[go: up one dir, main page]

NO20005669L - Nye derivater av 3,3-difenylpropylaminer - Google Patents

Nye derivater av 3,3-difenylpropylaminer

Info

Publication number
NO20005669L
NO20005669L NO20005669A NO20005669A NO20005669L NO 20005669 L NO20005669 L NO 20005669L NO 20005669 A NO20005669 A NO 20005669A NO 20005669 A NO20005669 A NO 20005669A NO 20005669 L NO20005669 L NO 20005669L
Authority
NO
Norway
Prior art keywords
compounds
diphenylpropylamines
novel
preparation
methods
Prior art date
Application number
NO20005669A
Other languages
English (en)
Other versions
NO20005669D0 (no
NO326872B1 (no
Inventor
Claus Meese
Bengt Ake Sparf
Original Assignee
Sanol Arznei Schwarz Gmbh
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=8231918&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO20005669(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanol Arznei Schwarz Gmbh filed Critical Sanol Arznei Schwarz Gmbh
Publication of NO20005669D0 publication Critical patent/NO20005669D0/no
Publication of NO20005669L publication Critical patent/NO20005669L/no
Publication of NO326872B1 publication Critical patent/NO326872B1/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/48—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C219/00—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C219/26—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/10—Drugs for disorders of the urinary system of the bladder
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • 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
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified 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
    • C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified 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 singly-bound oxygen atoms
    • C07C217/62—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified 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 singly-bound oxygen atoms 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C219/00—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C219/26—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified 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
    • C07C219/28—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified 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 having amino groups bound to acyclic carbon atoms of the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/34—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
    • C07C271/42—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/44—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
    • C07C271/42—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/52—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C307/00—Amides of sulfuric acids, i.e. compounds having singly-bound oxygen atoms of sulfate groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C307/02—Monoamides of sulfuric acids or esters thereof, e.g. sulfamic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Urology & Nephrology (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Neurosurgery (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Luminescent Compositions (AREA)
  • Photoreceptors In Electrophotography (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Saccharide Compounds (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
NO20005669A 1998-05-12 2000-11-10 Nye derivater av 3,3-difenylpropylaminer, farmasøytisk preparat inneholdende disse, samt fremgangsmåter for fremstilling derav NO326872B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP98108608A EP0957073A1 (en) 1998-05-12 1998-05-12 Novel derivatives of 3,3-diphenylpropylamines
PCT/EP1999/003212 WO1999058478A1 (en) 1998-05-12 1999-05-11 Novel derivatives of 3,3-diphenylpropylamines

Publications (3)

Publication Number Publication Date
NO20005669D0 NO20005669D0 (no) 2000-11-10
NO20005669L true NO20005669L (no) 2001-01-11
NO326872B1 NO326872B1 (no) 2009-03-09

Family

ID=8231918

Family Applications (2)

Application Number Title Priority Date Filing Date
NO20005669A NO326872B1 (no) 1998-05-12 2000-11-10 Nye derivater av 3,3-difenylpropylaminer, farmasøytisk preparat inneholdende disse, samt fremgangsmåter for fremstilling derav
NO2009015C NO2009015I2 (no) 1998-05-12 2009-07-17 Fesoterodine, eventuelt i form av et fysiologisk akseptabelt salt, inkludert hydrogenfumaratsaltet

Family Applications After (1)

Application Number Title Priority Date Filing Date
NO2009015C NO2009015I2 (no) 1998-05-12 2009-07-17 Fesoterodine, eventuelt i form av et fysiologisk akseptabelt salt, inkludert hydrogenfumaratsaltet

Country Status (32)

Country Link
US (6) US6713464B1 (no)
EP (3) EP0957073A1 (no)
JP (3) JP3929702B2 (no)
KR (1) KR100599004B1 (no)
CN (2) CN1207268C (no)
AT (1) ATE220056T1 (no)
AU (1) AU748057B2 (no)
BR (1) BRPI9910406B8 (no)
CA (1) CA2328920C (no)
CY (1) CY2007024I2 (no)
CZ (2) CZ296605B6 (no)
DE (2) DE122007000065I2 (no)
DK (1) DK1077912T3 (no)
ES (1) ES2181443T3 (no)
FR (1) FR07C0050I2 (no)
GE (1) GEP20084461B (no)
HK (1) HK1046269B (no)
HU (2) HU226490B1 (no)
IL (1) IL139110A0 (no)
IS (1) IS2044B (no)
LU (1) LU91365I2 (no)
MX (1) MXPA00011096A (no)
NL (1) NL300293I2 (no)
NO (2) NO326872B1 (no)
NZ (1) NZ507487A (no)
PL (3) PL218882B1 (no)
PT (1) PT1077912E (no)
RU (1) RU2199525C2 (no)
SK (1) SK286052B6 (no)
TR (1) TR200003319T2 (no)
WO (1) WO1999058478A1 (no)
ZA (1) ZA200005728B (no)

Families Citing this family (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0957073A1 (en) 1998-05-12 1999-11-17 Schwarz Pharma Ag Novel derivatives of 3,3-diphenylpropylamines
DE19955190A1 (de) * 1999-11-16 2001-06-21 Sanol Arznei Schwarz Gmbh Stabile Salze neuartiger Derivate von 3,3-Diphenylpropylaminen
SE9904850D0 (sv) * 1999-12-30 1999-12-30 Pharmacia & Upjohn Ab Novel 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
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
DE10315878B4 (de) * 2003-04-08 2009-06-04 Schwarz Pharma Ag Vorrichtung zur transdermalen Verabreichung von Fesoterodin und Verwendung
DE10315917A1 (de) * 2003-04-08 2004-11-18 Schwarz Pharma Ag Hochreine Basen von 3,3-Diphenylpropylaminmonoestern
WO2004091597A2 (en) * 2003-04-15 2004-10-28 Pharmacia & Upjohn Company Llc Method of treating irritable bowel syndrome (ibs)
WO2004096751A1 (en) 2003-04-25 2004-11-11 Pharmacia & Upjohn Company Llc Halogen substituted 3,3-diphenylpropylamines (tolterodine) having antimuscarinic activity
CA2522888C (en) 2003-05-23 2012-07-17 Bridge Pharma, Inc. Smooth muscle spasmolytic agents
WO2005012227A2 (en) * 2003-08-05 2005-02-10 Ranbaxy Laboratories Limited Process for preparation of 2-(3-diisopropylamino-1-phenylpropyl)-4-hydroxymethyl-phenol, a metabolite of tolterodine
WO2007039918A1 (en) * 2005-10-06 2007-04-12 Natco Pharma Limited Novel process for the preparation of tolterodine
TW200733975A (en) * 2005-12-20 2007-09-16 Pfizer Prod Inc Pharmaceutical combination for the treatment of luts
US8119667B2 (en) * 2005-12-29 2012-02-21 Schering-Plough Animal Health Corporation Carbonates of fenicol antibiotics
ATE480531T1 (de) * 2006-05-24 2010-09-15 Pfizer Ltd Verfahren zur herstellung von benzopyran-2- olderivaten
EP1862449A1 (en) * 2006-05-31 2007-12-05 Schwarz Pharma Ltd. A shortened synthesis of substituted hydroxymethyl phenols
EP1940774B1 (en) 2006-05-31 2014-03-05 Schwarz Pharma Ltd. New synthesis of substituted hydroxymethyl phenols
IES20060424A2 (en) * 2006-06-08 2007-10-31 Schwarz Pharma Ltd Accelerated synthesis of (3-Diisopropylamino-1-phenylpropyl)-4-(hydroxymethyl)phenol and its phenolic monoesters
US7807715B2 (en) 2006-06-09 2010-10-05 Ucb Pharma Gmbh Pharmaceutical compositions comprising fesoterodine
DE602007008389D1 (de) * 2006-06-09 2010-09-23 Schwarz Pharma Ltd Synthese von phenolischen estern von hydroxymethylphenolen
PE20120476A1 (es) * 2006-06-09 2012-04-20 Sanol Arznei Schwarz Gmbh Composiciones farmaceuticas estabilizadas que comprenden fesoterodina
PL2027103T3 (pl) 2006-06-12 2014-12-31 Ucb Pharma Gmbh Nowe, chiralne związki pośrednie, sposób ich wytwarzania i ich zastosowanie w wytwarzaniu tolterodyny, fesoterodyny lub ich aktywnych metabolitów
IES20060435A2 (en) * 2006-06-12 2007-12-12 Schwarz Pharma Ltd Shortened synthesis using paraformaldehyde or trioxane
CZ2006506A3 (cs) * 2006-08-09 2007-10-03 Zentiva, A. S. Farmaceutická kompozice s obsahem tolterodinu
WO2008059953A1 (en) * 2006-11-17 2008-05-22 Asahi Kasei Chemicals Corporation Method for producing isocyanate
TW200844080A (en) 2007-01-11 2008-11-16 Asahi Kasei Chemicals Corp Process for producing isocyanate
US20090005309A1 (en) * 2007-05-18 2009-01-01 Auspex Pharmaceuticals, Inc. Substituted piperidines
US20090005431A1 (en) * 2007-06-30 2009-01-01 Auspex Pharmaceuticals, Inc. Substituted pyrrolidines
US20090062385A1 (en) * 2007-08-29 2009-03-05 Protia, Llc Deuterium-enriched fesoterodine
US20090062398A1 (en) * 2007-08-29 2009-03-05 Protia, Llc Deuterium-enriched tolterodine
WO2009037569A2 (en) * 2007-09-21 2009-03-26 Actavis Group Ptc Ehf An improved process for the preparation of fesoterodine
US20100297241A1 (en) * 2007-10-01 2010-11-25 Actavis Group Ptc Ehf Amorphous Fesoterodine Fumarate
KR101270122B1 (ko) * 2007-11-01 2013-05-31 어큐셀라 인코포레이티드 안과 질환 및 장애를 치료하기 위한 아민 유도체 화합물
WO2009122303A2 (en) * 2008-04-04 2009-10-08 Actavis Group Ptc Ehf Novel mandelate salt of fesoterodine
KR20130127553A (ko) 2008-05-15 2013-11-22 아사히 가세이 케미칼즈 가부시키가이샤 탄산디아릴을 이용하는 이소시아네이트의 제조 방법
BRPI0822694B1 (pt) 2008-05-15 2018-11-27 Asahi Kasei Chemicals Corp processo para produzir um isocianato
US20110171274A1 (en) * 2008-07-21 2011-07-14 Actavis Group Ptc Ehf Fesoterodine Substantially Free of Dehydroxy Impurity
JP5381086B2 (ja) * 2008-10-06 2014-01-08 日本電気株式会社 通信システム及び通信制御方法
WO2010130392A1 (de) 2009-05-11 2010-11-18 Ratiopharm Gmbh Desfesoterodin in form eines weinsäuresalzes
IT1394217B1 (it) 2009-05-15 2012-06-01 Chemi Spa Metodo di preparazione di fesoterodina e/o fesoterodina fumarato.
IT1394219B1 (it) 2009-05-15 2012-06-01 Chemi Spa Metodo di preparazione di fesoterodina fumarato di elevata purezza.
ES2456866T3 (es) 2009-07-27 2014-04-23 Crystal Pharma, S.A.U. Procedimiento para la obtención de 3,3-difenilpropilaminas
IT1396373B1 (it) 2009-10-29 2012-11-19 Dipharma Francis Srl Procedimento per la preparazione di fesoterodina.
EP2316432A1 (de) 2009-10-30 2011-05-04 ratiopharm GmbH Zusammensetzung enthaltend Fesoterodin und Ballaststoffe
US20110124903A1 (en) * 2009-11-20 2011-05-26 Actavis Group Ptc Ehf Solid state forms of fesoterodine intermediates
IT1397521B1 (it) 2009-12-21 2013-01-16 Dipharma Francis Srl Procedimento per la preparazione di fesoterodina con un basso contenuto di impurezze.
EP2364966A1 (en) 2010-03-09 2011-09-14 LEK Pharmaceuticals d.d. Process for preparation of 3-(2-hydroxy-5-substituted phenyl)-3-phenylpropylamines, intermediates for making hydroxytolterodine
EP2549985A1 (en) 2010-03-22 2013-01-30 Cadila Healthcare Limited Stable pharmaceutical compositions comprising fesoterodine
US8729056B2 (en) 2010-03-31 2014-05-20 Ono Pharmaceutical Co., Ltd. Preventive and/or therapeutic agent of hand-foot syndrome
WO2011137054A1 (en) 2010-04-30 2011-11-03 Merck Sharp & Dohme Corp. Novel beta 3 adrenergic receptor agonists
US20110282094A1 (en) 2010-05-11 2011-11-17 Intas Pharmaceuticals Limited Process for preparation of phenolic monoesters of hydroxymethyl phenols
IT1401451B1 (it) 2010-06-10 2013-07-26 Chemi Spa Nuovo processo di preparazione di 2-idrossi-4-fenil-3,4-diidro-2h-cromen-6-il-metanolo e (r)-2-[3-(diisopropilammino)-1-fenilpropil]-4-(idrossimetil)fenolo.
WO2011158257A1 (en) 2010-06-18 2011-12-22 Panacea Biotec Ltd Preparation process of fesoterodine and intermediates
US9012678B2 (en) * 2010-08-25 2015-04-21 Cadila Healthcare Limited Processes for the preparation of fesoterodine
US8492557B2 (en) * 2010-09-16 2013-07-23 Allergan, Inc. Ester pro-drugs of [3-(1-(1H-imidazol-4-yl)ethyl)-2-methylphenyl] methanol
IT1403094B1 (it) 2010-12-09 2013-10-04 Dipharma Francis Srl Procedimento per la preparazione di fesoterodina o un suo sale
WO2012098560A2 (en) * 2011-01-17 2012-07-26 Msn Laboratories Limited Process for the preparation of muscarinic receptor antagonist
TWI590821B (zh) 2011-01-18 2017-07-11 輝瑞有限公司 固體分子分散液
WO2012137047A1 (en) 2011-04-07 2012-10-11 Alembic Pharmaceuticals Limited A process for preparing fesoterodine
EP2508173A1 (en) 2011-04-08 2012-10-10 LEK Pharmaceuticals d.d. Stabilized pharmaceutical composition comprising fesoterodine
EP2508175A1 (en) 2011-04-08 2012-10-10 LEK Pharmaceuticals d.d. Pharmaceutical composition comprising fesoterodine or a salt or a solvate thereof
WO2013021343A1 (en) 2011-08-05 2013-02-14 Ranbaxy Laboratories Limited Process for the optical resolution of () -3- (2 -benzyloxy- 5 - bromophenyl) - 3 - phenylpropionic
WO2013046135A1 (en) 2011-09-26 2013-04-04 Ranbaxy Laboratories Limited Process for the preparation of fesoterodine or its salts
WO2013035084A2 (en) 2012-01-07 2013-03-14 Alembic Pharmaceuticals Limited Process for the preparation of fesoterodine
CN103304356B (zh) * 2012-03-12 2016-01-20 北京乐威泰克医药技术有限公司 羟胺的合成方法
JP6234999B2 (ja) 2012-05-04 2017-11-22 クリスタル ファルマ、エセ、ア、ウＣｒｙｓｔａｌ Ｐｈａｒｍａ，Ｓ．Ａ．Ｕ． 光学的に活性な３，３−ジフェニルプロピルアミンを調製するための方法
EP2780317A2 (en) 2012-05-18 2014-09-24 Alembic Pharmaceuticals Limited The novel reference markers for fesoterodine fumarate
US9315450B2 (en) 2012-06-14 2016-04-19 Ratiopharm Gmbh Desfesoterodine salts
ITMI20121232A1 (it) * 2012-07-16 2014-01-17 Cambrex Profarmaco Milano Srl Procedimento per la preparazione di 2-(3-n,n-diisopropilamino-1-fenilpropil)-4-idrossimetil-fenolo e suoi derivati
CZ2014400A3 (cs) 2014-06-09 2015-12-16 Zentiva, K.S. Stabilizovaná formulace fesoterodinu
US9751828B2 (en) 2014-07-30 2017-09-05 Dipharma Francis S.R.L. Antimuscarinic compound having a low content of impurities
TR201721437A2 (tr) 2017-12-25 2019-07-22 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Fesoterodi̇ni̇n modi̇fi̇ye salim sağlayan formülasyonlari

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE766207C (de) 1940-07-08 1952-12-22 Ig Farbenindustrie Ag Verfahren zur Herstellung von basischen Verbindungen der Diarylmethanreihe
DE925468C (de) 1941-08-13 1955-03-21 Hoechst Ag Verfahren zur Herstellung von ª†, ª†-Diaryl-propyl-aminen
GB624117A (en) 1946-12-07 1949-05-27 Wellcome Found Improvements in and relating to the preparation of substituted allylamines and propylamines
GB627139A (en) 1947-05-28 1949-07-29 Wellcome Found Improvements in and relating to the preparation of quaternary ammonium salts of substituted propanolamines, allylamines and propylamines
NL70759C (no) 1947-10-28
US2567245A (en) * 1948-05-10 1951-09-11 Schering Corp Aryl-(2-pyridyl)-amino alkanes and their production
US2556636A (en) * 1948-06-23 1951-06-12 Schering Corp gamma-substituted propylamine type antihistamines
DE830193C (de) 1948-11-09 1952-02-04 Farbwerke Hoechst Vormals Meis Verfahren zur Herstellung von basischen Verbindungen
CH285387A (de) 1948-11-09 1952-08-31 Michael Dr Erlenbach Verfahren zur Herstellung einer basischen Verbindung.
GB685696A (en) 1948-11-23 1953-01-07 Schering Corp Process for the manufacture of anti-histaminic compounds
NL74271C (no) 1949-09-05
US2676964A (en) * 1950-06-07 1954-04-27 Schering Corp 3-pyridyl propylamine antihistamine substances
US3261841A (en) * 1961-05-03 1966-07-19 Sterling Drug Inc N-substituted 1,5-iminocycloalkanes and -alkenes
US3216841A (en) * 1962-04-30 1965-11-09 Clevite Corp Metal slip casting composition
DK111894A (no) 1962-11-15
GB1025041A (en) 1964-02-21 1966-04-06 Hoechst Ag Process for the manufacture of diphenylalkylamines
GB1169945A (en) 1966-08-25 1969-11-05 Geistlich Soehne Ag Pharmaceutical Compositions containing Diphenylalkyl-amine Derivatives
GB1169944A (en) 1966-08-25 1969-11-05 Geistlich Soehne Ag Novel 3,3-Diphenylpropylamines and processes for the preparation thereof
HU200591B (en) * 1986-07-11 1990-07-28 Chinoin Gyogyszer Es Vegyeszet Process for producing new diphenyl propylamine derivatives and pharmaceutical compositions comprising such compounds
SE8800207D0 (sv) 1988-01-22 1988-01-22 Kabivitrum Ab Nya aminer, deras anvendning och framstellning
US5382600A (en) * 1988-01-22 1995-01-17 Pharmacia Aktiebolag 3,3-diphenylpropylamines and pharmaceutical compositions thereof
US5693144A (en) * 1990-03-19 1997-12-02 3D Systems, Inc. Vibrationally enhanced stereolithographic recoating
FI945311A0 (fi) 1992-05-13 1994-11-11 Alza Corp Oksibutyniinin transdermaalinen annostelu
SE9203318D0 (sv) * 1992-11-06 1992-11-06 Kabi Pharmacia Ab Novel 3,3-diphenylpropylamines, their use and preparation
US6071970A (en) 1993-02-08 2000-06-06 Nps Pharmaceuticals, Inc. Compounds active at a novel site on receptor-operated calcium channels useful for treatment of neurological disorders and diseases
AU7994694A (en) 1994-10-21 1996-05-15 Leiras Oy Controlled release oral delivery system containing oxybutynin
CA2259012C (en) 1996-07-19 2008-05-13 Gunnar Aberg S(-)-tolterodine in the treatment of urinary and gastrointestinal disorders
BR9713702A (pt) 1996-12-12 2000-10-31 Dds Drug Delivery Service Ges Preparado na forma de um composto coadjuvante de material matriz contendo opcionalmente substância ativa
KR20000057548A (ko) * 1996-12-13 2000-09-25 알프레드 엘. 미첼슨 광학적 전송물질 및 결합재
SE9701144D0 (sv) 1997-03-27 1997-03-27 Pharmacia & Upjohn Ab Novel compounds, their use and preparation
EP0872233A1 (en) 1997-04-14 1998-10-21 Janssen Pharmaceutica N.V. Antiretroviral compositions with improved bioavailability
WO1998056359A2 (de) 1997-06-13 1998-12-17 Roland Bodmeier Zusammensetzungen, die die wirkstofffreisetzung verzögern
EP0957073A1 (en) * 1998-05-12 1999-11-17 Schwarz Pharma Ag Novel derivatives of 3,3-diphenylpropylamines
SE9803871D0 (sv) 1998-11-11 1998-11-11 Pharmacia & Upjohn Ab Therapeutic method and formulation
CA2311755C (en) 1998-08-27 2010-03-23 Pharmacia & Upjohn Ab Therapeutic formulation for administering tolterodine with controlled release
SE9802864D0 (sv) * 1998-08-27 1998-08-27 Pharmacia & Upjohn Ab Transdermally administered tolterodine as antimuscarinic agent for the treatment of overactive bladder
DE19922662C1 (de) * 1999-05-18 2000-12-28 Sanol Arznei Schwarz Gmbh Transdermales therapeutisches System (TTS) Tolterodin enthaltend
ES2245320T3 (es) * 1999-11-11 2006-01-01 Pfizer Health Ab Formulacion farmaceutica que contiene tolterodina y su uso.
DE19955190A1 (de) * 1999-11-16 2001-06-21 Sanol Arznei Schwarz Gmbh Stabile Salze neuartiger Derivate von 3,3-Diphenylpropylaminen
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
US20030086972A1 (en) 2000-08-09 2003-05-08 Appel Leah E. Hydrogel-driven drug dosage form
AR033711A1 (es) 2001-05-09 2004-01-07 Novartis Ag Composiciones farmaceuticas
US20030027856A1 (en) 2001-06-29 2003-02-06 Aberg A.K. Gunnar Tolterodine metabolites
GB0117619D0 (en) 2001-07-19 2001-09-12 Phoqus Ltd Pharmaceutical dosage form
CA2459265A1 (en) 2001-09-04 2003-03-13 Pfizer Inc. Affinity-assay for the human erg potassium channel
WO2003020241A2 (en) 2001-09-05 2003-03-13 Vectura Limited Functional powders for oral delivery
CN1558756A (zh) 2001-09-27 2004-12-29 �ź㴫 用于治疗泌尿疾病的药物组合物
BR0206207A (pt) 2001-10-26 2003-12-23 Pharmacia & Up John Company Compostos de amÈnio quaternário e seu uso como agentes antimuscarìnicos
JP2005511582A (ja) 2001-11-05 2005-04-28 ファルマシア アンド アップジョン カンパニー リミティド ライアビリティー カンパニー 抗ムスカリン・エアゾール
AU2002360717A1 (en) * 2001-12-20 2003-07-09 Pharmacia Corporation Controlled release dosage form having improved drug release properties
KR100540035B1 (ko) 2002-02-01 2005-12-29 주식회사 태평양 다단계 경구 약물 방출 제어 시스템
DE10224107A1 (de) 2002-05-29 2003-12-11 Gruenenthal Gmbh Kombination ausgewählter Opioide mit anderen Wirkstoffen zur Therapie der Harninkontinenz
US20060257482A1 (en) 2002-06-07 2006-11-16 Patrik Kumar Modified release, multiple unit drug delivery systems
ITMI20021329A1 (it) 2002-06-14 2003-12-15 Recordati Chem Pharm Nuove ossialchilammine sostituite
AU2003268361A1 (en) 2002-08-30 2004-03-19 Watson Pharmaceuticals, Inc. Drug delivery system for treating urinary incontinence
TW200408955A (en) * 2002-09-30 2004-06-01 Advent Networks Inc Implementing request/reply programming semantics using publish/subscribe middleware
DE10315878B4 (de) * 2003-04-08 2009-06-04 Schwarz Pharma Ag Vorrichtung zur transdermalen Verabreichung von Fesoterodin und Verwendung
DE10315917A1 (de) * 2003-04-08 2004-11-18 Schwarz Pharma Ag Hochreine Basen von 3,3-Diphenylpropylaminmonoestern
WO2004096751A1 (en) * 2003-04-25 2004-11-11 Pharmacia & Upjohn Company Llc Halogen substituted 3,3-diphenylpropylamines (tolterodine) having antimuscarinic activity

Also Published As

Publication number Publication date
EP1077912A1 (en) 2001-02-28
HU226490B1 (en) 2009-03-02
PT1077912E (pt) 2002-11-29
US7230030B2 (en) 2007-06-12
KR100599004B1 (ko) 2006-07-12
DE122007000065I1 (de) 2008-01-03
IS5670A (is) 2000-10-17
FR07C0050I2 (no) 2008-05-09
US6713464B1 (en) 2004-03-30
CY2007024I1 (el) 2010-07-28
HU230434B1 (hu) 2016-06-28
RU2199525C2 (ru) 2003-02-27
CZ299721B6 (cs) 2008-10-29
CY2007024I2 (el) 2010-07-28
BRPI9910406B8 (pt) 2021-05-25
NZ507487A (en) 2002-11-26
US7985772B2 (en) 2011-07-26
CZ296605B6 (cs) 2006-04-12
MXPA00011096A (es) 2002-06-04
CN100491336C (zh) 2009-05-27
HUP0100779A3 (en) 2002-11-28
US20110294882A1 (en) 2011-12-01
JP4658895B2 (ja) 2011-03-23
IS2044B (is) 2005-09-15
US20100256231A1 (en) 2010-10-07
US20040186061A1 (en) 2004-09-23
CN1354737A (zh) 2002-06-19
NO2009015I2 (no) 2012-11-12
SK286052B6 (sk) 2008-02-05
DE69902037T2 (de) 2003-02-06
NO2009015I1 (no) 2009-07-17
US20060270738A1 (en) 2006-11-30
PL347823A1 (en) 2002-04-22
NO20005669D0 (no) 2000-11-10
BR9910406A (pt) 2001-01-09
SK15472000A3 (sk) 2001-06-11
PL380081A1 (pl) 2002-04-22
LU91365I9 (no) 2018-12-31
HU0600760D0 (en) 2006-12-28
EP1254890A1 (en) 2002-11-06
DE122007000065I2 (de) 2010-03-25
FR07C0050I1 (no) 2007-11-16
NL300293I2 (nl) 2008-03-03
JP4833884B2 (ja) 2011-12-07
ES2181443T3 (es) 2003-02-16
JP2007204481A (ja) 2007-08-16
NL300293I1 (nl) 2007-11-01
HK1046269A1 (en) 2003-01-03
US8338478B2 (en) 2012-12-25
CA2328920A1 (en) 1999-11-18
NO326872B1 (no) 2009-03-09
KR20010082547A (ko) 2001-08-30
CN1207268C (zh) 2005-06-22
US7855230B2 (en) 2010-12-21
CZ20003774A3 (cs) 2001-03-14
JP2007084552A (ja) 2007-04-05
WO1999058478A1 (en) 1999-11-18
ATE220056T1 (de) 2002-07-15
DE69902037D1 (de) 2002-08-08
HK1046269B (zh) 2005-09-23
LU91365I2 (fr) 2007-11-14
JP3929702B2 (ja) 2007-06-13
AU748057B2 (en) 2002-05-30
CN1690041A (zh) 2005-11-02
US20090042981A1 (en) 2009-02-12
AU4141299A (en) 1999-11-29
HUP0100779A2 (hu) 2001-08-28
US7384980B2 (en) 2008-06-10
EP1077912B1 (en) 2002-07-03
DK1077912T3 (da) 2002-10-28
BR9910406B1 (pt) 2014-01-07
GEP20084461B (en) 2008-08-25
HK1084099A1 (en) 2006-07-21
CA2328920C (en) 2008-04-15
IL139110A0 (en) 2001-11-25
PL202489B1 (pl) 2009-06-30
JP2003519079A (ja) 2003-06-17
PL195581B1 (pl) 2007-10-31
PL380733A1 (pl) 2006-11-13
PL218882B1 (pl) 2015-02-27
TR200003319T2 (tr) 2001-12-21
ZA200005728B (en) 2001-03-05
EP0957073A1 (en) 1999-11-17

Similar Documents

Publication Publication Date Title
NO20005669D0 (no) Nye derivater av 3,3-difenylpropylaminer
CA2387517A1 (en) Novel biaryl ether derivatives useful as monoamine reuptake inhibitors
IL112880A0 (en) 9-deoxotaxane compounds
UA66852C2 (uk) Похідні та аналоги 3-арилпропіонової кислоти, спосіб їх отримання, фармацевтична композиція (варіанти) та спосіб профілактики та/або лікування асоційованих з резистентністю до інсуліну клінічних станів
GEP20043366B (en) Benzothiophene Derivative Compounds Process of Preparation and Use Thereof
DE60004671D1 (de) Neue piperazinylalkylthiopyrimidine derivate, diese enthaltende pharmazeutische zusammenstellungen und verfahren zu deren herstellung
ATE4203T1 (de) 4-aryloxy- und 4-arylthio-3-phenylpiperidinderivate, verfahren zur herstellung solcher verbindungen und diese enthaltende pharmazeutische zusammensetzungen.
BR9707004A (pt) Composto processo para preparar o mesmo composição farmacêutica utilização do composto e processos para tratamento de doenças do sistema endocinológico e para a manufatura de um medicamento
MA27070A1 (fr) Nouveaux derives de l'isoquinoleine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
AU2001295837A1 (en) Aminoalkylpyrrolidine serotonin receptor ligands and compositions, their pharmaceutical uses, and methods for their synthesis
NO20001140L (no) Fremgangsmõte ved fremstilling av epoksid intermediater
DE3262166D1 (en) A new p-chlorophenoxyacetic acid derivative, its method of preparation and pharmaceutical composition
TW200509889A (en) Aniline derivatives
GR3015212T3 (en) Ethanolaminebenzoate derivative, process for their preparation and pharmaceutical compositions containing them.
FR2655042B1 (fr) Nouvelles benzothiazolinones substituees, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
TH42960A (th) ไอโซควิโนลีนชนิดถูกแทนที่ซึ่งเป็นสารกีดขวางประสาทกล้ามเนื้อที่ออกฤทธิ์ระยะสั้นมาก
WO2002036554A3 (en) Amidino-urea serotonin receptor ligands and compositions, their pharmaceutical uses, and methods for their snythesis

Legal Events

Date Code Title Description
SPCG Granted supplementary protection certificate

Free format text: PRODUCT NAME: TOVIAZ; NAT. REG. NO/DATE: EU107386001/NO-010/NO 20070531; FIRST REG. NO/DATE: EU107386001-010 20070420

Spc suppl protection certif: 2009015

Filing date: 20090717

Extension date: 20220420

CHAD Change of the owner's name or address (par. 44 patent law, par. patentforskriften)

Owner name: UCB PHARMA GMBH, DE

Owner name: PFIZER INC., US

CREP Change of representative

Representative=s name: ZACCO NORWAY AS, POSTBOKS 2003 VIKA, 0125 OSLO

LIS Published licence

Free format text: EXCLUSIVE LICENSE

Name of requester: PFIZER INC., 235 EAST 42ND STREET, NY10017 NEW YOR

SPCK Change in the validity period of an spc

Free format text: PRODUCT NAME: FESOTERODINE, EVENTUELT I; NAT. REG. NO/DATE: EU107386001/NO-010/NO 20070531; FIRST REG. NO/DATE: EU/1/07/386/001-010 20070424

Spc suppl protection certif: 2009015

Filing date: 20090717

Extension date: 20220424

MK1K Patent expired
SPCX Expiry of an spc

Spc suppl protection certif: 2009015