FIELD: organic chemistry. SUBSTANCE: triazolopyrimidines of the formula (I) given in description where one of R1 and R2 is C1-6-alkyl, radical (CH2)p-OR where p = 1-6; R - C1-6-alkyl, hydrogen or benzyl and other - hydrogen, halide, C1-6-alkyl, N3,OR4,SR4,NR5-R6 or NH(CH2)n-NR5R6 where R4 - hydrogen or (CH2)m-OR where m = 1-4; R1 is C1-6-alkyl; R5 and R6 are similar or different and mean hydrogen, C1-6-alkyl, or together with nitrogen they form morpholine, pyrrolidine and piperidine group; n = 1-4; X and Y are different and mean: N and group C-R6R7-H,, C1-6-alkyl, radical (CH2)n′-OH where n′ = 0-4, radical SR′ where R′ - as indicated above, or NR5R6 where R5 and R6 are similar or different and mean hydrogen or C1-6-alkyl; R3 - aminocarbonylphenyl, carboxyphenyl or radical of the formula: where Z is N or CH; X′ is S or O; R5 - hydrogen or when Z′ is O, halide. Synthesized compounds show antagonistic property with respect to angiotensin-II receptors and antiproliferative property that ensures to use their in pharmaceutical composition. EFFECT: improved method of synthesis, enhanced effectiveness. 11 cl, 2 tbl
Title | Year | Author | Number |
---|---|---|---|
TRIAZOLEPYRIMIDINE DERIVATIVES AND PHARMACEUTICAL COMPOSITION SHOWING ANTAGONISTIC ACTIVITY WITH RESPECT TO ANGIOTENSIN II RECEPTORS | 1992 |
|
RU2103270C1 |
SUBSTITUTED AZOLES AND A METHOD OF THEIR SYNTHESIS | 1991 |
|
RU2047604C1 |
DERIVATIVE OF DI- AND TRIAZOLYLPROPANE, METHODS OF ITS SYNTHESIS AND PHARMACEUTICAL COMPOSITION BASED ON THEREOF | 1996 |
|
RU2145605C1 |
ADENOSINE DERIVATIVES, METHOD OF PREPARING THEREOF, PHARMACEUTICAL COMPOSITION, AND METHOD OF PREPARING THEREOF | 1992 |
|
RU2129560C1 |
AGENT FOR PROPHYLAXIS AND TREATMENT OF NEUROPATHY | 2003 |
|
RU2337682C2 |
PHARMACEUTICAL COMPOSITION INHIBITING 5-LIPOXYHENASE, 4-(4-PHENYL-1-PIPERAZINYL) PHENYL DERIVATIVE AND METHOD FOR ITS PRODUCTION | 1989 |
|
RU2107064C1 |
SUBSTITUTED ARYLALKYLTHIOALKYLTHIOPYRIDINES USED FOR CONTROL OF BACTERIUM HELICOBACTER | 1995 |
|
RU2139286C1 |
NEW PHOSPHORAMIDATE NUCLEOSIDE DERIVATIVES AND APPLICATION THEREOF | 2014 |
|
RU2621709C2 |
TETRAHYDROTRIAZOLOPYRIMIDINE DERIVATIVES AS INHIBITORS OF HUMAN NEUTROPHIL ELASTASE | 2012 |
|
RU2622643C2 |
METHOD OF SYNTHESIS OF 5-SUBSTITUTED PYRROLO[2,3-α]- -PYRIMIDINES | 1993 |
|
RU2127274C1 |
Authors
Dates
1998-07-27—Published
1993-02-18—Filed