AR071887A1 - Pirrolidin amidas sustituidas como moduladores del receptor histamina h3 - Google Patents
Pirrolidin amidas sustituidas como moduladores del receptor histamina h3Info
- Publication number
- AR071887A1 AR071887A1 ARP090101849A ARP090101849A AR071887A1 AR 071887 A1 AR071887 A1 AR 071887A1 AR P090101849 A ARP090101849 A AR P090101849A AR P090101849 A ARP090101849 A AR P090101849A AR 071887 A1 AR071887 A1 AR 071887A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- 4alkyl
- substituted
- heterocycloalkyl
- Prior art date
Links
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 title 2
- 229960001340 histamine Drugs 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 230000001149 cognitive effect Effects 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 125000001475 halogen functional group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 238000002483 medication Methods 0.000 abstract 1
- 239000002207 metabolite Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
- C07D403/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- 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
- 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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Composicion farmaceutica, uso para preparar medicamentos para trastornos cognitivo, del sueno, psiqui tricos, y metodo para preparar los compuestos. Reivindicacion 1: Un compuesto de formula (1) en la cual R1 y R2 tomados conjuntamente con el nitrogeno al cual est n unidos forman un compuesto como se muestra en las formulas (2) o (3) donde m es 1 o 2; n es 1 o 2; Ra es H, alquilo C1-6, cicloalquilo, heterocicloalquilo, o bencilo; y Rb y Rc son cada uno independientemente H o alquilo C1-4 o Rb y Rc tomados conjuntamente con el nitrogeno al cual est n unidos forman un anillo heterocicloalquilo; R3 es H; alquilo C1-6, alquilo C2-6 substituido con OH, -Oalquilo C1-4, fluor, o cicloalquilo; cicloalquilo; heterocicloalquilo; -COalquilo C1-6, -CO-(cicloalquilo); benzoilo; -CO2alquilo C1-4, -CO2-bencilo; -SO2alquilo C1-4, -SO2-(cicloalquilo); o -SO2-fenilo; R4, R5, y R6 se definen tal como uno de a), b) o c); a) R4 es -X-Rd y R5 y R6 son cada uno H; b) R5 es -X-Rd y R4 y R6 son cada uno H; c) R6 es -CH2-Re y R4 y R5 son cada uno H; X es O, S, o CH2; Rd es H o alquilo C1-6, o un grupo fenilo, bencilo, cicloalquilo, heterocicloalquilo, o heteroarilo monoc¡clico, estando cada grupo no sustituido o sustituido con uno o dos sustituyentes Rf, donde cada sustituyente Rf est seleccionado independientemente del grupo que consiste en: halo; -alquilo C1-4; -alquilo C2-4 sustituido con OH, F, o -Oalquilo C1-4; -CHF2, -CF3, -OH; -Oalquilo C1-4, -Salquilo C1-4, -SO2alquilo C1-4, -CN; -CONRgRh, y -NO2, o dos sustituyentes Rf forman conjuntamente -O(CH2)1-2-O-; donde Rg y Rh son cada uno independientemente -H o -alquilo C1-4; y Re es fenilo o heteroarilo monociclico, cada uno no sustituido o sustituido con uno o dos sustituyentes Rf, o una sal farmaceuticamente aceptable, o un prof rmaco farmaceuticamente aceptable, o un metabolito del mismo farmaceuticamente activo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5553808P | 2008-05-23 | 2008-05-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR071887A1 true AR071887A1 (es) | 2010-07-21 |
Family
ID=41026372
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090101849A AR071887A1 (es) | 2008-05-23 | 2009-05-22 | Pirrolidin amidas sustituidas como moduladores del receptor histamina h3 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8236792B2 (es) |
| AR (1) | AR071887A1 (es) |
| CL (1) | CL2009001282A1 (es) |
| PA (1) | PA8827501A1 (es) |
| PE (1) | PE20091948A1 (es) |
| TW (1) | TW201008928A (es) |
| UY (1) | UY31840A (es) |
| WO (1) | WO2009143153A1 (es) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200823204A (en) * | 2006-10-17 | 2008-06-01 | Arena Pharm Inc | Biphenyl sulfonyl and phenyl-heteroaryl sulfonyl modulators of the histamine H3-receptor useful for the treatment of disorders related thereto |
| GEP20125502B (en) | 2008-05-23 | 2012-04-25 | Novartis Ag | Derivatives of quinolines and quinoxalines as protein tyrosine kinase inhibitors |
| US8802864B2 (en) * | 2010-02-22 | 2014-08-12 | Glaxosmithkline Llc | Triazolones as fatty acid synthase inhibitors |
| WO2013076590A1 (en) | 2011-11-23 | 2013-05-30 | Oxygen Healthcare Research Pvt. Ltd | Benzothiazine compounds as h3 receptor ligands |
| CN104876917B (zh) * | 2015-06-16 | 2017-09-19 | 上海皓元医药股份有限公司 | 用作脂肪酸合成酶抑制剂的三唑酮的合成方法 |
| GB201518950D0 (en) * | 2015-10-27 | 2015-12-09 | Glaxosmithkline Ip Dev Ltd | Compound |
| WO2025211415A1 (ja) * | 2024-04-04 | 2025-10-09 | キッセイ薬品工業株式会社 | 置換スルホンアミド化合物 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ167792A3 (en) * | 1991-06-04 | 1995-12-13 | Sankyo Co | 1-methylcarbapenem derivatives process of their preparation and use |
| JP3091297B2 (ja) * | 1992-01-10 | 2000-09-25 | 住友製薬株式会社 | ピロリジン誘導体およびその製造方法 |
| AU2001277754B2 (en) | 2000-08-10 | 2005-09-29 | Mitsubishi Tanabe Pharma Corporation | Proline derivatives and use thereof as drugs |
| DE60122750T2 (de) | 2000-09-11 | 2006-12-21 | Genentech, Inc., South San Francisco | Amidin-Inhibitoren von Serin-Proteasen |
| US7067507B2 (en) * | 2001-06-12 | 2006-06-27 | Pharmacia & Upjohn Company | Macrocycles useful in the treatment of Alzheimer's disease |
| JP2005502623A (ja) | 2001-07-02 | 2005-01-27 | ノボ ノルディスク アクティーゼルスカブ | 置換ピペラジンおよびジアゼパン |
| GB0324159D0 (en) | 2003-10-15 | 2003-11-19 | Glaxo Group Ltd | Novel compounds |
| HRP20080227T3 (hr) | 2004-10-15 | 2008-06-30 | Glaxo Group Limited | Pirolidinski derivati kao ligandi histaminskih receptora |
| WO2007136668A2 (en) | 2006-05-19 | 2007-11-29 | Wyeth | N-benzoyl-and n-benzylpyrrolidin-3-ylamines as histamine-3 antagonists |
-
2009
- 2009-05-19 WO PCT/US2009/044518 patent/WO2009143153A1/en not_active Ceased
- 2009-05-19 US US12/468,632 patent/US8236792B2/en not_active Expired - Fee Related
- 2009-05-22 UY UY0001031840A patent/UY31840A/es unknown
- 2009-05-22 AR ARP090101849A patent/AR071887A1/es unknown
- 2009-05-22 TW TW098116965A patent/TW201008928A/zh unknown
- 2009-05-22 PA PA20098827501A patent/PA8827501A1/es unknown
- 2009-05-22 PE PE2009000722A patent/PE20091948A1/es not_active Application Discontinuation
- 2009-05-25 CL CL2009001282A patent/CL2009001282A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US8236792B2 (en) | 2012-08-07 |
| UY31840A (es) | 2009-12-14 |
| CL2009001282A1 (es) | 2009-10-23 |
| TW201008928A (en) | 2010-03-01 |
| US20090291903A1 (en) | 2009-11-26 |
| WO2009143153A1 (en) | 2009-11-26 |
| PE20091948A1 (es) | 2009-12-31 |
| PA8827501A1 (es) | 2009-12-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |