SE422941B - Analogiforfarande for framstellning av tetracykliska pyrido-bensazepinforeningar - Google Patents
Analogiforfarande for framstellning av tetracykliska pyrido-bensazepinforeningarInfo
- Publication number
- SE422941B SE422941B SE7603931A SE7603931A SE422941B SE 422941 B SE422941 B SE 422941B SE 7603931 A SE7603931 A SE 7603931A SE 7603931 A SE7603931 A SE 7603931A SE 422941 B SE422941 B SE 422941B
- Authority
- SE
- Sweden
- Prior art keywords
- preparation
- analogy procedure
- benzazepine compounds
- tetracyclic
- pyrido
- 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 (1)
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. |
Publications (2)
Publication Number | Publication Date |
---|---|
SE7603931L SE7603931L (sv) | 1976-10-06 |
SE422941B true SE422941B (sv) | 1982-04-05 |
Family
ID=19823518
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7603931A SE422941B (sv) | 1975-04-05 | 1976-04-02 | Analogiforfarande for framstellning av tetracykliska pyrido-bensazepinforeningar |
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 |
CA2326356C (fr) * | 1998-04-02 | 2008-06-03 | Akzo Nobel N.V. | Solution orale liquide exercant un effet antidepresseur |
US6545149B2 (en) | 1999-04-19 | 2003-04-08 | Teva Pharmaceutical Industries Ltd. | Synthesis and crystallization of piperazine ring-containing compounds |
SK14672001A3 (sk) * | 1999-04-19 | 2002-11-06 | Teva Pharmaceutical Industries Ltd. | Spôsob syntézy a kryštalizácie zlúčenín obsahujúcich piperazínový kruh |
EP1178805A4 (fr) * | 1999-04-19 | 2004-11-24 | Teva Pharma | Nouvelle synthese et cristallisation de composes contenant de la piperazine |
TR200103035T2 (tr) | 1999-04-19 | 2002-01-21 | Teva Pharmaceutical Industries Ltd. | Yeni piperazin halkası sentezi. |
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 |
AU6474200A (en) * | 1999-12-13 | 2001-06-18 | Sumika Fine Chemicals Co., Ltd. | Process for the preparation of a pyridinemethanol compound |
AU780817B2 (en) * | 2000-01-19 | 2005-04-21 | Akzo Nobel N.V. | Drug combination for the treatment of depression and related disorders comprising mirtazapine and gepirone |
DE60117122T2 (de) | 2000-02-11 | 2006-07-27 | Akzo Nobel N.V. | Verwendung von mirtazapin zur behandlung von schlafstörungen |
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 |
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 |
AU2002237847A1 (en) * | 2001-02-12 | 2002-08-28 | Akzo Nobel N.V | Methods for improving the treatment of major depression by genotyping for the gene for apolipoproteine 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 |
IL157607A0 (en) | 2001-03-01 | 2004-03-28 | Teva Pharma | Methods for the preparation of mirtazapine intermediates |
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 |
US20040192754A1 (en) * | 2003-03-24 | 2004-09-30 | Shapira Nathan Andrew | Methods for treating idiopathic hyperhidrosis and associated conditions |
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 |
EP1753460A2 (fr) * | 2004-05-11 | 2007-02-21 | Pfizer Products Inc. | Combinaison d'antipsychotiques atypiques et d'antagonistes du recepteur de 5-ht1b |
EP1776160A1 (fr) * | 2004-08-13 | 2007-04-25 | Omeros Corporation | Nouveaux ligands de recepteur de serotonine et leurs utilisations |
WO2006023702A2 (fr) * | 2004-08-20 | 2006-03-02 | Cypress Bioscience, Inc. | Methode de traitement de troubles respiratoires lies au sommeil a l'aide de setiptiline |
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 |
EP1783125A4 (fr) * | 2004-08-24 | 2008-06-18 | Sumitomo Chemical Co | Methode de production de 2-(4-methyl-2-phenylpiperazine-1-yl)-3-cyanopyridine |
TW200631584A (en) * | 2004-11-15 | 2006-09-16 | Akzo Nobel Nv | A medicament related to mirtazapine for the treatment of hot flush |
EP1827450A4 (fr) * | 2004-11-17 | 2009-04-22 | 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 |
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 |
AU2006308889A1 (en) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | GABA receptor mediated modulation of neurogenesis |
US20070225217A1 (en) | 2005-11-09 | 2007-09-27 | Combinatorx, Incorporated | Methods, compositions, and kits for the treatment of medical conditions |
ZA200804860B (en) * | 2005-11-14 | 2009-11-25 | Sumitomo Chemical Co | Method for producing 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 |
WO2007101832A1 (fr) * | 2006-03-06 | 2007-09-13 | 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 |
EP2021000A2 (fr) | 2006-05-09 | 2009-02-11 | Braincells, Inc. | Neurogenèse par modulation de l'angiotensine |
US7858611B2 (en) * | 2006-05-09 | 2010-12-28 | Braincells Inc. | Neurogenesis by modulating angiotensin |
MX2008014320A (es) | 2006-05-09 | 2009-03-25 | Braincells Inc | Neurogenesis mediada por el receptor de 5-hidroxitriptamina. |
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 |
MX2009002496A (es) * | 2006-09-08 | 2009-07-10 | Braincells Inc | Combinaciones que contienen un derivado de 4-acilaminopiridina. |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
US20080167363A1 (en) * | 2006-12-28 | 2008-07-10 | Braincells, Inc | Modulation of Neurogenesis By Melatoninergic Agents |
CA2675132A1 (fr) * | 2007-01-11 | 2008-07-17 | Braincells, Inc. | Modulation de la neurogenese en utilisant du 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 |
US7994314B2 (en) * | 2007-04-11 | 2011-08-09 | N.V. Organon | Method for the preparation of an enantiomerically pure benzazepine |
JP5635905B2 (ja) * | 2007-04-11 | 2014-12-03 | メルク・シャープ・エンド・ドーム・ベー・フェー | ミルタザピンの調製方法 |
MX2009010964A (es) * | 2007-04-11 | 2009-10-30 | Organon Nv | Un metodo para la preparacion de una benzazepina enantiomericamente pura. |
US20080255348A1 (en) * | 2007-04-11 | 2008-10-16 | N.V. Organon | Method for the preparation of an enantiomer of a tetracyclic benzazepine |
EP2167096A4 (fr) * | 2007-06-13 | 2010-07-14 | 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 |
EP2288345B1 (fr) | 2008-04-18 | 2015-06-10 | University College Dublin National University Of Ireland, Dublin | Produits psycho-pharmaceutiques |
EP2291181B9 (fr) | 2008-04-18 | 2013-09-11 | University College Dublin National University Of Ireland, Dublin | Utilisation de la captodiamine pour le traitement des symptômes de la dépression |
CA2727573A1 (fr) * | 2008-06-25 | 2009-12-30 | Pfizer Inc. | Composes diaryle et leurs utilisations |
US20110201804A1 (en) * | 2008-10-22 | 2011-08-18 | Watson Pharma Private Limited | Process for the preparation of 1- ( 3-hydroxymethylpyrid-2 -yl ) -2 -phenyl-4-methylpiperazine and mirtazapine |
WO2010099217A1 (fr) | 2009-02-25 | 2010-09-02 | Braincells, Inc. | Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine |
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 ZA ZA761756A patent/ZA761756B/xx unknown
- 1976-03-23 IE IE614/76A patent/IE42969B1/en 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 CA CA249,439A patent/CA1076571A/fr not_active Expired
- 1976-04-02 JP JP51037678A patent/JPS5942678B2/ja 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 LU LU74680A patent/LU74680A1/xx unknown
- 1976-04-02 ES ES446634A patent/ES446634A1/es not_active Expired
- 1976-04-02 BE BE165832A patent/BE840362A/fr not_active IP Right Cessation
- 1976-04-02 FR FR7609686A patent/FR2305986A1/fr active Granted
- 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 |
---|---|
LU74680A1 (fr) | 1976-11-11 |
NL940007I2 (nl) | 1994-10-17 |
FR2305986A1 (fr) | 1976-10-29 |
IE42969B1 (en) | 1980-11-19 |
NL189199C (nl) | 1993-02-01 |
NL7504075A (nl) | 1976-10-07 |
DE2614406C2 (fr) | 1992-02-20 |
FI760884A (fr) | 1976-10-06 |
JPS5942678B2 (ja) | 1984-10-16 |
FI62087B (fi) | 1982-07-30 |
NL940007I1 (nl) | 1994-06-01 |
US4062848A (en) | 1977-12-13 |
GB1543171A (en) | 1979-03-28 |
FI62087C (fi) | 1982-11-10 |
AU1236176A (en) | 1977-09-29 |
IE42969L (en) | 1976-10-05 |
NL189199B (nl) | 1992-09-01 |
DK142498B (da) | 1980-11-10 |
CA1076571A (fr) | 1980-04-29 |
ES446634A1 (es) | 1977-11-01 |
JPS51122099A (en) | 1976-10-25 |
DK142676A (fr) | 1976-10-06 |
CH622261A5 (fr) | 1981-03-31 |
HU179401B (en) | 1982-10-28 |
DE2614406A1 (de) | 1976-10-14 |
ES459348A1 (es) | 1978-03-16 |
ZA761756B (en) | 1977-03-30 |
SE7603931L (sv) | 1976-10-06 |
DK142498C (fr) | 1981-07-06 |
FR2305986B1 (fr) | 1980-06-13 |
BE840362A (fr) | 1976-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
SE422941B (sv) | Analogiforfarande for framstellning av tetracykliska pyrido-bensazepinforeningar | |
SE433208B (sv) | Forfarande for framstellning av fenoletrar | |
SE438853B (sv) | Forfarande for framstellning av 2-azetidinonforeningar | |
DK146205C (da) | Analogifremgangsmaade til fremstilling af 8alfa-ergolin-i-derivater | |
SE7605139L (sv) | Forfarande for framstellning av vattenupptagande cellulosaetrar | |
SE430336B (sv) | Forbettrat forfarande for framstellning av amoxicillinfrihydrat | |
SE427839B (sv) | Analogiforfaranden for framstellning av n-aryl-n-(1-l-4-piperidinyl)-aryl-acetamider | |
NO139555C (no) | Fremgangsmaate for fremstilling av fosgen | |
NO146058C (no) | Analogifremgangsmaate for fremstilling av substituerte benzamider | |
SE443142B (sv) | Forfarande for framstellning av rifamycinforeningar | |
SE7606116L (sv) | Forfarande for framstellning av 3-fenoxidbensaldehyder | |
SE427841B (sv) | Analogiforfarande for framstellning av tienamycinderivat | |
SE7604781L (sv) | Forfarande for framstellning av diarylhydroxibutylaminer | |
SE421793B (sv) | Analogiforfarande for framstellning naftyridinsubstituerade pyrrolderivat | |
SE420730B (sv) | Analogiforfarande for framstellning av nya pentacykliska foreningar | |
SE404186B (sv) | Forfarande for framstellning av cyklopropanolderivat | |
SE423814B (sv) | Forfarande for framstellning av dibensofenazin- eller acenaftokinoxalinderivat | |
SE427840B (sv) | Analogiforfarande for framstellning av tienamycinderivat | |
SE7610637L (sv) | Forfarande for framstellning av 2-alkylindaner | |
SE446726B (sv) | Forfarande for framstellning av 16-metoxiprostaglandiner | |
DK142845C (da) | Analogifremgangsmaade til fremstilling af imidazolderivater | |
DK140476A (da) | Fremgangsmade til fremstilling af trans-decalinderivater | |
SE7605427L (sv) | Forfarande for framstellning av klorcyan | |
SE7603682L (sv) | Forfarande for framstellning av en eteriskt substituerad monosackarid | |
NO149137C (no) | Analogifremgangsmaate ved fremsilling av diazepin-forbindelser |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
NAL | Patent in force |
Ref document number: 7603931-2 Format of ref document f/p: F |
|
SPCF | Application for supplementary protection certificate filed |
Free format text: 9690008, 960228 |
|
NUG | Patent has lapsed |
Ref document number: 7603931-2 Format of ref document f/p: F |
|
SPCG | Supplementary protection certificate granted |
Free format text: 9690008, 960228, EXPIRES: 20010402 |