HK82284A - Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine and pharmaceutical compositions thereof - Google Patents
Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine and pharmaceutical compositions thereofInfo
- Publication number
- HK82284A HK82284A HK822/84A HK82284A HK82284A HK 82284 A HK82284 A HK 82284A HK 822/84 A HK822/84 A HK 822/84A HK 82284 A HK82284 A HK 82284A HK 82284 A HK82284 A HK 82284A
- Authority
- HK
- Hong Kong
- Prior art keywords
- cis
- hydrogen
- formula
- methyl
- tetrahydro
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/14—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups
- C07C209/16—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/21—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing rings other than six-membered aromatic rings
-
- 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
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/30—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring the six-membered aromatic ring being part of a condensed ring system formed by two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/004—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with organometalhalides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/28—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of CHx-moieties
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
- C07C45/46—Friedel-Crafts reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
- C07C49/697—Unsaturated compounds containing a keto groups being part of a ring containing halogen containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/52—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
- C07C57/58—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/52—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
- C07C57/58—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
- C07C57/60—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings having unsaturation outside the rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Claims (10)
1. Cis-isomere Base der Formel
und deren pharmazeutisch annehmbare Säureadditionssalze, in der
R1 Wasserstoff oder n-Alkyl mit 1 bis 3 Kohlenstoffatomen,
R2 n-Alkyl mit 1 bis 3 Kohlenstoffatomen,
ist,
X und Y jeweils Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, Alkoxy mit 1 bis 3 Kohlenstoffatomen oder Cyano sind, wobei wenigstens eine der Gruppen X und Y eine andere Bedeutung als Wasserstoff hat, und
W Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl oder Alkoxy mit 1 bis 3 Kohlenstoffatomen ist.
2. Verbindung nach Anspruch 1, wobei die Verbindung entweder das (1 S)-Enantiomer oder das racemische Gemisch des (1 S)-Enantiomeren mit dem entsprechenden (1 R)-Enantiomeren ist.
3. Verbindung nach Anspruch 2, in der R, Wasserstoff oder Methyl, R2 Methyl und Z 3-Chlorphenyl, 4-Chlorphenyl, 4-Methoxyphenyl, 3-Trifluormethyl-phenyl, 4-Trifluormethyl-phenyl, 3,4-Dichlorphenyl, 3-Bromphenyl, 4-Bromphenyl oder 3-Trifluormethyl-4-chlorphenyl ist.
4. Verbindung nach Anspruch 3, in der W Wasserstoff ist.
5. Verbindung nach Anspruch 4, in der Z 3,4-Dichlorphenyl, 3-Trifluormethyl-phenyl, 4-Chlorphenyl, 4-Bromphenyl oder 3-Trifluormethyl-4-chlorphenyl ist.
6. Verbindung nach Anspruch 3, in der R1 Wasserstoff ist.
7. Verbindung nach Anspruch 1, in der die Verbindung
cis-N-Methyl-4-(3,4-dichlorphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin;
cis-N-Methyl-4-(4-bromphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin;
cis-N-Methyl-4-(4-chlorphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin;
cis-N-Methyl-4-(3-trifluormethyl-phenyl)-1,2,3,4-tetrahydro-1-naphthalinamin;
cis-N-Methyl-4-(3-trifluormethyl-4-chlorphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin;
cis-N,N-Dimethyl-4-(4-chlorphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin;
cis-N,N-Dimethyl-4-(3-trifluormethyl-phenyl)-1,2,3,4-tetrahydro-1-naphthalinamin oder
cis-N-Methyl-4-(4-chlorphenyl)-7-chlor-1,2,3,4-tetrahydro-1-naphthalinamin;
cis-N,N-Dimethyl-4-(3,4-dichlorphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin,
in entweder der (1 S)-enantiomeren oder der racemischen (1 S) (1 R)-Form ist, und deren pharmazeutisch annehmbare Säureadditionssalze.8. Verbindung nach Anspruch 6, wobei die Verbindung cis-(1S)-N-Methyl-4-(3,4-dichlorphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin ist.
9. Verbindung nach Anspruch 1, wobei die Verbindung das (1 R)-Enantiomer von cis-N-Methyl-4-(3,4-dichlorphenyl)-1,2,3,4-tetrahydro-1-naphthalinamin ist.
10. Pharmazeutische Zusammenstellung, umfassend eine Verbindung, wie in irgend einem der Ansprüche 1 bis 8 beansprucht, in einer zum Bekämpfen seelischer Depression als essentieller, aktiver Bestandteil wirksamen Menge, zusammen mit einem pharmazeutisch annehmbaren Verdünnungsmittel oder Träger.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/090,240 US4536518A (en) | 1979-11-01 | 1979-11-01 | Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK82284A true HK82284A (en) | 1984-11-09 |
Family
ID=22221931
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK822/84A HK82284A (en) | 1979-11-01 | 1984-11-01 | Antidepressant derivatives of cis-4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine and pharmaceutical compositions thereof |
Country Status (38)
| Country | Link |
|---|---|
| US (1) | US4536518A (de) |
| EP (1) | EP0030081B1 (de) |
| JP (1) | JPS605584B2 (de) |
| KR (2) | KR840002001B1 (de) |
| AT (1) | ATE2668T1 (de) |
| AU (1) | AU517357B2 (de) |
| BA (2) | BA97149B1 (de) |
| BG (1) | BG60333B2 (de) |
| CA (1) | CA1130815A (de) |
| CS (4) | CS238609B2 (de) |
| DD (2) | DD155615A5 (de) |
| DE (2) | DE3062225D1 (de) |
| DK (1) | DK153390C (de) |
| EG (1) | EG15527A (de) |
| ES (2) | ES496443A0 (de) |
| FI (1) | FI68806C (de) |
| GR (1) | GR70781B (de) |
| HK (1) | HK82284A (de) |
| HR (2) | HRP930199B1 (de) |
| HU (1) | HU182224B (de) |
| IE (1) | IE50395B1 (de) |
| IL (1) | IL61374A (de) |
| IN (2) | IN159643B (de) |
| LU (1) | LU88330I2 (de) |
| LV (2) | LV5456A3 (de) |
| MX (1) | MX5980E (de) |
| MY (1) | MY8500326A (de) |
| NL (1) | NL940018I1 (de) |
| NO (2) | NO148996C (de) |
| NZ (1) | NZ195407A (de) |
| PH (1) | PH17319A (de) |
| PT (1) | PT72004B (de) |
| SG (1) | SG56584G (de) |
| SI (2) | SI8012798A8 (de) |
| SU (2) | SU1014467A3 (de) |
| UA (2) | UA6301A1 (de) |
| YU (2) | YU41951B (de) |
| ZA (1) | ZA806726B (de) |
Families Citing this family (172)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE8004002L (sv) * | 1980-05-29 | 1981-11-30 | Arvidsson Folke Lars Erik | Terapeutiskt anvendbara tetralinderivat |
| US4777288A (en) * | 1987-06-11 | 1988-10-11 | Pfizer Inc. | Process for preparing a 4,4-diphenylbutanoic acid derivative |
| US4839104A (en) * | 1987-06-11 | 1989-06-13 | Pfizer, Inc. | Process for preparing sertraline intermediates |
| FR2623802B1 (fr) * | 1987-11-26 | 1990-05-04 | Lucien Laboratoires | Derives d'amino-4 trifluoromethyl-1 tetralines. leur preparation et leur application en therapeutique |
| US4855500A (en) * | 1988-05-04 | 1989-08-08 | Pfizer Inc. | Process for preparing a ketimine |
| FR2632633B1 (fr) * | 1988-06-08 | 1991-04-05 | Delalande Sa | Procede de preparation de 4-aryl-1-tetralones |
| US4981870A (en) * | 1989-03-07 | 1991-01-01 | Pfizer Inc. | Use of 4-phenyl-1,2,3,4-tetrahydro-1-naphthalenamine derivatives in the treatment of psychosis, inflammation and as immunosuppressants |
| US4940731A (en) * | 1989-08-30 | 1990-07-10 | Pfizer Inc. | Method of treating premature ejaculation using sertraline |
| DE69004529T2 (de) * | 1989-08-30 | 1994-02-24 | Pfizer | Verwendung von Sertralin zur Behandlung von Abhängigkeiten von chemischen Stoffen. |
| US5130338A (en) * | 1989-08-30 | 1992-07-14 | Pfizer Inc. | Method of treating chemical dependencies using sertraline |
| US4962128A (en) * | 1989-11-02 | 1990-10-09 | Pfizer Inc. | Method of treating anxiety-related disorders using sertraline |
| FR2665443B1 (fr) * | 1990-08-03 | 1992-11-06 | Lucien Laboratoires | Derives d'amino-4-methyl-1-tetralines, leur preparation et leur application en therapeutique. |
| US5082970A (en) * | 1991-03-06 | 1992-01-21 | Pfizer Inc. | Process for recycling amine isomer |
| GB9114948D0 (en) * | 1991-07-11 | 1991-08-28 | Pfizer Ltd | Process for preparing sertraline intermediates |
| GB9114947D0 (en) * | 1991-07-11 | 1991-08-28 | Pfizer Ltd | Process for preparing sertraline |
| US5196607A (en) * | 1992-02-14 | 1993-03-23 | Pfizer Inc. | Process for preparing ketone enantiomer |
| US5248699A (en) * | 1992-08-13 | 1993-09-28 | Pfizer Inc. | Sertraline polymorph |
| US5288916A (en) * | 1993-03-25 | 1994-02-22 | Bend Research, Inc. | Enantiomeric resolution of 4-(3,4-dichlorophenyl)-3,4-dihydro-1(2H)-naphthalenone |
| DE69406553T2 (de) * | 1993-11-30 | 1998-02-26 | Pfizer Inc., New York, N.Y. | Verfahren zur herstellung von chiralen tetralonen |
| US5597826A (en) | 1994-09-14 | 1997-01-28 | Pfizer Inc. | Compositions containing sertraline and a 5-HT1D receptor agonist or antagonist |
| US6410794B1 (en) | 1994-12-16 | 2002-06-25 | Uop Llc | Process for preparation of pharmaceutically desired chiral tetralone from tetralones |
| US6455736B1 (en) | 1994-12-16 | 2002-09-24 | Uop Llc | Process for preparation of pharmaceutically desired sertraline and sertraline analogs |
| WO1996041633A1 (en) * | 1995-06-08 | 1996-12-27 | Eli Lilly And Company | Methods of treating cold and allergic rhinitis |
| US6548084B2 (en) * | 1995-07-20 | 2003-04-15 | Smithkline Beecham Plc | Controlled release compositions |
| EP0759299B1 (de) * | 1995-08-16 | 2000-04-26 | Eli Lilly And Company | Potenzierung von Serotonin-Wirkstoffresponz |
| US5734083A (en) * | 1996-05-17 | 1998-03-31 | Torcan Chemical Ltd. | Sertraline polymorph |
| HU222341B1 (hu) * | 1996-12-18 | 2003-06-28 | Richter Gedeon Vegyészeti Gyár Rt. | Eljárás sertralin előállítására és az eljárásban alkalmazott intermedier |
| TW526195B (en) * | 1997-06-10 | 2003-04-01 | Novartis Ag | Crystal modifications of 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxamide and their use |
| EP0999830A1 (de) * | 1997-07-01 | 2000-05-17 | Pfizer Inc. | Sertraline salze und dozierungsformen für dauerverabreichung enthaltend sertraline |
| US20040208926A1 (en) * | 1997-07-01 | 2004-10-21 | Pfizer Inc | Solubilized sertraline compositions |
| US20030133974A1 (en) * | 1997-07-01 | 2003-07-17 | Curatolo William John | Encapsulated solution dosage forms of sertraline |
| DE69713353D1 (de) * | 1997-12-11 | 2002-07-18 | Torcan Chemical Ltd | Sertralin-Polymorph mit verbesserter Wasserlöslichkeit |
| IN191358B (de) * | 1998-01-16 | 2003-11-29 | Pfizer Prod Inc | |
| WO1999046233A1 (en) * | 1998-03-09 | 1999-09-16 | Sumika Fine Chemicals Co., Ltd. | Benzyl alcohol derivatives |
| HUP0101322A3 (en) * | 1998-03-18 | 2002-06-28 | Ciba Sc Holding Ag | Process for the cis-selective catalytic hydrogenation of cyclohexylidenamines |
| FR2777000B1 (fr) | 1998-04-01 | 2002-09-27 | Catalys | Procede de preparation de la sertraline racemique |
| ATE228119T1 (de) * | 1998-04-15 | 2002-12-15 | Pfizer Prod Inc | Heterocyclische carboxamide |
| US6054614A (en) * | 1998-04-23 | 2000-04-25 | Ciba Specialty Chemicals Corporation | Process for the preparation of tetralone imines for the preparation of active pharmaceutical compounds |
| HU226424B1 (en) * | 1998-05-05 | 2008-12-29 | Egis Gyogyszergyar Nyrt | Process for producing enantiomer mixture for preparation of sertraline |
| HU226423B1 (en) * | 1998-05-05 | 2008-12-29 | Egis Gyogyszergyar Nyrt | Process for producing a 1(2h)-naphtalene-1-ylidene derivative |
| IN182588B (de) | 1998-05-12 | 1999-05-08 | Sun Pharmaceutical Ind Ltd | |
| DE19830201A1 (de) * | 1998-07-07 | 2000-01-13 | Boehringer Ingelheim Pharma | Mittel mit antidepressiver Wirkung |
| US6727283B2 (en) | 1998-10-13 | 2004-04-27 | Pfizer Inc. | Sertraline oral concentrate |
| BR9914418A (pt) * | 1998-10-13 | 2001-06-26 | Pfizer Prod Inc | Concentrado oral de sertralina |
| IL132500A0 (en) | 1998-10-29 | 2001-03-19 | Pfizer Prod Inc | Stereoselective microbial reduction of a racemic tetralone |
| AU1031500A (en) * | 1998-11-03 | 2000-05-22 | Dandy A/S | Sucrose fatty acid esters for use as increased release of active ingredients |
| US6518284B2 (en) * | 1998-11-18 | 2003-02-11 | Faes, Fabrica Espanola De Productos Quimicos Y Farmaceuticos S.A. | 4-substituted piperidines |
| EP1133459B1 (de) * | 1998-11-27 | 2006-01-11 | Teva Pharmaceutical Industries Ltd. | Sertralin hydrochlorid form v |
| EP1632472A1 (de) * | 1998-11-27 | 2006-03-08 | Teva Pharmaceutical Industries Ltd | Polymorphe des Sertralin-Hydrochlorids |
| US6500987B1 (en) | 1998-11-27 | 2002-12-31 | Teva Pharmaceutical Industries Ltd. | Sertraline hydrochloride polymorphs |
| AU2315400A (en) * | 1999-03-01 | 2000-09-21 | Middleton, Donald Stuart | 1,2,3,4-tetrahydro-1-naphthalenamine compounds useful in therapy |
| US6245782B1 (en) | 1999-05-17 | 2001-06-12 | Heartdrug Research L.L.C. | Methods of inhibiting platelet activation with selective serotonin reuptake inhibitors |
| US6593496B1 (en) * | 1999-06-09 | 2003-07-15 | Pfizer Inc | Process for preparing sertraline from chiral tetralone |
| US6720454B1 (en) * | 1999-07-29 | 2004-04-13 | Ciba Specialty Chemicals Corporation | Process for the cis-selective catalytic hydrogenation of cyclohexylidenamines |
| US6495721B1 (en) * | 1999-08-09 | 2002-12-17 | Teva Pharmaceutical Industries Ltd. | Sertraline hydrochloride Form II and methods for the preparation thereof |
| IN185109B (de) * | 1999-09-01 | 2000-11-18 | Torrent Pharmaceuticals Ltd | |
| DK174219B1 (da) * | 1999-10-27 | 2002-09-30 | Gea Farmaceutisk Fabrik As | Forbedret syntese af racemisk sertralin |
| US20050119351A1 (en) * | 1999-10-29 | 2005-06-02 | Van Der Schaaf Paul A. | Polymorphic forms of sertraline hydrochloride |
| TWI260315B (en) | 1999-10-29 | 2006-08-21 | Ciba Sc Holding Ag | Polymorphic forms of sertraline hydrochloride |
| US7442838B2 (en) * | 1999-10-29 | 2008-10-28 | Ciba Specialty Chemicals Corp. | Polymorphic forms of sertraline hydrochloride |
| HUP0203384A3 (en) * | 1999-11-16 | 2006-02-28 | Ciba Sc Holding Ag | Process for the preparation of ketimines |
| IL149527A0 (en) * | 1999-11-16 | 2002-11-10 | Ciba Sc Holding Ag | Process for the preparation of ketimines |
| US6380200B1 (en) | 1999-12-07 | 2002-04-30 | Pfizer, Inc. | Combination of aldose reductase inhibitors and selective serotonin reuptake inhibitors for the treatment of diabetic complications |
| ATE354358T1 (de) | 1999-12-21 | 2007-03-15 | Teva Pharma | Neue sertralinhydrochlorid polymorphe, verfahren zur herstellung und zur verwendung und diese enthaltende zusammensetzungen |
| WO2001047498A2 (en) | 1999-12-23 | 2001-07-05 | Pfizer Products Inc. | Hydrogel-driven layered drug dosage form comprising sertraline |
| IN187170B (de) | 2000-01-04 | 2002-02-23 | Sun Pharmaceutical Ind Ltd | |
| WO2001068566A1 (en) * | 2000-03-14 | 2001-09-20 | Teva Pharmaceutical Industries Ltd. | Novel process for preparing (+)-cis-sertraline |
| WO2001078721A1 (en) * | 2000-04-13 | 2001-10-25 | Mayo Foundation For Medical Education And Research | Aβ42 LOWERING AGENTS |
| IN192343B (de) * | 2000-05-26 | 2004-04-10 | Ranbaxy Lab Ltd | |
| US6630504B2 (en) | 2000-08-31 | 2003-10-07 | Pfizer Inc. | Phenoxyphenylheterocyclyl derivatives as SSRIs |
| DE60119047D1 (de) * | 2000-08-31 | 2006-06-01 | Pfizer | Phenoxyphenylheterozyklen als Serotonin-Wiederaufnahmehemmer |
| US6482440B2 (en) | 2000-09-21 | 2002-11-19 | Phase 2 Discovery, Inc. | Long acting antidepressant microparticles |
| US6645946B1 (en) | 2001-03-27 | 2003-11-11 | Pro-Pharmaceuticals, Inc. | Delivery of a therapeutic agent in a formulation for reduced toxicity |
| EP1397343A1 (de) * | 2001-05-31 | 2004-03-17 | Orion Corporation Fermion | Verfahren zur herstellung der polymorphen form ii von sertralinhydrochlorid |
| US6723878B2 (en) | 2001-06-15 | 2004-04-20 | Orion Corporation Fermion | Method for preparing sertraline |
| CA2448499A1 (en) * | 2001-06-15 | 2002-12-27 | Orion Corporation Fermion | A novel process for the preparation of (is-cis) -4-(3, 4-dichlorophenyl) -1, 2, 3, 4 - tetrahydro-n-methyl-1-naphthalenamine |
| NZ532033A (en) * | 2001-10-12 | 2006-11-30 | Azevan Pharmaceuticals Inc | 2-(azetidin-2-on-1-yl)alkanedioic acid derivatives as vasopressin V1a receptor antagonists |
| EP1490090A4 (de) | 2002-02-22 | 2006-09-20 | New River Pharmaceuticals Inc | Wirkstoff-abgabesystem und verfahren zum schutz und zur verabreichung von wirkstoffen |
| AU2003251290A1 (en) * | 2002-04-29 | 2003-11-17 | Teva Pharmaceutical Industries Ltd. | Process for preparation of polymorphic form ii of sertraline hydrochloride, pharmaceutical formulations and methods of administration thereof |
| AU2003254475A1 (en) * | 2002-07-29 | 2004-02-16 | Cipla Limited | Sertraline |
| PL376832A1 (pl) * | 2002-11-07 | 2006-01-09 | Torrent Pharmaceuticals Ltd. | Sposób wytwarzania polimorficznej postaci chlorowodorku sertraliny |
| US20040131672A1 (en) * | 2003-01-07 | 2004-07-08 | Nilobon Podhipleux | Direct compression pharmaceutical composition containing a pharmaceutically active ingredient with poor flowing properties |
| EP1603548A4 (de) * | 2003-02-05 | 2007-10-10 | Myriad Genetics Inc | Verfahren und zusammensetzung zur behandlung neurodegenerativer erkrankungen |
| WO2004087732A2 (en) * | 2003-03-11 | 2004-10-14 | Sun Pharmaceutical Industries Limited | Process for the preparation of (1s, 4s)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-n-methyl-1-naphthylamine |
| US7276629B2 (en) * | 2003-04-14 | 2007-10-02 | Teva Pharmaceutical Industries Ltd. | Hydrogenation of imine intermediates of sertraline with catalysts |
| JP2007502329A (ja) * | 2003-05-23 | 2007-02-08 | トランスフォーム・ファーマシューティカルズ・インコーポレイテッド | セルトラリン組成物 |
| US20050070577A1 (en) * | 2003-07-03 | 2005-03-31 | Pfizer Inc. | Compositions containing a serotonin selective reuptake inhibitor and a 5-HT2A receptor antagonist |
| US20050042284A1 (en) * | 2003-07-11 | 2005-02-24 | Myriad Genetics, Incorporated | Pharmaceutical methods, dosing regimes and dosage forms for the treatment of Alzheimer's disease |
| US7189876B2 (en) * | 2003-07-15 | 2007-03-13 | Recordati Industria Chimica E Farmaceutica S.P.A. | Methods for preparing sertraline hydrochloride polymorphs |
| WO2005012224A1 (en) * | 2003-07-15 | 2005-02-10 | Recordati Industria Chimica E Farmaceutica S.P.A. | Sertraline hydrochloride form ii and methods for the preparation thereof |
| HU227495B1 (en) * | 2003-07-21 | 2011-07-28 | Egis Gyogyszergyar Nyilvanosan Muekoedoe Reszvenytarsasag | Process for producing of imine intermediate |
| WO2005023752A2 (en) * | 2003-09-05 | 2005-03-17 | Teva Pharmaceutical Industries Ltd. | A recycling process for preparing sertraline |
| BRPI0414347A (pt) * | 2003-09-12 | 2006-11-07 | Warner Lambert Co | associação compreendendo um ligando de alfa-2-delta e um ssri e/ou snri para tratamento de depressão e distúrbios da ansiedade |
| ATE449633T1 (de) | 2003-09-12 | 2009-12-15 | Pfizer | Kombinationen aus alpha-2-delta liganden und serotonin / noradrenalin-wiederaufnahmehemmern |
| SI1668014T1 (sl) * | 2003-09-17 | 2009-06-30 | Janssen Pharmaceutica Nv | Kondenzirane heterociklične spojine kot modulatorji serotoninskih receptorjev |
| EP1682483B1 (de) * | 2003-11-04 | 2010-05-26 | Cipla Ltd. | Verfahren zur herstellung von polymorphen von sertralin hydrochlorid |
| DE602004028150D1 (de) * | 2003-11-26 | 2010-08-26 | Pfizer Prod Inc | Aminopyrazolderivate als gsk-3-inhibitoren |
| US20050250803A1 (en) * | 2003-11-26 | 2005-11-10 | Pfizer Inc | Combination of dopamine agonists and monoamine reuptake inhibitors |
| WO2005060968A1 (en) | 2003-12-11 | 2005-07-07 | Sepracor Inc. | Combination of a sedative and a neurotransmitter modulator, and methods for improving sleep quality and treating depression |
| WO2006001877A2 (en) * | 2004-04-13 | 2006-01-05 | Myriad Genetics, Inc. | Combination treatment for neurodegenerative disorders comprising r-flurbiprofen |
| WO2005102366A2 (en) * | 2004-04-19 | 2005-11-03 | Philip Maxwell Satow | Lithium combinations, and uses related thereto |
| MXPA06012777A (es) * | 2004-05-06 | 2007-02-14 | Cydex Inc | Formulaciones de sabor enmascarado que contienen sertralina y eter sulfoalquilico-ciclodextrina. |
| PE20060437A1 (es) | 2004-06-18 | 2006-06-08 | Novartis Ag | COMPUESTOS AZA-BICICLONONANOS COMO LIGANDOS COLINERGICOS DE nAChR |
| GB0415746D0 (en) | 2004-07-14 | 2004-08-18 | Novartis Ag | Organic compounds |
| WO2006020852A2 (en) * | 2004-08-11 | 2006-02-23 | Myriad Genetics, Inc. | Pharmaceutical composition and method for treating neurodegenerative disorders |
| BRPI0514303A (pt) * | 2004-08-11 | 2008-06-10 | Myriad Genetics Inc | composição farmacêutica e método para tratar distúrbios neurodegenerativos |
| WO2006020850A2 (en) * | 2004-08-11 | 2006-02-23 | Myriad Genetics, Inc. | Pharmaceutical composition and method for treating neurodegenerative disorders |
| TW200640836A (en) * | 2005-02-23 | 2006-12-01 | Teva Pharma | Processes for preparing sertraline |
| EP1868434A4 (de) | 2005-03-22 | 2011-10-26 | Azevan Pharmaceuticals Inc | Beta-lactamylalkansäuren zur behandlung von prämenstruellen störungen |
| JP2006265169A (ja) * | 2005-03-24 | 2006-10-05 | Tokuyama Corp | アルキリデンコハク酸化合物の製造方法 |
| GB0507090D0 (en) * | 2005-04-07 | 2005-05-11 | Sandoz Ag | Process for preparing polymorphic form ll of sertraline hydrochloride |
| GB0507298D0 (en) | 2005-04-11 | 2005-05-18 | Novartis Ag | Organic compounds |
| CN101203218A (zh) * | 2005-04-22 | 2008-06-18 | 惠氏公司 | 苯并呋喃基链烷胺衍生物和其作为5-ht2c激动剂的用途 |
| CN101203216A (zh) * | 2005-04-22 | 2008-06-18 | 惠氏公司 | 二氢苯并呋喃衍生物及其用途 |
| TW200716595A (en) * | 2005-04-22 | 2007-05-01 | Wyeth Corp | Chromane and chromene derivatives and uses thereof |
| AU2006239920A1 (en) | 2005-04-22 | 2006-11-02 | Wyeth | Dihydrobenzofuran derivatives and uses thereof |
| MX2007013179A (es) * | 2005-04-22 | 2008-01-16 | Wyeth Corp | Formas cristalinas de clorhidrato de {[(2r)-7-(diclorofenil)-5- fluoro-2,3-dihidro-1-benzofurano-2-il]metil}amina. |
| CA2576097C (en) * | 2005-06-03 | 2009-10-27 | Hetero Drugs Limited | A highly stereoselective synthesis of sertraline |
| US20070100165A1 (en) * | 2005-06-09 | 2007-05-03 | Ronen Borochovitz | Process for preparation of sertraline hydrochloride form I |
| AU2006261788B2 (en) | 2005-06-27 | 2012-05-31 | Valeant International Bermuda | Modified-release formulations of a bupropion salt |
| SG163588A1 (en) | 2005-07-08 | 2010-08-30 | Braincells Inc | Methods for identifying agents and conditions that modulate neurogenesis |
| US20070015832A1 (en) * | 2005-07-14 | 2007-01-18 | Myriad Genetics, Incorporated | Methods of treating overactive bladder and urinary incontinence |
| PL1910346T3 (pl) * | 2005-07-19 | 2019-09-30 | Azevan Pharmaceuticals, Inc. | Beta-laktamowy antagonista wazopresyny fenyloalaniny, cysteiny i seryny |
| US7598255B2 (en) | 2005-08-04 | 2009-10-06 | Janssen Pharmaceutica Nv | Pyrimidine compounds as serotonin receptor modulators |
| JP2009512711A (ja) | 2005-10-21 | 2009-03-26 | ブレインセルス,インコーポレイティド | Pde阻害による神経新生の調節 |
| JP2009513672A (ja) | 2005-10-31 | 2009-04-02 | ブレインセルス,インコーポレイティド | 神経発生のgaba受容体媒介調節 |
| GB0525672D0 (en) | 2005-12-16 | 2006-01-25 | Novartis Ag | Organic compounds |
| GB0525673D0 (en) | 2005-12-16 | 2006-01-25 | Novartis Ag | Organic compounds |
| ES2566479T3 (es) * | 2006-01-06 | 2016-04-13 | Sunovion Pharmaceuticals Inc. | Inhibidores de reabsorción de monoamina con base en tetralona |
| US20070213562A1 (en) * | 2006-01-23 | 2007-09-13 | Ami Zoran | Recycling process for preparing sertraline |
| FR2912057B1 (fr) * | 2007-02-07 | 2009-04-17 | Sanofi Aventis Sa | Composition pharmaceutique contenant en association le saredutant et un inhibiteur selectif de la recapture de la serotonine ou un inhibiteur de la recapture de la serotonine/norepinephrine |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| RU2008135326A (ru) * | 2006-03-24 | 2010-04-27 | Вайет (Us) | Терапевтические композиции для лечения депрессии |
| WO2007119247A2 (en) * | 2006-04-17 | 2007-10-25 | Unichem Laboratories Limited | Improved manufacturing procedure for the preparation of polymorphic form ii of cis-(1s)-n-methyl-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-1-napthleneamine hydrochloride (sertraline hydrochloride) |
| TR200808115T1 (tr) * | 2006-04-28 | 2009-03-23 | Sandoz Ag | 4(S,R)-(3,4-diklorofenil)-3,4-dihidro-l(2H)-naftalin-l-ilid n]metilamin'ın Hazırlanması için Proses.@ |
| AU2007249399A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
| WO2007134077A2 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | 5 ht receptor mediated neurogenesis |
| US7858611B2 (en) * | 2006-05-09 | 2010-12-28 | Braincells Inc. | Neurogenesis by modulating angiotensin |
| US7518019B2 (en) | 2006-06-01 | 2009-04-14 | Hetero Drugs Limited | Processes for preparing sertraline hydrochloride crystalline forms |
| US20100279990A1 (en) * | 2006-06-13 | 2010-11-04 | Ramot At Tel-Aviv University Ltd. | Antiproliferative compounds, compositions and methods of use |
| US7893053B2 (en) * | 2006-06-16 | 2011-02-22 | Theracos, Inc. | Treating psychological conditions using muscarinic receptor M1 antagonists |
| US20080033045A1 (en) * | 2006-07-07 | 2008-02-07 | Myriad Genetics, Incorporated | Treatment of psychiatric disorders |
| TW200817003A (en) * | 2006-07-31 | 2008-04-16 | Sanofi Aventis | Pharmaceutical composition comprising, in combination, saredutant and a selective serotonin peuptake inhibitor or a serotonin/norepinephrine reuptake inhibitor |
| US20060257475A1 (en) * | 2006-08-17 | 2006-11-16 | Boehringer Ingelheim International Gmbh | Stable Sertraline Hydrochloride Formulation and Method |
| MX2009002496A (es) | 2006-09-08 | 2009-07-10 | Braincells Inc | Combinaciones que contienen un derivado de 4-acilaminopiridina. |
| WO2008034032A2 (en) * | 2006-09-14 | 2008-03-20 | Azevan Pharmaceuticals, Inc. | Beta-lactam cannabinoid receptor modulators |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| FR2909376A1 (fr) * | 2006-11-30 | 2008-06-06 | Cerep Sa | Procedes de preparation de la desmethulsertraline ou d'un de ses sels pharmaceutiquement acceptables |
| WO2008083204A2 (en) * | 2006-12-28 | 2008-07-10 | Braincells, Inc. | Modulation of neurogenesis by melatoninergic ligands |
| CA2675132A1 (en) * | 2007-01-11 | 2008-07-17 | Braincells, Inc. | Modulation of neurogenesis with use of modafinil |
| CA2594198A1 (en) * | 2007-07-20 | 2009-01-20 | Apotex Pharmachem Inc. | A novel process for the preparation of sertraline hydrochloride form ii |
| US20090062399A1 (en) * | 2007-08-29 | 2009-03-05 | Protia, Llc | Deuterium-enriched sertraline |
| US8461389B2 (en) | 2008-04-18 | 2013-06-11 | University College Dublin, National University Of Ireland, Dublin | Psycho-pharmaceuticals |
| WO2009128058A1 (en) | 2008-04-18 | 2009-10-22 | UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN et al | Psycho-pharmaceuticals |
| WO2010099217A1 (en) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
| US9260413B2 (en) * | 2010-03-04 | 2016-02-16 | Merck Sharp & Dohme Corp. | Inhibitors of catechol O-methyl transferase and their use in the treatment of psychotic disorders |
| EP2380595A1 (de) | 2010-04-19 | 2011-10-26 | Nlife Therapeutics S.L. | Zusammensetzungen und Verfahren zur selektiven Abgabe von Oligonukleotidmolekülen an spezifische Neuronentypen |
| US8440655B2 (en) | 2010-06-21 | 2013-05-14 | Theracos, Inc. | Combination therapy for the treatment of diabetes |
| WO2012003436A1 (en) | 2010-07-01 | 2012-01-05 | Azevan Pharmaceuticals, Inc. | Methods for treating post traumatic stress disorder |
| WO2012123922A1 (en) | 2011-03-17 | 2012-09-20 | Lupin Limited | Controlled release pharmaceutical compositions of selective serotonin reuptake inhibitor |
| KR101340270B1 (ko) * | 2011-11-10 | 2013-12-10 | 보령제약 주식회사 | (+)-시스-서트랄린의 선택적인 제조방법 |
| NZ703537A (en) * | 2012-10-18 | 2018-06-29 | Hoffmann La Roche | Ethynyl derivatives |
| MX2021005502A (es) | 2014-03-28 | 2023-01-16 | Azevan Pharmaceuticals Inc | Composiciones y metodos para tratar enfermedades neurodegenerativas. |
| US10266481B2 (en) | 2014-06-20 | 2019-04-23 | Council Of Scientific & Industrial Research | Organocatalytic asymmetric synthesis of antidepressants |
| JP6695323B2 (ja) * | 2014-08-11 | 2020-05-20 | ハイドラ・バイオサイエンシーズ・リミテッド・ライアビリティ・カンパニーHydra Biosciences, LLC | ピリド[3,4−d]ピリミジン−2,4(1H,3H)−ジオン誘導体 |
| WO2016023830A1 (en) * | 2014-08-11 | 2016-02-18 | Hydra Biosciences, Inc. | Pyrido[2,3-d]pyrimidine-2,4(1h,3h)-dione derivatives |
| EP3180345B1 (de) * | 2014-08-11 | 2018-10-10 | Hydra Biosciences, Inc. | Thieno- und furo[2,3-d]pyrimidin-2,4[1h,3h]-dion derivate als trpc5 modulatoren zur behandlung von neuropsychiatrischen erkrankungen |
| JP6667092B2 (ja) * | 2014-08-11 | 2020-03-18 | ハイドラ・バイオサイエンシーズ・リミテッド・ライアビリティ・カンパニーHydra Biosciences, LLC | ピロロ[3,2−d]ピリミジン−2,4(3H,5H)−ジオン誘導体 |
| EP4166237A1 (de) | 2015-09-21 | 2023-04-19 | S.C. Johnson & Son, Inc. | Misch- und abgabesystem |
| BR112020005107A2 (pt) | 2017-09-15 | 2020-11-03 | Azevan Pharmaceuticals, Inc. | composições e métodos para o tratamento de lesão cerebral |
| WO2020043716A1 (en) | 2018-08-27 | 2020-03-05 | Katholieke Universiteit Leuven | Pharmacological targeting of de novo serine/glycine synthesis |
| GB2630572A (en) | 2023-05-29 | 2024-12-04 | Novumgen Ltd | An orally disintegrating tablet of sertraline and its process of preparation |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2887509A (en) * | 1956-11-05 | 1959-05-19 | Lilly Co Eli | Hydroxybenzoyl benzoate salt of beta-(o-chlorophenyl)-beta-hydroxyethyl isopropylamine |
| US3704323A (en) * | 1969-12-23 | 1972-11-28 | Squibb & Sons Inc | Indane derivatives |
| US4045488A (en) * | 1974-11-06 | 1977-08-30 | Pfizer Inc. | Aminophenyltetralin compounds |
| US4029731A (en) * | 1974-11-06 | 1977-06-14 | Pfizer Inc. | Aminophenyltetralin compounds |
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