Method for producing salts of tolperisone
The invention relates to a method for producing an addition salt of 2,4′-dimethyl-3-piperidino-propiophenone (tolperisone) with a pharmaceutically acceptable acid, of formula (I). According to the invention, 4-methylpropiophenone is reacted with piperidine hydrochloride and 1,2-dioxolane in the presence of an acid serving as a catalyst, and the tolperisone obtained in the form of an acid addition salt is separated by filtering after the reaction mixture has cooled down
1. A method for manufacturing pharmaceutically acceptable acid addition salts of 2,4′-dimethyl-3-piperidinopropiophenone (tolperisone), of formula (A)
said acid addition salts having a formula (B)
comprising reacting 4-methylpropiophenone of the formula
with piperidine hydrochloride of the formula
and 1,2-dioxolane of the formula
in the presence of a catalytic amount of an acid, wherein tolperisone is separated as an acid addition salt in accordance with the general formula (B) after cooling the reaction mixture by addition of ethyl acetate and tert-butylmethylether to cause precipitation.
2. A method according to claim 1 , wherein the acid is an inorganic acid.
3. A method according to claim 1 , wherein the acid is aqueous hydrochloric acid.
4. A method according to claim 1 , wherein the reaction is carried out in a solvent.
5. A method according to claim 4 , wherein the reaction is accomplished in 1,2-dioxolane as a solvent in a concentration range from 1 to 6 mol/lit.
6. A method according to claim 5 , wherein the reaction is accomplished in 1,2-dioxolane as a solvent at a concentration of 3.6 mol/lit.