AR040261A1 - AMIDES OF 2-HETEROARILCARBOXILIC ACIDS - Google Patents
AMIDES OF 2-HETEROARILCARBOXILIC ACIDSInfo
- Publication number
- AR040261A1 AR040261A1 ARP030102069A AR040261A1 AR 040261 A1 AR040261 A1 AR 040261A1 AR P030102069 A ARP030102069 A AR P030102069A AR 040261 A1 AR040261 A1 AR 040261A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- optionally
- cyano
- halogen
- Prior art date
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La presente trata de amidas de ácidos 2-heteroarilcarboxilicos y de su uso para la preparación de medicamentos para el tratamiento y/o la profilaxis de enfermedades y para mejorar la capacidad perceptiva, la capacidad de concentración, la capacidad de aprendizaje y/o la capacidad de memoria. Son objeto también de esta solicitud medicamentos, procedimientos para preparar los compuestos y uso para preparar los medicamentos. Reivindicación 1: Compuestos de la fórmula (1) en la que R1 representa 1-aza-biciclo[2.2.2]oct-3-ilo, que está sustituido, opcionalmente, a través del átomo de N por un resto seleccionado entre el grupo alquilo C1-4, bencilo y oxi; R2 es H o alquilo C1-6; R3 es H, halógeno o alquilo C1-6; R4 es H, halógeno, ciano, amino, trifluorometilo, trifluorometoxi, alquilo C1-6, alquilcarbonilo C1-6, alquilamino C1-6, formilo, hidroxicarbonilo, alcoxi C1-6, alcoxicarbonilo C1-6, alquiltio C1-6,alquilcarbonilamino C1-6, alquilaminocarbonilo C1-6,alquilsulfonilamino C1-6, cicloalquilcarbonilamino C3-8,cicloalquilaminocarbonilo C3-6, pirrolilo, alquilaminocarbonilamino C1-6, heterociclilcarbonilo, heterociclilcarbonilamino, heteroarilcarbonilamino, hidroxi, fenilo o heterociclilo, pudiendo estar sustituido alquilo C1-6, opcionalmente con hidroxi, ciano, amino, alquilaminocarbonilamino C1-6, alquilaminocarboxilo C1-6, heterociclilo o arilo, alquilaminocarbonilo C1-6, opcionalmente , alcoxi C1-6 o alquilamino C1-6, alquilcarbonilamino C1-6, opcionalmente, con alcoxi C1-6 y heterociclilo, opcionalmente. Con oxo, A representa O o S; el anillo B es benzo o pirido, que están sustituidos, opcionalmente, con restos de la serie halógeno, ciano, formilo, trifluorometilo, trifluorometoxi, nitro, amino, alquilo C1-6, y alcoxi C1-6, respectivamente; y E, C:::C, arileno y heteroarileno, pudiendo estar sustituidos arileno y heteroarileno por restos de la serie de halógeno, ciano, trifluorometilo, trifluorometoxi, nitro, amino, alcoxi C1-6 y alquilo C1-6, así como los solvatos, sales o solvatos de sales de estos compuestos.The present invention concerns amides of 2-heteroarylcarboxylic acids and their use for the preparation of medicaments for the treatment and / or prophylaxis of diseases and to improve the perceptual capacity, the concentration capacity, the learning capacity and / or the capacity of memory Also subject to this application are medications, procedures for preparing the compounds and use for preparing the medications. Claim 1: Compounds of the formula (1) wherein R 1 represents 1-aza-bicyclo [2.2.2] oct-3-yl, which is optionally substituted through the N atom by a moiety selected from the group C1-4 alkyl, benzyl and oxy; R2 is H or C1-6 alkyl; R3 is H, halogen or C1-6 alkyl; R4 is H, halogen, cyano, amino, trifluoromethyl, trifluoromethoxy, C1-6 alkyl, C1-6 alkylcarbonyl, C1-6 alkylamino, formyl, hydroxycarbonyl, C1-6 alkoxy, C1-6 alkoxycarbonyl, C1-6 alkylthio, C1 alkylcarbonylamino -6, C 1-6 alkylaminocarbonyl, C 1-6 alkylsulfonylamino, C 3-8 cycloalkylcarbonylamino, C 3-6 cycloalkylaminocarbonyl, pyrrolyl, C 1-6 alkylaminocarbonylamino, heterocyclylcarbonyl, heterocyclylcarbonylamino, heteroarylcarbonylamino, hydroxy, phenyl- or C 1-6 alkylalkyl optionally with hydroxy, cyano, amino, C 1-6 alkylaminocarbonylamino, C 1-6 alkylaminocarboxy, heterocyclyl or aryl, C 1-6 alkylaminocarbonyl, optionally, C 1-6 alkoxy or C 1-6 alkylamino, C 1-6 alkylcarbonylamino, optionally, with C 1- alkoxy 6 and heterocyclyl, optionally. With oxo, A represents O or S; Ring B is benzo or pyrido, which are optionally substituted with halogen, cyano, formyl, trifluoromethyl, trifluoromethoxy, nitro, amino, C1-6 alkyl, and C1-6 alkoxy, respectively; and E, C ::: C, arylene and heteroarylene, arylene and heteroarylene may be substituted by halogen, cyano, trifluoromethyl, trifluoromethoxy, nitro, amino, C1-6 alkoxy and C1-6 alkyl series, as well as the solvates, salts or solvates of salts of these compounds.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10225536 | 2002-06-10 | ||
DE10257078A DE10257078A1 (en) | 2002-12-06 | 2002-12-06 | New N-azabicyclooctyl bicyclic heteroaryl carboxamides, are alpha 7-nicotinic acetylcholine receptor ligands useful for improving attention, concentration, learning and/or memory performance |
DE2002157537 DE10257537A1 (en) | 2002-12-10 | 2002-12-10 | New N-azabicyclooctyl bicyclic heteroaryl carboxamides, are alpha 7-nicotinic acetylcholine receptor ligands useful for improving attention, concentration, learning and/or memory performance |
DE10305922A DE10305922A1 (en) | 2002-06-10 | 2003-02-13 | New N-azabicyclooctyl bicyclic heteroaryl carboxamides, are alpha 7-nicotinic acetylcholine receptor ligands useful for improving attention, concentration, learning and/or memory performance |
Publications (1)
Publication Number | Publication Date |
---|---|
AR040261A1 true AR040261A1 (en) | 2005-03-23 |
Family
ID=41259016
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP030102069 AR040261A1 (en) | 2002-06-10 | 2003-06-10 | AMIDES OF 2-HETEROARILCARBOXILIC ACIDS |
Country Status (6)
Country | Link |
---|---|
AR (1) | AR040261A1 (en) |
DO (1) | DOP2003000657A (en) |
HN (1) | HN2003000166A (en) |
HR (1) | HRP20050012A2 (en) |
PE (1) | PE20040557A1 (en) |
TW (1) | TW200410967A (en) |
-
2003
- 2003-06-09 TW TW92115481A patent/TW200410967A/en unknown
- 2003-06-09 DO DO2003000657A patent/DOP2003000657A/en unknown
- 2003-06-09 HN HN2003000166A patent/HN2003000166A/en unknown
- 2003-06-10 PE PE2003000576A patent/PE20040557A1/en not_active Application Discontinuation
- 2003-06-10 AR ARP030102069 patent/AR040261A1/en unknown
-
2005
- 2005-01-07 HR HR20050012A patent/HRP20050012A2/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
HRP20050012A2 (en) | 2006-04-30 |
DOP2003000657A (en) | 2004-01-31 |
PE20040557A1 (en) | 2004-10-01 |
TW200410967A (en) | 2004-07-01 |
HN2003000166A (en) | 2004-07-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20230249A1 (en) | BICYCLIC HETEROARYL COMPOUNDS AND THEIR USES | |
ES2525763T3 (en) | Derivatives of substituted phenylalcanoic acid and its uses for the treatment of respiratory diseases | |
PE20060921A1 (en) | PROCEDURE TO PREPARE CHIRAL 8- (3-AMINO-PIPERIDIN-1-IL) -XANTHINES | |
AR050698A1 (en) | BENZAZEPINE COMPOUND, PHARMACEUTICAL COMPOSITION THAT INCLUDES IT, ITS USE FOR THE MANUFACTURE OF A MEDICINAL PRODUCT AND PROCEDURE FOR THE PREPARATION OF SUCH COMPOUND | |
AR043187A1 (en) | PIPERIDINE-BENCENSULFONAMIDE DERIVATIVES, MEDICINES CONTAINING THEM AND USES FOR THE TREATMENT OF CNS DISORDERS. | |
PE20060437A1 (en) | AZA-BICYCLONONE COMPOUNDS AS CHOLINERGIC LINKS OF nAChR | |
AR073348A1 (en) | CYCLE INHIBITORS OF 11 BETA-HYDROXIESTEROID DEHYDROGENASE 1 | |
AR047531A1 (en) | DERIVATIVES 1H-TIENO (2,3-C) PIRAZOL USEFUL AS QUINASE INHIBITORS | |
AR071577A1 (en) | PIRAZOLO-PYRIMIDINONE FOR THE TREATMENT OF DISORDERS OF THE CENTRAL NERVOUS SYSTEM | |
CU20090184A7 (en) | AMINO-HETEROCYCLIC COMPOUNDS | |
PE20020721A1 (en) | QUINUCLIDINE DERIVATIVES AS ANTIMUSCARINAL AGENTS M3 | |
PE20040450A1 (en) | HETEROARYLOXY-ARYL-SPIRO-PYRIMIDINE-2,4,6-TRIONA N-SUBSTITUTED AS METALOPROTEINASE INHIBITORS | |
AR041134A1 (en) | PIRAZOLOPIRIMIDINAS AS INHIBITORS OF THE CYCLINE-DEPENDENT KINASE | |
CO6501182A2 (en) | DERIVATIVES OF 1-HETEROCICLIL-1,5-DIHIDRO-PIRAZOLO [3,4-D] PIRIMIDIN-4-ONA AND ITS USE AS PDE9A MODULATORS | |
AR043199A1 (en) | USEFUL HETEROCICLIC COMPONENTS FOR THE TREATMENT OF INFLAMMATORY AND ALLERGIC DISEASES, PROCESS FOR OPERATION AND PHARMACEUTICAL COMPOSITION CONTAINING SUCH COMPONENTS | |
PE20060531A1 (en) | DERIVATIVES OF PYRIDAZIN-3- (2H) -ONE AS INHIBITORS OF PHOSPHODIESTERASE 4 | |
UY28526A1 (en) | GLUCOCORTICOID MIMETICS, METHODS OF PREPARATION PHARMACEUTICAL COMPOSITIONS AND USES OF THE SAME | |
DOP2006000169A (en) | BETA-SECRETASE SPIROPIPERIDINE INHIBITORS FOR THE TREATMENT OF ALZHEIMER'S DISEASE | |
AR037740A1 (en) | SUBSTITUTED AZABICICLIC COMPOUNDS OF FUSIONED HETEROARILES FOR THE TREATMENT OF DISEASES, PHARMACEUTICAL COMPOSITIONS, THEIR USE IN THE PREPARATION OF MEDICINES | |
DOP2005000046A (en) | ALFA ARILO OR HETEROARIL METHYL BETA PIPERIDINE PROPANOIC ACID COMPOUNDS AS ANOTHONIST OF THE ENT RECEIVER1 | |
AR052938A1 (en) | N-SULFONYLAMINOFENILETIL-2-PHENOXYACETAMIDE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS THAT INCLUDE THEM AND THEIR USE IN THE PREPARATION OF MEDICINES FOR THE TREATMENT OF DISEASES MEDIATED BY RECEIVER VR1 | |
PE20071090A1 (en) | 5-PIRAZOLPIPERIDINES- (SUBSTITUTED) | |
UY28333A1 (en) | CASPASA INHIBITORS AND THEIR USES. | |
AR053435A1 (en) | DERIVATIVES OF 5-AMMINOINDOL, A METHOD FOR THEIR PREPARATION, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND THEIR USE IN THE MANUFACTURE OF A MADICAMENT FOR THE TREATMENT OF DISEASES ASSOCIATED WITH THE MODULATION OF H3 RECEPTORS. | |
UY27786A1 (en) | ISOQUINOLINE DERIVATIVES. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |