NO20042101L - N-Formylderivater av paroksetin - Google Patents

N-Formylderivater av paroksetin

Info

Publication number
NO20042101L
NO20042101L NO20042101A NO20042101A NO20042101L NO 20042101 L NO20042101 L NO 20042101L NO 20042101 A NO20042101 A NO 20042101A NO 20042101 A NO20042101 A NO 20042101A NO 20042101 L NO20042101 L NO 20042101L
Authority
NO
Norway
Prior art keywords
paroxetine
compound
formylparoxetine
formula
composition
Prior art date
Application number
NO20042101A
Other languages
English (en)
Norwegian (no)
Inventor
Hans Jan Hoorn
Theodorus Hendricus Ant Peters
Frantisek Picha
Original Assignee
Synthon Bv
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 Synthon Bv filed Critical Synthon Bv
Publication of NO20042101L publication Critical patent/NO20042101L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P39/00General protective or antinoxious agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic 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
    • C07D211/08Heterocyclic 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
    • C07D211/18Heterocyclic 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
    • C07D211/20Heterocyclic 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
    • C07D211/22Heterocyclic 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

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Toxicology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
NO20042101A 2001-10-22 2004-05-21 N-Formylderivater av paroksetin NO20042101L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US33043001P 2001-10-22 2001-10-22
PCT/NL2002/000654 WO2003044012A1 (en) 2001-10-22 2002-10-15 N-formyl derivatives of paroxetine

Publications (1)

Publication Number Publication Date
NO20042101L true NO20042101L (no) 2004-05-21

Family

ID=23289741

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20042101A NO20042101L (no) 2001-10-22 2004-05-21 N-Formylderivater av paroksetin

Country Status (15)

Country Link
US (3) US6703408B2 (de)
EP (1) EP1440067B1 (de)
AR (1) AR036860A1 (de)
AT (1) ATE285408T1 (de)
AU (1) AU2002330771A1 (de)
CA (1) CA2464327A1 (de)
DE (2) DE60202381T2 (de)
DK (1) DK1440067T3 (de)
ES (1) ES2230516T3 (de)
HU (1) HUP0401895A2 (de)
IL (1) IL161521A0 (de)
NO (1) NO20042101L (de)
NZ (1) NZ532432A (de)
PT (1) PT1440067E (de)
WO (1) WO2003044012A1 (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6777554B2 (en) 2001-02-05 2004-08-17 Teva Pharmaceutical Industries Ltd. Preparation of N-methylparoxetine and related intermediate compounds
EP1778183B1 (de) * 2004-08-18 2018-06-27 Synthon B.V. Flüssige paroxetinzusammensetzungen
WO2007058998A2 (en) * 2005-11-14 2007-05-24 Auspex Pharmaceuticals, Inc. Substituted phenylpiperidines with serotoninergic activity and enhanced therapeutic properties
US9138430B2 (en) * 2007-12-27 2015-09-22 Mylan Specialty L.P. Formulation and method for the release of paroxetine in the large intestine
CN109507349A (zh) * 2017-09-15 2019-03-22 万全万特制药江苏有限公司 液相色谱法分离测定帕罗西汀中间体光学异构体的方法

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1422263A (en) 1973-01-30 1976-01-21 Ferrosan As 4-phenyl-piperidine compounds
EP0223403B1 (de) * 1985-10-25 1993-08-04 Beecham Group Plc Piperidinderivat, seine Herstellung und seine Verwendung als Arzneimittel
GB9325644D0 (en) * 1993-12-15 1994-02-16 Smithkline Beecham Plc Novel formulation
US5856493A (en) * 1995-02-06 1999-01-05 Smithkline Beecham Corporation Process for making novel form of paroxeting hydrochloride anhydrate
JP3446468B2 (ja) 1996-04-15 2003-09-16 旭硝子株式会社 ピペリジンカルビノール類の製造方法
EP0812829A1 (de) 1996-06-14 1997-12-17 Ontogen Corporation Substituierte Imidazole als Modulatoren für Mehrfachresistenz gegen Medikamente
PL337513A1 (en) 1997-05-29 2000-08-28 Smithkline Beecham Corp Novel method of obtaining pharmaceutically active compounds and their associated intermediate products
GB9810181D0 (en) * 1998-05-13 1998-07-08 Smithkline Beecham Plc Novel formulations
WO2000026187A1 (en) 1998-11-02 2000-05-11 Synthon B.V. Process for producing 4-arylpiperidine-3-carbinols and related compounds
US6239126B1 (en) * 1998-12-17 2001-05-29 American Home Products Corporation Arylpiperidine and aryl-1,2,5,6-tetra-hydropyridine urea derivatives
GB9916392D0 (en) 1999-07-13 1999-09-15 Smithkline Beecham Plc Novel process
IT1313702B1 (it) 1999-08-02 2002-09-09 Chemi Spa Processo per la preparazione di derivati 3-sostituiti di 4-fenil-piperidine.
WO2002017921A2 (en) * 2000-08-28 2002-03-07 Synthon B.V. Paroxetine compositions and processes for making the same
US6755653B2 (en) * 2001-10-25 2004-06-29 Cubic Defense Systems, Inc. System and method for preventing cheating in a simulated combat exercise

Also Published As

Publication number Publication date
IL161521A0 (en) 2004-09-27
AU2002330771A1 (en) 2003-06-10
DE60202381T2 (de) 2005-12-08
HUP0401895A2 (hu) 2004-12-28
EP1440067B1 (de) 2004-12-22
US6703408B2 (en) 2004-03-09
DE20220955U1 (de) 2004-09-02
NZ532432A (en) 2005-02-25
AR036860A1 (es) 2004-10-06
WO2003044012A1 (en) 2003-05-30
PT1440067E (pt) 2005-02-28
CA2464327A1 (en) 2003-05-30
EP1440067A1 (de) 2004-07-28
US20040266825A1 (en) 2004-12-30
DE60202381D1 (de) 2005-01-27
US20040147497A1 (en) 2004-07-29
DK1440067T3 (da) 2005-04-11
ATE285408T1 (de) 2005-01-15
US20030125560A1 (en) 2003-07-03
ES2230516T3 (es) 2005-05-01

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