FI991477A0 - Menetelmä tolterodiinin valmistamiseksi - Google Patents
Menetelmä tolterodiinin valmistamiseksiInfo
- Publication number
- FI991477A0 FI991477A0 FI991477A FI991477A FI991477A0 FI 991477 A0 FI991477 A0 FI 991477A0 FI 991477 A FI991477 A FI 991477A FI 991477 A FI991477 A FI 991477A FI 991477 A0 FI991477 A0 FI 991477A0
- Authority
- FI
- Finland
- Prior art keywords
- tolterodine
- preparation
- benzopyran
- dihydro
- phenyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/20—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 hydrogenated in the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C215/48—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups
- C07C215/54—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Pyrane Compounds (AREA)
- Optical Integrated Circuits (AREA)
- Saccharide Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3396196P | 1996-12-31 | 1996-12-31 | |
| PCT/US1997/022521 WO1998029402A1 (fr) | 1996-12-31 | 1997-12-18 | Procede de preparation de la tolterodine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FI991477A0 true FI991477A0 (fi) | 1999-06-29 |
| FI991477A FI991477A (fi) | 1999-06-29 |
Family
ID=21873473
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI991477A FI991477A (fi) | 1996-12-31 | 1999-06-29 | Menetelmä tolterodiinin valmistamiseksi |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US5922914A (fr) |
| EP (1) | EP0960109B1 (fr) |
| JP (1) | JP4199310B2 (fr) |
| KR (2) | KR20000057548A (fr) |
| CN (1) | CN1151141C (fr) |
| AT (1) | ATE226949T1 (fr) |
| AU (1) | AU717985B2 (fr) |
| CA (1) | CA2273789C (fr) |
| CZ (1) | CZ295477B6 (fr) |
| DE (1) | DE69716767T2 (fr) |
| DK (1) | DK0960109T3 (fr) |
| ES (1) | ES2186018T3 (fr) |
| FI (1) | FI991477A (fr) |
| HK (1) | HK1023566A1 (fr) |
| HU (1) | HUP0000527A3 (fr) |
| NO (1) | NO317158B1 (fr) |
| NZ (1) | NZ336533A (fr) |
| PL (1) | PL191603B1 (fr) |
| PT (1) | PT960109E (fr) |
| RU (1) | RU2176246C2 (fr) |
| SI (1) | SI0960109T1 (fr) |
| SK (1) | SK283591B6 (fr) |
| WO (1) | WO1998029402A1 (fr) |
Families Citing this family (59)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000515525A (ja) * | 1996-07-19 | 2000-11-21 | アベーグ，グンナー | 尿と胃腸の疾患の治療におけるｓ（―）―トルテロジン |
| EP0957073A1 (fr) * | 1998-05-12 | 1999-11-17 | Schwarz Pharma Ag | Dérivés de 3,3-diphénylpropylamines |
| CA2643231A1 (fr) * | 1999-07-01 | 2001-01-11 | Pharmacia & Upjohn Company | Inhibiteurs de recapture de la noradrenaline et methodes d'utilisation connexes |
| SE9904850D0 (sv) * | 1999-12-30 | 1999-12-30 | Pharmacia & Upjohn Ab | Novel process and intermediates |
| US6566537B2 (en) | 1999-12-30 | 2003-05-20 | Pharmacia Ab | Process and intermediates |
| DE10028443C1 (de) * | 2000-06-14 | 2002-05-29 | Sanol Arznei Schwarz Gmbh | Verfahren zur Herstellung von 3,3-Diarylpropylaminen, (R,S)- und (R)-4-Phenyl-2-chromanon-6-carbonsäure sowie (R)-4-Phenyl-2-chromanon-carbonsäure-cinchonidinsalz und deren Verwendung zur Herstellung eines rechtsdrehenden Hydroxybenzylalkohols und von pharmazeutischen Zusammensetzungen |
| DE10033016A1 (de) * | 2000-07-07 | 2002-01-24 | Sanol Arznei Schwarz Gmbh | Verfahren zur Herstellung von 3,3-Diarylpropylaminen |
| PE20020547A1 (es) | 2000-10-24 | 2002-06-12 | Upjohn Co | Uso de la tolterodina en tratamientos del asma |
| US20030027856A1 (en) * | 2001-06-29 | 2003-02-06 | Aberg A.K. Gunnar | Tolterodine metabolites |
| IN191835B (fr) * | 2001-08-03 | 2004-01-10 | Ranbaxy Lab Ltd | |
| DK1461306T3 (da) | 2001-10-26 | 2009-03-09 | Pharmacia & Upjohn Co Llc | Kvaternære ammoniumforbindelser og deres anvendelse som antimuscarin-midler |
| US7005449B2 (en) | 2002-04-23 | 2006-02-28 | Pharmacia & Upjohn Company | Tolterodine salts |
| WO2004004629A2 (fr) | 2002-07-08 | 2004-01-15 | Ranbaxy Laboratories Limited | Derives d'azabicyclo[3.1.0]hexanes 3,6-disubstitues utiles comme antagonistes des recepteurs muscariniques |
| ATE396969T1 (de) | 2002-07-31 | 2008-06-15 | Ranbaxy Lab Ltd | 3,6-disubstituierte azabicyclo (3.1.0)hexanderivate, die sich als muscarinrezeptorantagonisten eignen |
| AU2002321711A1 (en) | 2002-08-09 | 2004-02-25 | Ranbaxy Laboratories Limited | 3,6-disubstituted azabicyclo (3.1.0) hexane derivatives useful as muscarinic receptor antagonist |
| DE60231341D1 (de) | 2002-08-23 | 2009-04-09 | Ranbaxy Lab Ltd | Fluor- und sulfonylaminohaltige, 3,6-disubstituierptorantagonisten |
| MXPA05002302A (es) * | 2002-08-28 | 2005-06-08 | Pharmacia Corp | Composicion liquida oral de tolterodina. |
| AU2002353286A1 (en) | 2002-12-10 | 2004-06-30 | Ranbaxy Laboratories Limited | 3,6-disubstituted azabicyclo (3.1.0) hexane derivatives as muscarinic receptor antagonists |
| WO2004056767A1 (fr) | 2002-12-23 | 2004-07-08 | Ranbaxy Laboratories Limited | Derives de 1-substitues-3-pyrrolidines comme antagonistes de recepteurs muscariniques |
| AU2002347553A1 (en) | 2002-12-23 | 2004-07-14 | Ranbaxy Laboratories Limited | Flavaxate derivatives as muscarinic receptor antagonists |
| US7488748B2 (en) | 2003-01-28 | 2009-02-10 | Ranbaxy Laboratories Limited | 3,6-Disubstituted azabicyclo hexane derivatives as muscarinic receptor antagonists |
| CA2517824A1 (fr) * | 2003-03-06 | 2004-09-16 | Neela Praveen Kumar | Derives de 3,3-diarylpropylamine et procedes permettant de les isoler |
| AU2003304037A1 (en) * | 2003-04-08 | 2004-11-01 | Hetero Drugs Limited | Novel polymorphs of tolterodine tartrate |
| DE10315917A1 (de) * | 2003-04-08 | 2004-11-18 | Schwarz Pharma Ag | Hochreine Basen von 3,3-Diphenylpropylaminmonoestern |
| EP1618091A1 (fr) | 2003-04-09 | 2006-01-25 | Ranbaxy Laboratories, Ltd. | Derives d'azabicyclo hexane substitues en tant qu'antagonistes de recepteurs muscariniques |
| EP1615887A1 (fr) | 2003-04-10 | 2006-01-18 | Ranbaxy Laboratories, Ltd. | Derives d'azabicyclo hexanes en tant qu'antagonistes des recepteurs muscariniques |
| ATE362364T1 (de) | 2003-04-10 | 2007-06-15 | Ranbaxy Lab Ltd | Substituierte azabicyclo hexane derivate als muscarin rezeptor antagonisten |
| JP2006522787A (ja) | 2003-04-11 | 2006-10-05 | ランバクシー ラボラトリーズ リミテッド | ムスカリン様受容体アンタゴニストとしてのアザビシクロ誘導体 |
| ITMI20031354A1 (it) * | 2003-07-02 | 2005-01-03 | Istituto Di Chimica Biomolecolare D El Cnr Sezione | Sintesis enantioselettiva di composti enantiomericamente arricchiti. |
| ES2235648B1 (es) * | 2003-12-22 | 2006-11-01 | Ragactives, S.L. | Procedimiento para la obtencion de tolterodina. |
| JP5250205B2 (ja) * | 2003-12-24 | 2013-07-31 | シプラ・リミテッド | トルテロジン、その組成物及び使用、及びその製造方法 |
| EP1629834A1 (fr) | 2004-08-27 | 2006-03-01 | KRKA, D.D., Novo Mesto | Composition pharmaceutique de tolterodine avec liberation soutenue |
| ITMI20041920A1 (it) * | 2004-10-11 | 2005-01-11 | Chemi Spa | Processo per la preparazione di n, n-diisopropil-3-2-idrossi-5-metilfenil-3-fenil-propabammina |
| US7355077B2 (en) * | 2004-10-28 | 2008-04-08 | Dr. Reddy's Laboratories Limited | Process for preparing tolterodine |
| JP4513535B2 (ja) * | 2004-12-03 | 2010-07-28 | 住友化学株式会社 | トルテロジンの製造方法 |
| EP1836156A1 (fr) * | 2005-01-10 | 2007-09-26 | Teva Gyogyszergyar Reszvenytarsasag | Tartrate de tolterodine sensiblement pur et procede de fabrication |
| US7528267B2 (en) | 2005-08-01 | 2009-05-05 | Girindus America, Inc. | Method for enantioselective hydrogenation of chromenes |
| ES2268987B1 (es) | 2005-08-05 | 2008-02-01 | Ragactives, S.L. | Procedimiento para la obtencion de 3,3-difenilpropilaminas. |
| WO2007039918A1 (fr) * | 2005-10-06 | 2007-04-12 | Natco Pharma Limited | Nouveau procede de preparation de tolterodine |
| RU2008119323A (ru) | 2005-10-19 | 2009-11-27 | Рэнбакси Лабораториз Лимитед (In) | Фармацевтические композиции мускаринового рецептора |
| KR100686351B1 (ko) * | 2006-01-12 | 2007-02-22 | 주식회사 카이로제닉스 | 톨테로딘 라세미체의 제조방법 |
| ITMI20060110A1 (it) * | 2006-01-24 | 2007-07-25 | Dipharma Spa | Procedimento per la purificazione di tolterodina |
| DE602007009096D1 (de) * | 2006-05-24 | 2010-10-21 | Pfizer Ltd | Verfahren zur herstellung von benzopyran-2-olderivaten |
| US7268257B1 (en) | 2006-05-31 | 2007-09-11 | Sumitomo Chemical Company, Limited | Process for producing tolterodine |
| CZ302585B6 (cs) * | 2007-02-26 | 2011-07-20 | Zentiva, A. S. | Krystalická sul 2-[(1R)-3-[bis(1-methylethyl)amino]-1-fenylpropyl]-4-methylfenolu s kyselinou (2R,3R)-2,3-dihydroxybutandiovou |
| US8486452B2 (en) * | 2007-07-20 | 2013-07-16 | Mylan Pharmaceuticals Inc. | Stabilized tolterodine tartrate formulations |
| US8871275B2 (en) | 2007-08-08 | 2014-10-28 | Inventia Healthcare Private Limited | Extended release compositions comprising tolterodine |
| KR101188333B1 (ko) | 2008-02-20 | 2012-10-09 | 에스케이케미칼주식회사 | 안정성이 우수하고 경피제로 유용한 톨테로딘 결정성산부가염 |
| US20090214665A1 (en) * | 2008-02-26 | 2009-08-27 | Lai Felix S | Controlled Release Muscarinic Receptor Antagonist Formulation |
| ITMI20082055A1 (it) * | 2008-11-19 | 2009-02-18 | Dipharma Francis Srl | Procedimento per la preparazione di (r)-tolterodina base libera |
| WO2010092500A2 (fr) | 2009-02-12 | 2010-08-19 | Alembic Limited | Procédé de préparation du tartrate de toltérodine |
| WO2010094292A1 (fr) * | 2009-02-17 | 2010-08-26 | Pharmathen S.A. | Procédé perfectionné pour la préparation de (r)-2-(3-diisopropylamino)-1-phénylpropyl)-4-méthylphénol et de sels de celui-ci |
| WO2011125763A1 (fr) | 2010-03-31 | 2011-10-13 | 小野薬品工業株式会社 | Agent préventif et/ou remède pour le syndrome d'enflure douloureuse des mains et des pieds |
| EP2476665A1 (fr) | 2011-01-17 | 2012-07-18 | Cambrex Profarmaco Milano S.r.l. | Procédé pour la préparation de N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)- 3-phenyl propylamine et ses sels démarrant à partir d'un nouvel intermédiaire |
| WO2012098044A1 (fr) | 2011-01-17 | 2012-07-26 | Cambrex Profarmaco Milano S.R.L. | Procédé pour la préparation de n,n-diisopropyl-3-(2-hydroxy-5-méthylphényl)-3-phénylpropylamine et de ses sels à partir d'un nouvel intermédiaire |
| CN102516098B (zh) * | 2011-12-09 | 2014-06-18 | 北京联本医药化学技术有限公司 | 酒石酸托特罗定制备方法 |
| CN103044274B (zh) * | 2012-11-29 | 2014-10-22 | 珠海保税区丽珠合成制药有限公司 | 一种无溶剂合成酒石酸托特罗定的方法 |
| GB201402556D0 (en) | 2014-02-13 | 2014-04-02 | Crystec Ltd | Improvements relating to inhalable particles |
| CN110229072B (zh) * | 2019-06-25 | 2022-04-08 | 中国药科大学 | 一种托特罗定及其对映体的合成方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5382600A (en) * | 1988-01-22 | 1995-01-17 | Pharmacia Aktiebolag | 3,3-diphenylpropylamines and pharmaceutical compositions thereof |
| SE8800207D0 (sv) * | 1988-01-22 | 1988-01-22 | Kabivitrum Ab | Nya aminer, deras anvendning och framstellning |
| EP0585913B1 (fr) * | 1992-09-04 | 1997-12-29 | Takeda Chemical Industries, Ltd. | Composés hétérocycliques condensés, leur production et usage |
-
1997
- 1997-11-21 KR KR1019990705269A patent/KR20000057548A/ko not_active Application Discontinuation
- 1997-12-18 SI SI9730426T patent/SI0960109T1/xx unknown
- 1997-12-18 PL PL334375A patent/PL191603B1/pl not_active IP Right Cessation
- 1997-12-18 HU HU0000527A patent/HUP0000527A3/hu unknown
- 1997-12-18 AU AU59569/98A patent/AU717985B2/en not_active Ceased
- 1997-12-18 DE DE69716767T patent/DE69716767T2/de not_active Expired - Lifetime
- 1997-12-18 JP JP53003098A patent/JP4199310B2/ja not_active Expired - Fee Related
- 1997-12-18 CA CA002273789A patent/CA2273789C/fr not_active Expired - Fee Related
- 1997-12-18 SK SK815-99A patent/SK283591B6/sk not_active IP Right Cessation
- 1997-12-18 AT AT97954678T patent/ATE226949T1/de active
- 1997-12-18 US US08/993,257 patent/US5922914A/en not_active Expired - Lifetime
- 1997-12-18 NZ NZ336533A patent/NZ336533A/xx not_active IP Right Cessation
- 1997-12-18 ES ES97954678T patent/ES2186018T3/es not_active Expired - Lifetime
- 1997-12-18 DK DK97954678T patent/DK0960109T3/da active
- 1997-12-18 WO PCT/US1997/022521 patent/WO1998029402A1/fr active IP Right Grant
- 1997-12-18 CZ CZ19992272A patent/CZ295477B6/cs not_active IP Right Cessation
- 1997-12-18 KR KR10-1999-7005910A patent/KR100463614B1/ko not_active IP Right Cessation
- 1997-12-18 PT PT97954678T patent/PT960109E/pt unknown
- 1997-12-18 EP EP97954678A patent/EP0960109B1/fr not_active Expired - Lifetime
- 1997-12-18 CN CNB971801479A patent/CN1151141C/zh not_active Expired - Fee Related
- 1997-12-18 RU RU99116356/04A patent/RU2176246C2/ru not_active IP Right Cessation
-
1999
- 1999-06-29 FI FI991477A patent/FI991477A/fi unknown
- 1999-06-29 NO NO19993247A patent/NO317158B1/no not_active IP Right Cessation
-
2000
- 2000-04-28 HK HK00102580A patent/HK1023566A1/xx not_active IP Right Cessation
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