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CL2008000703A1 - Compuestos derivados de pirimidinas sustituidas; procedimiento para la preparacion de dichos compuestos; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar transtornos hematologicos. - Google Patents

Compuestos derivados de pirimidinas sustituidas; procedimiento para la preparacion de dichos compuestos; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar transtornos hematologicos.

Info

Publication number
CL2008000703A1
CL2008000703A1 CL200800703A CL2008000703A CL2008000703A1 CL 2008000703 A1 CL2008000703 A1 CL 2008000703A1 CL 200800703 A CL200800703 A CL 200800703A CL 2008000703 A CL2008000703 A CL 2008000703A CL 2008000703 A1 CL2008000703 A1 CL 2008000703A1
Authority
CL
Chile
Prior art keywords
compounds
pyrimidins
substituted
procedure
preparation
Prior art date
Application number
CL200800703A
Other languages
English (en)
Inventor
Stephan Siegel Dr Andreas W Dr
Original Assignee
Bayer Healthcare 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 Bayer Healthcare Ag filed Critical Bayer Healthcare Ag
Publication of CL2008000703A1 publication Critical patent/CL2008000703A1/es

Links

Classifications

    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
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  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
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  • Urology & Nephrology (AREA)
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CL200800703A 2007-03-16 2008-03-10 Compuestos derivados de pirimidinas sustituidas; procedimiento para la preparacion de dichos compuestos; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar transtornos hematologicos. CL2008000703A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102007012645A DE102007012645A1 (de) 2007-03-16 2007-03-16 Substituierte Imidazo- und Triazolopyrimidine

Publications (1)

Publication Number Publication Date
CL2008000703A1 true CL2008000703A1 (es) 2008-09-26

Family

ID=39688187

Family Applications (1)

Application Number Title Priority Date Filing Date
CL200800703A CL2008000703A1 (es) 2007-03-16 2008-03-10 Compuestos derivados de pirimidinas sustituidas; procedimiento para la preparacion de dichos compuestos; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar transtornos hematologicos.

Country Status (13)

Country Link
US (2) US8273752B2 (es)
EP (1) EP2137188B1 (es)
JP (1) JP5400626B2 (es)
AR (1) AR065719A1 (es)
CA (1) CA2680697C (es)
CL (1) CL2008000703A1 (es)
DE (1) DE102007012645A1 (es)
ES (1) ES2387223T3 (es)
PA (1) PA8772101A1 (es)
PE (1) PE20081806A1 (es)
TW (1) TW200904819A (es)
UY (1) UY30956A1 (es)
WO (1) WO2008113469A2 (es)

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DE102007012645A1 (de) 2007-03-16 2008-09-18 Bayer Healthcare Ag Substituierte Imidazo- und Triazolopyrimidine
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DE102008035552A1 (de) * 2008-07-30 2010-02-04 Bayer Schering Pharma Aktiengesellschaft Substituierte Pyridine und ihre Verwendung
CA2752114C (en) * 2009-02-13 2017-06-20 Bayer Pharma Aktiengesellschaft Fused pyrimidines as akt inhibitors
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PH12012500355A1 (en) * 2009-09-24 2019-11-29 Hoffmann La Roche Imidazopyridine or imidazopyrimidine derivatives as phosphodiesterase 10a inhibitors
WO2011044637A1 (en) 2009-10-15 2011-04-21 Monash University Affinity ligands and methods for protein purification
EP2526102B1 (en) 2010-01-22 2017-03-08 Fundación Centro Nacional de Investigaciones Oncológicas Carlos III Inhibitors of PI3 kinase
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
CN102791692B (zh) * 2010-03-12 2015-05-27 日本曹达株式会社 叔丁氧基羰基胺化合物的制造方法
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TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
AU2011338339A1 (en) 2010-12-08 2013-06-27 Vanderbilt University Bicyclic pyrazole compounds as allosteric modulators of mGluR5 receptors
WO2013037390A1 (en) 2011-09-12 2013-03-21 Sanofi 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors
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US9527835B2 (en) 2014-02-13 2016-12-27 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
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CN106255689B (zh) 2014-03-19 2019-09-17 勃林格殷格翰国际有限公司 杂芳基syk抑制剂
US9695180B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted imidazo[1,2-a]pyrazines as LSD1 inhibitors
WO2016007722A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines and triazolopyrazines as lsd1 inhibitors
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EP3626720A1 (en) 2015-04-03 2020-03-25 Incyte Corporation Heterocyclic compounds as lsd1 inhibitors
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