AU2002254114A1 - Non-imidazole aryl alkylamines compounds as histamine h3 receptor antagonists, preparation and therapeutic uses - Google Patents
Non-imidazole aryl alkylamines compounds as histamine h3 receptor antagonists, preparation and therapeutic usesInfo
- Publication number
- AU2002254114A1 AU2002254114A1 AU2002254114A AU2002254114A AU2002254114A1 AU 2002254114 A1 AU2002254114 A1 AU 2002254114A1 AU 2002254114 A AU2002254114 A AU 2002254114A AU 2002254114 A AU2002254114 A AU 2002254114A AU 2002254114 A1 AU2002254114 A1 AU 2002254114A1
- Authority
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- Australia
- Prior art keywords
- histamine
- imidazole
- compounds
- preparation
- receptor antagonists
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
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- C07C233/68—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/73—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
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- 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
- C07C237/08—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 atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
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- C07C237/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to an acyclic carbon atom of a hydrocarbon radical substituted by oxygen atoms
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- C07C271/34—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
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- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
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PCT/US2002/006644 WO2002076925A2 (en) | 2001-03-23 | 2002-03-21 | Non-imidazole aryl alkylamines compounds as histamine h3 receptor antagonists, preparation and therapeutic uses |
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DE10235312A1 (en) * | 2002-08-01 | 2004-02-12 | Basf Ag | Process for the preparation of aminoalkoxybenzylamines and aminoalkoxybenzonitriles as intermediates |
GB0224084D0 (en) * | 2002-10-16 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
GB0224083D0 (en) * | 2002-10-16 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
GB0224557D0 (en) * | 2002-10-22 | 2002-11-27 | Glaxo Group Ltd | Novel compounds |
JP2006512404A (en) * | 2002-10-22 | 2006-04-13 | グラクソ グループ リミテッド | Aryloxyalkylamine derivatives as H3 receptor ligands |
JP2006505590A (en) | 2002-10-23 | 2006-02-16 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Phenylpiperidine and phenylpyrrolidine as histamine H3 receptor modulators |
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PT1615909E (en) | 2003-04-23 | 2008-10-30 | Glaxo Group Ltd | Piperazine derivatives and their use for the treatment of neurological and psychiatric diseases |
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JP4173191B2 (en) * | 2004-05-07 | 2008-10-29 | ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー | 3- or 4-monosubstituted phenol and thiophenol derivatives useful as H3 ligands |
US7456164B2 (en) | 2004-05-07 | 2008-11-25 | Pfizer, Inc | 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands |
EP1593679A1 (en) * | 2004-05-07 | 2005-11-09 | Warner-Lambert Company LLC | 3- Or 4-monosubstituted phenol derivatives useful as H3 ligands |
JP2007536270A (en) | 2004-05-07 | 2007-12-13 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Scalable synthesis of imidazole derivatives |
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WO2005117865A1 (en) | 2004-06-02 | 2005-12-15 | F. Hoffmann-La Roche Ag | Naphthaline derivatives useful as histamine-3-receptor ligands |
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PT1786790E (en) | 2004-07-26 | 2009-08-18 | Lilly Co Eli | Oxazole derivatives as histamine h3 receptor agents, preparation and therapeutic uses |
AU2005277518B2 (en) | 2004-08-23 | 2011-08-04 | Eli Lilly And Company | Histamine H3 receptor agents, preparation and therapeutic uses |
SI1805169T1 (en) | 2004-10-18 | 2009-06-30 | Lilly Co Eli | Histamine h3 receptor inhibitors, their preparation and therapeutic uses |
BRPI0518222A (en) * | 2004-10-19 | 2008-11-04 | Hoffmann La Roche | compound, process for their manufacture, pharmaceutical compositions comprising them, method for treating and / or preventing diseases that are associated with modulating h3 receptors and using them |
ES2335305T3 (en) * | 2005-03-17 | 2010-03-24 | Eli Lilly And Company | PIRROLIDINE DERIVATIVES AS ANTAGONISTS OF H3 HISTAMINE RECEIVER. |
EP1868991B1 (en) * | 2005-04-01 | 2014-07-30 | Eli Lilly And Company | Histamine h3 receptor agents, preparation and therapeutic uses |
EP1707204A1 (en) * | 2005-04-01 | 2006-10-04 | Bioprojet | Treatment of epilepsy with non-imidazole alkylamines histamine H3-receptor ligands |
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US2810719A (en) * | 1954-10-19 | 1957-10-22 | Abbott Lab | Morpholino alkyl ethers of hydroxybenzoic acid esters |
HU187208B (en) * | 1982-12-28 | 1985-11-28 | Richter Gedeon Vegyeszet | Process for production of new dialcil-amino-alcoxi-benzoalcohole derivates, their acid additional and quaterner soils and medical preparates consisting of them |
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EP0982300A3 (en) * | 1998-07-29 | 2000-03-08 | Societe Civile Bioprojet | Non-imidazole alkylamines as histamine H3 - receptor ligands and their therapeutic applications |
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DE60142355D1 (en) * | 2000-11-20 | 2010-07-22 | Biovitrum Ab Publ | PIPERAZINYLPYRAZIN COMPOUNDS AS AGONISTS OR ANTAGONISTS ON THE SEROTONIN 5HT-2 RECEPTOR |
-
2002
- 2002-03-21 AU AU2002254114A patent/AU2002254114A1/en not_active Abandoned
- 2002-03-21 JP JP2002576188A patent/JP2004532834A/en not_active Withdrawn
- 2002-03-21 CA CA002441080A patent/CA2441080A1/en not_active Abandoned
- 2002-03-21 WO PCT/US2002/006644 patent/WO2002076925A2/en not_active Application Discontinuation
- 2002-03-21 EP EP02723329A patent/EP1379493A2/en not_active Withdrawn
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JP2004532834A (en) | 2004-10-28 |
WO2002076925A2 (en) | 2002-10-03 |
EP1379493A2 (en) | 2004-01-14 |
CA2441080A1 (en) | 2002-10-03 |
WO2002076925A3 (en) | 2003-09-18 |
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