AU1794697A - 7-alkyl-pyrrolo{2,3-d}pyrimidines - Google Patents

7-alkyl-pyrrolo{2,3-d}pyrimidines

Info

Publication number
AU1794697A
AU1794697A AU17946/97A AU1794697A AU1794697A AU 1794697 A AU1794697 A AU 1794697A AU 17946/97 A AU17946/97 A AU 17946/97A AU 1794697 A AU1794697 A AU 1794697A AU 1794697 A AU1794697 A AU 1794697A
Authority
AU
Australia
Prior art keywords
pyrimidines
pyrrolo
alkyl
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
AU17946/97A
Inventor
Eva Altmann
Martin Missbach
Leo Widler
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
Ciba Geigy AG
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
Application filed by Ciba Geigy AG, Novartis AG filed Critical Ciba Geigy AG
Publication of AU1794697A publication Critical patent/AU1794697A/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AU17946/97A 1996-03-06 1997-02-24 7-alkyl-pyrrolo{2,3-d}pyrimidines Abandoned AU1794697A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP96810137 1996-03-06
EP96810137 1996-03-06
PCT/EP1997/000874 WO1997032879A1 (en) 1996-03-06 1997-02-24 7-ALKYL-PYRROLO[2,3-d]PYRIMIDINES

Publications (1)

Publication Number Publication Date
AU1794697A true AU1794697A (en) 1997-09-22

Family

ID=8225559

Family Applications (1)

Application Number Title Priority Date Filing Date
AU17946/97A Abandoned AU1794697A (en) 1996-03-06 1997-02-24 7-alkyl-pyrrolo{2,3-d}pyrimidines

Country Status (2)

Country Link
AU (1) AU1794697A (en)
WO (1) WO1997032879A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU753555B2 (en) * 1998-09-18 2002-10-24 Abbott Gmbh & Co. Kg Pyrrolopyrimidines as protein kinase inhibitors

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9704948D0 (en) 1997-03-11 1997-04-30 Knoll Ag Therapeutic agents
DE69815317T2 (en) * 1997-03-19 2005-04-07 Abbott Gmbh & Co. Kg PYRROLO [2,3-D] PYRIMIDINE AND ITS USE AS TYROSINE KINASE INHIBITORS
US7863444B2 (en) 1997-03-19 2011-01-04 Abbott Laboratories 4-aminopyrrolopyrimidines as kinase inhibitors
PA8474101A1 (en) 1998-06-19 2000-09-29 Pfizer Prod Inc PYROLEUM [2,3-D] PIRIMIDINE COMPOUNDS
AU3951899A (en) 1998-06-19 2000-01-05 Pfizer Products Inc. Pyrrolo(2,3-d)pyrimidine compounds
US6713474B2 (en) 1998-09-18 2004-03-30 Abbott Gmbh & Co. Kg Pyrrolopyrimidines as therapeutic agents
US7071199B1 (en) 1999-09-17 2006-07-04 Abbott Gmbh & Cco. Kg Kinase inhibitors as therapeutic agents
JP4078074B2 (en) 1999-12-10 2008-04-23 ファイザー・プロダクツ・インク Pyrrolo [2,3-d] pyrimidine compound
WO2001072751A1 (en) * 2000-03-29 2001-10-04 Knoll Gesellschaft Mit Beschraenkter Haftung Pyrrolopyrimidines as tyrosine kinase inhibitors
CN100351253C (en) 2000-06-26 2007-11-28 辉瑞产品公司 Pyrrolo [2,3-d] pyrimidine compounds as immunosuppressive agents
US7301023B2 (en) 2001-05-31 2007-11-27 Pfizer Inc. Chiral salt resolution
CN1523991A (en) 2001-08-10 2004-08-25 ��˹��ŵ�� Use of c-Src inhibitors alone or in combination with STI571 for the treatment of leukaemia
GB0206215D0 (en) 2002-03-15 2002-05-01 Novartis Ag Organic compounds
KR20050086784A (en) 2002-11-26 2005-08-30 화이자 프로덕츠 인크. Method of treatment of transplant rejection
UA80171C2 (en) 2002-12-19 2007-08-27 Pfizer Prod Inc Pyrrolopyrimidine derivatives
JP2007530541A (en) * 2004-03-22 2007-11-01 ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド Α-Trifluoromethyl alcohol or amine as glucocorticoid mimetics
GB0512324D0 (en) 2005-06-16 2005-07-27 Novartis Ag Organic compounds
JP5147401B2 (en) * 2005-09-06 2013-02-20 塩野義製薬株式会社 Indolecarboxylic acid derivatives having PGD2 receptor antagonist activity
EP1973917B1 (en) * 2005-12-29 2015-06-10 AbbVie Inc. Protein kinase inhibitors
RU2536040C2 (en) 2007-11-01 2014-12-20 Акусела Инк. Amine derivatives and their use for treatment of ophthalmological diseases and illnesses
CA2733359C (en) 2008-08-20 2014-08-05 Pfizer Inc. Pyrrolo[2,3-d]pyrimidine compounds
US8426428B2 (en) 2008-12-05 2013-04-23 Principia Biopharma, Inc. EGFR kinase knockdown via electrophilically enhanced inhibitors
US20120165310A1 (en) 2009-09-10 2012-06-28 Novartis Ag Ether derivatives of bicyclic heteroaryls
US20120289501A1 (en) 2009-11-25 2012-11-15 Novartis Ag Benzene-fused 6-membered oxygen-containing heterocyclic derivatives of bicyclic heteroaryls
EP2582680A1 (en) 2010-06-17 2013-04-24 Novartis AG Biphenyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
EP2582681A1 (en) 2010-06-17 2013-04-24 Novartis AG Piperidinyl substituted 1,3-dihydro-benzoimidazol-2-ylideneamine derivatives
WO2012120469A1 (en) 2011-03-08 2012-09-13 Novartis Ag Fluorophenyl bicyclic heteroaryl compounds
CN104169425A (en) 2011-03-09 2014-11-26 理查德·G·佩斯泰尔 Prostate cancer cell line, gene signatures and uses thereof
CA2873743C (en) 2012-05-14 2022-12-06 Prostagene, Llc Using modulators of ccr5 for treating cancer
EP3194572B1 (en) 2014-07-30 2023-10-25 Yeda Research and Development Co. Ltd. Media for culturing pluripotent stem cells
US11602534B2 (en) 2017-12-21 2023-03-14 Hefei Institutes Of Physical Science, Chinese Academy Of Sciences Pyrimidine derivative kinase inhibitors
EP3914698A1 (en) 2019-01-23 2021-12-01 Yeda Research and Development Co. Ltd Culture media for pluripotent stem cells
US20220395553A1 (en) 2019-11-14 2022-12-15 Cohbar, Inc. Cxcr4 antagonist peptides

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3036390A1 (en) * 1980-09-26 1982-05-13 Troponwerke GmbH & Co KG, 5000 Köln Antiinflammatory intermediate 7H-pyrrolo-(2,3-D)-pyrimidine derivs. - prepd. by dealkylation of 7-phenyl:ethyl derivs. by reaction with hydrochloric, phosphoric or poly:phosphoric acid
NO169490C (en) * 1988-03-24 1992-07-01 Takeda Chemical Industries Ltd ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVE PYRROLOPYRIMIDINE DERIVATIVES
EP0514540B1 (en) * 1989-09-19 1996-07-17 Teijin Limited PYRROLO 2,3-d]PYRIMIDINE DERIVATIVE, PROCESS FOR PREPARING THE SAME, AND PHARMACEUTICAL PREPARATION COMPRISING THE DERIVATIVE AS ACTIVE INGREDIENT

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU753555B2 (en) * 1998-09-18 2002-10-24 Abbott Gmbh & Co. Kg Pyrrolopyrimidines as protein kinase inhibitors
AU753555C (en) * 1998-09-18 2003-07-03 Abbott Gmbh & Co. Kg Pyrrolopyrimidines as protein kinase inhibitors

Also Published As

Publication number Publication date
WO1997032879A1 (en) 1997-09-12

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