FIELD: organic chemistry, heterocyclic compounds, pharmacy. SUBSTANCE: invention relates to novel biologically active compounds, namely, spiroazobicyclic heterocyclic compounds of the formula (I): where n = 0 or 1; m = 0 or 1; p = 0; X presents oxygen or sulfur atom; Y presents CH, N or NO; W presents oxygen atom or H2; A presents N or C(R2); G presents N or C(R3); D presents N or C(R4) under condition that only one among A, G and D presents nitrogen atom but at least one among Y, A, G and D presents nitrogen atom or NO; R1 presents hydrogen atom or C1-C4-alkyl; R2, R3, R4 present independently hydrogen, halogen atom, C1-C4-alkyl, C2-C4-alkenyl, C2-C4- alkynyl, aryl, heteroaryl including 5- or 6-membered aromatic ring with 1 or 2 nitrogen atoms and also furyl or morpholyl, OH, OC1-C4-alkyl, CO2R1, - CN, -NO2, -NR5R6; or R2 and R3 or R3 and R4, respectively, can form in common with A and G or G and D, respectively, another 6-membered aromatic ring; R5 and R6 present independently hydrogen atom, C1-C4-alkyl, and phenyl or they can present in common (CH2)jQ(CH2)k where Q means linkage; j = 2; k = 0-2; R7, R8, R9, R10 present independently C1-C44-alkyl, NH2, aryl or its enantiomer; and their pharmaceutically acceptable salts. Invention relates also to methods of their synthesis, intermediate compounds and pharmaceutical composition that shows activating effect with regards to nicotine α7-receptors of acetylcholine and can be used in treatment and prophylaxis of psychotic disturbances or attenuation of mental activity. Invention provides synthesis of novel compounds eliciting valuable biological and medicinal properties. EFFECT: improved methods of synthesis. 17 cl, 43 ex
Title |
Year |
Author |
Number |
FUROPYRIDINE ARALKYLAMINES, METHOD FOR THEIR PREPARING, PHARMACEUTICAL COMPOSITION BASED ON THEREOF AND INTERMEDIATE SUBSTANCES |
1999 |
- Lok Dzhejms Iii
- Mallen Dzhordzh
- Fillips Ehjfion
|
RU2233282C2 |
SPIRO-AZABICYCLIC COMPOUNDS, METHODS OF THEIR SYNTHESIS AND INTERMEDIATE COMPOUNDS |
1995 |
- Majkl Balestra
- Dzhon Charlz Gordon
- Ronald Konrad Griffit
- Robert Dzhon Mjurrej
|
RU2148058C1 |
CARBAMIC ACID AZABICYCLIC ESTERS, METHODS OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION AND INTERMEDIATE COMPOUNDS |
1997 |
|
RU2172739C2 |
NICOTINIC RECEPTOR LIGANDS |
2007 |
- Chang Gui-Fang
- Khol'Mkvist Kristofer
- Fillips Ehjfion
- Pajzer Timoti
- Simpson Tomas
- Urbanek Rebekka
- Vuds Dzhejms
- Ksiong Gui
|
RU2441007C2 |
PHENYLETHYL- AND PHENYLPROPYLAMINE COMPOUNDS, METHOD OF THEIR SYNTHESIS AND PHARMACEUTICAL PREPARATION |
1994 |
- Stefan Bengtsson
- Sven Khell'Berg
- Nina Mokhell'
- Lian Zhang
- Gerd Khall'Nemo
- Dejvid Dzhekson
- Bengt Ul'Ff
|
RU2133735C1 |
COMPOUNDS, MEDICINAL AGENTS, TREATMENT METHODS, METHOD FOR PREPARING COMPOUNDS |
2001 |
- Fillips Ehjfion
- Shmizing Richard
|
RU2263114C2 |
DERIVATIVES OF 1,2,3,4-TETRAHYDRONAPHTHALENE, METHODS OF THEIR SYNTHESIS, PHARMACEUTICAL COMPOSITION BASED ON THEREOF AND METHOD OF TREATMENT |
1998 |
- Berg Stefan
- Linderberg Mats
- Ross Svante
- Torberg Set-Olov
- Ul'Ff Bengt
|
RU2194696C2 |
THROMBIN INHIBITORS, PHARMACEUTICAL COMPOSITION BASED ON THEREOF, METHOD OF TREATMENT, METHOD OF THEIR SYNTHESIS (VERSIONS) AND PROTECTED DERIVATIVE |
1996 |
- Gustafsson David
- Njustrem Jan-Ehrik
|
RU2176645C2 |
DERIVATIVES OF IMIDAZO[1,2-A]PYRIDINE, METHODS OF THEIR SYNTHESIS, PHARMACEUTICAL PREPARATION BASED ON THEREOF, METHOD OF INHIBITION OF GASTRIC ACID SECRETION, METHOD OF TREATMENT OF GASTROENTERIC INFLAMMATORY DISEASES AND METHOD OF TREATMENT OF STATES WITH HELICOBACTER PYLORI INFECTION |
1998 |
- Amin Kosrat
- Dal'Strem Mikaehl'
- Nordberg Peter
- Starke Ingemar
|
RU2193036C2 |
NOVEL COMPOUNDS |
1997 |
- Amin Kosrat
- Dakhl'Strem Mikaehl'
- Nordberg Peter
- Starke Ingemar
|
RU2184113C2 |