ATE453634T1 - Regioselektives verfahren zur zubereitung von benzimidazol-thiophenen - Google Patents

Regioselektives verfahren zur zubereitung von benzimidazol-thiophenen

Info

Publication number
ATE453634T1
ATE453634T1 AT06813938T AT06813938T ATE453634T1 AT E453634 T1 ATE453634 T1 AT E453634T1 AT 06813938 T AT06813938 T AT 06813938T AT 06813938 T AT06813938 T AT 06813938T AT E453634 T1 ATE453634 T1 AT E453634T1
Authority
AT
Austria
Prior art keywords
thiophenes
preparing benzimidazole
regioselective process
preparing
benzimidazole
Prior art date
Application number
AT06813938T
Other languages
English (en)
Inventor
Keith Hornberger
Mui Cheung
Mark Pobanz
Kyle Emmitte
Kevin Kuntz
Jennifer Badiang
Original Assignee
Smithkline Beecham Corp
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 Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Application granted granted Critical
Publication of ATE453634T1 publication Critical patent/ATE453634T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur 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
    • C07D333/38Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D333/40Thiophene-2-carboxylic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
AT06813938T 2005-09-06 2006-08-28 Regioselektives verfahren zur zubereitung von benzimidazol-thiophenen ATE453634T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US71430105P 2005-09-06 2005-09-06
PCT/US2006/033793 WO2007030366A1 (en) 2005-09-06 2006-08-28 Regioselective process for preparing benzimidazole thiophenes

Publications (1)

Publication Number Publication Date
ATE453634T1 true ATE453634T1 (de) 2010-01-15

Family

ID=37605702

Family Applications (1)

Application Number Title Priority Date Filing Date
AT06813938T ATE453634T1 (de) 2005-09-06 2006-08-28 Regioselektives verfahren zur zubereitung von benzimidazol-thiophenen

Country Status (18)

Country Link
US (1) US20080249301A1 (de)
EP (1) EP1924572B1 (de)
JP (1) JP2009507022A (de)
KR (1) KR20080045266A (de)
CN (1) CN101304986A (de)
AT (1) ATE453634T1 (de)
AU (1) AU2006287771A1 (de)
BR (1) BRPI0615705A2 (de)
CA (1) CA2621073A1 (de)
DE (1) DE602006011482D1 (de)
EA (1) EA200800549A1 (de)
ES (1) ES2338590T3 (de)
IL (1) IL189769A0 (de)
MA (1) MA29781B1 (de)
MX (1) MX2008003172A (de)
NO (1) NO20081101L (de)
WO (1) WO2007030366A1 (de)
ZA (1) ZA200801950B (de)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
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US7595330B2 (en) * 2005-09-06 2009-09-29 Smithkline Beecham Corporation Benzimidazole thiophene compounds
JP2009507020A (ja) * 2005-09-06 2009-02-19 スミスクライン ビーチャム コーポレーション Plk調節物質としてのルベンゾイミダゾールチオフェン化合物
WO2007087283A2 (en) * 2006-01-23 2007-08-02 Vertex Pharmaceuticals Incorporated Thiophene-carboxamides useful as inhibitors of protein kinases
CN101466708A (zh) 2006-04-13 2009-06-24 弗特克斯药品有限公司 可用作蛋白激酶抑制剂的噻吩甲酰胺
AU2007268056A1 (en) 2006-05-23 2007-12-06 Vertex Pharmaceuticals Incorporated Thiophene-carboxamides useful as inhibitors of protein kinases
AU2007267986A1 (en) 2006-05-23 2007-12-06 Vertex Pharmaceuticals Incorporated Thiophene-carboxamides useful as inhibitors of protein kinases
US7615643B2 (en) 2006-06-02 2009-11-10 Smithkline Beecham Corporation Benzimidazole thiophene compounds
WO2009002916A2 (en) * 2007-06-26 2008-12-31 Smithkline Beecham Corporation Processes for preparing benzimidazole thiophenes
EP2100894A1 (de) 2008-03-12 2009-09-16 4Sc Ag Pyridopyrimidinone verwendbar als Plk1 (polo-like kinase) Hemmen
MX357614B (es) * 2010-04-12 2018-07-17 Supernus Pharmaceuticals Inc Métodos para producir sales de viloxazina y polimorfos novedosos de las mismas.
US20130315895A1 (en) 2010-07-01 2013-11-28 Takeda Pharmaceutical Company Limited COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET
US8754114B2 (en) 2010-12-22 2014-06-17 Incyte Corporation Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3
EP2565186A1 (de) 2011-09-02 2013-03-06 Hybrigenics S.A. Spezifische und reversible Inhibitoren von ubiquitinspezifischer Protease 7
RU2014144951A (ru) 2012-04-10 2016-06-10 Сумитомо Дайниппон Фарма Ко., Лтд. Новое 1-замещенное производное индазола
EA036592B1 (ru) 2012-06-13 2020-11-26 Инсайт Холдингс Корпорейшн Замещенные трициклические соединения как ингибиторы fgfr
WO2014026125A1 (en) 2012-08-10 2014-02-13 Incyte Corporation Pyrazine derivatives as fgfr inhibitors
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
WO2014172644A2 (en) 2013-04-19 2014-10-23 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
WO2016134294A1 (en) 2015-02-20 2016-08-25 Incyte Corporation Bicyclic heterocycles as fgfr4 inhibitors
ES2895769T3 (es) 2015-02-20 2022-02-22 Incyte Corp Heterociclos bicíclicos como inhibidores de FGFR
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
BR112020012635A2 (pt) 2017-12-22 2020-12-01 Ravenna Pharmaceuticals, Inc. derivados de aminopiridina como inibidores de fosfatidilinositol fosfato quinase
US11174257B2 (en) 2018-05-04 2021-11-16 Incyte Corporation Salts of an FGFR inhibitor
CA3099287A1 (en) 2018-05-04 2019-11-07 Incyte Corporation Solid forms of an fgfr inhibitor and processes for preparing the same
US11628162B2 (en) 2019-03-08 2023-04-18 Incyte Corporation Methods of treating cancer with an FGFR inhibitor
CN109988098A (zh) * 2019-05-23 2019-07-09 常州工程职业技术学院 一种(r)-n-叔丁氧羰基-3-羟甲基哌啶的合成方法
WO2021007269A1 (en) 2019-07-09 2021-01-14 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
CR20220169A (es) 2019-10-14 2022-10-27 Incyte Corp Heterociclos bicíclicos como inhibidores de fgfr
WO2021076728A1 (en) 2019-10-16 2021-04-22 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
EP4069696A1 (de) 2019-12-04 2022-10-12 Incyte Corporation Tricyclische heterocyclen als fgfr-inhibitoren
BR112022010664A2 (pt) 2019-12-04 2022-08-16 Incyte Corp Derivados de um inibidor de fgfr
EP4352059A1 (de) 2021-06-09 2024-04-17 Incyte Corporation Tricyclische heterocyclen als fgfr-inhibitoren

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US5990146A (en) * 1997-08-20 1999-11-23 Warner-Lambert Company Benzimidazoles for inhibiting protein tyrosine kinase mediated cellular proliferation
US6162804A (en) * 1997-09-26 2000-12-19 Merck & Co., Inc. Tyrosine kinase inhibitors
GB0005642D0 (en) * 2000-03-10 2000-05-03 Astrazeneca Uk Ltd Chemical compounds
US7244744B2 (en) * 2001-11-01 2007-07-17 Icagen, Inc. Piperidines
KR20050071471A (ko) * 2002-08-08 2005-07-07 스미스클라인 비참 코포레이션 티오펜 화합물
CA2502178A1 (en) * 2002-10-30 2004-05-21 Merck & Co., Inc. Heteroarylpiperidine modulators of chemokine receptor activity
JP2007509070A (ja) * 2003-10-16 2007-04-12 スミスクライン ビーチャム コーポレーション チオフェン化合物

Also Published As

Publication number Publication date
AU2006287771A1 (en) 2007-03-15
ES2338590T3 (es) 2010-05-10
ZA200801950B (en) 2009-09-30
CA2621073A1 (en) 2007-03-15
EP1924572B1 (de) 2009-12-30
EP1924572A1 (de) 2008-05-28
JP2009507022A (ja) 2009-02-19
MX2008003172A (es) 2008-03-18
WO2007030366A1 (en) 2007-03-15
NO20081101L (no) 2008-04-04
EA200800549A1 (ru) 2008-08-29
IL189769A0 (en) 2008-08-07
MA29781B1 (fr) 2008-09-01
KR20080045266A (ko) 2008-05-22
DE602006011482D1 (de) 2010-02-11
BRPI0615705A2 (pt) 2016-08-23
CN101304986A (zh) 2008-11-12
US20080249301A1 (en) 2008-10-09

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