NO20081617L - Metoder for fremstilling av Glutaminsyrederivater - Google Patents
Metoder for fremstilling av GlutaminsyrederivaterInfo
- Publication number
- NO20081617L NO20081617L NO20081617A NO20081617A NO20081617L NO 20081617 L NO20081617 L NO 20081617L NO 20081617 A NO20081617 A NO 20081617A NO 20081617 A NO20081617 A NO 20081617A NO 20081617 L NO20081617 L NO 20081617L
- Authority
- NO
- Norway
- Prior art keywords
- preparation
- glutamic acid
- acid derivatives
- methods
- novel methods
- Prior art date
Links
- 150000002306 glutamic acid derivatives Chemical class 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C269/06—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups by reactions not involving the formation of carbamate groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- C07C237/06—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2603/00—Systems containing at least three condensed rings
- C07C2603/02—Ortho- or ortho- and peri-condensed systems
- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US72644105P | 2005-10-13 | 2005-10-13 | |
| PCT/US2006/026892 WO2007044100A1 (en) | 2005-10-13 | 2006-07-11 | Methods for preparing glutamic acid derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20081617L true NO20081617L (no) | 2008-05-06 |
Family
ID=37119907
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20081617A NO20081617L (no) | 2005-10-13 | 2008-04-02 | Metoder for fremstilling av Glutaminsyrederivater |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7541485B2 (es) |
| EP (1) | EP1934171A1 (es) |
| JP (1) | JP2009511578A (es) |
| KR (1) | KR20080058436A (es) |
| CN (1) | CN101282927A (es) |
| AR (1) | AR057451A1 (es) |
| AU (1) | AU2006299918A1 (es) |
| BR (1) | BRPI0617348A2 (es) |
| CA (1) | CA2624866A1 (es) |
| CR (1) | CR9885A (es) |
| EC (1) | ECSP088360A (es) |
| GT (1) | GT200600305A (es) |
| IL (1) | IL190729A0 (es) |
| NO (1) | NO20081617L (es) |
| PE (1) | PE20070526A1 (es) |
| RU (1) | RU2008113222A (es) |
| TW (1) | TW200740729A (es) |
| WO (1) | WO2007044100A1 (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200808715A (en) * | 2006-06-02 | 2008-02-16 | Wyeth Corp | Methods for preparing glutamic acid derivatives and intermediates thereof |
| US20100216886A1 (en) * | 2006-11-09 | 2010-08-26 | Wyeth | Polymorphs of n2-(1,1'-biphenyl-4-ylcarbonyl)-n1-[2-(4-fluorophenyl)-1,1-dimethylethyl]-l-alpha-glutamine |
| RU2609245C2 (ru) * | 2011-09-30 | 2017-01-31 | Кемира Ойй | Предотвращение деградации крахмала при производстве целлюлозы, бумаги или картона |
| EP3054936B1 (en) | 2013-10-10 | 2023-10-18 | Eastern Virginia Medical School | 4-((2-hydroxy-3-methoxybenzyl)amino) benzenesulfonamide derivatives as 12-lipoxygenase inhibitors |
| WO2016172496A1 (en) | 2015-04-23 | 2016-10-27 | Constellation Pharmaceuticals, Inc. | Lsd1 inhibitors and uses thereof |
| ES2961499T3 (es) | 2016-10-26 | 2024-03-12 | Constellation Pharmaceuticals Inc | Inhibidores de LSD1 y usos médicos de los mismos |
| WO2022175747A1 (en) | 2021-02-19 | 2022-08-25 | Sudo Biosciences Limited | Tyk2 inhibitors and uses thereof |
| MX2023009685A (es) | 2021-02-19 | 2023-10-30 | Sudo Biosciences Ltd | Inhibidores de tyk2 y sus usos. |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2440649A (en) * | 1948-04-27 | Quinazoline | ||
| GB1108819A (en) | 1964-07-31 | 1968-04-03 | Rotta Research Lab | Derivatives of 2-acylaminobicarboxylic acids and method for preparing same |
| DE3332633A1 (de) | 1983-09-09 | 1985-04-04 | Luitpold-Werk Chemisch-pharmazeutische Fabrik GmbH & Co, 8000 München | Substituierte carbonsaeurederivate, verfahren zu ihrer herstellung, und arzneimittel |
| DE4102024A1 (de) * | 1991-01-24 | 1992-07-30 | Thomae Gmbh Dr K | Biphenylderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
| US5424334A (en) | 1991-12-19 | 1995-06-13 | G. D. Searle & Co. | Peptide mimetic compounds useful as platelet aggregation inhibitors |
| WO1994012181A1 (en) | 1992-12-01 | 1994-06-09 | Merck & Co., Inc. | Fibrinogen receptor antagonists |
| JPH06192199A (ja) | 1992-12-25 | 1994-07-12 | Mitsubishi Kasei Corp | ケトン誘導体 |
| US5563127A (en) * | 1993-03-24 | 1996-10-08 | The Dupont Merck Pharmaceutical Company | Boronic acid and ester inhibitors of thrombin |
| EP0751765B1 (en) * | 1994-03-11 | 2003-05-07 | Pharmacopeia, Inc. | Sulfonamide derivatives and their use |
| GB2292149A (en) | 1994-08-09 | 1996-02-14 | Ferring Res Ltd | Peptide inhibitors of pro-interleukin-1beta converting enzyme |
| US6306840B1 (en) * | 1995-01-23 | 2001-10-23 | Biogen, Inc. | Cell adhesion inhibitors |
| KR19990035780A (ko) | 1995-07-24 | 1999-05-25 | 후지야마 아키라 | Ｐｌａ２ 억제제로서의 에스테르 및 아미드 |
| ATE377006T1 (de) | 1995-11-28 | 2007-11-15 | Cephalon Inc | Aus d-aminosäuren abgeleitete cystein- und serinproteasehemmer |
| ATE320249T1 (de) | 1997-07-08 | 2006-04-15 | Ono Pharmaceutical Co | Aminosäurederivate |
| JP4129069B2 (ja) | 1997-09-16 | 2008-07-30 | 株式会社Ａｄｅｋａ | アシル化ペプチド類の製造方法 |
| JP4090541B2 (ja) | 1997-10-15 | 2008-05-28 | 株式会社Ａｄｅｋａ | アシル化ペプチド類の製造方法 |
| EP1063888A1 (en) | 1998-03-27 | 2001-01-03 | The Regents of the University of California | Novel hiv integrase inhibitors and hiv therapy based on drug combinations including integrase inhibitors |
| TWI245035B (en) * | 1998-06-26 | 2005-12-11 | Ono Pharmaceutical Co | Amino acid derivatives and a pharmaceutical composition comprising the derivatives |
| US7157430B2 (en) * | 1998-10-22 | 2007-01-02 | Idun Pharmaceuticals, Inc. | (Substituted)acyl dipeptidyl inhibitors of the ICE/CED-3 family of cysteine proteases |
| US6242422B1 (en) | 1998-10-22 | 2001-06-05 | Idun Pharmacueticals, Inc. | (Substituted)Acyl dipeptidyl inhibitors of the ice/ced-3 family of cysteine proteases |
| DE19851184A1 (de) | 1998-11-06 | 2000-05-11 | Aventis Pharma Gmbh | N-Arylsulfonyl-aminosäure-omega-amide |
| US6265610B1 (en) * | 1999-01-12 | 2001-07-24 | The University Of North Carolina At Chapel Hill | Contrast media for angiography |
| US6723711B2 (en) | 1999-05-07 | 2004-04-20 | Texas Biotechnology Corporation | Propanoic acid derivatives that inhibit the binding of integrins to their receptors |
| AU4826900A (en) | 1999-05-07 | 2000-11-21 | Texas Biotechnology Corporation | Propanoic acid derivatives that inhibit the binding of integrins to their receptors |
| US6493791B1 (en) * | 1999-12-20 | 2002-12-10 | Intel Corporation | Prioritized content addressable memory |
| CA2377629A1 (en) | 2000-04-25 | 2001-11-08 | Hae-Young Bae | Biphenyl butyric acid derivative as a matrix metalloproteinase inhibitor |
| US6723733B2 (en) | 2000-05-19 | 2004-04-20 | Guilford Pharmaceuticals, Inc. | Sulfonamide and carbamide derivatives of 6(5H)phenanthridinones and their uses |
| CA2321348A1 (en) * | 2000-09-27 | 2002-03-27 | Blaise Magloire N'zemba | Aromatic derivatives with hiv integrase inhibitory properties |
| JP2002145849A (ja) | 2000-11-10 | 2002-05-22 | Kyorin Pharmaceut Co Ltd | アルキニルアミノ酸誘導体及びその製造法 |
| US20050049242A1 (en) * | 2000-12-21 | 2005-03-03 | W. Edward Robinson | Novel HIV integrase inhibitors and HIV therapy based on drug combinations including integrase inhibitors |
| WO2003093498A1 (en) | 2002-04-29 | 2003-11-13 | The Ohio State University | Inhibition of protein tyrosine phosphatases and sh2 domains by a neutral phosphotyrosine mimetic |
| MXPA06001636A (es) | 2003-08-13 | 2006-04-28 | Amgen Inc | Antagonista del receptor de la hormona concentradora de melanina. |
| JP2007527412A (ja) | 2003-10-24 | 2007-09-27 | エグゼリクシス， インコーポレイテッド | Ｔａｏキナーゼモジュレーターおよび使用方法 |
| WO2005061459A1 (en) | 2003-12-04 | 2005-07-07 | Wyeth | Biaryl sulfonamides and methods for using same |
| ZA200605247B (en) | 2003-12-15 | 2007-10-31 | Japan Tobacco Inc | N-substituted-n-sulfonylaminocyclopropane compounds and pharmaceutical use thereof |
| EP1734942A1 (en) | 2004-03-09 | 2006-12-27 | Elan Pharmaceuticals, Inc. | Substituted urea and carbamate, phenacyl-2-hydroxy-3-diaminoalkane, and benzamide-2-hydroxy-3-diaminoalkane aspartyl-protease inhibitors |
| EP1902014A2 (en) * | 2005-07-11 | 2008-03-26 | Wyeth | Glutamate aggrecanase inhibitors |
| DE102006018250A1 (de) | 2006-04-13 | 2007-10-18 | Aicuris Gmbh & Co. Kg | Verfahren zum Herstellen von cyclischen Depsipeptiden |
| TW200808715A (en) * | 2006-06-02 | 2008-02-16 | Wyeth Corp | Methods for preparing glutamic acid derivatives and intermediates thereof |
-
2006
- 2006-07-11 GT GT200600305A patent/GT200600305A/es unknown
- 2006-07-11 CA CA002624866A patent/CA2624866A1/en not_active Abandoned
- 2006-07-11 US US11/484,217 patent/US7541485B2/en not_active Expired - Fee Related
- 2006-07-11 AR ARP060102975A patent/AR057451A1/es unknown
- 2006-07-11 EP EP06786899A patent/EP1934171A1/en not_active Withdrawn
- 2006-07-11 CN CNA2006800376761A patent/CN101282927A/zh active Pending
- 2006-07-11 PE PE2006000824A patent/PE20070526A1/es not_active Application Discontinuation
- 2006-07-11 BR BRPI0617348-9A patent/BRPI0617348A2/pt not_active IP Right Cessation
- 2006-07-11 JP JP2008535516A patent/JP2009511578A/ja not_active Withdrawn
- 2006-07-11 TW TW095125251A patent/TW200740729A/zh unknown
- 2006-07-11 KR KR1020087010057A patent/KR20080058436A/ko not_active Withdrawn
- 2006-07-11 AU AU2006299918A patent/AU2006299918A1/en not_active Abandoned
- 2006-07-11 WO PCT/US2006/026892 patent/WO2007044100A1/en not_active Ceased
- 2006-07-11 RU RU2008113222/04A patent/RU2008113222A/ru not_active Application Discontinuation
-
2008
- 2008-04-02 NO NO20081617A patent/NO20081617L/no not_active Application Discontinuation
- 2008-04-08 IL IL190729A patent/IL190729A0/en unknown
- 2008-04-10 EC EC2008008360A patent/ECSP088360A/es unknown
- 2008-04-11 CR CR9885A patent/CR9885A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| GT200600305A (es) | 2007-02-26 |
| AR057451A1 (es) | 2007-12-05 |
| KR20080058436A (ko) | 2008-06-25 |
| RU2008113222A (ru) | 2009-11-20 |
| JP2009511578A (ja) | 2009-03-19 |
| US7541485B2 (en) | 2009-06-02 |
| IL190729A0 (en) | 2008-11-03 |
| TW200740729A (en) | 2007-11-01 |
| US20070088172A1 (en) | 2007-04-19 |
| ECSP088360A (es) | 2008-05-30 |
| CR9885A (es) | 2008-06-16 |
| CA2624866A1 (en) | 2007-04-19 |
| CN101282927A (zh) | 2008-10-08 |
| WO2007044100A1 (en) | 2007-04-19 |
| EP1934171A1 (en) | 2008-06-25 |
| BRPI0617348A2 (pt) | 2011-07-26 |
| AU2006299918A1 (en) | 2007-04-19 |
| PE20070526A1 (es) | 2007-06-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |