FIELD: medicine, pharmaceutics.
SUBSTANCE: invention relates to pharmacology and organic chemistry and deals with novel quaternary ammonium derivative of Novocain of formula which possesses anti-arrhythmic activity, and method of its obtaining by interaction of Novocain base with bromide allyl in medium of isopropyl alcohol at temperature 57-63°C, holding at said temperature during 5-6 hours with following cooling of reaction mixture to room temperature and separation of N-allyl-N-(2-oxiethylcarboxy-4-aminophenyl)-diethylamine of bromide.
EFFECT: compound possesses useful biological properties.
2 cl, 2 tbl
Title | Year | Author | Number |
---|---|---|---|
QUATERNARY AMMONIUM DERIVATIVE OF LIDOCAINE ELICITING ANTI-ARRHYTHMIC ACTIVITY AND METHOD FOR ITS PREPARING | 2004 |
|
RU2258700C1 |
10-BR-N(4) PROPYLIMALINIUM BENZENESULFONATE HAVING ANTIARRHYTUMEL ACTIVITY | 1995 |
|
RU2083578C1 |
COMPOUND OF NIBENTANE AND AMINO ACID POSSESSING ANTIARHYTHMIC ACTIVITY AND METHOD FOR PRODUCING IT | 2014 |
|
RU2572710C1 |
PHARMACEUTICAL COMPOSITION POSSESSING PROLONGED ANTIARRHYTHMIC ACTIVITY | 2012 |
|
RU2538674C2 |
APPLICATION OF GLUTARIC ACID DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS AS ANTIARRHYTHMIC DRUG | 2008 |
|
RU2373934C1 |
COMPOSITION OF AMINO ACIDS WITH TRACE ELEMENTS ELICITING ANTIARRHYTHMIC ACTIVITY | 1999 |
|
RU2173553C2 |
SALTS OF MESIDIDES OF ALPHA-PIPERIDINCARBOXYLIC ACIDS POSSESSING LOCALLYANESTHETIC, ANTIARYTHMIC AND ANTIFIBRILLATORY ACTIVITY AND MESIDIDES OF ALPHA-PUPERIDINCARBOXYLIC ACIDS AS INTERMEDIATE PRODUCTS FOR SYNTHESIS OF SALTS OF MESIDIDES OF PIPERIDINCARBOXYLIC ACIDS | 0 |
|
SU1120654A1 |
DERIVATIVE OF 4-HYDROXYBUTYRIC ACID BENZYLAMIDE SHOWING LOCAL ANESTHETIC, ANTIARRHYTHMIC, ANTIANGIAL AND ANTINECROTIC ACTIVITY | 1988 |
|
SU1601984A1 |
DERIVATIVES OF AMINO ACIDS SHOWING ANTIARRHYTHMIC ACTIVITY | 1999 |
|
RU2164512C1 |
N-[2-(ADAMANT-2-YL)AMINOCARBONYLMETHYL]-N'-(DIALKYLAMINO)ALKYLNITROBENZAMIDES POSSESSING ANTIARHYTHMIC ACTIVITY | 2013 |
|
RU2547096C2 |
Authors
Dates
2011-03-27—Published
2009-11-11—Filed