FIELD: organic chemistry, chemical technology, medicine, pharmacy.
SUBSTANCE: invention relates to new derivatives of indole of the formula (I): wherein R1 means phenyl substituted or unsubstituted radical R2 and/or R4; R2, R4 R5 and R6 in each case and independently of one another mean Hal; R3 mean substituted or unsubstituted radical R5 and/or R6 or means Het wherein Het means 2-furyl, 3-furyl, 2-thienyl or 3-thienyl; Hal means fluorine atom (F), chlorine atom (Cl), bromine atom (Br) or iodine atom (J), and their physiologically acceptable salts and solvates also. Compounds of the formula (I) are prepared by interaction of compound of the formula (I): wherein L means Cl, Br, J or free or reactive functional modified group OH; R3 has value indicated in the formula (I) with compound of the formula (III): . Compounds of the formula (I) show affinity to 5-HT2A receptors that allow their using in the pharmaceutical composition.
EFFECT: valuable medicinal and pharmacological properties of compounds.
4 cl, 10 ex
Title | Year | Author | Number |
---|---|---|---|
N-(INDOLCARBONYL)PIPERAZINE DERIVATIVES, METHODS FOR PRODUCTION THE SAME, PHARMACEUTICAL COMPOSITION, AND COMPOUNDS | 2000 |
|
RU2251548C2 |
USING DERIVATIVES OF N-(INDOLCARBONYL)PIPERAZINE | 2002 |
|
RU2317083C2 |
COMPOUNDS, METHOD FOR THEIR PREPARING, PHARMACEUTICAL COMPOSITION, SELECTIVE ANTAGONISTS OF 5-HT -RECEPTOR | 2001 |
|
RU2280034C2 |
METHOD FOR PREPARING (3-CYANO-1H-INDOLE-7-YL)-[4-(4-FLUOROPHENETHYL)-PIPERAZINE-1-YL]METHANONE AND ITS SALTS | 2001 |
|
RU2295519C2 |
INDOL-3-YL-CARBONYL-PIPERADINE-BENZIMIDAZOLE DERIVATIVES AS V1A RECEPTOR ANTAGONISTS | 2006 |
|
RU2415139C2 |
INDOLE-3-YL-CARBONYL-PIPERIDINE AND PIPERAZINE DERIVATIVES | 2006 |
|
RU2422442C2 |
SELECTIVE HISTAMINE H4 RECEPTOR ANTAGONISTS FOR TREATING VESTIBULAR DISORDERS | 2009 |
|
RU2589846C2 |
HETEROCYCLIC INHIBITORS OF Hh-SYGNAL CASCADE, BASED ON THEM MEDICINAL COMPOSITIONS AND METHOD OF TREATING DISEASES INDUCED BY ABBARANT ACTIVITY OF Hh-SIGNAL SYSTEM | 2007 |
|
RU2364597C1 |
DERIVATIVES OF AMIDES AND UREA AS INHIBITORS OF REUPTAKE OF 5-HT AND LIGANDS OF 5-HT1B/1D | 1998 |
|
RU2211216C2 |
CYCLIC (AZA)INDOLYSINCARBOXAMIDES, PREPARING AND USING THEM AS PHARMACEUTICAL AGENTS | 2010 |
|
RU2539574C2 |
Authors
Dates
2005-07-20—Published
2000-07-07—Filed