FIELD: chemistry.
SUBSTANCE: invention relates to an improved highly-selective method of producing deserpidine (Ia) through demethylation of 11-methoxy group of 11-O-methyl reserpic acid lactone, with subsequent stages for reduction, hydrolysis and esterification of the obtained methyldeserpidate 3,4,5-trimethoxybenzoic acid. Output is 40%.
EFFECT: method for semisynthesis of deserpidine is described.
6 cl, 7 ex
Title | Year | Author | Number |
---|---|---|---|
DERIVATIVES OF TAXANE FUNCTIONED BY POSITION 14 AND METHOD FOR THEIR PREPARING | 2003 |
|
RU2320652C2 |
METHODS FOR SYNTHESIS OF APLIDINE AND NOVEL ANTI-TUMOR DERIVATIVES, METHODS FOR THEIR INDUSTRIAL PREPARING AND USING | 2001 |
|
RU2299887C2 |
IMIDES AS TNF-ALPHA INHIBITORS | 1994 |
|
RU2174516C2 |
3-HALOGEN-6-(ARYL)-IMINOTETRAHYDROPICOLINATES AND THEIR APPLICATION AS HERBICIDES | 2010 |
|
RU2527954C2 |
NOVEL POLYCYCLIC COMPOUNDS | 2006 |
|
RU2434006C2 |
INHIBITOR COMPOUNDS | 2013 |
|
RU2673079C2 |
METHOD FOR OBTAINING DISPYROINDOLINONES BASED ON 5-INDOLIDENE-2-THIOHIDANTOINES | 2020 |
|
RU2756463C1 |
SEMISYNTHETIC METHOD AND NEW COMPOUNDS | 2000 |
|
RU2237063C9 |
NOVEL OXAZOLIDINONE DERIVATIVES WITH CYCLIC AMIDOXIM OR CYCLIC AMIDRAZONE AND CONTAINING THEM PHARMACEUTICAL COMPOSITIONS | 2009 |
|
RU2468023C1 |
MACROCYCLIC INTEGRASE INHIBITORS | 2011 |
|
RU2567385C2 |
Authors
Dates
2009-11-10—Published
2005-03-02—Filed