FIELD: organic chemistry, pharmacy. SUBSTANCE: products: derivatives of pyrazolo-[1,5-a] -pyridine of the general formula (I)  where R1 - phenyl; R2 - lower (alkanoyl) lower alkyl carboxy (lower) alkyl, or substituted carboxy (lower) alkyl; A - lower alkenylene, or their pharmaceutically acceptable salts and method of their synthesis. Reagent 1: compounds of the formula (II)
 where R1 - phenyl; R2 - lower (alkanoyl) lower alkyl carboxy (lower) alkyl, or substituted carboxy (lower) alkyl; A - lower alkenylene, or their pharmaceutically acceptable salts and method of their synthesis. Reagent 1: compounds of the formula (II)  . Reagent 2: piperidine derivatives of the formula (III)
. Reagent 2: piperidine derivatives of the formula (III)  . Method involves optional stages of carboxy-protective groups removing and/or synthesis of compounds of the formula (I)
. Method involves optional stages of carboxy-protective groups removing and/or synthesis of compounds of the formula (I)  where R2 means amidated carboxy (lower) alkyl. Synthesized compounds are adenosine antagonists. ???EFFECT: improved method of synthesis. 6 cl
 where R2 means amidated carboxy (lower) alkyl. Synthesized compounds are adenosine antagonists. ???EFFECT: improved method of synthesis. 6 cl
| Title | Year | Author | Number | 
|---|---|---|---|
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 | RU2007403C1 | 
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 | SU1795971A3 | 
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 | RU2073683C1 | 
| METHOD OF SYNTHESIS OF CEPHEM COMPOUNDS OR THEIR ACID-ADDITIVE SALTS | 1988 | 
 | RU2017744C1 | 
| DERIVATIVES OF INDOLYLPYPERIDINE OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS | 1991 | 
 | RU2039056C1 | 
| CEPHEM COMPOUND OR ITS PHARMACEUTICALLY ACCEPTABLE SALT | 1992 | 
 | RU2024530C1 | 
| ANTIBIOTIC COMPOSITION | 1988 | 
 | RU2029549C1 | 
Authors
Dates
1996-11-27—Published
1992-04-09—Filed