EA199800449A1 - Способ получения 7-альфа-карбоксил-9,11-эпоксистероидов, используемые в этом способе промежуточные соединения и общий способ эпоксидирования двойных этиленовых связей - Google Patents
Способ получения 7-альфа-карбоксил-9,11-эпоксистероидов, используемые в этом способе промежуточные соединения и общий способ эпоксидирования двойных этиленовых связейInfo
- Publication number
- EA199800449A1 EA199800449A1 EA199800449A EA199800449A EA199800449A1 EA 199800449 A1 EA199800449 A1 EA 199800449A1 EA 199800449 A EA199800449 A EA 199800449A EA 199800449 A EA199800449 A EA 199800449A EA 199800449 A1 EA199800449 A1 EA 199800449A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- sup
- group
- chr
- hydroxyalkyl
- alpha
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004104 aryloxy group Chemical group 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000001475 halogen functional group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 3
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000005041 acyloxyalkyl group Chemical group 0.000 abstract 2
- 125000002837 carbocyclic group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- JUKPWJGBANNWMW-VWBFHTRKSA-N eplerenone Chemical compound C([C@@H]1[C@]2(C)C[C@H]3O[C@]33[C@@]4(C)CCC(=O)C=C4C[C@H]([C@@H]13)C(=O)OC)C[C@@]21CCC(=O)O1 JUKPWJGBANNWMW-VWBFHTRKSA-N 0.000 abstract 1
- 229960001208 eplerenone Drugs 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J21/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J21/00—Normal steroids containing carbon, hydrogen, halogen or oxygen having an oxygen-containing hetero ring spiro-condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J21/001—Lactones
- C07J21/003—Lactones at position 17
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J31/00—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring
- C07J31/006—Normal steroids containing one or more sulfur atoms not belonging to a hetero ring not covered by C07J31/003
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J53/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
- C07J53/002—Carbocyclic rings fused
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J71/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
- C07J71/0005—Oxygen-containing hetero ring
- C07J71/001—Oxiranes
- C07J71/0015—Oxiranes at position 9(11)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P33/00—Preparation of steroids
- C12P33/005—Degradation of the lateral chains at position 17
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P33/00—Preparation of steroids
- C12P33/06—Hydroxylating
- C12P33/08—Hydroxylating at 11 position
- C12P33/10—Hydroxylating at 11 position at 11 alpha-position
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/02—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Genetics & Genomics (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Analytical Chemistry (AREA)
- Immunology (AREA)
- Physics & Mathematics (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Epoxy Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
В заявке описаны многочисленные новые схемы реакций, новые стадии способов и новые промежуточные продукты для синтеза эпоксимексренона и других соединений формулы (I),в которой -А-А- обозначает группу -CHR-CHR- или -CR=CR-; R, Rи Rнезависимо друг от друга выбирают из группы, включающей водород, галоген, гидроксил, (низш.)алкил, (низш.)алкоксигруппу, гидроксиалкил, алкоксиалкил, гидроксикарбонил, цианогруппу и арилоксигруппу; Rобозначает альфа-ориентированный (низш.)алкоксикарбонильный или гидроксиалкильный радикал; -В-В- обозначает группу -CHR-CHR- или альфа- или бета-ориентированную группу формулы (III),где Rи Rнезависимо друг от друга выбирают из группы, включающей водород, галоген, (низш.)алкоксигруппу, ацил, гидроксиалкил, алкоксиалкил, гидроксикарбонил, алкил, алкоксикарбонил, ацилоксиалкил, цианогруппу и арилоксигруппу, а Rи Rнезависимо друг от друга выбирают из группы, включающей водород, галоген, (низш.)алкоксигруппу, ацил, гидроксиалкил, алкоксиалкил, гидроксикарбонил, алкил, алкоксикарбонил, ацилоксиалкил, цианогруппу и арилоксигруппу, или Rи Rсовместно образуют карбоциклическую или гетероциклическую структуру, или либо R, либо Rсовместно с Rили с Rобразуют карбоциклическую или гетероциклическую структуру, конденсированную с пентациклическим D-кольцом.Международная заявка была опубликована вместе с отчетом о международном поиске.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US845595P | 1995-12-11 | 1995-12-11 | |
| PCT/US1996/020780 WO1997021720A2 (en) | 1995-12-11 | 1996-12-11 | Processes for preparation of 7 alpha-carboxyl 9,11-epoxy steroids and intermediates useful therein and a general process for the epoxidation of olifinic double bonds |
| US08/763,910 US5981744A (en) | 1995-12-11 | 1996-12-11 | Processes for preparation of 9,11-epoxy steroids and intermediates useful therein |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA199800449A1 true EA199800449A1 (ru) | 1999-02-25 |
| EA009176B1 EA009176B1 (ru) | 2007-12-28 |
Family
ID=26678218
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA199800449A EA009176B1 (ru) | 1995-12-11 | 1996-12-11 | Способ получения 7-альфа-карбоксил-9,11-эпоксистероидов и промежуточных продуктов, используемых для их получения, и общий способ эпоксидирования по олефиновым двойным связям |
Country Status (12)
| Country | Link |
|---|---|
| US (13) | US5981744A (ru) |
| EP (1) | EP0973791B1 (ru) |
| JP (2) | JP4146897B2 (ru) |
| CN (1) | CN100384866C (ru) |
| AT (1) | ATE365171T1 (ru) |
| DE (1) | DE69637140T2 (ru) |
| DK (1) | DK0973791T3 (ru) |
| EA (1) | EA009176B1 (ru) |
| ES (1) | ES2287943T3 (ru) |
| IL (2) | IL124631A (ru) |
| PT (1) | PT973791E (ru) |
| WO (1) | WO1997021720A2 (ru) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050267302A1 (en) * | 1995-12-11 | 2005-12-01 | G.D. Searle & Co. | Eplerenone crystalline form exhibiting enhanced dissolution rate |
| PT973791E (pt) | 1995-12-11 | 2007-09-26 | Searle Llc | Processo para a preparação de um composto epoxi |
| US20020038021A1 (en) * | 1995-12-11 | 2002-03-28 | Barton Kathleen P. | Eplerenone crystalline form exhibiting enhanced dissolution rate |
| US20020045746A1 (en) * | 1995-12-11 | 2002-04-18 | Barton Kathleen P. | Eplerenone crystalline form |
| ATE225367T1 (de) | 1996-12-11 | 2002-10-15 | Searle & Co | Verfahren zur herstellung von 3-keto-7alpha- alkoxycarbonyl- delta4,5-steroiden sowie zwischenprodukte |
| EP1223174A3 (en) * | 1996-12-11 | 2005-03-16 | G.D. Searle & Co. | Processes for preparation of 3-keto-7alpha-alkoxycarbonyl-delta-4,5- steroids and intermediates useful therein |
| US6887991B1 (en) | 1996-12-11 | 2005-05-03 | G. D. Searle & Company | Processes for preparation of 9, 11-epoxy steroids and intermediates useful therein |
| EP1228083A2 (en) * | 1999-09-30 | 2002-08-07 | Hollis-Eden Pharmaceuticals Inc. | Therapeutic treatment of androgen receptor driven conditions |
| IL144757A0 (en) * | 1999-12-08 | 2002-06-30 | Pharmacia Corp | Eplerenone crystalline form |
| US20030083493A1 (en) * | 1999-12-08 | 2003-05-01 | Barton Kathleen P. | Eplerenone drug substance having high phase purity |
| US6716829B2 (en) | 2000-07-27 | 2004-04-06 | Pharmacia Corporation | Aldosterone antagonist and cyclooxygenase-2 inhibitor combination therapy to prevent or treat inflammation-related cardiovascular disorders |
| EP1487859B1 (en) * | 2002-03-22 | 2008-08-13 | Pharmacia & Upjohn Company LLC | Process to prepare eplerenone |
| US7235655B2 (en) | 2002-03-22 | 2007-06-26 | Pharmacia & Upjohn Company | Processes to prepare eplerenone |
| DE60308388T2 (de) * | 2002-08-16 | 2007-09-20 | Pharmacia & Upjohn Co. Llc, Kalamazoo | 5-Androsten-3beta-ol-Steroide und Verfahren für ihre Herstellung |
| US20070066579A1 (en) * | 2002-08-16 | 2007-03-22 | White Michael J | 5-androsten-3beta-ol steroid intermediates and processs for their preparation |
| CN1694897A (zh) * | 2002-11-06 | 2005-11-09 | 法玛西亚普强责任有限公司 | 7-羧基取代的甾族化合物的制备方法 |
| RU2289586C2 (ru) * | 2002-11-07 | 2006-12-20 | Фармация Энд Апджон Компани Ллс | Способ получения 7-замещенных стероидных соединений, соединения, способы получения эплеренона, продукт |
| CL2004000574A1 (es) * | 2003-03-21 | 2005-02-11 | Pharmacia Corp Sa Organizada B | Proceso para preparar un compuesto 17-espirolactona o la sal de lactona abierta por carbonilacion del correspondiente 17-alquenil o alquinil derivado, los intermediarios que se usan y su proceso de obtencion. |
| US20040265948A1 (en) * | 2003-06-27 | 2004-12-30 | White Michael Jon | Microbial method for hydrolysis and oxidation of androst-5-ene and pregn-5-ene steroid esters |
| WO2005016912A1 (en) * | 2003-08-19 | 2005-02-24 | Pfizer Inc. | An efficient microbial preparation of capravirine metabolites m4 and m5 |
| TW200602352A (en) * | 2004-03-22 | 2006-01-16 | Upjohn Co | Improved process for the preparation of 9,11 epoxy steroids |
| CN1321128C (zh) * | 2005-07-15 | 2007-06-13 | 浙江医药股份有限公司新昌制药厂 | 孕甾-4-烯-7,21-二甲酸,9,11-环氧-17-羟基-3-氧代,γ-内酯,甲酯,(7α,11α,17α)-的制备方法 |
| WO2007025780A2 (en) * | 2005-09-02 | 2007-03-08 | Recordati Ireland Limited | Aldosterone receptor antagonists |
| WO2008045323A2 (en) * | 2006-10-06 | 2008-04-17 | Health Research Inc. | Method for determination of dht levels in tissue samples |
| US20080242856A1 (en) * | 2007-04-02 | 2008-10-02 | Funci Biotechnology Co., Ltd. | Extracts of taiwanofungus camphoratus with a capacity for inhibiting the activity of matrix metalloproteinases and method for preparing the same |
| HU227304B1 (en) * | 2007-07-04 | 2011-02-28 | Richter Gedeon Nyrt | Process for producing 9alpha-hydroxy-steroids |
| US8222237B2 (en) * | 2008-11-25 | 2012-07-17 | Evestra, Inc. | Progestational 3-(6,6-ethylene-17B-hydroxy-3-oxo-17A-pregna-4-ene-17A-yl)propionic acid G-lactones |
| ES2641144T3 (es) | 2010-05-10 | 2017-11-07 | Inserm (Institut National De La Santé Et De La Recherche Medicale) | Métodos y composiciones para el tratamiento de la acumulación de líquido en y/o bajo la retina |
| US9241944B2 (en) | 2010-06-16 | 2016-01-26 | Institut National De La Santé Et De La Recherche Médicale (Inserm) | Methods and compositions for stimulating reepithelialisation during wound healing |
| CN104262450A (zh) * | 2014-09-19 | 2015-01-07 | 江苏嘉逸医药有限公司 | 依普利酮的制备及精制方法 |
| US9562068B2 (en) | 2014-10-17 | 2017-02-07 | Industriale Chimica, S.R.L. | Process for the preparation of 7 α-(methoxycarbonyl)-3-OXO-17alpha-pregn-4,9(11)-dien-21,17-carbolactone, a useful intermediate for the synthesis of molecules with pharmacological activity |
| WO2016063269A1 (en) | 2014-10-20 | 2016-04-28 | Prendergast Patrick T | Use of antagonists to the nuclear steroid receptor alone or in combination as direct antiviral agents to inhibit alphavirus, togaviridae, arenaviridae, filoviridae, bunyaviridae, flaviviridae and rhabdoviridae |
| WO2017055248A1 (en) | 2015-09-28 | 2017-04-06 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of heart failure |
| JP6835836B2 (ja) | 2015-10-13 | 2021-02-24 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 脈絡膜血管新生の処置のための方法及び医薬組成物 |
| CN105753930A (zh) * | 2016-03-30 | 2016-07-13 | 北京万全德众医药生物技术有限公司 | 依普利酮的一种合成方法 |
| US20190262363A1 (en) | 2016-07-26 | 2019-08-29 | INSERM (Institut National de la Santé et de la Recherche Médicale | Antagonist of mineralocorticoid receptor for the treatment of osteoarthritis |
| CN106501388A (zh) * | 2016-09-22 | 2017-03-15 | 北京万全德众医药生物技术有限公司 | 一种用气相色谱法分离测定依普利酮中三氯乙酰胺的方法 |
| CN108085359B (zh) * | 2016-11-22 | 2020-07-24 | 保定九孚生化有限公司 | 一种11α-羟基-4-烯-3,17-雄甾二酮的生产方法 |
| CN110698529A (zh) * | 2019-11-19 | 2020-01-17 | 湖南新合新生物医药有限公司 | 一种依普利酮中间体△9,11烯酯的制备方法 |
| WO2023031277A1 (en) | 2021-08-31 | 2023-03-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of ocular rosacea |
| CN114235976B (zh) * | 2021-11-09 | 2023-11-03 | 暨南大学 | 一种含氮杂环有机化合物中间产物的合成和分析方法 |
| US12060148B2 (en) | 2022-08-16 | 2024-08-13 | Honeywell International Inc. | Ground resonance detection and warning system and method |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2602769A (en) | 1952-02-23 | 1952-07-08 | Upjohn Co | Oxygenation of steroids by mucorales fungi |
| US2691030A (en) * | 1952-03-28 | 1954-10-05 | Upjohn Co | 11 alpha-hydroxy-6-dehydroprogesterone and esters thereof |
| US3053856A (en) * | 1958-10-29 | 1962-09-11 | Shell Oil Co | Epoxidation of ethylenic compounds with peroxycarboximidic acids |
| US3095412A (en) * | 1961-12-19 | 1963-06-25 | Searle & Co | 9alpha, 11alpha-epoxy and 11beta-chloro-9alpha-hydroxy 17alpha-(2-carboxyethyl)-17beta-hydroxyandrost-4-en-3-one gamma-lactones and delta1 and delta6 analogs |
| US3120515A (en) * | 1962-05-31 | 1964-02-04 | Sterling Drug Inc | 5-cyano steroids, their preparation, and derivatives thereof |
| US3200113A (en) * | 1963-01-09 | 1965-08-10 | Sterling Drug Inc | 7-cyano steroids and derivatives thereof |
| US3300489A (en) * | 1964-07-24 | 1967-01-24 | Smith Kline French Lab | Steroidal c-17 spirolactones and processes and intermediates used in the preparation thereof |
| US3413288A (en) * | 1965-07-07 | 1968-11-26 | Parke Davis & Co | Process for the production of steroidal c-17 spirolactones |
| US3741990A (en) * | 1969-07-28 | 1973-06-26 | Upjohn Co | Organic compounds and processes |
| US3759791A (en) * | 1970-12-10 | 1973-09-18 | Searle & Co | Selective microbiological preparation of androst-4-ene-3,17-dione |
| FR2216273B1 (ru) * | 1973-02-06 | 1977-07-22 | Roussel Uclaf | |
| DE2404948C2 (de) * | 1973-02-06 | 1983-04-14 | Roussel-Uclaf, 75007 Paris | 7α-Acylthio-Steroidspirolactonderivate |
| GB1455220A (ru) * | 1973-09-14 | 1976-11-10 | Searle & Co | |
| DE2349022A1 (de) * | 1973-09-26 | 1975-04-10 | Schering Ag | Neue d-homo-steroide |
| FR2260569B1 (ru) | 1974-02-08 | 1978-06-16 | Ugine Kuhlmann | |
| US3972871A (en) * | 1975-09-22 | 1976-08-03 | G. D. Searle & Co. | 6β,17-Dihydroxy-7α-(lower alkoxy)carbonyl-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactones and congeners |
| CH631462A5 (de) * | 1976-03-05 | 1982-08-13 | Schering Ag | Verfahren zur herstellung von neuen steroiden der androstan- oder oestranreihe. |
| US4069219A (en) | 1976-12-27 | 1978-01-17 | G. D. Searle & Co. | 7ξ-(Alkoxycarbonyl)-6ξ-alkyl/halo-17-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactones and corresponding 21-carboxylic acids, their salts, and esters |
| YU41412B (en) * | 1978-08-15 | 1987-04-30 | Gist Brocades Nv | Process for obtaining 17 beta-hydroxy -3-dxo-17 alpha-pregn-4-en-21-carboxylic acid |
| US4270994A (en) | 1980-02-20 | 1981-06-02 | G. D. Searle & Co. | Electrochemical dehydrogenation of steroidal Δ3,5 enol ethers under basic conditions to provide steroidal Δ4,6 dienones |
| JPS56120697A (en) * | 1980-02-28 | 1981-09-22 | Mitsubishi Chem Ind Ltd | Preparation of 4,6-diene-3-oxosteroid |
| JPS58179498A (ja) * | 1982-04-13 | 1983-10-20 | Dainippon Ink & Chem Inc | 微生物による11α−ヒドロキシル化アンドロスタン系化合物の製造方法 |
| US4559332A (en) * | 1983-04-13 | 1985-12-17 | Ciba Geigy Corporation | 20-Spiroxanes and analogues having an open ring E, processes for their manufacture, and pharmaceutical preparations thereof |
| EP0123734A1 (en) * | 1983-04-29 | 1984-11-07 | Gist-Brocades N.V. | 17-(Isocyano-sulfonylmethylene)-steroids, 17-(formamido-sulfonylmethylene)-steroids and their preparation |
| US4670551A (en) * | 1984-06-21 | 1987-06-02 | Ciba-Geigy Corporation | Epoxy steroids |
| HU204063B (en) | 1986-10-10 | 1991-11-28 | Gist Brocades Nv | Process for producing 9-alpha-hydroxy steroids |
| US5502222A (en) * | 1994-06-01 | 1996-03-26 | Schering Corporation | Process for preparing delta 9,11 and 21-chloro corticosteroids |
| US5565558A (en) * | 1994-12-30 | 1996-10-15 | Mccully; Kilmer S. | Thioretinaco ozonide and enhanced biological activity of thioretinaco ozonide in combination with interferon |
| PT973791E (pt) | 1995-12-11 | 2007-09-26 | Searle Llc | Processo para a preparação de um composto epoxi |
-
1996
- 1996-12-11 PT PT96945103T patent/PT973791E/pt unknown
- 1996-12-11 DE DE69637140T patent/DE69637140T2/de not_active Expired - Fee Related
- 1996-12-11 ES ES96945103T patent/ES2287943T3/es not_active Expired - Lifetime
- 1996-12-11 IL IL12463196A patent/IL124631A/en not_active IP Right Cessation
- 1996-12-11 WO PCT/US1996/020780 patent/WO1997021720A2/en not_active Ceased
- 1996-12-11 EA EA199800449A patent/EA009176B1/ru not_active IP Right Cessation
- 1996-12-11 JP JP52230497A patent/JP4146897B2/ja not_active Expired - Fee Related
- 1996-12-11 DK DK96945103T patent/DK0973791T3/da active
- 1996-12-11 AT AT96945103T patent/ATE365171T1/de not_active IP Right Cessation
- 1996-12-11 CN CNB961999616A patent/CN100384866C/zh not_active Expired - Fee Related
- 1996-12-11 EP EP96945103A patent/EP0973791B1/en not_active Expired - Lifetime
- 1996-12-11 US US08/763,910 patent/US5981744A/en not_active Expired - Fee Related
-
1999
- 1999-02-08 US US09/246,204 patent/US6331622B1/en not_active Expired - Fee Related
- 1999-02-09 US US09/246,908 patent/US6180780B1/en not_active Expired - Fee Related
-
2000
- 2000-05-30 US US09/583,137 patent/US6258946B1/en not_active Expired - Fee Related
- 2000-05-30 US US09/583,158 patent/US6335441B1/en not_active Expired - Fee Related
-
2001
- 2001-04-03 US US09/826,406 patent/US20020016455A1/en not_active Abandoned
- 2001-04-04 US US09/826,434 patent/US20020019522A1/en not_active Abandoned
- 2001-08-07 US US09/923,977 patent/US6630587B2/en not_active Expired - Fee Related
- 2001-08-31 US US09/943,117 patent/US6586591B2/en not_active Expired - Fee Related
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2003
- 2003-06-27 US US10/608,101 patent/US7038040B2/en not_active Expired - Fee Related
- 2003-09-26 US US10/672,680 patent/US6953851B2/en not_active Expired - Fee Related
-
2005
- 2005-06-20 US US11/156,418 patent/US7129345B2/en not_active Expired - Fee Related
-
2006
- 2006-04-27 IL IL175299A patent/IL175299A0/en unknown
- 2006-07-21 US US11/459,040 patent/US20070060746A1/en not_active Abandoned
-
2007
- 2007-10-12 JP JP2007265977A patent/JP2008100996A/ja not_active Withdrawn
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