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PE20061158A1 - 2-anilinopirimidinas sustituidas como inhibidores de la quinasa del ciclo celular o del receptor de la tirosina quinasa y su preparacion - Google Patents

2-anilinopirimidinas sustituidas como inhibidores de la quinasa del ciclo celular o del receptor de la tirosina quinasa y su preparacion

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Publication number
PE20061158A1
PE20061158A1 PE2005001148A PE2005001148A PE20061158A1 PE 20061158 A1 PE20061158 A1 PE 20061158A1 PE 2005001148 A PE2005001148 A PE 2005001148A PE 2005001148 A PE2005001148 A PE 2005001148A PE 20061158 A1 PE20061158 A1 PE 20061158A1
Authority
PE
Peru
Prior art keywords
kinase
alkyl
inhibitors
tirosine
bencensulfonamide
Prior art date
Application number
PE2005001148A
Other languages
English (en)
Inventor
Arwed Cleve
Ulrich Lucking
Hans Briem
Martin Kruger
Philip Lienau
Rolf Jautelat
Gerhard Siemeister
Christopher West
Original Assignee
Schering 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=35447860&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20061158(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from DE102004049622A external-priority patent/DE102004049622A1/de
Application filed by Schering Ag filed Critical Schering Ag
Publication of PE20061158A1 publication Critical patent/PE20061158A1/es

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    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
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    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen atoms

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Abstract

REFERIDA A UN COMPUESTO DERIVADO DE ANILINOPIRIMIDINA DE FORMULA I, DONDE A Y D SON HALOGENO, OH, CIANO, ALQUILO C1-C4, ENTRE OTROS; X ES NH, N(ALQUILO C1-C3) U O EN DONDE EL RADICAL ALQUILO PUEDE SER RAMIFICADO; R1 ES HALOGENO O CIANO; R2 ES HIDROXIALQUILO C1-C8, CICLOALQUILO C3-C7, ENTRE OTROS; R3 Y R4 SON H, ALQUILO C1-C3, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 4-[5-BROMO-4-((R)-2-HIDROXI-1-METIL-ETIL-AMINO)PIRIMIDIN-2-ILAMINO]-2,6-DIMETIL-BENCENSULFONAMIDA, 4-(5-CIANO-4-CICLOHEXILAMINO-PIRIMIDIN-2-ILAMINO)-2,6-DIMETIL-BENCENSULFONAMIDA, 4-[5-BROMO-4-((1R,2R)-2-HIDROXI-1-METIL-PROPOXI)PIRIMIDIN-2-ILAMINO]-2,6-DIMETIL-BENCENSULFONAMIDA, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS SON INHIBIDORES DE LAS QUINASAS DEPENDIENTES DE LAS CICLINAS, TALES COMO CDK2, CDK3, CDK4, CDK5, CDK6, CDK7, CDK8 Y CDK9, ASI COMO DE LOS RECEPTORES DE VEGF DE TIROSINA QUINASAS Y SON UTILES PARA EL TRATAMIENTO DEL CANCER, ENFERMEDADES CAUSADAS POR TRASTORNOS DE LA PROLIFERACION CELULAR, ENTRE OTRAS
PE2005001148A 2004-09-29 2005-09-29 2-anilinopirimidinas sustituidas como inhibidores de la quinasa del ciclo celular o del receptor de la tirosina quinasa y su preparacion PE20061158A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US61396404P 2004-09-29 2004-09-29
DE102004049622A DE102004049622A1 (de) 2004-10-06 2004-10-06 Subtituierte 2-Anilinopyrimidine als Zellzyklus-kinase oder Rezeptortyrosin-kinase Inhibitoren, deren Herstellung und Verwendung als Arzneimittel

Publications (1)

Publication Number Publication Date
PE20061158A1 true PE20061158A1 (es) 2006-11-12

Family

ID=35447860

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2005001148A PE20061158A1 (es) 2004-09-29 2005-09-29 2-anilinopirimidinas sustituidas como inhibidores de la quinasa del ciclo celular o del receptor de la tirosina quinasa y su preparacion

Country Status (11)

Country Link
US (1) US20060111378A1 (es)
EP (1) EP1794134A1 (es)
JP (1) JP2008514571A (es)
AR (1) AR052312A1 (es)
GT (1) GT200500272A (es)
PA (1) PA8647401A1 (es)
PE (1) PE20061158A1 (es)
SV (1) SV2006002245A (es)
TW (1) TW200628452A (es)
UY (1) UY29145A1 (es)
WO (1) WO2006034872A1 (es)

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TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
GB0205688D0 (en) 2002-03-09 2002-04-24 Astrazeneca Ab Chemical compounds
GB0205690D0 (en) 2002-03-09 2002-04-24 Astrazeneca Ab Chemical compounds
GB0205693D0 (en) 2002-03-09 2002-04-24 Astrazeneca Ab Chemical compounds
US7442697B2 (en) 2002-03-09 2008-10-28 Astrazeneca Ab 4-imidazolyl substituted pyrimidine derivatives with CDK inhibitory activity
RS51752B (sr) 2002-07-29 2011-12-31 Rigel Pharmaceuticals Metode tretiranja i prevencije autoimunih oboljenja jedinjenjima 2,4-pirimidindiamina
GB0311274D0 (en) 2003-05-16 2003-06-18 Astrazeneca Ab Chemical compounds
GB0311276D0 (en) 2003-05-16 2003-06-18 Astrazeneca Ab Chemical compounds
RS53109B (sr) 2003-07-30 2014-06-30 Rigel Pharmaceuticals Inc. Jedinjenja 2,4 pirimidindiamina za upotrebu u tretmanu ili prevenciji autoimunih bolesti
BRPI0517426A (pt) * 2004-12-17 2008-10-07 Astrazeneca Ab composto, processo para preparar o mesmo, composição farmacêutica, uso de um composto, e, métodos para produzir um efeito anti-proliferação celular, para produzir um efeito inibitório de cdk2, e para tratar uma doença em um animal de sangue quente
KR101278397B1 (ko) 2005-01-19 2013-06-25 리겔 파마슈티칼스, 인크. 2,4-피리미딘디아민 화합물의 전구약물 및 이의 용도
GB0504753D0 (en) * 2005-03-08 2005-04-13 Astrazeneca Ab Chemical compounds
CN105348203B (zh) * 2005-06-08 2018-09-18 里格尔药品股份有限公司 抑制jak途径的组合物和方法
US20070203161A1 (en) * 2006-02-24 2007-08-30 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the jak pathway
WO2007015064A1 (en) * 2005-07-30 2007-02-08 Astrazeneca Ab Imidazolyl-pyrimidine compounds for use in the treatment of proliferative disorders
US7745428B2 (en) * 2005-09-30 2010-06-29 Astrazeneca Ab Imidazo[1,2-A]pyridine having anti-cell-proliferation activity
DE102005062742A1 (de) * 2005-12-22 2007-06-28 Bayer Schering Pharma Ag Sulfoximin substituierte Pyrimidine, Verfahren zu deren Herstellung und ihre Verwendung als Arzneimittel
ES2439948T3 (es) 2006-02-17 2014-01-27 Rigel Pharmaceuticals, Inc. Compuestos de 2,4-pirimidindiamina para el tratamiento o la prevención de enfermedades autoinmunitarias
US8962643B2 (en) 2006-02-24 2015-02-24 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the JAK pathway
TW200811169A (en) * 2006-05-26 2008-03-01 Astrazeneca Ab Chemical compounds
EP2179991A1 (de) * 2008-10-21 2010-04-28 Bayer Schering Pharma Aktiengesellschaft Sulfoximinsubstituierte Anilino-Pyrimidinderivate als CDK-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel
GB0821537D0 (en) * 2008-11-25 2008-12-31 Union Life Sciences Ltd Therapeutic target
CN102470135A (zh) * 2009-07-28 2012-05-23 里格尔药品股份有限公司 抑制jak途径的组合物和方法
US8466155B2 (en) * 2009-10-02 2013-06-18 Boehringer Ingelheim International Gmbh Pyrimidines
CN102574782B (zh) * 2009-10-21 2014-10-08 拜耳知识产权有限责任公司 取代的卤代苯氧基苯甲酰胺衍生物
EP2353591A1 (en) 2010-02-04 2011-08-10 Laboratorios Del. Dr. Esteve, S.A. Sigma ligands for potentiating the analgesic effect of opioids and opiates in post-operative pain and attenuating the dependency thereof
MX2016007898A (es) 2013-12-20 2016-10-07 Signal Pharm Llc Compuestos diaminopirimidilo sustituidos, las composiciones de estos y los metodos de tratamiento con estos.
CA3130706A1 (en) 2019-04-04 2020-10-08 Dana-Farber Cancer Institute, Inc. Cdk2/5 degraders and uses thereof

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JPS58183665A (ja) * 1982-04-19 1983-10-26 Sumitomo Chem Co Ltd スルホニルクロリドの製造方法
GB0016877D0 (en) * 2000-07-11 2000-08-30 Astrazeneca Ab Chemical compounds
MEP13408A (en) * 2001-05-29 2010-06-10 Bayer Schering Pharma Ag Cdk inhibiting pyrimidines, production thereof and their use as medicaments
JP2005526765A (ja) * 2002-03-11 2005-09-08 シエーリング アクチエンゲゼルシャフト Cdk−阻害性2−ヘテロアリール−ピリミジン類、それらの生成及び医薬としての使用
US7288547B2 (en) * 2002-03-11 2007-10-30 Schering Ag CDK-inhibitory 2-heteroaryl-pyrimidines, their production and use as pharmaceutical agents

Also Published As

Publication number Publication date
JP2008514571A (ja) 2008-05-08
PA8647401A1 (es) 2006-07-03
AR052312A1 (es) 2007-03-14
WO2006034872A1 (de) 2006-04-06
GT200500272A (es) 2006-06-06
US20060111378A1 (en) 2006-05-25
UY29145A1 (es) 2006-04-28
TW200628452A (en) 2006-08-16
SV2006002245A (es) 2006-05-25
EP1794134A1 (de) 2007-06-13

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