AR013206A1 - DERIVATIVES INDOL AND 2,3-DIHIDROINDOL, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS AND THE USE OF SUCH COMPOUNDS FOR THE PREPARATION OF A MEDICINAL PRODUCT FOR THE TREATMENT OF SENSITIVE DISORDERS TO THE INHIBITION OF SEROTONIN REABSORPTION AND ANTAGON 5. - Google Patents

DERIVATIVES INDOL AND 2,3-DIHIDROINDOL, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS AND THE USE OF SUCH COMPOUNDS FOR THE PREPARATION OF A MEDICINAL PRODUCT FOR THE TREATMENT OF SENSITIVE DISORDERS TO THE INHIBITION OF SEROTONIN REABSORPTION AND ANTAGON 5.

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Publication number
AR013206A1
AR013206A1 ARP980103400A AR013206A1 AR 013206 A1 AR013206 A1 AR 013206A1 AR P980103400 A ARP980103400 A AR P980103400A AR 013206 A1 AR013206 A1 AR 013206A1
Authority
AR
Argentina
Prior art keywords
compounds
treatment
aryl
inhibition
alkyl
Prior art date
Application number
Other languages
Spanish (es)
Original Assignee
Lundbeck & Co As H
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 by Lundbeck & Co As H filed Critical Lundbeck & Co As H
Publication of AR013206A1 publication Critical patent/AR013206A1/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Indol y derivados de 2,3-dihidroindol que tienen la formula (I) cualquiera de su enantiomeros o cualquier mezcla de los mismos, o una sal de ácido de losmismos, donde X es -O-, -S-, O-CR4R5- y Y es -CR6-R7-, CR8R7-CR8R9-, O -CR6=CR7-, o Xe Y conjuntamente forman un grupo -CR4=CR5-CR6R7-; Z es -O-, o-S-; W es N, C o CH; A es un grupo seleccionado de un grupo de formula (II), (III) y (IV) donde las líneas de puntos se refieren a un enlace opcional; R1,R2, R3, R13, R14, R15, R16 Yr17 están independientemente seleccionados de hidrogeno, halogeno, trifluormetilo, alquilo, alquenilo, alquinilo,cicloalquilo, alcoxi, hidroxi, formilo, acilo, amino, alquilamino, dialquilamino, acilamino, alcoxicarbonilamino,aminocar bonlamino,alquilaminocarbonilamino, dialquilaminocarbonilamino, nitro, ciano y arilo o arilalquilo, donde arilo puede ser sustituido con halogeno, trifluormetilo,alcoxi, hidroxi, amino, alquilamino, nitro y ciano; R4, R5, R6, R7 R8 y R9están cada uno independientemente seleccionados de hidrogeno y alquilo; y R11está seleccionado de hidrogeno, alquilo, alquenilo, alquinilo, cicloalquilo, arilo, arilalquilo, acilo y formilo; composiciones farmacéuticas que contienenlos compuestosanter iormene mencionados y el uso de dichos compuestos para la preparacion de un medicamento para el tratamiento de desordenes sensibles a lainhibicion de la reabsorcion de seotonina y antagonismo de receptores 5-HT1A (por ejemplo, desordenesafectiv os, incluyendo depresion, sicosis, desordenesde pánico y desorden compulsivo obsesivo). Estos compuestos son considerados particularmente utiles como principio rápido de la accion de medicamentos parael tratamietno de desordenes afectivoscomo dep resion.Indole and 2,3-dihydroindole derivatives having formula (I) any of its enantiomers or any mixture thereof, or an acid salt thereof, where X is -O-, -S-, O-CR4R5- and Y is -CR6-R7-, CR8R7-CR8R9-, O -CR6 = CR7-, or Xe Y together form a group -CR4 = CR5-CR6R7-; Z is -O-, o-S-; W is N, C or CH; A is a group selected from a group of formula (II), (III) and (IV) where the dotted lines refer to an optional bond; R1, R2, R3, R13, R14, R15, R16 Yr17 are independently selected from hydrogen, halogen, trifluoromethyl, alkyl, alkenyl, alkynyl, cycloalkyl, alkoxy, hydroxy, formyl, acyl, amino, alkylamino, dialkylamino, acylamino, alkoxycarbonylamino, aminocar bonlamino, alkylaminocarbonylamino, dialkylaminocarbonylamino, nitro, cyano and aryl or arylalkyl, where aryl can be substituted with halogen, trifluoromethyl, alkoxy, hydroxy, amino, alkylamino, nitro and cyano; R4, R5, R6, R7, R8 and R9 are each independently selected from hydrogen and alkyl; and R11 is selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, arylalkyl, acyl, and formyl; Pharmaceutical compositions containing the above mentioned compounds and the use of said compounds for the preparation of a medicament for the treatment of disorders sensitive to the inhibition of seotonin reuptake and antagonism of 5-HT1A receptors (for example, affective disorders, including depression, psychosis , panic disorder and obsessive compulsive disorder). These compounds are considered particularly useful as a quick start of action for medications for the treatment of affective disorders such as depression.

ARP980103400 1997-07-25 1998-07-13 DERIVATIVES INDOL AND 2,3-DIHIDROINDOL, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS AND THE USE OF SUCH COMPOUNDS FOR THE PREPARATION OF A MEDICINAL PRODUCT FOR THE TREATMENT OF SENSITIVE DISORDERS TO THE INHIBITION OF SEROTONIN REABSORPTION AND ANTAGON 5. AR013206A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DK89297 1997-07-25

Publications (1)

Publication Number Publication Date
AR013206A1 true AR013206A1 (en) 2000-12-13

Family

ID=8098721

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980103400 AR013206A1 (en) 1997-07-25 1998-07-13 DERIVATIVES INDOL AND 2,3-DIHIDROINDOL, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS AND THE USE OF SUCH COMPOUNDS FOR THE PREPARATION OF A MEDICINAL PRODUCT FOR THE TREATMENT OF SENSITIVE DISORDERS TO THE INHIBITION OF SEROTONIN REABSORPTION AND ANTAGON 5.

Country Status (13)

Country Link
CN (3) CN1127501C (en)
AR (1) AR013206A1 (en)
BR (1) BR9810790A (en)
EA (1) EA001890B1 (en)
HK (3) HK1030220A1 (en)
IL (1) IL133990A (en)
IS (1) IS2024B (en)
NO (1) NO318610B1 (en)
PL (1) PL190924B1 (en)
SK (1) SK284866B6 (en)
TR (1) TR200000231T2 (en)
UA (1) UA59408C2 (en)
ZA (1) ZA986237B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103420989B (en) * 2012-05-15 2016-03-23 华中科技大学 Benzodioxane derivative and application thereof

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8830312D0 (en) * 1988-12-28 1989-02-22 Lundbeck & Co As H Heterocyclic compounds
DE4127849A1 (en) * 1991-08-22 1993-02-25 Merck Patent Gmbh BENZODIOXAN DERIVATIVES
FR2692264B1 (en) * 1992-06-12 1994-08-05 Adir NOVEL 1,4-DISUBSTITUTED PIPERAZINES, THEIR PREPARATION PROCESS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM.

Also Published As

Publication number Publication date
PL338194A1 (en) 2000-10-09
NO318610B1 (en) 2005-04-18
CN1265107A (en) 2000-08-30
SK952000A3 (en) 2001-03-12
CN1127501C (en) 2003-11-12
IL133990A (en) 2003-09-17
NO20000372L (en) 2000-03-21
SK284866B6 (en) 2006-01-05
HK1066807A1 (en) 2005-04-01
BR9810790A (en) 2000-07-25
IS5334A (en) 2000-01-11
CN1293075C (en) 2007-01-03
NO20000372D0 (en) 2000-01-25
EA001890B1 (en) 2001-10-22
IS2024B (en) 2005-08-15
HK1066806A1 (en) 2005-04-01
UA59408C2 (en) 2003-09-15
TR200000231T2 (en) 2000-07-21
IL133990A0 (en) 2001-04-30
HK1030220A1 (en) 2001-04-27
CN1515568A (en) 2004-07-28
CN1515569A (en) 2004-07-28
EA200000162A1 (en) 2000-10-30
PL190924B1 (en) 2006-02-28
ZA986237B (en) 1999-03-31
CN1286833C (en) 2006-11-29

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