PE20141191A1 - Compuestos como inhibidores de bace - Google Patents

Compuestos como inhibidores de bace

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Publication number
PE20141191A1
PE20141191A1 PE2013001452A PE2013001452A PE20141191A1 PE 20141191 A1 PE20141191 A1 PE 20141191A1 PE 2013001452 A PE2013001452 A PE 2013001452A PE 2013001452 A PE2013001452 A PE 2013001452A PE 20141191 A1 PE20141191 A1 PE 20141191A1
Authority
PE
Peru
Prior art keywords
compounds
chroman
imidazol
alkyl
inhibitors
Prior art date
Application number
PE2013001452A
Other languages
English (en)
Inventor
Gabor Csjernyik
Sofia Karlstrom
Annika Kers
Karin Kolmodin
Martin Nylof
Liselotte Ohberg
Laszlo Rakos
Lars Sandberg
Fernando Sehgelmeble
Peter Soderman
Britt-Marie Swahn
Berg Stefan Von
Original Assignee
Astrazeneca Ab
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=46314249&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20141191(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of PE20141191A1 publication Critical patent/PE20141191A1/es

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    • C07D235/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
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    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/10Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
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    • 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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41881,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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  • Chemical & Material Sciences (AREA)
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  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
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  • Animal Behavior & Ethology (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Psychiatry (AREA)
  • Psychology (AREA)
  • Vascular Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pyridine Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Furan Compounds (AREA)

Abstract

REFERIDO A COMPUESTOS DE FORMULA (I), DONDE: A ES -O- O -CH2-; n ES 0 O 1; R1 ES ALQUILO C1-6 O HALOALQUILO C1-6; R2 ES H, CIANO, HALOGENO, CIANO, ENTRE OTROS; R5 Y R6 SON INDEPENDIENTEMENTE HETEROCICLILO, ARILO, HETEROARILO, CICLOALQUILO C3-6, ALQUILO C1-6 OPCIONALMENTE SUSTITUIDOS, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 6-(3,5-DICLOROFENIL)-5�-METILESPIRO[CROMAN-4,2�-IMIDAZOL]-4�-AMINA; N-(4�-AMINO-5�-METIL-ESPIRO[CROMANO-4,2�-IMIDAZOL]-6-IL)-5-CLORO-PIRIDINA-2-CARBOXAMIDA; ENTRE OTROS. REFERIDO ADEMAS A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA BETA-SECRETASA, SIENDO UTILES PARA EL TRATAMIENTO DEL MAL DEL ALZHEIMER, DEMENCIA SENIL, HEMORRAGIA CEREBRAL HEREDITARIA, PERDIDA DE MEMORIA
PE2013001452A 2010-12-22 2011-12-21 Compuestos como inhibidores de bace PE20141191A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201061425852P 2010-12-22 2010-12-22
US201161529620P 2011-08-31 2011-08-31

Publications (1)

Publication Number Publication Date
PE20141191A1 true PE20141191A1 (es) 2014-09-21

Family

ID=46314249

Family Applications (2)

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PE2013001452A PE20141191A1 (es) 2010-12-22 2011-12-21 Compuestos como inhibidores de bace
PE2017001273A PE20171342A1 (es) 2010-12-22 2011-12-21 Compuestos y su uso como inhibidores de bace

Family Applications After (1)

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PE2017001273A PE20171342A1 (es) 2010-12-22 2011-12-21 Compuestos y su uso como inhibidores de bace

Country Status (38)

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US (6) US8415483B2 (es)
EP (2) EP2655378B1 (es)
JP (3) JP6180325B2 (es)
KR (1) KR101916975B1 (es)
CN (2) CN103380133B (es)
AR (1) AR084553A1 (es)
AU (3) AU2011345389B2 (es)
BR (1) BR112013016030B1 (es)
CA (1) CA2822378C (es)
CL (1) CL2013001849A1 (es)
CO (1) CO6781485A2 (es)
CR (1) CR20130308A (es)
CY (1) CY1119211T1 (es)
DK (1) DK2655378T3 (es)
DO (3) DOP2013000147A (es)
EA (2) EA025746B9 (es)
EC (1) ECSP13012708A (es)
ES (2) ES2780928T3 (es)
GT (1) GT201300165A (es)
HR (1) HRP20170723T1 (es)
HU (1) HUE033274T2 (es)
LT (1) LT2655378T (es)
ME (1) ME02728B (es)
MX (1) MX342477B (es)
MY (1) MY178156A (es)
NI (1) NI201300055A (es)
NZ (2) NZ612041A (es)
PE (2) PE20141191A1 (es)
PL (1) PL2655378T3 (es)
PT (1) PT2655378T (es)
RS (1) RS55961B1 (es)
SA (2) SA111330107B1 (es)
SG (2) SG10201602241SA (es)
SI (1) SI2655378T1 (es)
TW (2) TWI633092B (es)
UY (1) UY33829A (es)
WO (1) WO2012087237A1 (es)
ZA (1) ZA201305495B (es)

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TWI557112B (zh) 2012-03-05 2016-11-11 百靈佳殷格翰國際股份有限公司 β-分泌酶抑制劑
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AR107783A1 (es) 2016-03-15 2018-06-06 Lilly Co Eli Terapia de combinación
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