DERIVATIVES OF TETRAHYDROQUINOLINE SHOWING PROTECTIVE ACTION FROM HIV-INFECTION Russian patent published in 2009 - IPC C07D215/38 C07D403/04 A61K31/47 A61P31/12 

Abstract RU 2350604 C2

FIELD: medicine.

SUBSTANCE: invention concerns bonds of the general formula , where t it is peer 0, 1 or 2; everyone R independently represents H, alkyl, alkenyl, alkinyl, halogenalkyl, cycloalkyl, -RaAy, -RaOR5; n it is peer O; R2 it is chosen from the group consisting from H, probably substituted alkyl, alkenyl, alkinyl, cycloalkyl, -RaAy,-RaOR5, and R2 is not an amine or an alkylamin, or it is not substituted by an amine or an alkylamin; R3 represents H, probably substituted alkyl, alkenyl, alkinyl, halogenalkyl, cycloalkyl, -RaAy, -RaOR5 where when p it is peer 0, R3 is not amine or an alkylamin, or it is not replaced by amine or an alkylamin; everyone R4 independently represents halogen, alkyl, alkenyl, alkinyl, halogenalkyl, cycloalkyl, cycloalkenyl, -Ay, -NHAy, -Het, -NHHet, -NR6R7, -RaNR6R7, -RaC(O)R10, -C(O)R10, -CO2R10, -RaCO2R10, -C(O)NR6R7, -C(O)Ay, -C(O)Het; m it is peer 0, 1 or 2; every R5 independently represents H, alkyl, alkenyl, alkinyl, cycloalkyl, -RaAy or -Ay; p it is peer 0 or 1; Y represents -NR10-, -C(O)NR10-, -NR10C(O)-, -C(O)-, -C(O)O-, -NR10C(O)N(R10)2-, X represents -N(R10)2, -RaN(R10)2, -AyN(R10)2, -RaAyN(R10)2, -AyRaN(R10)2, -RaAyRaN(R10)2, -Het, -RaHet, -HetN(R10)2, -RaHetN(R10)2, -HetRaN(R10)2, -RaHetRaN(R10)2, HetRaAy or HetRaHet, where, when p it is peer 0 then X is not -N(R10)2; everyone Ra independently represents probably replaced alkylene, cycloalkylene, alkenylene, cycloalkenylene or alkinilene; every R10 independently represents H, alkyl, cycloalkyl, alkenyl, alkinyl, cycloalkenyl, -racycloalkyl, -RaOH, -RaOR5, -RaNR6R7 or -RaHet; each of R6 and R7 is independently chosen from H, alkyl, cycloalkyl, alkenyl, alkinyl, cycloalkenyl, groups-racycloalkyl, -RaOH, -RaOR5, -Het, -RaHet; every Ay independently represents probably substituted aryl group; and every Het independently represents probably substituted 4, 5 either 6-termed heterocycle or eheteroaryl group where heteroatoms are chosen from N and O; to a pharmaceutical composition for treatment and HIV-infection preventive maintenance, to application of bonds formulas I, in medical product manufacturing, and also to ways of reception of bond of the formula I.

EFFECT: rising of efficiency of a composition and the method of treatment.

55 cl, 2 tbl, 185 ex

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RU 2 350 604 C2

Authors

Gudmundsson Krist'Jan

Sebakhar Pol Richard

Richardson Lija D`Avrora

Dates

2009-03-27Published

2005-08-12Filed