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AU2002218167A1 - N-phenyl-2-pyrimidine-amine derivatives - Google Patents

N-phenyl-2-pyrimidine-amine derivatives

Info

Publication number
AU2002218167A1
AU2002218167A1 AU2002218167A AU1816702A AU2002218167A1 AU 2002218167 A1 AU2002218167 A1 AU 2002218167A1 AU 2002218167 A AU2002218167 A AU 2002218167A AU 1816702 A AU1816702 A AU 1816702A AU 2002218167 A1 AU2002218167 A1 AU 2002218167A1
Authority
AU
Australia
Prior art keywords
pyrimidine
phenyl
amine derivatives
preparation
medicaments
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
AU2002218167A
Inventor
Werner Breitenstein
Hans Michael Buerger
Giorgio Caravatti
Margaret Amelia Cudd
Paul William Manley
Juerg Zimmermann
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.)
Novartis AG
Original Assignee
Novartis AG
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9899367&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AU2002218167(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis AG filed Critical Novartis AG
Publication of AU2002218167A1 publication Critical patent/AU2002218167A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen 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
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Liquid Crystal Substances (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention relates to N-phenyl-2-pyrimidine-amine derivatives of formula I wherein the substituents are defined as indicated in the description, to processes for the preparation thereof, to medicaments comprising those compounds, and to the use thereof in the preparation of pharmaceutical compositions for the therapeutic treatment of warm-blooded animals, including humans.
AU2002218167A 2000-09-13 2001-09-11 N-phenyl-2-pyrimidine-amine derivatives Abandoned AU2002218167A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0022438 2000-09-13
GBGB0022438.6A GB0022438D0 (en) 2000-09-13 2000-09-13 Organic Compounds
PCT/EP2001/010503 WO2002022597A1 (en) 2000-09-13 2001-09-11 N-phenyl-2-pyrimidine-amine derivatives

Publications (1)

Publication Number Publication Date
AU2002218167A1 true AU2002218167A1 (en) 2002-03-26

Family

ID=9899367

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2002218167A Abandoned AU2002218167A1 (en) 2000-09-13 2001-09-11 N-phenyl-2-pyrimidine-amine derivatives

Country Status (13)

Country Link
US (3) US7081532B2 (en)
EP (1) EP1322634B1 (en)
JP (1) JP2004509111A (en)
CN (2) CN100406452C (en)
AT (1) ATE452129T1 (en)
AU (1) AU2002218167A1 (en)
BR (1) BR0113838A (en)
CA (2) CA2416274C (en)
DE (1) DE60140814D1 (en)
ES (1) ES2336891T3 (en)
GB (1) GB0022438D0 (en)
PT (1) PT1322634E (en)
WO (1) WO2002022597A1 (en)

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GB0022438D0 (en) * 2000-09-13 2000-11-01 Novartis Ag Organic Compounds
WO2003000186A2 (en) 2001-06-21 2003-01-03 Ariad Pharmaceuticals, Inc. Novel phenylamino-pyrimidines and uses thereof
GB0201508D0 (en) * 2002-01-23 2002-03-13 Novartis Ag Organic compounds
US7494997B2 (en) 2002-06-28 2009-02-24 Nippon Shinyaku Co., Ltd. Amide derivative
CA2494061C (en) * 2002-07-31 2011-06-14 Wayne R. Danter Protein tyrosine kinase inhibitors
CA2439440A1 (en) 2002-09-05 2004-03-05 Emory University Treatment of tuberous sclerosis associated neoplasms
GB0222514D0 (en) 2002-09-27 2002-11-06 Novartis Ag Organic compounds
WO2004033446A1 (en) * 2002-10-09 2004-04-22 Danter Wayne R Protein tyrosine kinase inhibitors
AU2003232650A1 (en) * 2003-05-06 2004-11-26 Il Yang Pharm Co., Ltd. N-phenyl-2-pyrimidine-amine derivatives and process for the preparation thereof
WO2004108699A1 (en) * 2003-06-06 2004-12-16 Natco Pharma Limited Process for the preparation of the anti-cancer drug imatinib and its analogues
JP2006527230A (en) * 2003-06-13 2006-11-30 ノバルティス アクチエンゲゼルシャフト 2-Aminopyrimidine derivatives as RAF kinase inhibitors
MXPA06007237A (en) 2003-12-25 2006-08-18 Nippon Shinyaku Co Ltd Amide derivative and medicine.
JPWO2005063720A1 (en) * 2003-12-25 2007-07-19 日本新薬株式会社 Amide derivatives and pharmaceuticals
PE20051096A1 (en) * 2004-02-04 2006-01-23 Novartis Ag SALT FORMS OF 4- (4-METHYLPIPERAZIN-1-ILMETHYL) -N- [4-METHYL-3- (4-PYRIDIN-3-IL) PYRIMIDIN-2-ILAMINO) PHENYL] -BENZAMIDE
WO2006017353A2 (en) * 2004-07-13 2006-02-16 GOVERNMENT OF THE UNITED STATES, as represented byTHE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES Treatment of viral infections
US8735415B2 (en) 2004-09-09 2014-05-27 Natco Pharma Limited Acid addition salts of (3,5-Bis trifluoromethyl)-N-[4-methyl-3-(4-pyridin-3yl-pyrimidin-2ylamino)-phenyl]-benzamide
EA013328B1 (en) 2004-09-09 2010-04-30 Натко Фарма Лимитед Novel phenylaminopyrimidine derivatives as inhibitors of bcr-abl kinase
US7939541B2 (en) * 2004-09-09 2011-05-10 Natco Pharma Limited Intermediates and a process employing the intermediates for the preparation of (3-trifluoromethylsulfonyl)-N-[4-methyl-3-(4-pyridin-3yl-pyrimidin-2ylamino)-phenyl]-benzamide
CN1939910A (en) * 2004-12-31 2007-04-04 孙飘扬 Amino-metadiazine compound and its salt, its preparation and pharmaceutical use
CN1972917B (en) * 2004-12-31 2010-08-25 孙飘扬 Aminopyrimidine compound and its salt, its preparation method and pharmaceutical use
GB0512091D0 (en) * 2005-06-14 2005-07-20 Novartis Ag Organic compounds
JP2008546729A (en) * 2005-06-23 2008-12-25 ノバルティス アクチエンゲゼルシャフト Treatment of solid tumor disease comprising administering imatinib and an inhibitor of an efflux pump active at the blood brain barrier or a combination comprising demethylimatinib
KR100674813B1 (en) * 2005-08-05 2007-01-29 일양약품주식회사 N-phenyl-2-pyrimidine-amine derivatives and preparation method thereof
NZ566862A (en) * 2005-09-27 2010-12-24 Irm Llc Diarylamine-containing compounds and compositions, and their use as modulators of C-kit receptors
US8067421B2 (en) * 2006-04-27 2011-11-29 Sicor Inc. Polymorphic forms of imatinib mesylate and processes for preparation of novel crystalline forms as well as amorphous and form α
US7977348B2 (en) * 2006-04-27 2011-07-12 Sicor Inc. Polymorphic forms of imatinib mesylate and processes for preparation of novel crystalline forms as well as amorphous and form α
UA93548C2 (en) 2006-05-05 2011-02-25 Айерем Елелсі Compounds and compositions as hedgehog pathway modulators
MX2009002336A (en) * 2006-09-01 2009-03-20 Teva Pharma Imatinib compositions.
CA2662677C (en) 2006-09-05 2016-05-31 Emory University Kinase inhibitors for preventing or treating pathogen infection and method of use thereof
KR20090061055A (en) * 2006-10-26 2009-06-15 시코르, 인크. Crystalline and amorphous imatinib bases, imatinib mesylate and methods for their preparation
EP1988089A1 (en) 2006-10-26 2008-11-05 Sicor, Inc. Imatinib base, and imatinib mesylate and processes for preparation thereof
US8034815B2 (en) 2007-01-11 2011-10-11 Critical Outcome Technologies, Inc. Compounds and method for treatment of cancer
KR101122481B1 (en) * 2007-05-04 2012-02-29 아이알엠 엘엘씨 Pyrimidine derivatives and compositions as c-kit and pdgfr kinase inhibitors
US20090012296A1 (en) * 2007-05-29 2009-01-08 Alexandr Jegorov Processes for the preparation of crystalline form beta of imatinib mesylate
CA2689989A1 (en) * 2007-06-04 2008-12-11 Avila Therapeutics, Inc. Heterocyclic compounds and uses thereof
BRPI0815572A2 (en) 2007-08-22 2015-02-18 Irm Llc COMPOUNDS AND COMPOSITIONS AS KINASE INHIBITORS
WO2009026276A1 (en) * 2007-08-22 2009-02-26 Irm Llc 5- (4- (haloalkoxy) phenyl) pyrimidine-2-amine compounds and compositions as kinase inhibitors
US20090087489A1 (en) * 2007-09-25 2009-04-02 Bella Gerber Imatinib compositions
CA2710039C (en) 2007-12-26 2018-07-03 Critical Outcome Technologies, Inc. Semicarbazones, thiosemicarbazones and related compounds and methods for treatment of cancer
EP2240175B1 (en) * 2008-02-11 2013-01-02 The Government of the United States of America as represented by the Secretary of the Department of Health and Human Services Compounds with mdr1-inverse activity
MX2010008926A (en) 2008-02-15 2011-02-23 Rigel Pharmaceuticals Inc Pyrimidine-2-amine compounds and their use as inhibitors of jak kinases.
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
PL2300013T5 (en) 2008-05-21 2025-04-28 Takeda Pharmaceutical Company Limited Phosphorous derivatives as kinase inhibitors
KR20160011713A (en) * 2008-06-27 2016-02-01 인디애나 유니버시티 리서치 앤드 테크놀로지 코포레이션 Materials and methods for suppressing and/or treating neurofibroma and related tumors
WO2010006438A1 (en) 2008-07-17 2010-01-21 Critical Outcome Technologies Inc. Thiosemicarbazone inhibitor compounds and cancer treatment methods
CN101417995B (en) * 2008-11-21 2012-06-06 陈依军 Phenoxy pyrimidine derivates and preparation method and use thereof
EP2419425A4 (en) 2009-04-15 2012-08-29 Astrazeneca Ab Imidazole substituted pyrimidines useful in the treatment of glycogen synthase kinase 3 related disorders such as alzheimer's disease
US8816077B2 (en) 2009-04-17 2014-08-26 Nektar Therapeutics Oligomer-protein tyrosine kinase inhibitor conjugates
WO2010120386A1 (en) 2009-04-17 2010-10-21 Nektar Therapeutics Oligomer-protein tyrosine kinase inhibitor conjugates
US8987272B2 (en) 2010-04-01 2015-03-24 Critical Outcome Technologies Inc. Compounds and method for treatment of HIV
CN102212057B (en) * 2011-04-13 2013-11-27 合肥工业大学 A kind of carboxylic acid non-steroidal anti-inflammatory drug derivative and its preparation method and application
EP2704572B1 (en) 2011-05-04 2015-12-30 Ariad Pharmaceuticals, Inc. Compounds for inhibiting cell proliferation in egfr-driven cancers
CN102796110B (en) * 2011-05-23 2016-03-30 复旦大学 Aniline pyrimidine compound and its production and use
JP6469567B2 (en) 2012-05-05 2019-02-13 アリアド・ファーマシューティカルズ・インコーポレイテッド Compound for inhibiting cell proliferation of EGFR-activated cancer
CN103044394A (en) * 2012-12-20 2013-04-17 北京理工大学 Phenyl aminopyrimidine derivant and preparation method and application thereof
CN103058935B (en) * 2013-01-15 2015-05-06 四川大学 Pyrimidine compound as well as preparation method and use for same
US9611283B1 (en) 2013-04-10 2017-04-04 Ariad Pharmaceuticals, Inc. Methods for inhibiting cell proliferation in ALK-driven cancers
CN105859683B (en) * 2016-04-11 2018-09-28 连云港恒运药业有限公司 The high-purity technical preparation process of Imatinib
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CN107652266A (en) * 2017-10-27 2018-02-02 上海应用技术大学 One kind targeting EGFR-TK micromolecular inhibitor and its application
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CN110078708B (en) * 2019-05-08 2020-12-11 东南大学 Smo/Bcr-Abl dual-targeted inhibitor and its synthesis method and application

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US5521184A (en) * 1992-04-03 1996-05-28 Ciba-Geigy Corporation Pyrimidine derivatives and processes for the preparation thereof
TW225528B (en) 1992-04-03 1994-06-21 Ciba Geigy Ag
GB9914258D0 (en) 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
GB0022438D0 (en) * 2000-09-13 2000-11-01 Novartis Ag Organic Compounds

Also Published As

Publication number Publication date
CA2416274C (en) 2011-01-04
US7329661B2 (en) 2008-02-12
DE60140814D1 (en) 2010-01-28
CA2687476A1 (en) 2002-03-21
GB0022438D0 (en) 2000-11-01
BR0113838A (en) 2003-06-03
PT1322634E (en) 2010-02-22
US20060223818A1 (en) 2006-10-05
US7312216B2 (en) 2007-12-25
CN1525967A (en) 2004-09-01
US20040102453A1 (en) 2004-05-27
EP1322634B1 (en) 2009-12-16
US20070265292A1 (en) 2007-11-15
ATE452129T1 (en) 2010-01-15
US7081532B2 (en) 2006-07-25
HK1057752A1 (en) 2004-04-16
CN100406452C (en) 2008-07-30
EP1322634A1 (en) 2003-07-02
WO2002022597A1 (en) 2002-03-21
CN1872850A (en) 2006-12-06
CA2416274A1 (en) 2002-03-21
ES2336891T3 (en) 2010-04-19
JP2004509111A (en) 2004-03-25

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