PE20081806A1 - Imidazo- y triazolopirimidinas sustituidas - Google Patents
Imidazo- y triazolopirimidinas sustituidasInfo
- Publication number
- PE20081806A1 PE20081806A1 PE2008000448A PE2008000448A PE20081806A1 PE 20081806 A1 PE20081806 A1 PE 20081806A1 PE 2008000448 A PE2008000448 A PE 2008000448A PE 2008000448 A PE2008000448 A PE 2008000448A PE 20081806 A1 PE20081806 A1 PE 20081806A1
- Authority
- PE
- Peru
- Prior art keywords
- imidazo
- amino
- pyrimidin
- trifluoromethyl
- triazolopyrimidines
- Prior art date
Links
Classifications
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Virology (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Cardiology (AREA)
- Communicable Diseases (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Immunology (AREA)
- Psychiatry (AREA)
- Pulmonology (AREA)
- Molecular Biology (AREA)
- Ophthalmology & Optometry (AREA)
- Epidemiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Urology & Nephrology (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE IMIDAZO Y TRIAZOLOPIRIMIDINAS SUSTITUIDAS DE FORMULA (I) DONDE A ES N O CR15, EN DONDE R15 ES H, Br O Cl; R1 ES H, HIDROXI, NH2, TRIFLUOROMETILO, CN, ALQUILO(C1-C4), ENTRE OTROS; R2 ES ARILO(C6-C10) O HETEROARILO DE 5 A 10 MIEMBROS OPCIONALMENTE SUSTITUIDO CON HIDROXI, NH2, HALOGENO, CN, ENTRE OTROS; R4 ES H, HALOGENO, CN, TRIFLUOROMETILO, ENTRE OTROS; R16 ES UN COMPUESTO DE FORMULA (i), (ii), ENTRE OTROS, DONDE R3 ES 2-PIRIDILO, PIRIMID-2-ILO, 2-CICLOPROPILAMINOPIRIMID-4-ILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 6-[(2-{[7-(2,4-DICLOROFENIL)IMIDAZO[1,2-c]PIRIMIDIN-5-IL]AMINO}ETIL)AMINO]-NICOTINONITRILO, N-[7-(2,4-DICLOROFENIL)IMIDAZO[1,2-c]PIRIMIDIN-5-IL]-N'-[5-(TRIFLUOROMETIL)PIRIDIN-2-IL]ETANO-1,2-DIAMINA, 1-{6-[(2-{[7-(2,4-DICLOROFENIL)IMIDAZO[1,2-c]PIRIMIDIN-5-IL]AMINO}ETIL)AMINO]PIRIDIN-3-IL}ETANONA, ENTRE OTROS. SE REFIERE TAMBIEN A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA GLICOGENO SINTASA QUINASA 3B (GSK3B) SIENDO UTILES EN EL TRATAMIENTO DE TRASTORNOS HEMATOLOGICOS TALES COMO LEUCOPENIAS Y NEUTROPENIAS
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 |
---|---|
PE20081806A1 true PE20081806A1 (es) | 2009-02-07 |
Family
ID=39688187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008000448A PE20081806A1 (es) | 2007-03-16 | 2008-03-10 | Imidazo- y triazolopirimidinas sustituidas |
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) |
Families Citing this family (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007012645A1 (de) | 2007-03-16 | 2008-09-18 | Bayer Healthcare Ag | Substituierte Imidazo- und Triazolopyrimidine |
DE102008023801A1 (de) * | 2008-05-15 | 2009-11-19 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Imidazo- und Triazolopyrimidine, Imidazo- und Pyrazolopyrazine und Imidazotriazine |
DE102008035552A1 (de) * | 2008-07-30 | 2010-02-04 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Pyridine und ihre Verwendung |
CN102361872B (zh) * | 2009-02-13 | 2014-12-03 | 拜耳知识产权有限责任公司 | 作为akt抑制剂的稠合嘧啶 |
JP5503930B2 (ja) * | 2009-09-18 | 2014-05-28 | 住友化学株式会社 | 3−アミノ−1−tert−ブトキシカルボニルピペリジンの精製方法およびそのクエン酸塩 |
CA2770087C (en) * | 2009-09-24 | 2014-09-09 | F. Hoffmann-La Roche Ag | Imidazopyridine or imidazopyrimidine derivatives as phosphodiesterase 1oa inhibitors |
WO2011044637A1 (en) * | 2009-10-15 | 2011-04-21 | Monash University | Affinity ligands and methods for protein purification |
ES2627703T3 (es) | 2010-01-22 | 2017-07-31 | Fundación Centro Nacional De Investigaciones Oncológicas Carlos Iii | Inhibidores de PI3·quinasa |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
WO2011111705A1 (ja) | 2010-03-12 | 2011-09-15 | 日本曹達株式会社 | t-ブトキシカルボニルアミン化合物の製造方法 |
WO2011130146A1 (en) * | 2010-04-14 | 2011-10-20 | Array Biopharma Inc. | 5, 7-substituted-imidazo [1, 2-c] pyrimidines as inhibitors of jak kinases |
WO2011141713A1 (en) | 2010-05-13 | 2011-11-17 | Centro Nacional De Investigaciones Oncologicas (Cnio) | New bicyclic compounds as pi3-k and mtor inhibitors |
WO2011157827A1 (de) | 2010-06-18 | 2011-12-22 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
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 |
EP2648723A4 (en) | 2010-12-08 | 2014-04-02 | Univ Vanderbilt | Bicyclic pyrazole compounds as allergic Mglur5 receptor modulators |
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 |
EP2760862B1 (en) | 2011-09-27 | 2015-10-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
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DE102007012645A1 (de) | 2007-03-16 | 2008-09-18 | Bayer Healthcare Ag | Substituierte Imidazo- und Triazolopyrimidine |
DE102008023801A1 (de) * | 2008-05-15 | 2009-11-19 | Bayer Schering Pharma Aktiengesellschaft | Substituierte Imidazo- und Triazolopyrimidine, Imidazo- und Pyrazolopyrazine und Imidazotriazine |
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2007
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2008
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- 2008-03-04 US US12/529,711 patent/US8273752B2/en not_active Expired - Fee Related
- 2008-03-04 ES ES08716201T patent/ES2387223T3/es active Active
- 2008-03-04 JP JP2009553944A patent/JP5400626B2/ja not_active Expired - Fee Related
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- 2008-03-14 TW TW097108955A patent/TW200904819A/zh unknown
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PA8772101A1 (es) | 2009-02-09 |
EP2137188A2 (de) | 2009-12-30 |
WO2008113469A8 (de) | 2009-09-24 |
AR065719A1 (es) | 2009-06-24 |
JP5400626B2 (ja) | 2014-01-29 |
US8273752B2 (en) | 2012-09-25 |
US9051323B2 (en) | 2015-06-09 |
TW200904819A (en) | 2009-02-01 |
WO2008113469A2 (de) | 2008-09-25 |
DE102007012645A1 (de) | 2008-09-18 |
ES2387223T3 (es) | 2012-09-18 |
CL2008000703A1 (es) | 2008-09-26 |
EP2137188B1 (de) | 2012-06-06 |
CA2680697A1 (en) | 2008-09-25 |
CA2680697C (en) | 2016-09-20 |
US20130040946A1 (en) | 2013-02-14 |
US20100113441A1 (en) | 2010-05-06 |
JP2010521506A (ja) | 2010-06-24 |
WO2008113469A3 (de) | 2008-11-13 |
UY30956A1 (es) | 2008-10-31 |
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