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PE20030920A1 - Formas cristalinas de agonistas del receptor b3-adrenergico, procedimiento para su preparacion y sus usos - Google Patents

Formas cristalinas de agonistas del receptor b3-adrenergico, procedimiento para su preparacion y sus usos

Info

Publication number
PE20030920A1
PE20030920A1 PE2003000194A PE2003000194A PE20030920A1 PE 20030920 A1 PE20030920 A1 PE 20030920A1 PE 2003000194 A PE2003000194 A PE 2003000194A PE 2003000194 A PE2003000194 A PE 2003000194A PE 20030920 A1 PE20030920 A1 PE 20030920A1
Authority
PE
Peru
Prior art keywords
procedure
preparation
refers
diffraction
agonists
Prior art date
Application number
PE2003000194A
Other languages
English (en)
Inventor
Jennifer Anne Lafontaine
Joseph Francis Krzyzaniak
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of PE20030920A1 publication Critical patent/PE20030920A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics

Landscapes

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

Abstract

SE REFIERE A UNA FORMA CRISTALINA DE LA SAL DE p-TOLUENSULFONATO DEL (R)-2-(2-(4-OXAZOL-4-IL-FENOXI)-ETILAMINO)-1-PIRIDIN-3-IL-ETANOL QUE PRESENTA PICOS DE DIFRACCION DE RAYOS X DE ALTA INTENSIDAD A ANGULOS DE DIFRACCION (2 THETA) DE 6,0 Y 18,1 Y DISTANCIA (d) DE DIFRACCION DE RAYOS X DE POLVO DE 14,7 Y 4,9 RESPECTIVAMENTE. LA FORMA CRISTALINA TIENEN UNA TEMPERATURA DE FUSION DE 160°C. SE REFIERE TAMBIEN A UN PROCEDIMIENTO PARA LA PREPARACION QUE COMPRENDE PREPARAR UNA SOLUCION DE (R)-2-(2-(4-OXAZOL-4-IL-FENOXI)-ETILAMINO)-1-PIRIDIN-3-IL-ETANOL EN UN SOLVENTE INERTE PARA LA REACCION Y TRATAR DICHA SOLUCION CON ACIDO p-TOLUENSULFONICO MONOHIDRATO PARA OBTENER UNA RELACION ESTEQUIOMETRIA AL FINAL DE 1:1. EL PROCEDIMIENTO SE LLEVA A CABO EN UN SOLVENTE INERTE COMO TETRAHIDROFURANO. SE REFIERE TAMBIEN A METODOS PARA TRATAR LA DIABETES Y LA HIPOGLUCEMIA CON DICHAS FORMAS CRISTALINAS
PE2003000194A 2002-02-27 2003-02-27 Formas cristalinas de agonistas del receptor b3-adrenergico, procedimiento para su preparacion y sus usos PE20030920A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US36025202P 2002-02-27 2002-02-27

Publications (1)

Publication Number Publication Date
PE20030920A1 true PE20030920A1 (es) 2003-10-29

Family

ID=27766208

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2003000194A PE20030920A1 (es) 2002-02-27 2003-02-27 Formas cristalinas de agonistas del receptor b3-adrenergico, procedimiento para su preparacion y sus usos

Country Status (8)

Country Link
US (2) US6689800B2 (es)
AU (1) AU2003209527A1 (es)
GT (1) GT200300042A (es)
PA (1) PA8567501A1 (es)
PE (1) PE20030920A1 (es)
TW (1) TW200400962A (es)
UY (1) UY27677A1 (es)
WO (1) WO2003072573A1 (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US20050075323A1 (en) * 2003-03-05 2005-04-07 Pfizer Inc Beta3 adrenergic receptor agonists and uses thereof
DE102004050952A1 (de) * 2004-10-18 2006-04-20 Boehringer Ingelheim Pharma Gmbh & Co. Kg Pharmazeutische Zusammensetzung zur Behandlung von Beschwerden, die mit krankhaften Veränderungen oder Irritationen der Prostata verbunden sind
US8377465B2 (en) * 2005-02-11 2013-02-19 Kansas State University Research Foundation Product and process for elevating lipid blood levels in livestock
US20230219892A1 (en) * 2020-06-04 2023-07-13 Curasen Therapeutics, Inc. Forms and compositions of a beta adrenergic agonist

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GB8528633D0 (en) * 1985-11-21 1985-12-24 Beecham Group Plc Compounds
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US5030640A (en) * 1989-01-05 1991-07-09 Merck & Co., Inc. Novel β-adrenergic agonists and pharmaceutical compositions thereof
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US5776983A (en) * 1993-12-21 1998-07-07 Bristol-Myers Squibb Company Catecholamine surrogates useful as β3 agonists
ES2181772T3 (es) 1994-04-08 2003-03-01 Sumitomo Chemical Co Compuesto de eter, su utilizacion e intermediario para la obtencion de este compuesto.
US5705515A (en) 1994-04-26 1998-01-06 Merck & Co., Inc. Substituted sulfonamides as selective β-3 agonists for the treatment of diabetes and obesity
US5541197A (en) 1994-04-26 1996-07-30 Merck & Co., Inc. Substituted sulfonamides as selective β3 agonists for the treatment of diabetes and obesity
US5977124A (en) 1995-05-10 1999-11-02 Pfizer Inc. β-adrenergic agonists
US6075040A (en) 1996-09-05 2000-06-13 Eli Lilly And Company Selective β3 adrenergic agonists
PL325865A1 (en) 1995-09-21 1998-08-17 Lilly Co Eli Selective antagonists of beta3-adrenergic receptor
AU715233B2 (en) 1996-01-10 2000-01-20 Asahi Kasei Kogyo Kabushiki Kaisha Novel tricyclic compounds and drug compositions containing the same
EP0801060A1 (en) 1996-04-09 1997-10-15 Pfizer Inc. Heterocyclic Beta-3 Adrenergenic Agonists
US6008361A (en) 1996-04-09 1999-12-28 Pfizer Inc. Substituted pyridines
US5859044A (en) * 1996-07-31 1999-01-12 Pfizer Inc. β-adrenergic agonists
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US6001856A (en) 1997-06-13 1999-12-14 Pfizer Inc. β-adrenergic agonists to reduce a wasting condition
WO1999042455A1 (en) 1998-02-19 1999-08-26 Tularik Inc. Antiviral agents
GB9804426D0 (en) 1998-03-02 1998-04-29 Pfizer Ltd Heterocycles
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US6090942A (en) 1998-10-15 2000-07-18 Pfizer Inc. Process and intermediates for a β3 -adrenergic receptor agonist
AUPP796798A0 (en) 1998-12-30 1999-01-28 Fujisawa Pharmaceutical Co., Ltd. New compound
ATE280167T1 (de) 1999-07-23 2004-11-15 Pfizer Prod Inc Zwischenprodukte und ein verfahren zur herstellung von beta3-adrenergischer rezeptor- agoniste
US6451587B1 (en) 1999-09-29 2002-09-17 Pfizer Inc. Microbial asymmetric reduction of 2-chloro-1-[-6-(2,5-dimethyl-pyrrol-1-yl)-pyridin-3-yl]-ethanone
GB2356197A (en) * 1999-10-12 2001-05-16 Merck & Co Inc Amide derivatives as beta 3 agonists
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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

Also Published As

Publication number Publication date
US20030166686A1 (en) 2003-09-04
WO2003072573A1 (en) 2003-09-04
GT200300042A (es) 2003-09-22
TW200400962A (en) 2004-01-16
AU2003209527A1 (en) 2003-09-09
US20030199556A1 (en) 2003-10-23
US6689800B2 (en) 2004-02-10
PA8567501A1 (es) 2003-11-12
UY27677A1 (es) 2003-10-31

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