UY24774A1 - Procedimiento para piridinas sustituidas - Google Patents

Procedimiento para piridinas sustituidas

Info

Publication number
UY24774A1
UY24774A1 UY24774A UY24774A UY24774A1 UY 24774 A1 UY24774 A1 UY 24774A1 UY 24774 A UY24774 A UY 24774A UY 24774 A UY24774 A UY 24774A UY 24774 A1 UY24774 A1 UY 24774A1
Authority
UY
Uruguay
Prior art keywords
compound
procedure
useful
substituted pyridines
acetylaminopyridin
Prior art date
Application number
UY24774A
Other languages
English (en)
Inventor
Lee Dow Robert
Michael Devries Keith
Wayne Wright Stephen
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of UY24774A1 publication Critical patent/UY24774A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • C07D213/73Unsubstituted amino or imino radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • C07D213/75Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invención se refiere a un compuesto de fórmula (VIII) (figura 1) en la que Y5 es como se representa en la figura 2 y en la figura 3, donde Q3 es, entre otras posibilidades, un heterociclo seleccionado entre el grupo compuesto por -(CH2)n-piridilo, -(CHe)n-pirimidilo, entre otros. Como ejemplo no limitante: N-metil4-(2-(2-(2-acetilaminopiridin-5-il)-2-(R)-hidroxietil-N-terc-butiloxicarbonilamino)-etoxi)-fenilacetamida. Se describe además un procedimiento para preparar el compuesto. Los productos según la invención son útiles como agonistas de receptores beta-andrenérgicos, y en particular son útiles como agentes hipoglucemicos y contra la obesidad.
UY24774A 1996-11-14 1997-11-12 Procedimiento para piridinas sustituidas UY24774A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US3088096P 1996-11-14 1996-11-14

Publications (1)

Publication Number Publication Date
UY24774A1 true UY24774A1 (es) 1998-05-05

Family

ID=21856496

Family Applications (1)

Application Number Title Priority Date Filing Date
UY24774A UY24774A1 (es) 1996-11-14 1997-11-12 Procedimiento para piridinas sustituidas

Country Status (32)

Country Link
US (1) US6291489B1 (es)
EP (1) EP0938476B1 (es)
JP (1) JP3510635B2 (es)
KR (1) KR20000053314A (es)
CN (1) CN1237160A (es)
AP (1) AP805A (es)
AR (1) AR010584A1 (es)
AT (1) ATE319687T1 (es)
AU (1) AU4634697A (es)
BG (1) BG103393A (es)
BR (1) BR9712951A (es)
CA (1) CA2270386C (es)
CO (1) CO4930261A1 (es)
DE (1) DE69735433D1 (es)
EA (1) EA199900375A1 (es)
GT (1) GT199700118A (es)
HR (1) HRP970612A2 (es)
ID (1) ID18898A (es)
IL (1) IL129688A0 (es)
IS (1) IS5029A (es)
MA (1) MA24401A1 (es)
MY (1) MY132507A (es)
NO (1) NO992296D0 (es)
OA (1) OA11044A (es)
PA (1) PA8441401A1 (es)
PE (1) PE10299A1 (es)
TN (1) TNSN97172A1 (es)
TR (1) TR199901063T2 (es)
UY (1) UY24774A1 (es)
WO (1) WO1998021184A1 (es)
YU (1) YU22099A (es)
ZA (1) ZA9710186B (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU3605299A (en) * 1998-04-08 1999-11-01 Novartis Ag Novel herbicides
US6090942A (en) * 1998-10-15 2000-07-18 Pfizer Inc. Process and intermediates for a β3 -adrenergic receptor agonist
EP1153919A4 (en) * 1999-02-16 2002-10-02 Kaneka Corp SUBSTITUTED ACETYLPYRIDINE DERIVATIVES AND PROCESS FOR THE PREPARATION OF INTERMEDIATES FOR OPTICALLY ACTIVE BETA3 ADRENERGIC RECEPTOR AGONIST USING THE SAME
US6455734B1 (en) * 2000-08-09 2002-09-24 Magnesium Diagnostics, Inc. Antagonists of the magnesium binding defect as therapeutic agents and methods for treatment of abnormal physiological states
EP1078924B1 (en) * 1999-07-23 2004-10-20 Pfizer Products Inc. Intermediates and a process for producing beta-adrenergic receptor agonists
WO2003033468A1 (fr) * 2001-10-17 2003-04-24 Kaneka Corporation Procede de preparation de derives de (s)-$g(a)-halomethylpyridine-methanol
WO2003072573A1 (en) * 2002-02-27 2003-09-04 Pfizer Products Inc. Crystal forms of (r)-2-(2-(4-oxazol-4-yl-phenoxy)-ethylamino)-1-pyridin-3-yl-ethanol
US6864268B2 (en) 2002-02-27 2005-03-08 Pfizer Inc. β3 adrenergic receptor agonists
MXPA04008298A (es) * 2002-02-27 2004-11-26 Pfizer Prod Inc Procesos e intermedios utiles en la preparacion de agonistas de receptor beta-3 adrenergico.
EP1424079A1 (en) * 2002-11-27 2004-06-02 Boehringer Ingelheim International GmbH Combination of a beta-3-receptor agonist and of a reuptake inhibitor of serotonin and/or norepinephrine
ATE406363T1 (de) 2003-05-09 2008-09-15 Hoffmann La Roche Methylindole und methylpyrrolopyridine als alpha- 1-adrenerge agonisten
US7977359B2 (en) 2005-11-04 2011-07-12 Amira Pharmaceuticals, Inc. 5-lipdxygenase-activating protein (FLAP) inhibitors
US8399666B2 (en) 2005-11-04 2013-03-19 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
GB2431927B (en) 2005-11-04 2010-03-17 Amira Pharmaceuticals Inc 5-Lipoxygenase-activating protein (FLAP) inhibitors
CA2724726C (en) 2008-05-23 2018-02-27 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein inhibitor

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4358455A (en) 1980-12-23 1982-11-09 Merck & Co., Inc. Aralkylamindethanol heterocyclic compounds
US5019578A (en) 1987-11-27 1991-05-28 Merck & Co., Inc. β-adrenergic agonists
AU675536B2 (en) 1993-06-14 1997-02-06 Pfizer Inc. Secondary amines as antidiabetic and antiobesity agents
IL113410A (en) * 1994-04-26 1999-11-30 Merck & Co Inc Substituted sulfonamides having an asymmetric center and pharmaceutical compositions containing them
US5977124A (en) * 1995-05-10 1999-11-02 Pfizer Inc. β-adrenergic agonists
CA2220538A1 (en) 1995-05-10 1996-11-14 Pfizer Inc. .beta.-adrenergic agonists

Also Published As

Publication number Publication date
US6291489B1 (en) 2001-09-18
WO1998021184A1 (en) 1998-05-22
KR20000053314A (ko) 2000-08-25
NO992296L (no) 1999-05-12
PE10299A1 (es) 1999-02-10
IS5029A (is) 1999-04-16
CA2270386A1 (en) 1998-05-22
JP2000504347A (ja) 2000-04-11
CA2270386C (en) 2004-08-03
IL129688A0 (en) 2000-02-29
CO4930261A1 (es) 2000-06-27
MA24401A1 (fr) 1998-07-01
BR9712951A (pt) 1999-12-07
AP805A (en) 2000-01-28
NO992296D0 (no) 1999-05-12
TR199901063T2 (xx) 1999-08-23
AU4634697A (en) 1998-06-03
EP0938476A1 (en) 1999-09-01
HRP970612A2 (en) 1998-08-31
PA8441401A1 (es) 2000-05-24
ID18898A (id) 1998-05-20
AP9701147A0 (en) 1998-01-31
ZA9710186B (en) 1999-05-12
EA199900375A1 (ru) 1999-12-29
TNSN97172A1 (fr) 2005-03-15
OA11044A (en) 2002-02-20
AR010584A1 (es) 2000-06-28
EP0938476B1 (en) 2006-03-08
GT199700118A (es) 1999-05-05
MY132507A (en) 2007-10-31
JP3510635B2 (ja) 2004-03-29
ATE319687T1 (de) 2006-03-15
YU22099A (sh) 2001-09-28
BG103393A (en) 2000-07-31
DE69735433D1 (de) 2006-05-04
CN1237160A (zh) 1999-12-01

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Legal Events

Date Code Title Description
ABAN Application deemed to be withdrawn (no publication fee paid)

Effective date: 20001222