline based EGFR inhibitors containing a zinc binding moiety
US8604044B2 (en) 2006-09-11 2013-12-10 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
CL2008003749A1 (es) 2007-12-17 2010-01-15 Janssen Pharmaceutica Nv Compuestos derivados de imidazol, oxazol, y tiazol pirimidina, moduladores de trpv1, proceso de preparacion, composicion farmaceutica y su uso en el tratamiento de enfermedades, trastornos o condicion de dolor, prurito, artritis, tos, asma, trastorno del oido interno y enfermedad inflamatoria intestinal, entre otras.
KR20110005828A (ko) * 2008-03-28 2011-01-19 콘서트 파마슈티컬즈, 인크. 퀴나졸린 유도체 및 치료방법
WO2009137714A2 (en) * 2008-05-07 2009-11-12 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
MX2011002278A (es) * 2008-08-29 2011-04-14 Concert Pharmaceuticals Inc Derivados de triazolo-piridazina sustituidos.
JP5586606B2 (ja) * 2008-09-02 2014-09-10 アクチミス ファーマシューティカルズ インコーポレーテッド Crth2アンタゴニストとしての同位体富化されたピリミジン−5−イル酢酸誘導体
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
ES2535176T3 (es) 2009-09-28 2015-05-06 Qilu Pharmaceutical Co., Ltd Derivados de 4-(anilino sustituido)quinazolina como inhibidores de la tirosina quinasa
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
JP6013359B2 (ja) * 2010-12-17 2016-10-25 ノバルティス アーゲー 組合せ
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
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
CZ2012712A3 (cs) 2012-10-17 2014-04-30 Zentiva, K.S. Nový způsob výroby klíčového intermediátu výroby lapatinibu
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
ITVI20130003A1 (it) * 2013-01-14 2014-07-14 F I S Fabbrica Italiana Sint I S P A Procedimento per la preparazione di lapatinib e suoi sali mediante nuovi intermedi.
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
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
GB201611580D0 (en) * 2016-07-01 2016-08-17 Aslan Pharmaceuticals Pte Ltd Method
EP3687981A4 (en) * 2017-09-26 2021-03-31 The Regents of the University of California COMPOSITIONS AND METHODS OF TREATMENT OF CANCER
CN107827877B (zh) * 2017-11-21 2021-05-07 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
CN108187055B (zh) * 2018-03-06 2019-12-27 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

Family Cites Families (19)

* Cited by examiner, † Cited by third party
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
WO1998002434A1 (en) * 1996-07-13 1998-01-22 Glaxo Group Limited Fused heterocyclic compounds as protein tyrosine kinase inhibitors
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
DE60001623T2 (de) * 1999-12-03 2003-12-18 Pfizer Products Inc., Groton Sulfamoylheteroarylpyrazolverbindungen zur Verwendung als analgetisches/entzündungshemmendes Mittel
TW200413273A (en) * 2002-11-15 2004-08-01 Wako Pure Chem Ind Ltd Heavy hydrogenation method of heterocyclic rings
US7410974B2 (en) * 2003-08-08 2008-08-12 Ulysses Pharmaceutical Products, Inc. Halogenated Quinazolinyl nitrofurans as antibacterial agents
EP1682123A1 (en) * 2003-11-07 2006-07-26 SmithKline Beecham (Cork) Limited Cancer treatment method
US20100063074A1 (en) * 2004-06-03 2010-03-11 Berger Mark S Cancer Treatment Method
CA2569139A1 (en) * 2004-06-04 2005-12-22 Smithkline Beecham (Cork) Limited Lapatinib with letrozole for use in a treatment of breast cancer
JP2008504292A (ja) * 2004-06-24 2008-02-14 ノバルティス ヴァクシンズ アンド ダイアグノスティクス, インコーポレイテッド 免疫増強用の化合物
BRPI0617987A2 (pt) * 2005-10-06 2011-08-16 Auspex Pharmaceuticals Inc composição, composição farmacêutica, forma de dosagem efervescente, composição farmacêutica oral de comprimidos unitários múltiplos, forma de dosagem farmacêutica de liberação prolongada, forma de dosagem farmacêutica revestida entérica, forma de dosagem farmacêutica estável para administração oral a sujeitos mamìferos, método para tratamento de doenças relacionadas a ácido gástrico pela inibição de secreção de ácido gástrico, método para tratamento de uma infecção bacteriana provocada ou mediada por helicobacter pylori, processo para preparar um composto da fórmula 3, processo para preparar um composto da fórmula 5, uso de um composto da fórmula 1 para a preparação de um medicamento para tratamento de doenças relacionadas a ácido gástrico, pela inibição de secreção de ácido gástrico, uso de um composto da fórmula 1 para a preparação de um medicamento para tratamento de uma infecção bacteriana provocada ou mediada por helicobacter pylori uso de um composto da fórmula 1 para a preparação de um medicamento para tratamento de doenças relecionadas a ácido gástrico pela inibição de secreção de ácido gástrico
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
KR20090042994A (ko) * 2006-08-22 2009-05-04 콘서트 파마슈티컬즈, 인크. 4-아미노퀴나졸린 유도체 및 이의 사용방법
CA2661404A1 (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

Also Published As

Publication number Publication date
US20110097320A1 (en) 2011-04-28
CN101594870A (zh) 2009-12-02
AU2007288204A1 (en) 2008-02-28
US20080051422A1 (en) 2008-02-28
EP2054063A4 (en) 2010-10-27
KR20090042994A (ko) 2009-05-04
MX2009001814A (es) 2009-03-02
WO2008024439A2 (en) 2008-02-28
WO2008024439A3 (en) 2009-02-26
JP2010501572A (ja) 2010-01-21
EP2054063A2 (en) 2009-05-06

Similar Documents

Publication Publication Date Title
CA2661223A1 (en) 4-aminoquinazoline derivatives and methods of use thereof
US20110053964A1 (en) 4-aminoquinazoline derivatives and methods of use thereof
KR102738278B1 (ko) 글루카곤-유사 펩티드 1 수용체 효능제
JP6728447B2 (ja) Ret(rearranged during transfection)キナーゼ阻害剤としてのピリジン誘導体
DK2566327T3 (en) indoles
TWI604844B (zh) 新的羥基酯衍生物,其製備之方法及含其之醫藥組成物
JP6924794B2 (ja) 結晶質n−{(1s)−2−アミノ−1−[(3−フルオロフェニル)メチル]エチル}−5−クロロ−4−(4−クロロ−1−メチル−1h−ピラゾール−5−イル)−2−チオフェンカルボキサミド塩酸塩
CN106083714B (zh) N-(4-{[6,7-双(甲基氧基)喹啉-4-基]氧基}苯基)-n′-(4-氟苯基)环丙烷-1,1-二甲酰胺苹果酸盐及其结晶型
JP6016284B2 (ja) ジスピロピロリジン誘導体の結晶
CN104768555B (zh) 用于治疗癌症的联合治疗
US9382234B2 (en) Enhancer of Zeste Homolog 2 inhibitors
NO317093B1 (no) Substituerte kinazolinderivater og anvendelse derav som tyrosin-kinase-inhibitorer
CN102112465A (zh) 6-[(4s)-2-甲基-4-(2-萘基)-1,2,3,4-四氢异喹啉-7-基]哒嗪-3-胺的晶型
US20160130261A1 (en) Enhancer of zeste homolog 2 inhibitors
CN110603256A (zh) 可用作wee-1激酶抑制剂的嘧啶并嘧啶酮
KR20170068603A (ko) 제스트 인핸서 상동체 2 억제제
WO2011153942A1 (zh) 氰基喹啉衍生物
WO2013177349A2 (en) Quinazolinediones as tankyrase inhibitors
US9718810B2 (en) Solid state forms of a quinazoline derivative and its use as a BRAF inhibitor
CN110573503A (zh) 作为plk1抑制剂的吡咯衍生物
KR101789934B1 (ko) 상피세포성장인자수용체 변이체를 가진 종양 진단 및 종양 성장 억제 활성을 갖는 신규 화합물 및 이를 포함하는 의학적 용도
Yu et al. Design, synthesis and antitumor activity of 4-aminoquinazoline derivatives targeting VEGFR-2 tyrosine kinase
AU2006315684A1 (en) Substituted phenylpiperidines with serotoninergic activity and enhanced therapeutic properties
KR100843533B1 (ko) 신규한 디아진 유도체, 이의 제조 및 약학적 제제로서의용도
JP2006515347A (ja) 新規アニリン誘導体類、それらの製造及び医薬剤としての使用

Legal Events

Date Code Title Description
EEER Examination request
FZDE Discontinued

Effective date: 20150310