ES2176329T3 - Procedimientos para preparar formas anhidras e hidratadas de derivados antihistaminicos de piperidina, sus polimeros y pseudomorfos. - Google Patents
Procedimientos para preparar formas anhidras e hidratadas de derivados antihistaminicos de piperidina, sus polimeros y pseudomorfos.Info
- Publication number
- ES2176329T3 ES2176329T3 ES95918278T ES95918278T ES2176329T3 ES 2176329 T3 ES2176329 T3 ES 2176329T3 ES 95918278 T ES95918278 T ES 95918278T ES 95918278 T ES95918278 T ES 95918278T ES 2176329 T3 ES2176329 T3 ES 2176329T3
- Authority
- ES
- Spain
- Prior art keywords
- antihistaminic
- anhydrate
- piperidine
- derivatives
- pseudomorphes
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
Classifications
-
- 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
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
- C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A NUEVOS PROCESOS PARA PREPARAR FORMAS ANHIDRAS E HIDRATOS DE DERIVADOS DE PIPERIDINA, POLIMORFOS Y PSUDOMORFOS DE LOS MISMOS DE FORMULAS (I) Y (II) QUE SON UTILES COMO ANTIHISTAMINICOS, AGENTES ANTIALERGICOS Y BRONCODILATADORES.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24573194A | 1994-05-18 | 1994-05-18 | |
| US41716195A | 1995-04-11 | 1995-04-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2176329T3 true ES2176329T3 (es) | 2002-12-01 |
Family
ID=26937420
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES95918278T Expired - Lifetime ES2176329T3 (es) | 1994-05-18 | 1995-04-28 | Procedimientos para preparar formas anhidras e hidratadas de derivados antihistaminicos de piperidina, sus polimeros y pseudomorfos. |
Country Status (17)
| Country | Link |
|---|---|
| US (12) | US20010025106A1 (es) |
| EP (3) | EP0766668B1 (es) |
| JP (7) | JPH10500134A (es) |
| CN (3) | CN1148849A (es) |
| AT (1) | ATE220667T1 (es) |
| AU (1) | AU693892B2 (es) |
| CA (3) | CA2585705C (es) |
| DE (1) | DE69527429T2 (es) |
| DK (1) | DK0766668T3 (es) |
| ES (1) | ES2176329T3 (es) |
| FI (1) | FI964565A0 (es) |
| HU (1) | HU227676B1 (es) |
| IL (3) | IL134917A (es) |
| MX (1) | MX9605613A (es) |
| NO (1) | NO315319B1 (es) |
| PT (1) | PT766668E (es) |
| WO (1) | WO1995031437A1 (es) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9400555D0 (en) * | 1994-01-13 | 1994-03-09 | Short Brothers Plc | Boundery layer control in aerodynamic low drag structures |
| CA2585705C (en) | 1994-05-18 | 2012-04-17 | Aventis Pharmaceuticals Inc. | Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof |
| PT812195E (pt) * | 1995-02-28 | 2003-03-31 | Aventis Pharma Inc | Composicao farmaceutica para compostos de piperidinoalcanol |
| PT998272E (pt) * | 1997-08-26 | 2003-09-30 | Aventis Pharma Inc | Composicao farmaceutica para combinacao do descongestionante piperidinoalcanol |
| IN191492B (es) * | 1999-05-25 | 2003-12-06 | Ranbaxy Lab Ltd | |
| US6613906B1 (en) | 2000-06-06 | 2003-09-02 | Geneva Pharmaceuticals, Inc. | Crystal modification |
| CH695216A5 (de) * | 2001-02-23 | 2006-01-31 | Cilag Ag | Verfahren zur Herstellung eines nicht hydratisierten Salzes eines Piperidinderivats und eine so erhältliche neue kristalline Form eines solchen Salzes. |
| US20030021849A1 (en) * | 2001-04-09 | 2003-01-30 | Ben-Zion Dolitzky | Polymorphs of fexofenadine hydrochloride |
| EP1392303A4 (en) * | 2001-04-09 | 2005-01-26 | Teva Pharma | FEXOFENADINE HYDROCHLORIDE POLYMORPHS |
| US7700779B2 (en) * | 2001-06-18 | 2010-04-20 | Dr. Reddy's Laboratories Limited | Crystalline forms of fexofenadine and its hydrochloride |
| KR20040015734A (ko) * | 2001-06-18 | 2004-02-19 | 닥터 레디스 레보러터리즈 리미티드 | 4-[4-[4-(히드록실디페닐메틸)-1-피페리디닐]-1-히드록시부틸]-α,α-디메틸벤젠 아세트산 및 그 염산염의 신규 결정형태 |
| PT1414453E (pt) * | 2001-07-31 | 2008-05-29 | Texcontor Ets | Polimorfo de cloridrato de fexofenadina |
| US20030158227A1 (en) * | 2001-11-08 | 2003-08-21 | Barnaba Krochmal | Polymorphs of fexofenadine base |
| AU2003248657A1 (en) * | 2002-06-10 | 2003-12-22 | Teva Pharmaceutical Industries Ltd. | Polymorphic form xvi of fexofenadine hydrochloride |
| JP3910907B2 (ja) * | 2002-10-29 | 2007-04-25 | 新光電気工業株式会社 | キャパシタ素子及びこの製造方法、半導体装置用基板、並びに半導体装置 |
| ATE425170T1 (de) * | 2003-07-03 | 2009-03-15 | Teva Pharma | Kristallformen der zoledronsäure und deren natrioumsalze, amorphes natriumzoledronat und verfahren zu deren herstellung |
| GB0319935D0 (en) | 2003-08-26 | 2003-09-24 | Cipla Ltd | Polymorphs |
| EP1628959A2 (en) * | 2004-04-26 | 2006-03-01 | Teva Pharmaceutical Industries Ltd | Crystalline forms of fexofenadine hydrochloride and processes for their preparation |
| ITMI20041143A1 (it) | 2004-06-08 | 2004-09-08 | Dipharma Spa | Polimorfi di fexofenadina e procedimento per la loro preparazione |
| EP1616861A3 (en) * | 2004-06-15 | 2006-02-08 | Dipharma S.p.A. | A process for the preparation of keto compounds |
| ITMI20041568A1 (it) * | 2004-07-30 | 2004-10-30 | Dipharma Spa | "polimorfi di fexofenadina base" |
| US20060148851A1 (en) * | 2004-09-28 | 2006-07-06 | Shlomit Wizel | Fexofenadine crystal form and processes for its preparation thereof |
| DOP2006000274A (es) * | 2005-12-14 | 2007-10-15 | Sanofi Aventis Us Llc | Formulación de suspensión de fexofenadina |
| EP2046299A1 (en) * | 2006-07-11 | 2009-04-15 | Mutual Pharmaceutical Company, Inc. | Controlled-release formulations |
| US20090076080A1 (en) * | 2007-09-19 | 2009-03-19 | Protia, Llc | Deuterium-enriched fexofenadine |
| EP2105134A1 (en) | 2008-03-24 | 2009-09-30 | Ranbaxy Laboratories Limited | Stable amorphous fexofenadine hydrochloride |
| WO2010083360A2 (en) * | 2009-01-16 | 2010-07-22 | Mutual Pharmaceutical Company, Inc. | Controlled-release formulations |
| WO2011054741A2 (en) | 2009-11-06 | 2011-05-12 | Basf Se | Crystalline complexes of 4-hydroxy benzoic acid and selected pesticides |
| IT1400965B1 (it) | 2010-06-15 | 2013-07-05 | Dipharma Francis Srl | Polimorfi di fexofenadina |
| WO2011158262A1 (en) | 2010-06-15 | 2011-12-22 | Chemelectiva S.R.L. | Polymorphic form of fexofenadine hydrochloride, intermediates and process for its preparation |
| US9420872B2 (en) * | 2010-08-23 | 2016-08-23 | Jason Bird | Apparatus and system for holding game-calling devices |
| JP2012087100A (ja) * | 2010-10-21 | 2012-05-10 | Sumitomo Chemical Co Ltd | 形態iのフェキソフェナジン一塩酸塩の製造方法 |
| CN104072402B (zh) * | 2014-07-16 | 2016-08-17 | 昆山龙灯瑞迪制药有限公司 | 一种新结晶形式的盐酸非索非那定化合物及其制备方法 |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US631375A (en) * | 1899-04-12 | 1899-08-22 | Ephraim Musselman | Face-protector. |
| US3448152A (en) * | 1966-11-03 | 1969-06-03 | Jefferson Chem Co Inc | Amine recovery |
| BE794598A (fr) | 1972-01-28 | 1973-05-16 | Richardson Merrell Inc | Nouveaux derives olefiniques de piperidines substituees en 4 et leur procede de preparation |
| US3965257A (en) | 1972-01-28 | 1976-06-22 | Richardson-Merrell Inc. | Compositions and methods for the treatment of the symptoms of histamine induced allergic reactions |
| US3878217A (en) * | 1972-01-28 | 1975-04-15 | Richardson Merrell Inc | Alpha-aryl-4-substituted piperidinoalkanol derivatives |
| US4285957A (en) * | 1979-04-10 | 1981-08-25 | Richardson-Merrell Inc. | 1-Piperidine-alkanol derivatives, pharmaceutical compositions thereof, and method of use thereof |
| US4254130A (en) * | 1979-04-10 | 1981-03-03 | Richardson-Merrell Inc. | Piperidine derivatives |
| US4285958A (en) * | 1979-04-10 | 1981-08-25 | Richardson-Merrell Inc. | 1-Piperidine-alkylene ketones, pharmaceutical compositions thereof and method of use thereof |
| US4254129A (en) | 1979-04-10 | 1981-03-03 | Richardson-Merrell Inc. | Piperidine derivatives |
| IL63968A (en) | 1980-10-01 | 1985-10-31 | Glaxo Group Ltd | Form 2 ranitidine hydrochloride,its preparation and pharmaceutical compositions containing it |
| US4742175A (en) | 1986-05-07 | 1988-05-03 | Merrell Dow Pharmaceuticals Inc. | Preparation of polymorphically pure terfenadine |
| JPH02213431A (ja) * | 1989-02-13 | 1990-08-24 | Kobe Steel Ltd | SiCウィスカ強化Al合金複合材料 |
| DE4034218A1 (de) | 1990-10-27 | 1992-04-30 | Merck Patent Gmbh | Verfahren zur herstellung von carebastin |
| TW198008B (es) | 1991-04-08 | 1993-01-11 | Green Cross Corp | |
| US5631375A (en) | 1992-04-10 | 1997-05-20 | Merrell Pharmaceuticals, Inc. | Process for piperidine derivatives |
| EP0635004B1 (en) * | 1992-04-10 | 2002-07-17 | Merrell Pharmaceuticals Inc. | 4-diphenylmethyl piperidine derivatives and process for their preparation |
| EP0639976B1 (en) * | 1992-05-11 | 2000-07-26 | Merrell Pharmaceuticals Inc. | Use of terfenadine derivatives as antihistaminics in a hepatically impaired patient |
| WO1994003170A1 (en) | 1992-08-03 | 1994-02-17 | Sepracor Inc. | Terfenadine metabolites and their optically pure isomers for treating allergic disorders |
| US5315016A (en) | 1992-10-13 | 1994-05-24 | Nycomed Dak A/S | Process for preparing pure podophyllotoxin |
| DK1026147T3 (da) | 1993-06-24 | 2004-03-22 | Albany Molecular Res Inc | Forbindelser, der er anvendelige som mellemprodukter i fremstillingen af piperidinderivater |
| CA2254506C (en) | 1993-06-24 | 2000-11-28 | Albany Molecular Research, Inc. | Piperidine derivatives and process for their production |
| HU226037B1 (en) | 1993-06-25 | 2008-03-28 | Aventis Inc | Process for producing antihistaminic 4-diphenylmethyl/diphenylmethoxy piperidine derivatives and novel intermediates |
| US6147216A (en) | 1993-06-25 | 2000-11-14 | Merrell Pharmaceuticals Inc. | Intermediates useful for the preparation of antihistaminic piperidine derivatives |
| CA2585705C (en) * | 1994-05-18 | 2012-04-17 | Aventis Pharmaceuticals Inc. | Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof |
| US5576610A (en) | 1994-07-05 | 1996-11-19 | Motorola, Inc. | Method and apparatus for determining battery characteristics |
| IL134772A (en) | 1995-02-28 | 2002-02-10 | Aventis Pharma Inc | Pharmaceutical compositions of piperidinoalkanol compounds in solid unit dosage form |
| PT812195E (pt) | 1995-02-28 | 2003-03-31 | Aventis Pharma Inc | Composicao farmaceutica para compostos de piperidinoalcanol |
| US5574045A (en) * | 1995-06-06 | 1996-11-12 | Hoechst Marion Roussel, Inc. | Oral pharmaceutical composition of piperidinoalkanol compounds in solution form |
| PT998272E (pt) * | 1997-08-26 | 2003-09-30 | Aventis Pharma Inc | Composicao farmaceutica para combinacao do descongestionante piperidinoalcanol |
| US6214427B1 (en) * | 1998-08-28 | 2001-04-10 | General Electric Company | Method of making an electronic device having a single crystal substrate formed by solid state crystal conversion |
| US6613906B1 (en) * | 2000-06-06 | 2003-09-02 | Geneva Pharmaceuticals, Inc. | Crystal modification |
| US20020177680A1 (en) * | 2000-08-23 | 2002-11-28 | Hubbell Jeffrey A. | Novel polymer compounds |
| US6475942B1 (en) * | 2000-09-05 | 2002-11-05 | General Electric Company | Conversion of polycrystalline alumina to single crystal sapphire using molybdenum doping |
| EP1392303A4 (en) * | 2001-04-09 | 2005-01-26 | Teva Pharma | FEXOFENADINE HYDROCHLORIDE POLYMORPHS |
| US7700779B2 (en) * | 2001-06-18 | 2010-04-20 | Dr. Reddy's Laboratories Limited | Crystalline forms of fexofenadine and its hydrochloride |
| US20090211514A1 (en) * | 2008-02-26 | 2009-08-27 | Lehigh University | Single crystal conversion process |
-
1995
- 1995-04-28 CA CA2585705A patent/CA2585705C/en not_active Expired - Lifetime
- 1995-04-28 CN CN95193122A patent/CN1148849A/zh active Pending
- 1995-04-28 WO PCT/US1995/004942 patent/WO1995031437A1/en not_active Ceased
- 1995-04-28 DK DK95918278T patent/DK0766668T3/da active
- 1995-04-28 EP EP95918278A patent/EP0766668B1/en not_active Expired - Lifetime
- 1995-04-28 DE DE69527429T patent/DE69527429T2/de not_active Expired - Lifetime
- 1995-04-28 PT PT95918278T patent/PT766668E/pt unknown
- 1995-04-28 CN CN2006101031426A patent/CN1907967B/zh not_active Expired - Lifetime
- 1995-04-28 FI FI964565A patent/FI964565A0/fi unknown
- 1995-04-28 JP JP7529654A patent/JPH10500134A/ja not_active Withdrawn
- 1995-04-28 CA CA2449419A patent/CA2449419C/en not_active Expired - Lifetime
- 1995-04-28 CN CNA2003101007654A patent/CN1623985A/zh active Pending
- 1995-04-28 HU HU9603167A patent/HU227676B1/hu unknown
- 1995-04-28 EP EP01124314A patent/EP1178041A1/en not_active Withdrawn
- 1995-04-28 ES ES95918278T patent/ES2176329T3/es not_active Expired - Lifetime
- 1995-04-28 EP EP10180285A patent/EP2354125A1/en not_active Withdrawn
- 1995-04-28 AT AT95918278T patent/ATE220667T1/de active
- 1995-04-28 AU AU24265/95A patent/AU693892B2/en not_active Expired
- 1995-04-28 MX MX9605613A patent/MX9605613A/es unknown
- 1995-04-28 CA CA002189007A patent/CA2189007C/en not_active Expired - Lifetime
- 1995-05-16 IL IL13491795A patent/IL134917A/en not_active IP Right Cessation
- 1995-05-16 IL IL11374795A patent/IL113747A/en not_active IP Right Cessation
-
1996
- 1996-11-15 NO NO19964859A patent/NO315319B1/no not_active IP Right Cessation
-
2000
- 2000-03-07 IL IL13491700A patent/IL134917A0/xx unknown
-
2001
- 2001-03-09 US US09/803,476 patent/US20010025106A1/en not_active Abandoned
- 2001-03-09 US US09/803,389 patent/US20010012896A1/en not_active Abandoned
- 2001-03-09 US US09/803,390 patent/US20010014741A1/en not_active Abandoned
-
2002
- 2002-03-01 JP JP2002055434A patent/JP4503909B2/ja not_active Expired - Lifetime
- 2002-03-01 JP JP2002055431A patent/JP2002308849A/ja active Pending
- 2002-03-01 JP JP2002055433A patent/JP4503908B2/ja not_active Expired - Lifetime
- 2002-03-01 JP JP2002055435A patent/JP2002316978A/ja not_active Withdrawn
- 2002-03-01 JP JP2002055432A patent/JP4503907B2/ja not_active Expired - Lifetime
- 2002-04-24 US US10/128,926 patent/US20020193600A1/en not_active Abandoned
- 2002-06-03 US US10/162,011 patent/US7138524B2/en not_active Expired - Fee Related
- 2002-06-03 US US10/160,883 patent/US7135571B2/en not_active Expired - Fee Related
- 2002-08-07 US US10/214,262 patent/US20030045721A1/en not_active Abandoned
-
2003
- 2003-03-10 US US10/386,812 patent/US20040014976A1/en not_active Abandoned
-
2006
- 2006-09-25 US US11/534,828 patent/US7666881B2/en not_active Expired - Fee Related
- 2006-09-25 US US11/534,839 patent/US7662835B2/en not_active Expired - Fee Related
-
2007
- 2007-10-30 US US11/978,669 patent/US20080167469A1/en not_active Abandoned
- 2007-10-30 US US11/978,670 patent/US20080167471A1/en not_active Abandoned
-
2010
- 2010-02-24 JP JP2010038971A patent/JP2010120969A/ja active Pending
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