FIELD: chemistry.
SUBSTANCE: invention relates to novel compounds of formula (I) and their pharmaceutically acceptable addition salts having HIV replication inhibiting properties. In formula (I), R1 is halogen; R2 and R3 each independently denotes C1-6-alkyl. The invention also relates to a method for synthesis of said compounds and a pharmaceutical composition.
EFFECT: increased effectiveness of derivatives.
7 cl, 6 ex
Title | Year | Author | Number |
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|
RU2403245C2 |
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|
RU2410379C2 |
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HIV-INHIBITING 5-AMIDO-SUBSTITUTED PYRIMIDINES | 2007 |
|
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HIV INHIBITING 5-HETEROCYCLYL PYRIMIDINES | 2005 |
|
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1,5,6-SUBSTITUTED 2-OXO-3-CYANO-1,6A-DIAZATETRAHYDROFLUORANTHENES | 2006 |
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RU2389730C2 |
(1,10b-DIHYDRO-2-(AMINOALKYLPHENYL)-5H-PYRAZOLO[1,5-c][1,3] BENZOXAZIN-5-YL) PHENYLMETHANONE DERIVATIVES AS HIV VIRAL REPLICATION INHIBITORS | 2006 |
|
RU2416615C2 |
6,7,8,9-SUBSTITUTED 1-PHENYL-1,5-DIHYDROPYRIDO (3,2-b) INDOLE-2-ONES EFFECTIVE AS ANTIINFECTIOUS PHARMACEUTICAL AGENTS | 2005 |
|
RU2377243C2 |
Authors
Dates
2010-10-10—Published
2006-03-02—Filed