MA30089B1 - (arylsulfonyl)-pyrasolopiperidines - Google Patents

(arylsulfonyl)-pyrasolopiperidines

Info

Publication number
MA30089B1
MA30089B1 MA31080A MA31080A MA30089B1 MA 30089 B1 MA30089 B1 MA 30089B1 MA 31080 A MA31080 A MA 31080A MA 31080 A MA31080 A MA 31080A MA 30089 B1 MA30089 B1 MA 30089B1
Authority
MA
Morocco
Prior art keywords
formula
compounds
pyrasolopiperidines
arylsulfonyl
alzheimer
Prior art date
Application number
MA31080A
Other languages
English (en)
Inventor
Albert W Garofalo
Jacek J Jagodzinski
Andrei W Konradi
Christopher M Semko
Jenifer L Smith
Ying-Zi Xu
Xiaocong Michael Ye
Original Assignee
Elan Pharm Inc
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 Elan Pharm Inc filed Critical Elan Pharm Inc
Publication of MA30089B1 publication Critical patent/MA30089B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-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
    • A61K31/435Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/96Sulfur atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Abstract

La présente invention concerne des composés de sulfonamido N-cycliques de formule I dans laquelle A, B, R1, R1a, R2, R2a, R3 et R3a sont tels que décrits dans le mémoire descriptif. Les composés de formule I sont utiles pour le traitement ou la prévention de troubles de la cognition tels que la maladie d'Alzheimer. L'invention concerne également des compositions pharmaceutiques qui comprennent des composés de formule I, des procédés de préparation de composés de formule I et de procédés de traitement de troubles de la cognition tels que la maladie d'Alzheimer.
MA31080A 2005-12-01 2008-06-26 (arylsulfonyl)-pyrasolopiperidines MA30089B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US74136605P 2005-12-01 2005-12-01

Publications (1)

Publication Number Publication Date
MA30089B1 true MA30089B1 (fr) 2008-12-01

Family

ID=38092841

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31080A MA30089B1 (fr) 2005-12-01 2008-06-26 (arylsulfonyl)-pyrasolopiperidines

Country Status (18)

Country Link
US (2) US7732609B2 (fr)
EP (1) EP1957458A2 (fr)
JP (1) JP2009518301A (fr)
KR (1) KR20080073359A (fr)
CN (1) CN101370776A (fr)
AR (1) AR057959A1 (fr)
AU (1) AU2006320423B2 (fr)
BR (1) BRPI0619633A2 (fr)
CA (1) CA2632227A1 (fr)
EA (1) EA014906B1 (fr)
EC (1) ECSP088593A (fr)
IL (1) IL190608A0 (fr)
MA (1) MA30089B1 (fr)
MY (1) MY149422A (fr)
NZ (1) NZ568109A (fr)
PE (1) PE20071090A1 (fr)
TW (1) TW200736255A (fr)
WO (1) WO2007064914A2 (fr)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009538877A (ja) * 2006-05-31 2009-11-12 ガラパゴス・ナムローゼ・フェンノートシャップ 変性疾患及び炎症性疾患の治療に有用なトリアゾロピラジン化合物
BRPI0812014A2 (pt) 2007-05-25 2014-11-18 Elan Pharm Inc Pirazolopirrolidinas como inibidores de gama secretase, composição farmacêutica compreendendo as mesmas e uso dos referidos compostos
EP2271625B1 (fr) 2008-04-01 2012-09-12 Abbott GmbH & Co. KG Tétrahydroisoquinoléines, compositions pharmaceutiques les contenant et leur utilisation en thérapie
TW201038569A (en) * 2009-02-16 2010-11-01 Abbott Gmbh & Co Kg Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy
AR075442A1 (es) 2009-02-16 2011-03-30 Abbott Gmbh & Co Kg Derivados de aminotetralina, composiciones farmaceuticas que las contienen y sus usos en terapia
AU2010229954A1 (en) * 2009-03-25 2011-10-06 Elan Pharmaceuticals, Inc. Process for the production of fused, tricyclic sulfonamides
US8846743B2 (en) 2010-08-13 2014-09-30 Abbott Laboratories Aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapy
US8883839B2 (en) 2010-08-13 2014-11-11 Abbott Laboratories Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
US9051280B2 (en) 2010-08-13 2015-06-09 AbbVie Deutschland GmbH & Co. KG Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy
US8877794B2 (en) 2010-08-13 2014-11-04 Abbott Laboratories Phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapy
US9045459B2 (en) 2010-08-13 2015-06-02 AbbVie Deutschland GmbH & Co. KG Phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapy
US9309200B2 (en) 2011-05-12 2016-04-12 AbbVie Deutschland GmbH & Co. KG Benzazepine derivatives, pharmaceutical compositions containing them, and their use in therapy
CA2844275A1 (fr) 2011-08-05 2013-02-14 AbbVie Deutschland GmbH & Co. KG Derives d'aminochromane, d'aminothiochromane et d'amino-1,2,3,4-tetrahydroquinoleine, compositions pharmaceutiques contenant ceux-ci et leur utilisation therapeutique
MX2014006004A (es) 2011-11-18 2015-04-16 Abbvie Deutschland Derivados de aminobenzociclohepteno, aminotetralina, aminoindano y fenalcilamina n-sustituidas, composiciones farmaceuticas que los contienen, y su uso en terapia.
US9365512B2 (en) 2012-02-13 2016-06-14 AbbVie Deutschland GmbH & Co. KG Isoindoline derivatives, pharmaceutical compositions containing them, and their use in therapy
US9656955B2 (en) 2013-03-15 2017-05-23 Abbvie Inc. Pyrrolidine derivatives, pharmaceutical compositions containing them, and their use in therapy
US9650334B2 (en) 2013-03-15 2017-05-16 Abbvie Inc. Pyrrolidine derivatives, pharmaceutical compositions containing them, and their use in therapy
AU2014336154A1 (en) 2013-10-17 2016-04-28 AbbVie Deutschland GmbH & Co. KG Aminotetraline and aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapy
SG11201602982YA (en) 2013-10-17 2016-05-30 Abbvie Deutschland Aminochromane, aminothiochromane and amino-1,2,3,4-tetrahydroquinoline derivatives, pharmaceutical compositions containing them, and their use in therapy
CN104059063A (zh) * 2014-04-03 2014-09-24 丽水绿氟科技有限公司 7,7-二氟-4,5,6,7-四氢吡唑并[4,3-c]吡啶及其衍生物的制备方法
IL277071B1 (en) 2018-03-08 2024-03-01 Incyte Corp Aminopyrizine diol compounds as PI3K–y inhibitors
US11046658B2 (en) 2018-07-02 2021-06-29 Incyte Corporation Aminopyrazine derivatives as PI3K-γ inhibitors

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL319758A1 (en) * 1994-10-20 1997-08-18 Pfizer Bicyclic tetrahydropyrasole pyridines and their application as medicines
EA006381B1 (ru) * 2000-08-10 2005-12-29 Фармация Италия С.П.А. Бициклопиразолы, активные в качестве ингибиторов киназы, способ их получения и включающие их фармацевтические композиции
EP1443046B1 (fr) * 2001-10-09 2008-12-17 Kyorin Pharmaceutical Co., Ltd. Nouvelles 4-(2-furoyl)aminopiperidines, intermediaires utilises dans la synthese de ces dernieres, leur procede de production et leur utilisation medicale
AU2003292724A1 (en) * 2002-12-27 2004-07-29 Japan Tobacco Inc. Fused n-containing heterocyclic compounds and medicinal use thereof
US20060035884A1 (en) * 2004-05-20 2006-02-16 Elan Pharmaceuticals, Inc. N-cyclic sulfonamido inhibitors of gamma secretase
CA2585925C (fr) * 2004-10-27 2014-04-22 Janssen Pharmaceutica, N.V. Agents regulateurs de cannabinoides de type tetrahydropyridinylpyrazole
DE102005002500A1 (de) * 2005-01-19 2006-07-27 Sanofi-Aventis Deutschland Gmbh Tetrahydrofuranderivate als Inhibitoren von Matrix-Metalloproteinasen
WO2006101434A1 (fr) * 2005-03-22 2006-09-28 Astrazeneca Ab Nouveaux derives de tetrahydro-1h-pyrido [4,3-b]indole utilises comme ligands du recepteur cb1'
DE102005016170A1 (de) * 2005-04-07 2006-10-12 Grünenthal GmbH 4,5,6,7- Tetrahydro-isoxazolo(4,5c)pyridin-Verbindungen und deren Verwendung zur Herstellung von Arzneimitteln
AU2006283567A1 (en) * 2005-08-19 2007-03-01 Elan Pharmaceuticals, Inc. Bridged N-bicyclic sulfonamido inhibitors of gamma secretase

Also Published As

Publication number Publication date
US20100267747A1 (en) 2010-10-21
WO2007064914A3 (fr) 2007-12-27
US7732609B2 (en) 2010-06-08
WO2007064914A2 (fr) 2007-06-07
CA2632227A1 (fr) 2007-06-07
PE20071090A1 (es) 2007-10-24
ECSP088593A (es) 2008-08-29
EP1957458A2 (fr) 2008-08-20
EA014906B1 (ru) 2011-02-28
AU2006320423A1 (en) 2007-06-07
MY149422A (en) 2013-08-30
IL190608A0 (en) 2008-11-03
JP2009518301A (ja) 2009-05-07
TW200736255A (en) 2007-10-01
EA200801481A1 (ru) 2009-02-27
NZ568109A (en) 2011-07-29
BRPI0619633A2 (pt) 2011-10-04
WO2007064914A8 (fr) 2008-05-15
CN101370776A (zh) 2009-02-18
US20070155753A1 (en) 2007-07-05
AR057959A1 (es) 2007-12-26
KR20080073359A (ko) 2008-08-08
AU2006320423B2 (en) 2012-06-21

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