WO2004078748A3 - Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders - Google Patents

Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders Download PDF

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Publication number
WO2004078748A3
WO2004078748A3 PCT/US2004/006287 US2004006287W WO2004078748A3 WO 2004078748 A3 WO2004078748 A3 WO 2004078748A3 US 2004006287 W US2004006287 W US 2004006287W WO 2004078748 A3 WO2004078748 A3 WO 2004078748A3
Authority
WO
WIPO (PCT)
Prior art keywords
disorders
cancer
treatment
urea derivatives
derivatives useful
Prior art date
Application number
PCT/US2004/006287
Other languages
French (fr)
Other versions
WO2004078748A2 (en
Inventor
Jacques Dumas
Stephen Boyer
Sharad Verma
Lila Adnane
Yuanwei Chen
Wendy Lee
Barton Phillips
Roger A Smith
William J Scott
Jennifer Burke
Jianqing Chen
Zhi Chen
Jianmei Fan
Karl Miranda
Brian Raudenbush
Aniko Redman
Jianxing Shao
Ning Su
Gan Wang
Lin Yi
Qingming Zhu
Original Assignee
Bayer Pharmaceuticals Corp
Jacques Dumas
Stephen Boyer
Sharad Verma
Lila Adnane
Yuanwei Chen
Wendy Lee
Barton Phillips
Roger A Smith
William J Scott
Jennifer Burke
Jianqing Chen
Zhi Chen
Jianmei Fan
Karl Miranda
Brian Raudenbush
Aniko Redman
Jianxing Shao
Ning Su
Gan Wang
Lin Yi
Qingming Zhu
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 Bayer Pharmaceuticals Corp, Jacques Dumas, Stephen Boyer, Sharad Verma, Lila Adnane, Yuanwei Chen, Wendy Lee, Barton Phillips, Roger A Smith, William J Scott, Jennifer Burke, Jianqing Chen, Zhi Chen, Jianmei Fan, Karl Miranda, Brian Raudenbush, Aniko Redman, Jianxing Shao, Ning Su, Gan Wang, Lin Yi, Qingming Zhu filed Critical Bayer Pharmaceuticals Corp
Priority to MXPA05009104A priority Critical patent/MXPA05009104A/en
Priority to JP2006508978A priority patent/JP5229853B2/en
Priority to EP04716166A priority patent/EP1608639A2/en
Priority to CA2516931A priority patent/CA2516931C/en
Publication of WO2004078748A2 publication Critical patent/WO2004078748A2/en
Publication of WO2004078748A3 publication Critical patent/WO2004078748A3/en

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    • 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
    • C07D401/12—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 linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • 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
    • C07D401/14—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 three or more hetero 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
    • C07D405/12—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 chain containing hetero atoms as chain links
    • 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
    • C07D405/14—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 three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pyridine Compounds (AREA)

Abstract

This invention relates to novel diary) ureas, pharmaceutical compositions containing such compounds and the use of those compounds or compositions for treating hyper-proliferative and angiogenesis disorders, as a sole agent or in combination with cytotoxic therapies.
PCT/US2004/006287 2003-02-28 2004-03-01 Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders WO2004078748A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
MXPA05009104A MXPA05009104A (en) 2003-02-28 2004-03-01 Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders.
JP2006508978A JP5229853B2 (en) 2003-02-28 2004-03-01 Novel bicyclic urea derivatives useful for the treatment of cancer and other diseases
EP04716166A EP1608639A2 (en) 2003-02-28 2004-03-01 Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders
CA2516931A CA2516931C (en) 2003-02-28 2004-03-01 Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US45034803P 2003-02-28 2003-02-28
US60/450,348 2003-02-28

Publications (2)

Publication Number Publication Date
WO2004078748A2 WO2004078748A2 (en) 2004-09-16
WO2004078748A3 true WO2004078748A3 (en) 2004-11-11

Family

ID=32962496

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2004/006287 WO2004078748A2 (en) 2003-02-28 2004-03-01 Novel bicyclic urea derivatives useful in the treatment of cancer and other disorders

Country Status (5)

Country Link
EP (1) EP1608639A2 (en)
JP (1) JP5229853B2 (en)
CA (1) CA2516931C (en)
MX (1) MXPA05009104A (en)
WO (1) WO2004078748A2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7897623B2 (en) 1999-01-13 2011-03-01 Bayer Healthcare Llc ω-carboxyl aryl substituted diphenyl ureas as p38 kinase inhibitors
US8637553B2 (en) 2003-07-23 2014-01-28 Bayer Healthcare Llc Fluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions
US9181188B2 (en) 2002-02-11 2015-11-10 Bayer Healthcare Llc Aryl ureas as kinase inhibitors

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8124630B2 (en) 1999-01-13 2012-02-28 Bayer Healthcare Llc ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
EP2324825A1 (en) 2002-02-11 2011-05-25 Bayer Healthcare LLC Aryl ureas with angiogenesis inhibiting activity
ATE384264T1 (en) 2003-05-20 2008-02-15 Bayer Pharmaceuticals Corp DIARYL UREAS WITH KINASE-INHIBITING EFFECT
US7071182B2 (en) * 2003-12-23 2006-07-04 Abbott Laboratories Antagonists of melanin concentrating hormone effects on the melanin concentrating hormone receptor
JP2007523929A (en) * 2004-02-26 2007-08-23 メルク　パテント　ゲゼルシャフト　ミット　ベシュレンクテル　ハフトング Benzimidazolyl derivatives
EP1799661A1 (en) * 2004-10-08 2007-06-27 AstraZeneca AB New hydroxymethylbenzothiazoles amides
KR101335932B1 (en) 2005-03-07 2013-12-04 바이엘 헬스케어 엘엘씨 Pharmaceutical composition comprising an omega-carboxyaryl substituted diphenyl urea for the treatment of cancer
BRPI0502016B8 (en) * 2005-06-03 2021-05-25 Univ Federal Do Rio De Janeiro Ufrj ureid compounds, pharmaceutical compositions containing them and their use in the treatment of inflammatory diseases
MX2008011857A (en) 2006-03-23 2008-12-15 Prolysis Ltd Antibacterial agents.
DE102006029795A1 (en) * 2006-06-27 2008-01-03 Schebo Biotech Ag New urea derivatives and their uses
EP2134677B1 (en) 2006-12-20 2011-10-12 Bayer HealthCare LLC 4-{4-[({3-tert-butyl-1-[3-(hydroxymethyl)phenyl]-1h-pyrazol-5-yl}carbamoyl)-amino]-3-chlorophenoxy}-n-methylpyridine-2-carboxamide as an inhibitor of the vegfr kinase for the treatment of cancer
WO2009021965A2 (en) 2007-08-15 2009-02-19 Glaxo Group Limited Substituted quinoline derivatives as h1 receptor antagonists
CN102295600A (en) * 2011-09-08 2011-12-28 天津大学 Method for preparing 5-amino-8-hydroxyquinoline
US9725427B2 (en) 2012-03-16 2017-08-08 Biohaven Pharmaceutical Holding Company Limited Prodrugs of riluzole and their method of use
CN103508961B (en) * 2012-06-26 2015-07-22 中美冠科生物技术（太仓）有限公司 Antitumor drug
CN104250226B (en) * 2013-06-27 2019-04-26 常州方楠医药技术有限公司 A method of preparing Rui Gefeini intermediate
WO2017047803A1 (en) * 2015-09-17 2017-03-23 三栄源エフ・エフ・アイ株式会社 Production method for polysaccharide thickener-containing preparation
WO2018035346A1 (en) * 2016-08-17 2018-02-22 Ichan School Of Medicine At Mount Sinal Kinase inhibitor compounds, compositions, and methods of treating cancer

Citations (6)

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WO1999024035A1 (en) * 1997-11-10 1999-05-20 Bristol-Myers Squibb Company Benzothiazole protein tyrosine kinase inhibitors
WO1999032106A1 (en) * 1997-12-22 1999-07-01 Bayer Corporation Inhibition of raf kinase using substituted heterocyclic ureas
WO2000042012A1 (en) * 1999-01-13 2000-07-20 Bayer Corporation φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS
WO2001036403A1 (en) * 1999-11-16 2001-05-25 Boehringer Ingelheim Pharmaceuticals, Inc. Urea derivatives as anti-inflammatory agents
WO2002062763A2 (en) * 2001-02-07 2002-08-15 Bayer Corporation Inhibition of raf kinase using quinolyl isoquinolyl or pyridyl ureas
WO2003068228A1 (en) * 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Aryl ureas with angiogenesis inhibiting activity

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US6001930A (en) 1997-03-13 1999-12-14 Acushnet Company Golf ball forming compositions comprising polyamide blended with sulfonated or phosphonated polymers
DK1043995T3 (en) 1997-12-22 2007-03-05 Bayer Pharmaceuticals Corp Inhibition of p38 kinase activity using aryl- and heteroaryl-substituted heterocyclic ureas
IL136738A0 (en) 1997-12-22 2001-06-14 Bayer Ag Inhibition of p38 kinase activity using substituted heterocyclic ureas
AU1939999A (en) 1997-12-22 1999-07-12 Bayer Corporation Inhibition of p38 kinase using symmetrical and unsymmetrical diphenyl ureas
AU765412B2 (en) 1997-12-22 2003-09-18 Bayer Healthcare Llc Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas
CA2315646C (en) 1997-12-22 2010-02-09 Bayer Corporation Inhibition of raf kinase using symmetrical and unsymmetrical substituted diphenyl ureas
IL144144A0 (en) * 1999-01-13 2002-05-23 Bayer Ag Omega-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors
ME00275B (en) * 1999-01-13 2011-02-10 Bayer Corp ?-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
US20020065296A1 (en) * 1999-01-13 2002-05-30 Bayer Corporation Heteroaryl ureas containing nitrogen hetero-atoms as p38 kinase inhibitors
PT1598340E (en) 2001-04-18 2009-04-13 Euro Celtique Sa 1-(4-piperidinyl)-1,3-dihydro-2h-benzoxazole-2-one derivatives and related compounds as nociceptin analogs and orl1 ligands for the treatment of pain
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MXPA05009102A (en) * 2003-02-28 2006-05-31 Bayer Pharmaceuticals Corp Substituted pyridine derivatives useful in the treatment of cancer and other disorders.

Patent Citations (6)

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WO1999024035A1 (en) * 1997-11-10 1999-05-20 Bristol-Myers Squibb Company Benzothiazole protein tyrosine kinase inhibitors
WO1999032106A1 (en) * 1997-12-22 1999-07-01 Bayer Corporation Inhibition of raf kinase using substituted heterocyclic ureas
WO2000042012A1 (en) * 1999-01-13 2000-07-20 Bayer Corporation φ-CARBOXYARYL SUBSTITUTED DIPHENYL UREAS AS RAF KINASE INHIBITORS
WO2001036403A1 (en) * 1999-11-16 2001-05-25 Boehringer Ingelheim Pharmaceuticals, Inc. Urea derivatives as anti-inflammatory agents
WO2002062763A2 (en) * 2001-02-07 2002-08-15 Bayer Corporation Inhibition of raf kinase using quinolyl isoquinolyl or pyridyl ureas
WO2003068228A1 (en) * 2002-02-11 2003-08-21 Bayer Pharmaceuticals Corporation Aryl ureas with angiogenesis inhibiting activity

Non-Patent Citations (2)

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Title
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HOTTE S J ET AL: "BAY 43-9006: EARLY CLINICAL DATA IN PATIENTS WITH ADVANCED SOLID MALIGNANCIES", CURRENT PHARMACEUTICAL DESIGN, BENTHAM SCIENCE PUBLISHERS, SCHIPHOL, NL, vol. 8, no. 25, 2002, pages 2249 - 2253, XP001145745, ISSN: 1381-6128 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7897623B2 (en) 1999-01-13 2011-03-01 Bayer Healthcare Llc ω-carboxyl aryl substituted diphenyl ureas as p38 kinase inhibitors
US9181188B2 (en) 2002-02-11 2015-11-10 Bayer Healthcare Llc Aryl ureas as kinase inhibitors
US8637553B2 (en) 2003-07-23 2014-01-28 Bayer Healthcare Llc Fluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions

Also Published As

Publication number Publication date
CA2516931A1 (en) 2004-09-16
JP2006519265A (en) 2006-08-24
EP1608639A2 (en) 2005-12-28
WO2004078748A2 (en) 2004-09-16
JP5229853B2 (en) 2013-07-03
MXPA05009104A (en) 2006-05-31
CA2516931C (en) 2014-09-09

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