AR060462A1 - Compuestos de ariloxietilamina apropiados para tratar trastornos que responden a la modulacion del receptor de dopamina d3 - Google Patents
Compuestos de ariloxietilamina apropiados para tratar trastornos que responden a la modulacion del receptor de dopamina d3Info
- Publication number
- AR060462A1 AR060462A1 ARP070101595A ARP070101595A AR060462A1 AR 060462 A1 AR060462 A1 AR 060462A1 AR P070101595 A ARP070101595 A AR P070101595A AR P070101595 A ARP070101595 A AR P070101595A AR 060462 A1 AR060462 A1 AR 060462A1
- Authority
- AR
- Argentina
- Prior art keywords
- fluorinated
- alkyl
- alkoxy
- cycloalkyl
- alkenyl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/76—Nitrogen atoms to which a second hetero atom is attached
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
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- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- 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
- A61P25/20—Hypnotics; Sedatives
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- 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
- A61P25/22—Anxiolytics
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- 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
- A61P25/24—Antidepressants
-
- 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
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- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/69—Benzenesulfonamido-pyrimidines
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Addiction (AREA)
- Anesthesiology (AREA)
- Pain & Pain Management (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
El uso de un compuesto de la formula (1) o una sal aceptable para uso farmacéutico del mismo para preparar una composicion farmacéutica para el tratamiento de un trastorno médico susceptible al tratamiento con un ligando del receptor do dopamina D3, SNC. Reivindicacion 1: Un compuesto ariloxietilamina de la formula (1) en donde Ar es fenilo o un radical heteroaromático unido por C de 5 o 6 miembros, en donde Ar puede llevar 1 radical Ra y en donde Ar también puede llevar 1 o 2 radicales Rb; Ra se selecciona entre el grupo formado por alquilo C1-6, alquilo fluorado C1-6, alquenilo C2-6, alquenilo fluorado C2-6, cicloalquilo C3-6, cicloalquilo fluorado C3-6, alcoxi C1-6, alcoxi fluorado C1-6, hidroxialquilo C1-6, alcoxi C1-6-alquilo C1-4, hidroxialcoxi C1-6, alcoxi- C1-6-alcoxi C1-4, COOH, NR4R5, CH2NR4R5, ONR4R5, NHC(O)NR4R5, C(O)NR4R5, SO2NR4R5, alquilcarbonilo C1-6, alquilcarbonilo fluorado C1-6, alquilcarbonilamino C1-6, alquilcarbonilamino fluorado C1-6, alquilcarboniloxi C1-6, alquilcarboniloxi fluorado C1-6, alcoxicarbonilo C1-6, alcoxicarbonilo fluorado C1-6, alquiltio C1-6, alquiltio fluorado C1-6, alquilsulfinilo C1-6, alquilsulfinilo fluorado C1-6, alquilsulfonilo C1-6, alquilsulfonilo fluorado C1-6, fenilsulfonilo, fenilo, fenoxi, benciloxi, piridin-2-iloxi y un radical heterocíclico de entre 3 y 7 miembros, en donde los grupos fenilo, el grupo piridilo y el grupo heterociclilo en los ultimos seis radicales mencionados pueden llevar 1 2, 3 o 4 radicales seleccionados entre halogeno, ciano, OH, oxo, CN, y un radical Raa, en donde Raa se selecciona entre alquilo C1-6, alquilo fluorado C1-6, alquenilo C2-6, alquenilo fluorado C2-6, cicloalquilo C3-6, cicloalquilo fluorado C3-6, alcoxi C1-6, alcoxi fluorado C1-6, hidroxialquilo C1-6 ,alcoxi C1-6-alquilo C1-4, hidroxialcoxi C1-6, alcoxi C1-6-alcoxi C1-4, COOH, NR4R5, CH2NR4R5, ONR4R5, NHC(O)NR4R5, C(O)NR4R5, SO2NR4R5, alquilcarbonilo C1-6, alquilcarbonilo fluorado C1-6, alquilcarbonilamino C1- 6, alquilcarbonilamino fluorado C1-6, alquilcarboniloxi C1-6, alquilcarboniloxi fluorado C1-6, alcoxicarbonilo C1-6, alcoxicarbonilo fluorado C1-6, alquiltio C1-6, alquiltio fluorado C1-6, alquilsulfinilo C1-6, alquilsulfinilo fluorado C1-6, alquilsulfonilo C1-6, alquilsulfonilo fluorado C1-6; cada Rb se selecciona entre halogeno, ciano, nitro, OH, metilo, metoxi, fluorometilo, difluorometilo, trifluorometilo, fluormetoxi, difluorometoxi y trifluorometoxi, o el radical Ra y un radical Rb, de estar presentes, unidos a dos átomos de carbono adyacentes de fenilo, pueden formar un anillo heterocíclico o carbocíclico de 5 o 6 miembros que está unido al anillo fenilo y que no está sustituido o que puede llevar 1, 2 o 3 radicales seleccionados entre halogeno, NO2, NH2, OH, CN, alquilo C1-6, alquilo fluorado C1-6, cicloalquilo C3-6, cicloalquilo fluorado C3-6, alcoxi C1-6, alcoxi fluorado C1-6, hidroxialquilo C1-6, alcoxi-C1-4-alquilo C2-4, hidroxialcoxi C1-6, alcoxi-C1-4- alcoxi C2-4, alquilcarbonilo C1-6, alquilcarbonilo fluorado C1-6, alquilamino C1-6, di-C1-6-alquilamino, alquilaminocarbonilo C1-6, di-C1-6 alquilaminocarbonilo, alquilcarbonilamino C1-6, alquilcarbonilamino fluorado C1-6, alquilcarboniloxi C1-6, alquilcarboniloxi fluorado C1-6, alcoxicarbonilo C1-6, alquiltio C1-6, alquiltio fluorado C1-6, alquilsulfinilo C1-6, alquilsulfinilo fluorado C1-6, alquilsulfonilo C1-6, y alquilsulfonilo fluorado C1-6, X es N o CH; R1 es H, alquilo C1-4, cicloalquilo C3-4, cicloalquilmetilo C3-4, alquenilo C3-4, alquilo fluorado C1-4, cicloalquilo fluorado C3-4, cicloalquilmetilo fluorado C3-4, alquenilo fluorado C3-4, formilo o alquilcarbonilo C1-3; R1a es H, alquilo C1-4, cicloalquilo C3-4, cicloalquilmetilo C3-4, alquenilo C3-4, alquilo fluorado C1-4, cicloalquilo fluorado C3-4, cicloalquilmetilo fluorado C3-4, o alquenilo fluorado C3-4, o R1 y R1a juntos son (CR6R7)r donde r es 3, 4 o 5; R2 y R2a son en forma independiente entre sí H, F, alquilo C1-4 o alquilo fluorado C1-4 o R2a y R2 juntos pueden formar un miembro del anillo (CR6R7)m donde m es 2, 3, 4 o 5; oR1a y R2a juntos son (CR6R7)n donde n es 2, 3 o 4; R3 es H o alquilo C1-4; R4, R5 en forma independiente entre sí y en forma independiente de cada aparicion se seleccionan entre H, alquilo C1-3, alcoxi C1-3 y alquilo fluorado C1-3; R6, R7 en forma independiente entre sí y en forma independiente de cada aparicion se seleccionan entre H, F, alquilo C1-4 y alquilo fluorado C1-4; R8, R8a en forma independiente entre sí son H, F, alquilo C1-4 o alquilo fluorado C1-4 o R8a y R8 juntos pueden formar un miembro del anillo (CR6R7)q donde q es 2, 3, 4 o 5, R1a y R8a juntos son (CR6R7)n donde n es 2 o 3; y R9 es H, alquilo C1-4, alquilo fluorado C1-4, alcoxi C1-4, o alcoxi fluorado C1-4; y las sales de adicion ácida fisiologicamente tolerables del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06007923 | 2006-04-14 | ||
US79367106P | 2006-04-20 | 2006-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR060462A1 true AR060462A1 (es) | 2008-06-18 |
Family
ID=38180343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070101595A AR060462A1 (es) | 2006-04-14 | 2007-04-13 | Compuestos de ariloxietilamina apropiados para tratar trastornos que responden a la modulacion del receptor de dopamina d3 |
Country Status (8)
Country | Link |
---|---|
US (1) | US8383641B2 (es) |
EP (1) | EP2013179B1 (es) |
JP (1) | JP5232987B2 (es) |
AR (1) | AR060462A1 (es) |
CA (1) | CA2648543C (es) |
MX (1) | MX2008013114A (es) |
UY (1) | UY30284A1 (es) |
WO (1) | WO2007118859A1 (es) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PE20142099A1 (es) | 2009-01-12 | 2014-12-13 | Icagen Inc | Derivados de sulfonamida |
AU2010231694A1 (en) | 2009-03-30 | 2011-10-06 | Astellas Pharma Inc. | Pyrimidine compound |
EP2590972B1 (en) | 2010-07-09 | 2015-01-21 | Pfizer Limited | N-sulfonylbenzamides as inhibitors of voltage-gated sodium channels |
WO2013074965A1 (en) * | 2011-11-16 | 2013-05-23 | Microbiotix, Inc. | Aminoalkyl phenol ether inhibitors of influenza a virus |
TW201512171A (zh) | 2013-04-19 | 2015-04-01 | Pfizer Ltd | 化學化合物 |
WO2018164192A1 (ja) * | 2017-03-08 | 2018-09-13 | 武田薬品工業株式会社 | 置換ピロリジン化合物およびその用途 |
CN118271298A (zh) | 2019-01-31 | 2024-07-02 | 武田药品工业株式会社 | 杂环化合物及其用途 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW450954B (en) | 1998-05-14 | 2001-08-21 | Pharmacia & Amp Upjohn Company | Phenylsulfonamide-phenylethylamines useful as dopamine receptors |
EP1809597B1 (en) * | 2004-10-14 | 2012-01-11 | Abbott GmbH & Co. KG | Aminoethylaromatic compounds suitable for treating disorders that respond to modulation of the dopamine d3 receptor |
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2007
- 2007-04-13 AR ARP070101595A patent/AR060462A1/es not_active Application Discontinuation
- 2007-04-13 MX MX2008013114A patent/MX2008013114A/es active IP Right Grant
- 2007-04-13 JP JP2009504760A patent/JP5232987B2/ja not_active Expired - Fee Related
- 2007-04-13 EP EP07728098A patent/EP2013179B1/en not_active Not-in-force
- 2007-04-13 UY UY30284A patent/UY30284A1/es not_active Application Discontinuation
- 2007-04-13 WO PCT/EP2007/053633 patent/WO2007118859A1/en active Application Filing
- 2007-04-13 US US12/296,739 patent/US8383641B2/en active Active
- 2007-04-13 CA CA2648543A patent/CA2648543C/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2009533397A (ja) | 2009-09-17 |
US8383641B2 (en) | 2013-02-26 |
EP2013179A1 (en) | 2009-01-14 |
US20090143383A1 (en) | 2009-06-04 |
CA2648543C (en) | 2015-06-02 |
UY30284A1 (es) | 2007-11-30 |
MX2008013114A (es) | 2008-10-21 |
JP5232987B2 (ja) | 2013-07-10 |
WO2007118859A1 (en) | 2007-10-25 |
CA2648543A1 (en) | 2007-10-25 |
EP2013179B1 (en) | 2011-01-19 |
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