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 usosInfo
- 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
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
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)
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 |
EP4161496A1 (en) * | 2020-06-04 | 2023-04-12 | Curasen Therapeutics, Inc. | Forms and compositions of a beta adrenergic agonist |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2965655D1 (en) * | 1978-06-28 | 1983-07-21 | Beecham Group Plc | Secondary amines, their preparation, pharmaceutical compositions containing them and their use |
US4358455A (en) | 1980-12-23 | 1982-11-09 | Merck & Co., Inc. | Aralkylamindethanol heterocyclic compounds |
GB8528633D0 (en) * | 1985-11-21 | 1985-12-24 | Beecham Group Plc | Compounds |
EP0295828A1 (en) * | 1987-06-13 | 1988-12-21 | Beecham Group Plc | Novel compounds |
US5019578A (en) * | 1987-11-27 | 1991-05-28 | Merck & Co., Inc. | β-adrenergic agonists |
US5051423A (en) | 1988-07-13 | 1991-09-24 | Schering Ag | Derivatized alkanolamines as cardiovascular agents |
US5030640A (en) | 1989-01-05 | 1991-07-09 | Merck & Co., Inc. | Novel β-adrenergic agonists and pharmaceutical compositions thereof |
DE3934436A1 (de) * | 1989-06-01 | 1991-04-18 | Thomae Gmbh Dr K | 2-hydroxy-n-propylamine, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
GB9111426D0 (en) * | 1991-05-28 | 1991-07-17 | Ici Plc | Chemical compounds |
NO179246C (no) | 1991-11-20 | 1996-09-04 | Sankyo Co | Aromatiske amino-alkoholderivater og mellomprodukter til fremstilling derav |
ATE154935T1 (de) * | 1993-06-14 | 1997-07-15 | Pfizer | Zweite amine als antidiabetische mittel und für die behandlung von fettleibigkeit |
US5776983A (en) * | 1993-12-21 | 1998-07-07 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
CN1079794C (zh) | 1994-04-08 | 2002-02-27 | 住友化学工业株式会社 | 醚类化合物,它们的应用以及其制备中所用的中间体 |
US5541197A (en) * | 1994-04-26 | 1996-07-30 | Merck & Co., Inc. | Substituted sulfonamides as selective β3 agonists for the treatment of diabetes and obesity |
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 |
CA2220399A1 (en) | 1995-05-10 | 1996-11-14 | Pfizer Inc. | .beta.-adrenergic agonists |
TR199800521T1 (xx) | 1995-09-21 | 1998-06-22 | Eli Lilly And Company | Se�imli beta3 adrenerjik agonistler. |
EP0882707B1 (en) | 1996-01-10 | 2003-10-08 | Asahi Kasei 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 |
US5808080A (en) * | 1996-09-05 | 1998-09-15 | Eli Lilly And Company | Selective β3 adrenergic agonists |
TR199901063T2 (xx) | 1996-11-14 | 1999-08-23 | Pfizer Inc. | �kame edilmi� piridinler i�in i�lem. |
US6001856A (en) | 1997-06-13 | 1999-12-14 | Pfizer Inc. | β-adrenergic agonists to reduce a wasting condition |
AU3289299A (en) | 1998-02-19 | 1999-09-06 | Tularik Inc. | Antiviral agents |
GB9804426D0 (en) | 1998-03-02 | 1998-04-29 | Pfizer Ltd | Heterocycles |
GB9812709D0 (en) | 1998-06-13 | 1998-08-12 | Glaxo Group Ltd | Chemical compounds |
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 |
DE60015036T2 (de) | 1999-07-23 | 2006-03-02 | Pfizer Products Inc., Groton | 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 |
US6465501B2 (en) | 2000-07-17 | 2002-10-15 | Wyeth | Azolidines as β3 adrenergic receptor agonists |
BR0114836A (pt) * | 2000-10-20 | 2003-07-01 | Pfizer Prod Inc | Agonistas de receptores beta-3 adrenérgicos e suas aplicações |
AR035605A1 (es) | 2000-12-11 | 2004-06-16 | Bayer Corp | Derivados de aminometil cromano di-sustituidos, un metodo para su preparacion, composiciones farmaceuticas y el uso de dichos derivados para la manufactura de medicamentos utiles como agonistas beta-3-adreno-receptores |
EP1236723A1 (en) | 2001-03-01 | 2002-09-04 | Pfizer Products Inc. | Sulfamide derivatives useful as beta3 agonists and pharmaceutical uses thereof |
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 |
-
2003
- 2003-02-17 AU AU2003209527A patent/AU2003209527A1/en not_active Abandoned
- 2003-02-17 WO PCT/IB2003/000737 patent/WO2003072573A1/en not_active Application Discontinuation
- 2003-02-25 US US10/373,473 patent/US6689800B2/en not_active Expired - Fee Related
- 2003-02-25 US US10/373,492 patent/US20030199556A1/en not_active Abandoned
- 2003-02-25 UY UY27677A patent/UY27677A1/es not_active Application Discontinuation
- 2003-02-26 GT GT200300042A patent/GT200300042A/es unknown
- 2003-02-26 PA PA20038567501A patent/PA8567501A1/es unknown
- 2003-02-26 TW TW092104065A patent/TW200400962A/zh unknown
- 2003-02-27 PE PE2003000194A patent/PE20030920A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
US20030199556A1 (en) | 2003-10-23 |
AU2003209527A1 (en) | 2003-09-09 |
GT200300042A (es) | 2003-09-22 |
PA8567501A1 (es) | 2003-11-12 |
US20030166686A1 (en) | 2003-09-04 |
TW200400962A (en) | 2004-01-16 |
US6689800B2 (en) | 2004-02-10 |
UY27677A1 (es) | 2003-10-31 |
WO2003072573A1 (en) | 2003-09-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FD | Application declared void or lapsed |