FI62087C - Foerfarande foer framstaellning av 1,2,3,4,10,14b-hexahydrobenso(c)pyrazino(1,2-a)pyridoazepinderivat med antihistamin- oc centralnervstimulerande aktivitet - Google Patents
Foerfarande foer framstaellning av 1,2,3,4,10,14b-hexahydrobenso(c)pyrazino(1,2-a)pyridoazepinderivat med antihistamin- oc centralnervstimulerande aktivitet Download PDFInfo
- Publication number
- FI62087C FI62087C FI760884A FI760884A FI62087C FI 62087 C FI62087 C FI 62087C FI 760884 A FI760884 A FI 760884A FI 760884 A FI760884 A FI 760884A FI 62087 C FI62087 C FI 62087C
- Authority
- FI
- Finland
- Prior art keywords
- formula
- compound
- mixture
- group
- salt
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NLAANVRAGE7504075,A NL189199C (nl) | 1975-04-05 | 1975-04-05 | Werkwijze ter bereiding van farmaceutische preparaten met werking op het centraal zenuwstelsel op basis van benz(aryl)azepinederivaten, de verkregen gevormde farmaceutische preparaten, alsmede werkwijze ter bereiding van de toe te passen benz(aryl)azepinederivaten. |
NL7504075 | 1975-04-05 |
Publications (3)
Publication Number | Publication Date |
---|---|
FI760884A FI760884A (fr) | 1976-10-06 |
FI62087B FI62087B (fi) | 1982-07-30 |
FI62087C true FI62087C (fi) | 1982-11-10 |
Family
ID=19823518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI760884A FI62087C (fi) | 1975-04-05 | 1976-04-01 | Foerfarande foer framstaellning av 1,2,3,4,10,14b-hexahydrobenso(c)pyrazino(1,2-a)pyridoazepinderivat med antihistamin- oc centralnervstimulerande aktivitet |
Country Status (17)
Country | Link |
---|---|
US (1) | US4062848A (fr) |
JP (1) | JPS5942678B2 (fr) |
BE (1) | BE840362A (fr) |
CA (1) | CA1076571A (fr) |
CH (1) | CH622261A5 (fr) |
DE (1) | DE2614406A1 (fr) |
DK (1) | DK142498B (fr) |
ES (2) | ES446634A1 (fr) |
FI (1) | FI62087C (fr) |
FR (1) | FR2305986A1 (fr) |
GB (1) | GB1543171A (fr) |
HU (1) | HU179401B (fr) |
IE (1) | IE42969B1 (fr) |
LU (1) | LU74680A1 (fr) |
NL (2) | NL189199C (fr) |
SE (1) | SE422941B (fr) |
ZA (1) | ZA761756B (fr) |
Families Citing this family (74)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4515792A (en) * | 1982-09-30 | 1985-05-07 | Ciba-Geigy Corporation | Tetracyclic heterocycles and antidepressant compositions thereof |
JPS6336682A (ja) * | 1986-07-31 | 1988-02-17 | Matsushita Electric Ind Co Ltd | カセツト方式文字放送受信機 |
JPS63177670A (ja) * | 1987-01-31 | 1988-07-21 | Fujitsu General Ltd | 文字放送受信装置 |
JPS63215179A (ja) * | 1987-03-03 | 1988-09-07 | Fujitsu General Ltd | 受信装置 |
JPH055746Y2 (fr) * | 1988-04-27 | 1993-02-15 | ||
NO175781C (no) * | 1989-10-05 | 1994-12-07 | Sankyo Co | Analogifremgangsmåte for fremstilling av terapeutisk aktive tetracykliske forbindelser |
EP0539164A1 (fr) * | 1991-10-23 | 1993-04-28 | Sankyo Company Limited | Composés tétracycliques contenant l'azote ayant des propriétés antiallergiques et antiasthmatiques, leur préparation et utilisation |
IL121076A (en) * | 1996-06-19 | 2000-10-31 | Akzo Nobel Nv | Pharmaceutical combinations comprising mirtazapine and one or more selective serotonin reuptake inhibitors |
DE69913116T2 (de) * | 1998-04-02 | 2004-06-03 | Akzo Nobel N.V. | Orale flüssige lösung enthaltend das antidepressivum mirtazapine |
EP1178972A4 (fr) | 1999-04-19 | 2002-06-12 | Teva Pharma | Nouvelle synthese de noyau piperazine |
US6545149B2 (en) | 1999-04-19 | 2003-04-08 | Teva Pharmaceutical Industries Ltd. | Synthesis and crystallization of piperazine ring-containing compounds |
AU781221B2 (en) * | 1999-04-19 | 2005-05-12 | Teva Pharmaceutical Industries Ltd. | Novel synthesis and crystallization of piperazine ring-containing compounds |
CA2368815A1 (fr) * | 1999-04-19 | 2000-10-26 | Claude Singer | Nouvelle synthese et cristallisation de composes contenant de la piperazine |
US6281207B1 (en) * | 1999-09-15 | 2001-08-28 | Reed Richter | Treatment of movement disorders by administration of mirtazapine |
AU6476300A (en) * | 1999-09-30 | 2001-05-10 | Sumika Fine Chemicals Co., Ltd. | Process for the preparation of a piperazine derivative |
WO2001038329A1 (fr) * | 1999-11-24 | 2001-05-31 | Sumika Fine Chemicals Co., Ltd. | Cristaux de mirtazapine anhydre et leur procede d'obtention |
WO2001042239A1 (fr) | 1999-12-13 | 2001-06-14 | Sumika Fine Chemicals Co., Ltd. | Procede de preparation d'un compose pyridinemethanol |
HUP0204050A3 (en) * | 2000-01-19 | 2004-09-28 | Akzo Nobel Nv | Drug combination for the treatment of depression and related disorders comprising mirtazapine and gepirone |
EP1257278B1 (fr) | 2000-02-11 | 2006-02-08 | Akzo Nobel N.V. | Utilisation de mirtazapine pour traiter des troubles du sommeil |
IN190478B (fr) * | 2000-11-07 | 2003-08-02 | Sun Pharmaceutical Ind Ltd | |
US6660730B2 (en) | 2000-11-27 | 2003-12-09 | Sumika Fine Chemicals Co., Ltd. | Anhydrous mirtazapine and process for preparing the same |
WO2002064735A2 (fr) * | 2001-02-12 | 2002-08-22 | Akzo Nobel N.V. | Methodes permettant d'ameliorer le traitement de depressions graves par genotypage visant a determiner le gene associe a l'apolipoproteine e4 et d'ameliorer la reponse therapeutique de personnes souffrant de depression grave et porteuses du gene associe a l'apolipoproteine e4 |
US6399310B1 (en) | 2001-02-12 | 2002-06-04 | Akzo Nobel N.V. | Methods for improving the therapeutic response of humans having major depression and carrying the gene for apolipoprotein E4 |
US20030105082A1 (en) * | 2001-12-03 | 2003-06-05 | Murphy Greer Marechal | Methods for improving the therapeutic response of humans having major depression and carrying the gene for apolipoprotein E4 |
JP2005501808A (ja) * | 2001-03-01 | 2005-01-20 | テバ ファーマシューティカル インダストリーズ リミティド | ミルタザピン中間体の製造方法 |
US7355042B2 (en) * | 2001-10-16 | 2008-04-08 | Hypnion, Inc. | Treatment of CNS disorders using CNS target modulators |
CZ296992B6 (cs) * | 2002-10-03 | 2006-08-16 | Zentiva, A.S. | Príprava a izolace 2-substituovaných-3-pyridylkarboxylových kyselin, jejich karboxylových solí a produktu redukce |
WO2004084905A2 (fr) * | 2003-03-24 | 2004-10-07 | University Of Florida | Methodes de traitement de l'hyperhidrose idiopathique et de pathologies associees |
UA83666C2 (ru) | 2003-07-10 | 2008-08-11 | Н.В. Органон | Способ получения энантиомерно чистого миртазапина |
US7838029B1 (en) * | 2003-07-31 | 2010-11-23 | Watson Laboratories, Inc. | Mirtazapine solid dosage forms |
TW200538100A (en) * | 2004-04-21 | 2005-12-01 | Akzo Nobel Nv | Mirtazapine salts |
CA2565996A1 (fr) * | 2004-05-11 | 2005-11-17 | Pfizer Products Inc. | Combinaison d'antipsychotiques atypiques et d'antagonistes du recepteur de 5-ht<sb>1b</sb> |
EP1776160A1 (fr) * | 2004-08-13 | 2007-04-25 | Omeros Corporation | Nouveaux ligands de recepteur de serotonine et leurs utilisations |
WO2006023703A2 (fr) * | 2004-08-20 | 2006-03-02 | Cypress Bioscience, Inc. | Methode de traitement de troubles respiratoires lies au sommeil |
JP4848704B2 (ja) * | 2004-08-24 | 2011-12-28 | 住友化学株式会社 | 2−(4−メチル−2−フェニルピペラジン−1−イル)−3−シアノピリジンの製造方法 |
US20080182987A1 (en) * | 2004-08-24 | 2008-07-31 | Sumitomo Chemical Company, Limited | Method For Producing 2-(4-Methyl-2-Phenylpiperazine-1-Yl)-3-Cyanopiridine |
TW200631584A (en) * | 2004-11-15 | 2006-09-16 | Akzo Nobel Nv | A medicament related to mirtazapine for the treatment of hot flush |
WO2006055854A2 (fr) * | 2004-11-17 | 2006-05-26 | Cypress Bioscience, Inc. | Methodes servant a limiter les effets secondaires d'un traitement par mirtazapine |
US20090306046A1 (en) * | 2005-06-27 | 2009-12-10 | N.V. Organon | Method of treatment of hormone depletion induced vasomotor symptoms |
EP1904843A2 (fr) * | 2005-07-08 | 2008-04-02 | Braincells, Inc. | Methodes destinees a identifier des agents et des conditions modulant la neurogenese |
CN1939918B (zh) * | 2005-09-30 | 2010-09-01 | 北京德众万全医药科技有限公司 | 一种米氮平的制备方法 |
WO2007047978A2 (fr) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation de la neurogenese par inhibition de la pde |
WO2007053596A1 (fr) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | Modulation de la neurogenese dont la mediation est assuree par recepteur gaba |
NZ568694A (en) | 2005-11-09 | 2011-09-30 | Zalicus Inc | Method, compositions, and kits for the treatment of medical conditions |
WO2007055423A1 (fr) * | 2005-11-14 | 2007-05-18 | Sumitomo Chemical Company, Limited | Procede de fabrication de 2-(4-methyl-2-phenylpiperazin- 1-yl)pyridine-3-methanol |
EP1792618A1 (fr) | 2005-11-30 | 2007-06-06 | Rainer Freynhagen | R-mirtazapine pour le traitement de la douleur |
EP1993556A1 (fr) * | 2006-03-06 | 2008-11-26 | N.V. Organon | Méthode perfectionnée pour sevrer d'un traitement hormonal de symptômes vasomoteurs induits par un épuisement hormonal |
US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
US7858611B2 (en) * | 2006-05-09 | 2010-12-28 | Braincells Inc. | Neurogenesis by modulating angiotensin |
EP2382975A3 (fr) | 2006-05-09 | 2012-02-29 | Braincells, Inc. | Neurogénèse par modulation d'angiotensine |
CA2651862A1 (fr) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenese induite par le recepteur 5ht |
US20070270413A1 (en) * | 2006-05-22 | 2007-11-22 | N.V. Organon | Mirtazapine for the treatment of neuropathic pain |
TW200815370A (en) * | 2006-06-16 | 2008-04-01 | Organon Nv | Stereoselective synthesis of (S)-1-methyl-3-phenylpiperazine |
KR20090064418A (ko) * | 2006-09-08 | 2009-06-18 | 브레인셀즈 인코퍼레이션 | 4-아실아미노피리딘 유도체 포함 조합물 |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
WO2008083204A2 (fr) * | 2006-12-28 | 2008-07-10 | Braincells, Inc. | Modulation de la neurogenèse par des ligands mélatoninergiques |
AU2008204800A1 (en) * | 2007-01-11 | 2008-07-17 | Braincells, Inc. | Modulation of neurogenesis with use of modafinil |
JP5192707B2 (ja) * | 2007-03-22 | 2013-05-08 | 住友化学株式会社 | ミルタザピンの製造方法 |
CN101679431B (zh) * | 2007-04-11 | 2013-08-14 | Msd欧斯股份有限公司 | 制备四环苯并氮杂卓的对映异构体的方法 |
US7994314B2 (en) * | 2007-04-11 | 2011-08-09 | N.V. Organon | Method for the preparation of an enantiomerically pure benzazepine |
EP2133350B1 (fr) * | 2007-04-11 | 2016-03-23 | Merck Sharp & Dohme B.V. | Procédé de préparation de benzazépine pure énantiomorphiquement |
US20080255348A1 (en) * | 2007-04-11 | 2008-10-16 | N.V. Organon | Method for the preparation of an enantiomer of a tetracyclic benzazepine |
WO2008157094A1 (fr) * | 2007-06-13 | 2008-12-24 | Cypress Bioscience, Inc. | Amélioration de la tolérance à la mirtazapine et à un second principe actif par utilisation combinée de ces derniers |
JP2009018992A (ja) * | 2007-07-10 | 2009-01-29 | Sumitomo Chemical Co Ltd | 光学活性ミルタザピンの製造方法 |
US8461389B2 (en) | 2008-04-18 | 2013-06-11 | University College Dublin, National University Of Ireland, Dublin | Psycho-pharmaceuticals |
WO2009128058A1 (fr) | 2008-04-18 | 2009-10-22 | UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN et al | Produits psycho-pharmaceutiques |
JP2011526881A (ja) * | 2008-06-25 | 2011-10-20 | ファイザー・インク | ジアリール化合物およびそれらの使用 |
WO2010046851A1 (fr) | 2008-10-22 | 2010-04-29 | Watson Pharma Private Limited | Procédé amélioré de synthèse de mirtazapine et de ses intermédiaires |
US20100216805A1 (en) | 2009-02-25 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
CN102432594B (zh) * | 2011-11-28 | 2013-09-11 | 山东鲁药制药有限公司 | 一种药物中间体1-(3-羟甲基吡啶-2-基)-2-苯基-4-甲基哌嗪的制备方法 |
CN103509020A (zh) * | 2013-10-21 | 2014-01-15 | 山东鲁药制药有限公司 | 一种米氮平的合成方法 |
CN104356133A (zh) * | 2014-11-25 | 2015-02-18 | 南京工业大学 | 一种制备抗抑郁药物米氮平的方法 |
JP6433809B2 (ja) * | 2015-02-20 | 2018-12-05 | 株式会社トクヤマ | 1−(3−ヒドロキシメチルピリジル−2−)−2−フェニル−4−メチルピペラジンの製造方法 |
KR102540021B1 (ko) | 2020-12-02 | 2023-06-07 | (주)유케이케미팜 | 대량 생산에 적합한 미르타자핀의 제조방법 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL129434C (fr) * | 1966-03-12 | |||
NL7202963A (fr) * | 1972-03-07 | 1973-09-11 | ||
US3959470A (en) * | 1972-11-28 | 1976-05-25 | Mikhail Davidovich Mashkovsky | Psychotropic medicinal preparation |
-
1975
- 1975-04-05 NL NLAANVRAGE7504075,A patent/NL189199C/xx not_active IP Right Cessation
-
1976
- 1976-03-23 US US05/669,544 patent/US4062848A/en not_active Expired - Lifetime
- 1976-03-23 IE IE614/76A patent/IE42969B1/en unknown
- 1976-03-23 ZA ZA761756A patent/ZA761756B/xx unknown
- 1976-03-26 GB GB12270/76A patent/GB1543171A/en not_active Expired
- 1976-03-29 CH CH388676A patent/CH622261A5/de not_active IP Right Cessation
- 1976-03-30 DK DK142676AA patent/DK142498B/da active Protection Beyond IP Right Term
- 1976-04-01 FI FI760884A patent/FI62087C/fi not_active IP Right Cessation
- 1976-04-02 JP JP51037678A patent/JPS5942678B2/ja not_active Expired
- 1976-04-02 FR FR7609686A patent/FR2305986A1/fr active Granted
- 1976-04-02 LU LU74680A patent/LU74680A1/xx unknown
- 1976-04-02 CA CA249,439A patent/CA1076571A/fr not_active Expired
- 1976-04-02 ES ES446634A patent/ES446634A1/es not_active Expired
- 1976-04-02 DE DE19762614406 patent/DE2614406A1/de active Granted
- 1976-04-02 SE SE7603931A patent/SE422941B/xx active Protection Beyond IP Right Term
- 1976-04-02 BE BE165832A patent/BE840362A/fr not_active IP Right Cessation
- 1976-04-05 HU HU76AO437A patent/HU179401B/hu unknown
-
1977
- 1977-05-31 ES ES459348A patent/ES459348A1/es not_active Expired
-
1994
- 1994-04-21 NL NL940007C patent/NL940007I2/nl unknown
Also Published As
Publication number | Publication date |
---|---|
DK142498B (da) | 1980-11-10 |
DK142498C (fr) | 1981-07-06 |
HU179401B (en) | 1982-10-28 |
CH622261A5 (fr) | 1981-03-31 |
CA1076571A (fr) | 1980-04-29 |
ZA761756B (en) | 1977-03-30 |
NL940007I1 (nl) | 1994-06-01 |
NL7504075A (nl) | 1976-10-07 |
NL189199B (nl) | 1992-09-01 |
FR2305986B1 (fr) | 1980-06-13 |
JPS51122099A (en) | 1976-10-25 |
FI62087B (fi) | 1982-07-30 |
JPS5942678B2 (ja) | 1984-10-16 |
SE7603931L (sv) | 1976-10-06 |
GB1543171A (en) | 1979-03-28 |
LU74680A1 (fr) | 1976-11-11 |
NL940007I2 (nl) | 1994-10-17 |
SE422941B (sv) | 1982-04-05 |
FI760884A (fr) | 1976-10-06 |
FR2305986A1 (fr) | 1976-10-29 |
NL189199C (nl) | 1993-02-01 |
US4062848A (en) | 1977-12-13 |
DE2614406A1 (de) | 1976-10-14 |
DK142676A (fr) | 1976-10-06 |
ES446634A1 (es) | 1977-11-01 |
AU1236176A (en) | 1977-09-29 |
IE42969B1 (en) | 1980-11-19 |
BE840362A (fr) | 1976-10-04 |
ES459348A1 (es) | 1978-03-16 |
IE42969L (en) | 1976-10-05 |
DE2614406C2 (fr) | 1992-02-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FI62087C (fi) | Foerfarande foer framstaellning av 1,2,3,4,10,14b-hexahydrobenso(c)pyrazino(1,2-a)pyridoazepinderivat med antihistamin- oc centralnervstimulerande aktivitet | |
JPS6134426B2 (fr) | ||
EP0047226B1 (fr) | Dérivés pipéridylidéniques, leur préparation et compositions pharmaceutiques les contenant | |
GB1593417A (en) | Carbocyclic-fused pyrazolopyridine derivatives | |
JPS58152885A (ja) | 薬理学的に活性なピラゾロ〔4,3−↓c〕ピリジン類 | |
DK157615B (da) | Analogifremgangsmaade til fremstilling af terapeutisk aktive imidazo oe1,5-aaaoe1,4aa diazepin-forbindelser eller farmaceutisk acceptable syreadditionssalte deraf | |
FI60563C (fi) | Foerfarande foer framstaellning av nya terapeutiskt anvaendbara tetracykliska piperidinoderivat | |
DE3780015T2 (de) | Kondensierte heterocyclische tetrahydroaminochinolinole und verwandte verbindungen, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel. | |
DE60218646T2 (de) | N-biphenylcarbonyl- und n-phenylpyridylcarbonyl substituierte bi- und tricyclische azepine und diazepine als vasopressin-agonisten | |
CS207619B2 (en) | Method of making the new derivatives of 5,11-dihydro-6h-pyrido 2,3-b 1,4 benzodiazepin-6-on | |
US4547496A (en) | Antiulcer [1] benzepino[3,4-b]pyridine and compositions | |
JPH0322390B2 (fr) | ||
FI91411B (fi) | Menetelmä terapeuttisesti käyttökelpoisten 4,5,6,7-tetrahydroisotiatsolo/4,5-c/pyridiini-johdannaisten ja niiden isomeerien ja happoadditiosuolojen valmistamiseksi | |
SU1272990A3 (ru) | Способ получени производных диазабицикло /3,3,1/ нонана или их солей | |
WO2002083685A1 (fr) | Cyclohexylphenyles ayant une activite d'agonistes de la vasopressine | |
Marchalin et al. | Thienoquinolizidinones. Synthesis and rearrangement into new piperidino [1, 2‐a][1, 3] or [1, 4] diazepinones fused to a thiophene ring | |
RU2057754C1 (ru) | Гетероциклические соединения или их кислотно-аддитивные соли | |
Huckle et al. | 4-Amino-2, 3, 4, 5-tetrahydro-1-benzoxepin-5-ols, 4-amino-2, 3, 4, 5-tetrahydro-1-benzothiepin-5-ols, and related compounds | |
PL90057B1 (en) | Piperdine derivatives[au6900774a] | |
Liepa | A synthesis of alkylated 3-aminoisoquinolines and related compounds | |
US3985751A (en) | Benzocycloheptaisoquinoline derivatives | |
US3555018A (en) | Thiazinopyridoindolone derivatives | |
FI89361C (fi) | Foerfarande foer framstaellning av farmaceutiskt anvaendbart 5,6,7,8-tetrahydro-4h-isoxazolo/4,5-c/azepinderivat | |
CA1082183A (fr) | Composes a base de diazepino-dibenzoxazepine et de diazepinodibenzazepine tetracyclique a activite biologique | |
US3419568A (en) | Derivatives of 1,2,3,4-tetrahydro-5h-pyrido[4,3b]indoles |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MA | Patent expired | ||
ND | Supplementary protection certificate (spc) granted | ||
SPCG | Supplementary protection certificate granted |
Spc suppl protection certif: L60 Extension date: 20010401 |
|
MA | Patent expired |
Owner name: AKZO N.V. |