ECSP003444A - DERIVATIVES OF CARBAMIC ACID - Google Patents

DERIVATIVES OF CARBAMIC ACID

Info

Publication number
ECSP003444A
ECSP003444A ECSP003444A ECSP003444A EC SP003444 A ECSP003444 A EC SP003444A EC SP003444 A ECSP003444 A EC SP003444A EC SP003444 A ECSP003444 A EC SP003444A
Authority
EC
Ecuador
Prior art keywords
lower alkyl
hydrogen
phenyl
trifluoromethyl
caused
Prior art date
Application number
Other languages
Spanish (es)
Inventor
Jurgen Wichmann
Eric Vieira
Vincent Mutel
Thomas Johannes Woltering
Konrad Bleicher
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed filed Critical
Priority to ECSP003444 priority Critical patent/ECSP003444A/en
Publication of ECSP003444A publication Critical patent/ECSP003444A/en

Links

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La presente invención se refiere a compuestos de fórmula: (gráfico), en donde R1 significa hidrógeno o alquilo inferior; R2, R2¿significan, independientemente entre si, hidrógeno, alquilo inferior, alcoxilo inferior, halógeno o trifluorometilo; X significa O, S ó dos átomos de hidrógeno que no forman un puente; A1/A2 significan, independientemente entre si, fenilo o heterociclo de 6 miembros que contiene 1 ó 2 átomos de nitrógeno; B es un grupo de fórmula (gráfico), en donde R3 significa alquilo inferior, alquenilo inferior, alquinilo inferior, bencilo, alquilo inferior-cicloalquilo, alquilo inferior-ciano, alquilo inferior-piridinilo, alquilo inferior-alcoxilo inferior-fenilo, alquilo inferior-fenilo, el cual está opcionalmente sustituido con alcoxilo inferior o fenilo, el cual está opcionalmente substituido mediante alcoxilo inferior o alquilo inferior-tienilo, cicloalquilo, alquilo inferior-trifluorometilo o alquilo inferior-morfolino; Y significa -O-, -S- ó un enlace; Z significa -O- ó -S-; ó B es un grupo heterociclico de 5 miembros, de f¿+ormula (gráficos), en donde R4 y R5 significan hidrógeno, alquilo inferior, alcoxilo inferior, ciclohexilo, alquilo inferior-ciclohexilo o trifluorometilo, con la condición de que por lo menos uno de R4 ó R5 tiene que ser hidrógeno; asi como sus sales farmacéuticamente aceptables. Estos compuestos pueden emplearse para el control o prevención de trastornos neurológicos agudos y/o crónicos tales como la función cerebral restringida ocasionada por operaciones de bypass o transplantes, pobre suministro sanguineo al cerebro, lesiones de la médula espinal, lesiones de la cabeza, hipoxia causada por el embarazo, pero cardiaco, hipoglucemia, enfermedad de Alzheimer, corea de Huntington, AlS, demencia causada por el SIDA, lesiones del ojo, retinopatia, transtornos cognitivos, déficits de memoria, esquizofrenia, parkinsonismo idiopático o parkisonismo causado por medicamentos asi como también condiciones que conducen a funciones con deficiencia de glutamato, tales como p.ej. espasmos musculares, convulsiones, migraña, incontinencia urinaria, adicción a la nicotina, psicosis, adicción a los opiáceos, ansiedad vómitos, dolor agudo y crónico disquinesis y depresión.The present invention relates to compounds of the formula: (graph), wherein R1 signifies hydrogen or lower alkyl; R2, R2¿ mean, independently of one another, hydrogen, lower alkyl, lower alkoxy, halogen or trifluoromethyl; X means O, S or two hydrogen atoms that do not form a bridge; A1 / A2 mean, independently of each other, phenyl or 6-membered heterocycle containing 1 or 2 nitrogen atoms; B is a group of the formula (graph), where R3 signifies lower alkyl, lower alkenyl, lower alkynyl, benzyl, lower alkyl-cycloalkyl, lower alkyl-cyano, lower alkyl-pyridinyl, lower alkyl-lower alkoxy-phenyl, lower alkyl -phenyl, which is optionally substituted by lower alkoxy or phenyl, which is optionally substituted by lower alkoxy or lower alkyl-thienyl, cycloalkyl, lower alkyl-trifluoromethyl or lower alkyl-morpholino; Y means -O-, -S- or a bond; Z means -O- or -S-; or B is a 5-membered heterocyclic group of f + formula (graphs), wherein R4 and R5 signify hydrogen, lower alkyl, lower alkoxy, cyclohexyl, lower alkyl-cyclohexyl, or trifluoromethyl, provided that at least one of R4 or R5 must be hydrogen; as well as its pharmaceutically acceptable salts. These compounds can be used for the control or prevention of acute and / or chronic neurological disorders such as restricted brain function caused by bypass or transplant operations, poor blood supply to the brain, spinal cord injuries, head injuries, hypoxia caused due to pregnancy, but cardiac, hypoglycemia, Alzheimer's disease, Huntington's chorea, AlS, dementia caused by AIDS, eye injuries, retinopathy, cognitive disorders, memory deficits, schizophrenia, idiopathic parkinsonism or parkisonism caused by medications as well as conditions leading to glutamate-deficient functions, such as eg muscle spasms, seizures, migraine, urinary incontinence, nicotine addiction, psychosis, opioid addiction, anxiety, vomiting, acute and chronic dyskinesis, and depression.

ECSP003444 2000-04-27 2000-04-27 DERIVATIVES OF CARBAMIC ACID ECSP003444A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
ECSP003444 ECSP003444A (en) 2000-04-27 2000-04-27 DERIVATIVES OF CARBAMIC ACID

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ECSP003444 ECSP003444A (en) 2000-04-27 2000-04-27 DERIVATIVES OF CARBAMIC ACID

Publications (1)

Publication Number Publication Date
ECSP003444A true ECSP003444A (en) 2000-11-24

Family

ID=42041072

Family Applications (1)

Application Number Title Priority Date Filing Date
ECSP003444 ECSP003444A (en) 2000-04-27 2000-04-27 DERIVATIVES OF CARBAMIC ACID

Country Status (1)

Country Link
EC (1) ECSP003444A (en)

Similar Documents

Publication Publication Date Title
AR029626A1 (en) DERIVATIVES OF CARBAMIC ACID, ITS EMPLOYMENT, A PROCEDURE TO OBTAIN THEM AND DRUGS THAT CONTAIN THEM
AR016129A1 (en) COMPOUNDS DERIVED FROM 5H-TIAZOLO [3,2-A] PYRIMIDINE; ITS USE, A PROCEDURE TO PREPARE THEM, MEDICATIONS CONTAINING THEM, AND USEFUL COMPOUNDS AS INTERMEDIARIES
PE20210040A1 (en) INTEGRATED STRESS TRAIL MODULATORS
AR038341A1 (en) COMPOUNDS THAT ARE ALFA-1 RECEIVER AGONISTS PREFERRED ALFA-1A / L RECEIVER AGONISTS
AR051202A1 (en) HETEROCICLIC DERIVATIVES AND THEIR USE AS INHIBITORS OF ESTEAROIL-COA DESATURASA
MY140039A (en) Pyrido-(2,1-a)-isoquinoline derivatives as dpp-iv inhibitors
AR051092A1 (en) HETEROCICLIC DERIVATIVES AND THEIR USE AS INHIBITORS OF ESTEAROIL-COA
PE20050429A1 (en) DERIVATIVES OF 2-PHENYLAMINE-4-AMINO-PYRIMIDINE AS KINASE INHIBITORS, PHARMACEUTICAL COMPOSITION CONTAINING THEM AND PREPARATION PROCESS
CO6160296A2 (en) BENZOAZEPIN-OXI-ACETIC ACID DERIVATIVES AS RECEPTOR AGONISTS ACTIVATED BY DELTA PEROXISONE PROLIFERATOR USED TO INCREASE HIGH-DENSITY LIPOPROTEIN-CHOLESTEROL-CHOLESTEROL REDUCE LIPOPROTEIN-LOW DENSITY-COLESTEROL
RU2008111991A (en) ORGANIC COMPOUNDS
PE20050896A1 (en) QUINOLINE INTERMEDIARIES AS INHIBITORS OF TIROSINE KINASES OF RECEPTORS AND THE SYNTHESIS OF THE SAME
PE20020338A1 (en) DERIVATIVES OF 3-INDOLYL-4-PHENYL-1H-PYRROL-2,5-DIONA WHICH INHIBIT GLUCOGEN SYNTHASE KINASE-3ß (GSK-3ß)
PE20010759A1 (en) BENZODIAZEPINE DERIVATIVES AS ANTAGONISTS OF THE METABOTROPIC GLUTAMATE RECEPTOR
DK0638073T3 (en) 1-piperazino-1,2-dihydroindene derivatives
AR058984A1 (en) CICLOHEXIL PIPERAZINIL METANONA DERIVATIVES
CO5200757A1 (en) DERIVATIVES OF 4-INDOL BENZAMIDAS WITH ACTIVITY AGAINST OSTEOPOROSIS, ITS PHARMACEUTICALLY ACCEPTABLE SALTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
SE0202134D0 (en) Therapeutic agents
AR076098A1 (en) BENZOFURAN DERIVATIVES
PE20021072A1 (en) DERIVATIVES OF DIHYDRO-BENZO (b) (1,4) -DIAZEPIN-2-ONA AS ANTAGONISTS I OF mGLUR2
ECSP066415A (en) 2-CARBONILAMINO-6-PIPERIDINAMINOPIRIDINAS REPLACED AND 1-CARBONILAMINO-3-PIPERIDINAMINOBENZENOS REPLACED AS 5-HT1F AGONISTS
AR057887A1 (en) COMPOSITIONS AND METHODS OF CNS DISORDER TREATMENT
PE20021067A1 (en) USE OF NK3 RECEIVER ANTAGONISTS
AR044478A1 (en) IMIDAZOL DERIVATIVES
PE20020882A1 (en) PIPERIDINE DERIVATIVES AS SELECTIVE ANTAGONISTS OF N-METHYL-D-ASPARTATE RECEPTOR SUBTYPES
CO4900047A1 (en) ACID AMIDES 4- (N -BENZOYLAMINE) -PENTEN-2-ENOIC WHICH HAVE ACTIVITY AS NEUROQUININE ANTAGONISTS