MY132507A - Process for substituted pyridines - Google Patents

Process for substituted pyridines

Info

Publication number
MY132507A
MY132507A MYPI97005396A MYPI9705396A MY132507A MY 132507 A MY132507 A MY 132507A MY PI97005396 A MYPI97005396 A MY PI97005396A MY PI9705396 A MYPI9705396 A MY PI9705396A MY 132507 A MY132507 A MY 132507A
Authority
MY
Malaysia
Prior art keywords
amino
formula
substituted pyridines
nitro
processes
Prior art date
Application number
MYPI97005396A
Other languages
English (en)
Inventor
Keith Michael Devries
Robert Lee Dow
Stephen Wayne Wright
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 MY132507A publication Critical patent/MY132507A/en

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
    • 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
    • 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
    • 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

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (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)
MYPI97005396A 1996-11-14 1997-11-12 Process for substituted pyridines MY132507A (en)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number Publication Date
MY132507A true MY132507A (en) 2007-10-31

Family

ID=21856496

Family Applications (1)

Application Number Title Priority Date Filing Date
MYPI97005396A MY132507A (en) 1996-11-14 1997-11-12 Process for substituted pyridines

Country Status (32)

Country Link
US (1) US6291489B1 (US06291489-20010918-C00046.png)
EP (1) EP0938476B1 (US06291489-20010918-C00046.png)
JP (1) JP3510635B2 (US06291489-20010918-C00046.png)
KR (1) KR20000053314A (US06291489-20010918-C00046.png)
CN (1) CN1237160A (US06291489-20010918-C00046.png)
AP (1) AP805A (US06291489-20010918-C00046.png)
AR (1) AR010584A1 (US06291489-20010918-C00046.png)
AT (1) ATE319687T1 (US06291489-20010918-C00046.png)
AU (1) AU4634697A (US06291489-20010918-C00046.png)
BG (1) BG103393A (US06291489-20010918-C00046.png)
BR (1) BR9712951A (US06291489-20010918-C00046.png)
CA (1) CA2270386C (US06291489-20010918-C00046.png)
CO (1) CO4930261A1 (US06291489-20010918-C00046.png)
DE (1) DE69735433D1 (US06291489-20010918-C00046.png)
EA (1) EA199900375A1 (US06291489-20010918-C00046.png)
GT (1) GT199700118A (US06291489-20010918-C00046.png)
HR (1) HRP970612A2 (US06291489-20010918-C00046.png)
ID (1) ID18898A (US06291489-20010918-C00046.png)
IL (1) IL129688A0 (US06291489-20010918-C00046.png)
IS (1) IS5029A (US06291489-20010918-C00046.png)
MA (1) MA24401A1 (US06291489-20010918-C00046.png)
MY (1) MY132507A (US06291489-20010918-C00046.png)
NO (1) NO992296D0 (US06291489-20010918-C00046.png)
OA (1) OA11044A (US06291489-20010918-C00046.png)
PA (1) PA8441401A1 (US06291489-20010918-C00046.png)
PE (1) PE10299A1 (US06291489-20010918-C00046.png)
TN (1) TNSN97172A1 (US06291489-20010918-C00046.png)
TR (1) TR199901063T2 (US06291489-20010918-C00046.png)
UY (1) UY24774A1 (US06291489-20010918-C00046.png)
WO (1) WO1998021184A1 (US06291489-20010918-C00046.png)
YU (1) YU22099A (US06291489-20010918-C00046.png)
ZA (1) ZA9710186B (US06291489-20010918-C00046.png)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ID26299A (id) * 1998-04-08 2000-12-14 Novartis Ag Herbisida baru
US6090942A (en) * 1998-10-15 2000-07-18 Pfizer Inc. Process and intermediates for a β3 -adrenergic receptor agonist
CA2362070A1 (en) * 1999-02-16 2000-08-24 Masaru Mitsuda Substituted acetylpyridine derivatives and process for the preparation of intermediates for optically active .beta.3 agonist by the use of 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
ATE280167T1 (de) * 1999-07-23 2004-11-15 Pfizer Prod Inc Zwischenprodukte und ein verfahren zur herstellung von beta3-adrenergischer rezeptor- agoniste
EP1454899A1 (en) * 2001-10-17 2004-09-08 Kaneka Corporation Process for preparation of (s)-alpha-halome thylpyridine methanol derivatives
AU2003209527A1 (en) * 2002-02-27 2003-09-09 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
CA2523253C (en) 2003-05-09 2010-06-22 F. Hoffmann-La Roche Ag Methyl indoles and methyl pyrrolopyridines as alpha-1 adrenergic agonists
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
US7977359B2 (en) 2005-11-04 2011-07-12 Amira Pharmaceuticals, Inc. 5-lipdxygenase-activating protein (FLAP) inhibitors
BRPI0912267A2 (pt) 2008-05-23 2015-10-13 Amira Pharmaceuticals Inc sal farmaceuticamente aceitável, composição farmacêutica, artigo de fabricação, métodos para tratar asma, rinite alérgica, doença, lesões gástricas e dor, métodos para prevenir broncoconstrição e rinite alérgica, uso de um sal farmaceuticamente aceitável, e, processo para a preparação de um sal farmaceuticamente aceitável.

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
CN1129443A (zh) * 1993-06-14 1996-08-21 美国辉瑞有限公司 仲胺用作治糖尿病和治肥胖病药物
IL113410A (en) * 1994-04-26 1999-11-30 Merck & Co Inc Substituted sulfonamides having an asymmetric center and pharmaceutical compositions containing them
WO1996035671A1 (en) * 1995-05-10 1996-11-14 Pfizer Inc. β-ADRENERGIC AGONISTS
JPH11504648A (ja) * 1995-05-10 1999-04-27 ファイザー・インコーポレーテッド β−アドレナリン作動性アゴニスト

Also Published As

Publication number Publication date
BR9712951A (pt) 1999-12-07
CA2270386C (en) 2004-08-03
CO4930261A1 (es) 2000-06-27
TR199901063T2 (xx) 1999-08-23
IL129688A0 (en) 2000-02-29
ID18898A (id) 1998-05-20
HRP970612A2 (en) 1998-08-31
PA8441401A1 (es) 2000-05-24
AU4634697A (en) 1998-06-03
AR010584A1 (es) 2000-06-28
PE10299A1 (es) 1999-02-10
KR20000053314A (ko) 2000-08-25
DE69735433D1 (de) 2006-05-04
ATE319687T1 (de) 2006-03-15
US6291489B1 (en) 2001-09-18
JP2000504347A (ja) 2000-04-11
EP0938476B1 (en) 2006-03-08
CA2270386A1 (en) 1998-05-22
YU22099A (sh) 2001-09-28
EA199900375A1 (ru) 1999-12-29
BG103393A (en) 2000-07-31
ZA9710186B (en) 1999-05-12
AP9701147A0 (en) 1998-01-31
EP0938476A1 (en) 1999-09-01
JP3510635B2 (ja) 2004-03-29
IS5029A (is) 1999-04-16
NO992296L (no) 1999-05-12
CN1237160A (zh) 1999-12-01
WO1998021184A1 (en) 1998-05-22
AP805A (en) 2000-01-28
OA11044A (en) 2002-02-20
TNSN97172A1 (fr) 2005-03-15
NO992296D0 (no) 1999-05-12
UY24774A1 (es) 1998-05-05
MA24401A1 (fr) 1998-07-01
GT199700118A (es) 1999-05-05

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