GB1422263A - 4-phenyl-piperidine compounds - Google Patents
4-phenyl-piperidine compoundsInfo
- Publication number
- GB1422263A GB1422263A GB449673A GB449673A GB1422263A GB 1422263 A GB1422263 A GB 1422263A GB 449673 A GB449673 A GB 449673A GB 449673 A GB449673 A GB 449673A GB 1422263 A GB1422263 A GB 1422263A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- phenyl
- jan
- alkoxy
- halogen
- 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
Links
- UTBULQCHEUWJNV-UHFFFAOYSA-N 4-phenylpiperidine Chemical class C1CNCCC1C1=CC=CC=C1 UTBULQCHEUWJNV-UHFFFAOYSA-N 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- -1 methylsulphonyl Chemical group 0.000 abstract 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical compound CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 239000000935 antidepressant agent Substances 0.000 abstract 1
- 229940005513 antidepressants Drugs 0.000 abstract 1
- 239000000939 antiparkinson agent Substances 0.000 abstract 1
- 229940125688 antiparkinson agent Drugs 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 abstract 1
- 125000004950 trifluoroalkyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic 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
- C07D405/02—Heterocyclic 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
- C07D405/12—Heterocyclic 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
-
- 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
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Public Health (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (25)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB449673A GB1422263A (en) | 1973-01-30 | 1973-01-30 | 4-phenyl-piperidine compounds |
| US435006A US3912743A (en) | 1973-01-30 | 1974-01-21 | 4-Phenylpiperidine compounds |
| CA191,106A CA1038390A (en) | 1973-01-30 | 1974-01-28 | Ethers of 2-hydroxymethyl-4-phenylpiperidine compounds |
| PH15445A PH10383A (en) | 1973-01-30 | 1974-01-29 | 4-phenylpiperidine compounds |
| LU69264A LU69264A1 (https=) | 1973-01-30 | 1974-01-29 | |
| FR7402823A FR2215233B1 (https=) | 1973-01-30 | 1974-01-29 | |
| AT69674*#A AT333759B (de) | 1973-01-30 | 1974-01-29 | Verfahren zur herstellung von neuen 3-subst.-4-phenylpiperidinen und von deren salzen |
| FI243/74A FI57932C (fi) | 1973-01-30 | 1974-01-29 | Foerfarande foer framstaellning av 3-substituerade 4-fenylpiperidiner med antidepressiv och anti-parkinson verkan |
| ES422734A ES422734A1 (es) | 1973-01-30 | 1974-01-29 | Metodo para la produccion de 1-alcohil-4-fenilpiperidinas sustituidas en la posicion 3. |
| DK045274A DK149843C (da) | 1973-01-30 | 1974-01-29 | Analogifremgangsmaade til fremstilling af 3-substituerede 4-fenylpiperidiner eller salte deraf med farmaceutisk acceptable syrer |
| IE166/74A IE38801B1 (en) | 1973-01-30 | 1974-01-29 | 4-phenylpiperidine compounds |
| SE7401101A SE401827B (sv) | 1973-01-30 | 1974-01-29 | Sett att framstella 1-och3-substituerade 4-fenylpiperidiner |
| DE2404113A DE2404113C2 (de) | 1973-01-30 | 1974-01-29 | 3-Substituierte 4-Phenylpiperidine und ihre Salze mit pharmazeutisch annehmbaren Säuren, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel |
| BE140304A BE810310A (fr) | 1973-01-30 | 1974-01-29 | 4-phenylpiperidines et leur preparation |
| CH121774A CH592059A5 (https=) | 1973-01-30 | 1974-01-29 | |
| NLAANVRAGE7401189,A NL179187C (nl) | 1973-01-30 | 1974-01-29 | Werkwijze voor het bereiden van een geneesmiddel; een aldus gevormd geneesmiddel; en een werkwijze voor het bereiden van geneeskrachtige verbindingen. |
| NO740272A NO144568C (no) | 1973-01-30 | 1974-01-29 | Analogifremgangsmaate til fremstilling av 3-substituerte 4-fenylpiperidiner |
| JP49011523A JPS5946216B2 (ja) | 1973-01-30 | 1974-01-29 | 4−フエニルピペリジン化合物の製法 |
| IT19998/74A IT1054157B (it) | 1973-01-30 | 1974-01-30 | Metodo per la preparazioni di composti della 4.fenilpiperidina |
| US05/598,146 US4007196A (en) | 1973-01-30 | 1975-07-23 | 4-Phenylpiperidine compounds |
| HK130/81A HK13081A (en) | 1973-01-30 | 1981-04-02 | 4-phenylpiperidine compounds |
| JP58025524A JPS5948826B2 (ja) | 1973-01-30 | 1983-02-19 | 4−フエニルピペリジン化合物の製法 |
| ES556013A ES556013A0 (es) | 1973-01-30 | 1986-06-13 | Procedimiento para la obtencion de trans-4-(p-fluorofenil)-3-((3,4-(metilendioxi)fenoxi)metil)piperidina |
| NL930003C NL930003I2 (nl) | 1973-01-30 | 1993-01-01 | Werkwijze voor het bereiden van een geneesmiddel; een aldus gevormd geneesmiddel; en een werkwijze voor het bereiden van geneeskrachtige verbindingen. |
| LU88398C LU88398I2 (fr) | 1973-01-30 | 1993-08-31 | Seroxat |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB449673A GB1422263A (en) | 1973-01-30 | 1973-01-30 | 4-phenyl-piperidine compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1422263A true GB1422263A (en) | 1976-01-21 |
Family
ID=9778288
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB449673A Expired GB1422263A (en) | 1973-01-30 | 1973-01-30 | 4-phenyl-piperidine compounds |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US3912743A (https=) |
| JP (2) | JPS5946216B2 (https=) |
| AT (1) | AT333759B (https=) |
| BE (1) | BE810310A (https=) |
| CA (1) | CA1038390A (https=) |
| CH (1) | CH592059A5 (https=) |
| DE (1) | DE2404113C2 (https=) |
| DK (1) | DK149843C (https=) |
| ES (2) | ES422734A1 (https=) |
| FI (1) | FI57932C (https=) |
| FR (1) | FR2215233B1 (https=) |
| GB (1) | GB1422263A (https=) |
| HK (1) | HK13081A (https=) |
| IE (1) | IE38801B1 (https=) |
| IT (1) | IT1054157B (https=) |
| LU (2) | LU69264A1 (https=) |
| NL (2) | NL179187C (https=) |
| NO (1) | NO144568C (https=) |
| PH (1) | PH10383A (https=) |
| SE (1) | SE401827B (https=) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0123832A1 (en) * | 1983-03-07 | 1984-11-07 | A/S Ferrosan | Process for the optical resolution of a mixture of the enantiomers of trans-3-((4-methoxyphenoxy)-methyl)-1-methyl-4-phenylpiperidine |
| EP0223334A1 (en) * | 1985-08-10 | 1987-05-27 | Beecham Group Plc | Process for the preparation of aryl-piperidine carbinols |
| EP0339579A3 (en) * | 1988-04-28 | 1991-12-18 | Novo Nordisk A/S | Piperidine compositions and their preparation and use |
| WO1992001672A1 (en) * | 1990-07-18 | 1992-02-06 | Novo Nordisk A/S | Piperidine compounds, their preparation and use |
| US5258517A (en) * | 1992-08-06 | 1993-11-02 | Sepracor, Inc. | Method of preparing optically pure precursors of paroxetine |
| US5874447A (en) * | 1997-06-10 | 1999-02-23 | Synthon B. V. | 4-Phenylpiperidine compounds for treating depression |
| US6063927A (en) * | 1998-07-02 | 2000-05-16 | Smithkline Beecham Plc | Paroxetine derivatives |
| EP2303859A4 (en) * | 2008-06-20 | 2012-08-22 | Metabolex Inc | ARYL GPR119 AGONISTS AND USES THEREOF |
| US8410127B2 (en) | 2009-10-01 | 2013-04-02 | Metabolex, Inc. | Substituted tetrazol-1-yl-phenoxymethyl-thiazol-2-yl-piperidinyl-pyrimidine salts |
| US8846675B2 (en) | 2007-07-19 | 2014-09-30 | Cymabay Therapeutics, Inc. | N-linked heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders |
| US8921350B2 (en) | 2006-12-28 | 2014-12-30 | Cymabay Therapeutics, Inc. | Heterocyclic receptor agonists for the treatment of diabetes and metabolic disorders |
| US9241924B2 (en) | 2010-06-23 | 2016-01-26 | Cymabay Therapeutics, Inc. | Compositions of 5-ethyl-2-{4-[4-(4-tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidin-1-yl}-pyrimidine |
| US10292983B2 (en) | 2016-08-03 | 2019-05-21 | Cymabay Therapeutics, Inc. | Oxymethylene aryl compounds for treating inflammatory gastrointestinal diseases or gastrointestinal conditions |
Families Citing this family (170)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3800378A (en) * | 1972-06-07 | 1974-04-02 | Rca Corp | Method of making a directly-heated cathode |
| US4442113A (en) * | 1981-05-07 | 1984-04-10 | A/S Ferrosan | Long-term weight reduction of obese patients using femoxetine |
| US4485109A (en) * | 1982-05-07 | 1984-11-27 | E. I. Du Pont De Nemours And Company | 4-Aryl-4-piperidinecarbinols |
| US4585777A (en) * | 1984-02-07 | 1986-04-29 | A/S Ferrosan | (-)-Trans-4-(4-fluorophenyl)-3-(4-methoxyphenoxy)methylpiperidine for potentiating 5-HT |
| US4593036A (en) * | 1984-02-07 | 1986-06-03 | A/S Ferrosan | (-)-Trans-4-(4-fluorophenyl)-3-[(4-methoxyphenoxy)methyl]-1-methylpiperidine useful as 5-HT potentiator |
| GB8430581D0 (en) * | 1984-12-04 | 1985-01-09 | Ferrosan As | Treatment |
| EP0190496A3 (en) * | 1984-12-13 | 1987-05-27 | Beecham Group Plc | Piperidine derivatives having a gastro-intestinal activity |
| GB8520154D0 (en) * | 1985-08-10 | 1985-09-18 | Beecham Group Plc | Chemical process |
| NO158038C (no) * | 1985-10-21 | 1988-06-29 | Standard Tel Kabelfab As | Kabel. |
| EP0223403B1 (en) * | 1985-10-25 | 1993-08-04 | Beecham Group Plc | Piperidine derivative, its preparation, and its use as medicament |
| US5017585A (en) * | 1986-11-03 | 1991-05-21 | Novo Nordisk A/S | Method of treating calcium overload |
| IE66332B1 (en) * | 1986-11-03 | 1995-12-27 | Novo Nordisk As | Piperidine compounds and their preparation and use |
| GB8626936D0 (en) * | 1986-11-11 | 1986-12-10 | Ferrosan As | Treatment |
| DK588289D0 (da) * | 1989-11-22 | 1989-11-22 | Ferrosan As | Ny heterocyklisk kemi |
| DK640289D0 (da) * | 1989-12-18 | 1989-12-18 | Ferrosan As | Ny heterocyklisk kemi |
| KR930702000A (ko) * | 1990-11-24 | 1993-09-08 | 데이빗 로버츠 | 노년기 치매, 식용항진, 편두통, 또는 식용불량의 치료를 위한 파로세틴의 사용 |
| US5512584A (en) * | 1991-04-16 | 1996-04-30 | Basf Aktiengesellschaft | 1,3,4-trisubstituted piperidine derivatives, the preparation and use thereof |
| DE4112353A1 (de) * | 1991-04-16 | 1992-10-22 | Basf Ag | 1,3,4-trisubstituierte piperidin-derivate, ihre herstellung und verwendung |
| GB9209687D0 (en) * | 1992-05-06 | 1992-06-17 | Smithkline Beecham Plc | Novel process |
| GB9305175D0 (en) * | 1993-03-13 | 1993-04-28 | Smithkline Beecham Plc | Novel process |
| US5276042A (en) * | 1993-04-16 | 1994-01-04 | Crenshaw Roger T | Treatment of premature ejaculation |
| EP0639568A1 (en) * | 1993-08-19 | 1995-02-22 | Novo Nordisk A/S | Piperidine compounds, their preparation and use in the treatment of neurodegenerative disorders |
| US5446057A (en) * | 1993-09-24 | 1995-08-29 | Warner-Lambert Company | Substituted tetrahydropyridine and piperidine carboxylic acids as muscarinic antagonists |
| US20020086053A1 (en) * | 1993-12-15 | 2002-07-04 | Smithkline Beecham Plc | Formulations, tablets of paroxetine and process to prepare them |
| GB9402029D0 (en) * | 1994-02-03 | 1994-03-30 | Smithkline Beecham Plc | Novel formulation |
| ES2102295B1 (es) * | 1994-03-18 | 1998-04-01 | Ferrer Int | Nuevos compuestos derivados de la n-benzoilmetil-piperidina. |
| US5856493A (en) * | 1995-02-06 | 1999-01-05 | Smithkline Beecham Corporation | Process for making novel form of paroxeting hydrochloride anhydrate |
| SK283608B6 (sk) * | 1995-02-06 | 2003-10-07 | Smithkline Beecham Plc | Bezvodý hydrochlorid paroxetínu, spôsob jeho výroby a použitie |
| HUP9900318A3 (en) * | 1995-05-17 | 2001-09-28 | Novo Nordisk As | Process for preparing 4-aryl-piperidine derivatives |
| US6548084B2 (en) * | 1995-07-20 | 2003-04-15 | Smithkline Beecham Plc | Controlled release compositions |
| ATE192042T1 (de) * | 1995-08-16 | 2000-05-15 | Lilly Co Eli | Potenzierung von serotonin-wirkstoffresponz |
| RU2167865C2 (ru) * | 1995-09-07 | 2001-05-27 | Ф. Хоффманн-Ля Рош Аг | Производные пиперидина, способ их получения, фармацевтическая композиция на их основе и промежуточные вещества |
| ZA9610738B (en) * | 1995-12-22 | 1997-06-24 | Warner Lambert Co | Subtype selective nmda receptor ligands and the use thereof |
| GB9526645D0 (en) * | 1995-12-28 | 1996-02-28 | Chiroscience Ltd | Stereoselective synthesis |
| GB9605828D0 (en) * | 1996-03-20 | 1996-05-22 | Smithkline Beecham Plc | Treatment method |
| ES2121685B1 (es) * | 1996-04-10 | 1999-09-16 | Vita Invest Sa | Procedimiento para la obtencion de (+)-trans-4(4-fluoro-fenil)-3-hidroximetil-1-metilpiperidina. |
| 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 |
| CA2206592A1 (en) * | 1996-05-30 | 1997-11-30 | Shu-Zhong Wang | Method of producing amorphous paroxetine hydrochloride |
| JP3882224B2 (ja) | 1996-05-31 | 2007-02-14 | 旭硝子株式会社 | パロキセチンの製造方法 |
| EP0812827B1 (en) | 1996-06-13 | 2009-09-02 | Sumitomo Chemical Company, Limited | Piperidine derivative as intermediates for the preparation of paroxetine and process for their preparation |
| HU221921B1 (hu) * | 1996-07-08 | 2003-02-28 | Richter Gedeon Vegyészeti Gyár Rt. | N-benzil-piperidin- és tetrahidropiridinszármazékok és eljárás azok előállítására |
| US6638948B1 (en) | 1996-09-09 | 2003-10-28 | Pentech Pharmaceuticals, Inc. | Amorphous paroxetine composition |
| US5672612A (en) * | 1996-09-09 | 1997-09-30 | Pentech Pharmaceuticals, Inc. | Amorphous paroxetine composition |
| GB9623359D0 (en) * | 1996-11-09 | 1997-01-08 | Smithkline Beecham Plc | Novel process |
| GB9700690D0 (en) * | 1997-01-15 | 1997-03-05 | Smithkline Beecham Plc | Novel process |
| ES2329739T3 (es) | 1997-04-07 | 2009-11-30 | Georgetown University | Analogos de cocaina. |
| GB9710004D0 (en) | 1997-05-17 | 1997-07-09 | Knoll Ag | Chemical process |
| BR9809687A (pt) | 1997-05-29 | 2000-07-11 | Smithkline Beecham Corp | Processo novo |
| CN1092654C (zh) * | 1997-06-10 | 2002-10-16 | 斯索恩有限公司 | 4-苯基哌啶类化合物 |
| CA2212451C (en) * | 1997-08-07 | 2001-10-02 | Brantford Chemicals Inc. | Stereoselective and useful preparation of 3-substituted 4-aryl piperidine compounds |
| ES2137131B1 (es) * | 1998-02-06 | 2000-09-16 | Vita Invest Sa | Derivado de piperidinona procedimiento de obtencion y procedimiento para su utilizacion. |
| PL342931A1 (en) * | 1998-03-16 | 2001-07-16 | Smithkline Beecham Plc | Crystalline form of paroxetine |
| GB9806312D0 (en) * | 1998-03-24 | 1998-05-20 | Smithkline Beecham Plc | Novel formulations |
| US6528529B1 (en) | 1998-03-31 | 2003-03-04 | Acadia Pharmaceuticals Inc. | Compounds with activity on muscarinic receptors |
| EA200001050A1 (ru) * | 1998-04-09 | 2001-04-23 | Смитклайн Бичам Плс | Малеат пароксетина |
| GB9808896D0 (en) * | 1998-04-25 | 1998-06-24 | Smithkline Beecham Plc | Novel compound |
| DE69910691T2 (de) | 1998-06-29 | 2004-07-08 | Sumika Fine Chemical Co. Ltd. | L-Tartrate von Trans-(-)-4-(4-Fluorphenyl)-3-Hydroxymethyl-Piperidin Verbindungen und Verfahren zu ihrer Herstellung |
| ES2138937B1 (es) | 1998-07-07 | 2000-10-01 | Medichem Sa | Polimorfo de maleato de paroxetina y formulaciones farmaceuticas que lo contienen. |
| AP2001002072A0 (en) * | 1998-08-07 | 2001-03-31 | Smithkline Becham P L C | Process for the preparation of a non-crystalline anhydrate form of paroxetine hydrochloride |
| AU769260B2 (en) | 1998-10-07 | 2004-01-22 | Georgetown University | Monomeric and dimeric heterocycles, and therapeutic uses thereof |
| DK1135383T3 (da) * | 1998-11-30 | 2004-04-05 | Smithkline Beecham Plc | Blandede paroxetin-propan-2-ol-solvater |
| GB9826171D0 (en) * | 1998-11-30 | 1999-01-20 | Smithkline Beecham Plc | Novel compounds |
| GB9826242D0 (en) * | 1998-11-30 | 1999-01-20 | Smithkline Beecham Plc | Novel process |
| GB9826178D0 (en) * | 1998-11-30 | 1999-01-20 | Smithkline Beecham Plc | Novel process |
| GB9827387D0 (en) * | 1998-12-11 | 1999-02-03 | Smithkline Beecham Plc | Novel process |
| WO2000037443A1 (en) * | 1998-12-22 | 2000-06-29 | Pentech Pharmaceuticals, Inc. | Process for preparing arylpiperidine carbinol intermediates and derivatives |
| GB9828767D0 (en) * | 1998-12-29 | 1999-02-17 | Smithkline Beecham Plc | Novel process |
| GB9914583D0 (en) * | 1999-06-22 | 1999-08-25 | Smithkline Beecham Plc | Novel process |
| GB9915303D0 (en) * | 1999-06-30 | 1999-09-01 | Smithkline Beecham Plc | Novel process |
| US6984632B1 (en) * | 1999-07-01 | 2006-01-10 | Italfarmaco S.P.A. | Complexes of paroxetine, with cyclodextrins or cyclodextrin derivatives |
| GB9915727D0 (en) * | 1999-07-03 | 1999-09-08 | Smithkline Beecham Plc | Novel compound and process |
| GB9916187D0 (en) * | 1999-07-09 | 1999-09-08 | Smithkline Beecham Plc | Novel process |
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| US2976291A (en) * | 1961-03-21 | Ethers of z | ||
| US3178438A (en) * | 1963-02-06 | 1965-04-13 | Sterling Drug Inc | 2-benzyl-3-hydroxy and lower alkoxy piperidines |
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1973
- 1973-01-30 GB GB449673A patent/GB1422263A/en not_active Expired
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1974
- 1974-01-21 US US435006A patent/US3912743A/en not_active Expired - Lifetime
- 1974-01-28 CA CA191,106A patent/CA1038390A/en not_active Expired
- 1974-01-29 BE BE140304A patent/BE810310A/xx not_active IP Right Cessation
- 1974-01-29 ES ES422734A patent/ES422734A1/es not_active Expired
- 1974-01-29 LU LU69264A patent/LU69264A1/xx unknown
- 1974-01-29 JP JP49011523A patent/JPS5946216B2/ja not_active Expired
- 1974-01-29 FR FR7402823A patent/FR2215233B1/fr not_active Expired
- 1974-01-29 NL NLAANVRAGE7401189,A patent/NL179187C/xx active Protection Beyond IP Right Term
- 1974-01-29 PH PH15445A patent/PH10383A/en unknown
- 1974-01-29 FI FI243/74A patent/FI57932C/fi active Protection Beyond IP Right Term
- 1974-01-29 CH CH121774A patent/CH592059A5/xx not_active IP Right Cessation
- 1974-01-29 DK DK045274A patent/DK149843C/da active Protection Beyond IP Right Term
- 1974-01-29 NO NO740272A patent/NO144568C/no unknown
- 1974-01-29 AT AT69674*#A patent/AT333759B/de active Protection Beyond IP Right Term
- 1974-01-29 SE SE7401101A patent/SE401827B/xx active Protection Beyond IP Right Term
- 1974-01-29 DE DE2404113A patent/DE2404113C2/de not_active Expired
- 1974-01-29 IE IE166/74A patent/IE38801B1/xx unknown
- 1974-01-30 IT IT19998/74A patent/IT1054157B/it active Protection Beyond IP Right Term
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1975
- 1975-07-23 US US05/598,146 patent/US4007196A/en not_active Expired - Lifetime
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1981
- 1981-04-02 HK HK130/81A patent/HK13081A/xx unknown
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1983
- 1983-02-19 JP JP58025524A patent/JPS5948826B2/ja not_active Expired
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1986
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1993
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- 1993-08-31 LU LU88398C patent/LU88398I2/fr unknown
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