AU2001249672A1 - Method for using 2- or 3-aryl substituted imidazo(1,2-a) pyridines as h3 antagonists - Google Patents
Method for using 2- or 3-aryl substituted imidazo(1,2-a) pyridines as h3 antagonistsInfo
- Publication number
- AU2001249672A1 AU2001249672A1 AU2001249672A AU4967201A AU2001249672A1 AU 2001249672 A1 AU2001249672 A1 AU 2001249672A1 AU 2001249672 A AU2001249672 A AU 2001249672A AU 4967201 A AU4967201 A AU 4967201A AU 2001249672 A1 AU2001249672 A1 AU 2001249672A1
- Authority
- AU
- Australia
- Prior art keywords
- pyridines
- antagonists
- aryl substituted
- substituted imidazo
- imidazo
- 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
Links
- 239000005557 antagonist Substances 0.000 title 1
- 150000005234 imidazo[1,2-a]pyridines Chemical class 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/12—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19407100P | 2000-03-31 | 2000-03-31 | |
US60194071 | 2000-03-31 | ||
US27229001P | 2001-02-28 | 2001-02-28 | |
US60272290 | 2001-02-28 | ||
PCT/US2001/010319 WO2001074813A2 (en) | 2000-03-31 | 2001-03-29 | METHOD FOR USING 2- OR 3-ARYL SUBSTITUTED IMIDAZO[1,2-a] PYRIDINES AS H3 ANTAGONISTS |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001249672A1 true AU2001249672A1 (en) | 2001-10-15 |
Family
ID=26889669
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001249672A Abandoned AU2001249672A1 (en) | 2000-03-31 | 2001-03-29 | Method for using 2- or 3-aryl substituted imidazo(1,2-a) pyridines as h3 antagonists |
Country Status (3)
Country | Link |
---|---|
US (1) | US6489337B1 (en) |
AU (1) | AU2001249672A1 (en) |
WO (1) | WO2001074813A2 (en) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7208497B2 (en) | 2001-07-02 | 2007-04-24 | Novo Nordisk A/S | Substituted piperazines and diazepanes |
EP1430027B1 (en) | 2001-09-14 | 2010-09-01 | High Point Pharmaceuticals, LLC | Novel aminoazetidine, -pyrrolidine and -piperidine derivatives |
US6673829B2 (en) | 2001-09-14 | 2004-01-06 | Novo Nordisk A/S | Aminoazetidine,-pyrrolidine and -piperidine derivatives |
DE10247271A1 (en) * | 2002-10-10 | 2004-08-26 | Grünenthal GmbH | Use of new and known 7-(methyl or trifluoromethyl)-imidazo-(1,2-a)-pyridines as nitrogen monoxide synthase inhibitors useful e.g. for treating migraine, neurodegenerative diseases, inflammatory pain, diabetes or cancer |
WO2004087938A1 (en) * | 2003-03-31 | 2004-10-14 | Meiji Seika Kaisha, Ltd. | Novel physiologically active substances pf1270a, b and c |
US8501739B2 (en) | 2005-07-04 | 2013-08-06 | High Point Pharmaceuticals, Llc | Medicaments |
AU2006326135A1 (en) * | 2005-12-15 | 2007-06-21 | F. Hoffmann-La Roche Ag | Pyrrolo[2,3-c]pyridine derivatives |
EP2019103B1 (en) * | 2006-05-19 | 2011-11-30 | Nihon Medi-Physics Co., Ltd. | Compound having affinity for amyloid |
JP5694661B2 (en) | 2006-05-29 | 2015-04-01 | ハイ ポイント ファーマシューティカルズ,リミティド ライアビリティ カンパニー | 3- (1,3-Benzodioxol-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salt, its solvate, and its use as a histamine H3 receptor antagonist Law |
TW200811175A (en) * | 2006-06-21 | 2008-03-01 | Nihon Mediphysics Co Ltd | Novel compound with affinity with amyloid |
EP2042501B1 (en) * | 2006-06-21 | 2017-04-12 | Nihon Medi-Physics Co., Ltd. | Compound having affinity for amyloid |
FR2903107B1 (en) | 2006-07-03 | 2008-08-22 | Sanofi Aventis Sa | IMIDAZOPYRIDINE-2-CARBOXAMIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2903105A1 (en) * | 2006-07-03 | 2008-01-04 | Sanofi Aventis Sa | 2-BENZOYL-IMIDAZOPYRIDINE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
FR2906250B1 (en) * | 2006-09-22 | 2008-10-31 | Sanofi Aventis Sa | DERIVATIVES OF 2-ARYL-6PHENYL-IMIDAZO (1,2-A) PYRIDINES, THEIR PREPARATION AND THEIR THERAPEUTIC USE |
US8207189B2 (en) | 2006-11-30 | 2012-06-26 | Nihon Medi-Physics Co., Ltd. | Compound having affinity for amyloid |
TWI406674B (en) | 2007-02-13 | 2013-09-01 | Nihon Mediphysics Co Ltd | Method for manufacturing diagnostic radiographic diagnostic agents |
EP2014656A3 (en) | 2007-06-11 | 2011-08-24 | High Point Pharmaceuticals, LLC | New heteocyclic h3 antagonists |
AU2008314870A1 (en) * | 2007-10-24 | 2009-04-30 | Nihon Medi-Physics Co., Ltd. | Novel compound having affinity for amyloid |
TW200918101A (en) | 2007-10-26 | 2009-05-01 | Nihon Mediphysics Co Ltd | Novel compound having affinity for amyloid |
WO2009057576A1 (en) * | 2007-10-30 | 2009-05-07 | Nihon Medi-Physics Co., Ltd. | Use of novel compound having affinity for amyloid, and process for production of the same |
KR20100101577A (en) * | 2007-10-30 | 2010-09-17 | 니혼 메디피직스 가부시키가이샤 | Utilization of novel compounds with amyloid affinity and method of producing the same |
WO2013151982A1 (en) | 2012-04-03 | 2013-10-10 | Arena Pharmaceuticals, Inc. | Methods and compounds useful in treating pruritus, and methods for identifying such compounds |
CN114874084B (en) * | 2022-01-28 | 2023-12-19 | 浙江普洛家园药业有限公司 | Preparation method of bupropion hydrochloride impurity F |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5910675B2 (en) * | 1976-03-22 | 1984-03-10 | ウェルファイド株式会社 | Aralkylamine derivatives |
US5182291A (en) | 1986-02-14 | 1993-01-26 | Sanofi | Pyrozala-pyridyl aminoabkoxyphenol compounds |
US4833149A (en) * | 1986-09-22 | 1989-05-23 | Ortho Pharmaceutical Corporation | 2- or 3-aryl substituted imidazo[1,2-a]pyridines |
US4727145A (en) | 1986-09-22 | 1988-02-23 | Ortho Pharmaceutical Corporation | 2- Or 3- aryl substituted imidazo [1,2-a]pyridines |
EP0289371B1 (en) * | 1987-03-27 | 1991-09-25 | Synthelabo | Imidazopyridine derivatives, their preparation and therapeutical use |
US4880824A (en) | 1987-09-21 | 1989-11-14 | Ortho Pharmaceutical Corporation | Phenyl and benzoyl substituted imidazo-fused heterocyclic calcium channel blockers |
EP0978512A1 (en) | 1998-07-29 | 2000-02-09 | Societe Civile Bioprojet | Non-imidazole aryloxy (or arylthio) alkylamines as histamine H3-receptor antagonists and their therapeutic applications |
DE60128211T2 (en) * | 2000-03-31 | 2008-01-10 | Ortho-Mcneil Pharmaceutical, Inc. | PHENYL-SUBSTITUTED IMIDAZOPYRIDINE |
-
2001
- 2001-03-29 WO PCT/US2001/010319 patent/WO2001074813A2/en active Application Filing
- 2001-03-29 US US09/820,418 patent/US6489337B1/en not_active Expired - Lifetime
- 2001-03-29 AU AU2001249672A patent/AU2001249672A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2001074813A2 (en) | 2001-10-11 |
US6489337B1 (en) | 2002-12-03 |
WO2001074813A3 (en) | 2002-03-21 |
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