WO2005028434A2 - Novel heterocyclic compounds as hsp90-inhibitors - Google Patents

Novel heterocyclic compounds as hsp90-inhibitors Download PDF

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Publication number
WO2005028434A2
WO2005028434A2 PCT/US2004/031248 US2004031248W WO2005028434A2 WO 2005028434 A2 WO2005028434 A2 WO 2005028434A2 US 2004031248 W US2004031248 W US 2004031248W WO 2005028434 A2 WO2005028434 A2 WO 2005028434A2
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WIPO (PCT)
Prior art keywords
compound
aryl
heteroaryl
group
tautomer
Prior art date
Application number
PCT/US2004/031248
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English (en)
French (fr)
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WO2005028434A3 (en
Inventor
Srinivas R. Kasibhatla
Marcus F. Boehm
Kevin D. Hong
Marco A. Biamonte
Jiandong Shi
Jean-Yves Le Brazidec
Lin Zhang
David Hurst
Original Assignee
Conforma Therapeutics Corporation
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
Priority to BRPI0414533-0A priority Critical patent/BRPI0414533A/pt
Priority to EA200600594A priority patent/EA010160B1/ru
Priority to MXPA06002997A priority patent/MXPA06002997A/es
Priority to CA002539548A priority patent/CA2539548A1/en
Priority to JP2006527162A priority patent/JP2007505933A/ja
Priority to EP04788954A priority patent/EP1670802A4/en
Priority to NZ546611A priority patent/NZ546611A/en
Priority to AU2004274507A priority patent/AU2004274507B2/en
Application filed by Conforma Therapeutics Corporation filed Critical Conforma Therapeutics Corporation
Priority to CN2004800335230A priority patent/CN1882589B/zh
Publication of WO2005028434A2 publication Critical patent/WO2005028434A2/en
Priority to IL174375A priority patent/IL174375A0/en
Publication of WO2005028434A3 publication Critical patent/WO2005028434A3/en
Priority to NO20061396A priority patent/NO20061396L/no
Priority to AU2010202750A priority patent/AU2010202750B2/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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    • AHUMAN NECESSITIES
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/18Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/24Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one nitrogen and one sulfur atom
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/32Nitrogen atom

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  • Plural Heterocyclic Compounds (AREA)
PCT/US2004/031248 2003-09-18 2004-09-20 Novel heterocyclic compounds as hsp90-inhibitors WO2005028434A2 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
NZ546611A NZ546611A (en) 2003-09-18 2004-09-20 Novel heterocyclic compounds as HSP90-inhibitors
MXPA06002997A MXPA06002997A (es) 2003-09-18 2004-09-20 Novedosos compuestos heterociclicos como inhibidores- hsp90.
CA002539548A CA2539548A1 (en) 2003-09-18 2004-09-20 Novel heterocyclic compounds as hsp90-inhibitors
JP2006527162A JP2007505933A (ja) 2003-09-18 2004-09-20 Hsp90インヒビターとしての新規なヘテロ環化合物
EP04788954A EP1670802A4 (en) 2003-09-18 2004-09-20 NOVEL HETEROCYCLIC COMPOUNDS AS INHIBITORS OF HSP90 PROTEIN
BRPI0414533-0A BRPI0414533A (pt) 2003-09-18 2004-09-20 composto, composição farmacêutica, e, métodos para inibir um hsp90 e para tratar um indivìduo tendo um distúrbio mediado por hsp90
AU2004274507A AU2004274507B2 (en) 2003-09-18 2004-09-20 Novel heterocyclic compounds as HSP90-inhibitors
EA200600594A EA010160B1 (ru) 2003-09-18 2004-09-20 Новые гетероциклические соединения - ингибиторы hsp90 и способы их получения
CN2004800335230A CN1882589B (zh) 2003-09-18 2004-09-20 作为hsp90-抑制剂的新的杂环化合物
IL174375A IL174375A0 (en) 2003-09-18 2006-03-16 Novel heterocyclic compounds as hsp90-inhibitors
NO20061396A NO20061396L (no) 2003-09-18 2006-03-27 Nye heterocykliske forbindelser som HSP90-inhibitorer
AU2010202750A AU2010202750B2 (en) 2003-09-18 2010-06-30 Novel heterocyclic compounds as HSP90-inhibitors

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US50413503P 2003-09-18 2003-09-18
US60/504,135 2003-09-18
US59146704P 2004-07-26 2004-07-26
US60/591,467 2004-07-26

Publications (2)

Publication Number Publication Date
WO2005028434A2 true WO2005028434A2 (en) 2005-03-31
WO2005028434A3 WO2005028434A3 (en) 2006-03-23

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Application Number Title Priority Date Filing Date
PCT/US2004/031248 WO2005028434A2 (en) 2003-09-18 2004-09-20 Novel heterocyclic compounds as hsp90-inhibitors

Country Status (14)

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US (8) US7138401B2 (US07138402-20061121-C00173.png)
EP (2) EP1670802A4 (US07138402-20061121-C00173.png)
JP (1) JP2007505933A (US07138402-20061121-C00173.png)
KR (1) KR20060070572A (US07138402-20061121-C00173.png)
CN (1) CN101906106A (US07138402-20061121-C00173.png)
AU (2) AU2004274507B2 (US07138402-20061121-C00173.png)
BR (1) BRPI0414533A (US07138402-20061121-C00173.png)
CA (1) CA2539548A1 (US07138402-20061121-C00173.png)
EA (1) EA010160B1 (US07138402-20061121-C00173.png)
IL (1) IL174375A0 (US07138402-20061121-C00173.png)
MX (1) MXPA06002997A (US07138402-20061121-C00173.png)
NO (1) NO20061396L (US07138402-20061121-C00173.png)
NZ (1) NZ546611A (US07138402-20061121-C00173.png)
WO (1) WO2005028434A2 (US07138402-20061121-C00173.png)

Cited By (88)

* Cited by examiner, † Cited by third party
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WO2008035629A1 (fr) 2006-09-19 2008-03-27 Daiichi Sankyo Company, Limited Dérivé de pyrazolopyrimidine
FR2907453A1 (fr) * 2006-10-24 2008-04-25 Sanofi Aventis Sa Nouveaux derives du fluorene,compositions les contenant et utilisation
WO2008093075A2 (en) * 2007-02-01 2008-08-07 Astrazeneca Ab 5,6,7,8-tetrahydropteridine derivatives as hsp90 inhibitors
JP2008536867A (ja) * 2005-04-14 2008-09-11 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 増殖疾患を処置する際に有用なhsp90インヒビターとしての2−アミノ−キナゾリン−5−オン
JP2008537751A (ja) * 2005-04-13 2008-09-25 アステックス、セラピューティックス、リミテッド 医薬化合物
EP2012791A2 (en) * 2006-02-07 2009-01-14 Conforma Therapeutics Corporation 7,9-dihydro-purin-8-one and related analogs as hsp90-inhibitors
WO2009114470A2 (en) * 2008-03-10 2009-09-17 Curis, Inc. Tetrahydroindole and tetrahdyroindazole as hsp90 inhibitors containing a zinc binding moiety
US7595401B2 (en) 2006-05-12 2009-09-29 Myriad Pharmaceuticals, Inc. Therapeutic compounds and their use in cancer
JP2010500870A (ja) * 2006-08-03 2010-01-14 セルゾーム アーゲー Pi3k相互作用分子の同定のための方法およびpi3kの精製のための方法
US7763624B2 (en) 2005-08-22 2010-07-27 Amgen Inc. Substituted pyrazolo[3,4-d]pyrimidines as ACK-1 and LCK inhibitors
WO2010098344A1 (ja) 2009-02-25 2010-09-02 第一三共株式会社 三環性ピラゾロピリミジン誘導体
US7960420B2 (en) 2007-12-21 2011-06-14 Joyant Pharmaceuticals, Inc Diazonamide analogs with improved solubility
WO2011076725A1 (en) 2009-12-21 2011-06-30 Bayer Cropscience Ag Thienylpyri (mi) dinylazole and their use for controlling phytopathogenic fungi
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WO2012026433A1 (ja) 2010-08-23 2012-03-01 第一三共株式会社 三環性ピラゾロピリミジン誘導体のフリー体結晶
WO2012026434A1 (ja) 2010-08-23 2012-03-01 第一三共株式会社 三環性ピラゾロピリミジン誘導体の結晶
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US9567326B2 (en) 2012-05-22 2017-02-14 The University Of North Carolina At Chapel Hill Pyrimidine compounds for the treatment of cancer
US9611267B2 (en) 2012-06-13 2017-04-04 Incyte Holdings Corporation Substituted tricyclic compounds as FGFR inhibitors
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US9663519B2 (en) 2013-03-15 2017-05-30 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
US9663502B2 (en) 2013-12-20 2017-05-30 Lycera Corporation 2-Acylamidomethyl and sulfonylamidomethyl benzoxazine carbamates for inhibition of RORgamma activity and the treatment of disease
US9670215B2 (en) 2014-06-05 2017-06-06 Vertex Pharmaceuticals Incorporated Compounds useful as inhibitors of ATR kinase
US9708318B2 (en) 2015-02-20 2017-07-18 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
US9745311B2 (en) 2012-08-10 2017-08-29 Incyte Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
US9771330B2 (en) 2012-11-27 2017-09-26 The University Of North Carolina At Chapel Hill Pyrimidine compounds for the treatment of cancer
US9783511B2 (en) 2013-12-20 2017-10-10 Lycera Corporation Carbamate benzoxazine propionic acids and acid derivatives for modulation of RORgamma activity and the treatment of disease
US9801889B2 (en) 2015-02-20 2017-10-31 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
US9809561B2 (en) 2013-12-20 2017-11-07 Merck Sharp & Dohme Corp. Tetrahydronaphthyridine, benzoxazine, aza-benzoxazine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease
US9890156B2 (en) 2015-02-20 2018-02-13 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
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