Tryptophane and 3-indolepyruvic acid, methods of production therefor
AssigneePolifarma S.p.A.
InventorsVincenzo Politi, Giovanna De Luca, Giovanni Di Stazio, Mario Materazzi
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Abstract
3-indolepyruvic acid derivatives substituted on the benzene moiety show good antagonizing activity on excitatory aminoacids and on free radicals, for which reason they are therapeutic agents in cerebral and peripheral degenerative pathologies. Their method of production by passage through the corresponding substituted triptophane.
Claims7
A process for the production of 3-indolepyruvic acid derivatives substituted on the benzene moiety, represented by formula I ##STR6## in which X is selected from the group consisting of hydrogen, halogen, methyl, methoxy and hydroxyl, comprising steps of:
- transforming a substituted indole of the formula ##STR7## in which X is selected from the group consisting of hydrogen, halogen, methyl, methoxy and hydroxyl, into the corresponding substituted tryptophan by reacting the substituted indole with methylamine and formaldehyde in an aqueous solution, at a temperature not greater than about 5.degree. C. to obtain the corresponding substituted gramine, then condensing said substituted gramine in a catalytic alkaline environment, in a per se known manner, with a derivative of malonic structure to obtain the corresponding substituted tryptophan, and transforming said substituted tryptophan into the corresponding substituted 3-indolepyruvic acid.
A process for the production of 3-indolepyruvic acid derivatives, substituted on the benzene moiety, represented by formula I ##STR8## in which X is a substituent chosen from the group consisting of hydrogen, halogen, methyl, methoxy and hydroxyl, comprising the steps of:
- (a) reacting in a condensation reaction a substituted indole of the formula ##STR9## in which X is a substituent as defined for formula I, with a lower alkyl ester oxime of 3-bromo-pyruvic acid, having the structural formula ##STR10## wherein R1 is a lower alkyl substituent, in a basic environment to obtain a lower alkyl-3-(substituted indole-3-yl)-2 hydroxylimine propionate as an intermediate compound having the structural formula ##STR11## (b) reacting said intermediate compound in an aqueous solution containing TiCl.sub.3 as a reducing agent to obtain a substituted tryptophan having the structural formula ##STR12## and (c) transforming said substituted tryptophan into the 3-indole pyruvic acid of formula I by reaction with an aromatic aldehyde in the presence of a basic, dehydrating proton acceptor agent in a solvent.
A process for the production of 3-indolepyruvic acid derivatives substituted on the benzene moiety, represented by formula I ##STR13## in which X is a substituent chosen from the group consisting of hydrogen, halogen, methyl, methoxy and hydroxyl, comprising the steps of:
- (a) reacting in a condensation reaction a substituted indole of the formula ##STR14## in which X is a substituent as defined for formula I, with a lower alkyl ester oxime of 3-bromo-pyruvic acid, having the structural formula ##STR15## wherein R1 is a lower alkyl substituent, in a basic environment to obtain a lower alkyl-3-(substituted indole-3-yl)-2 hydroxylimine propionate as an intermediate compound having the structural formula ##STR16## (b) reacting said intermediate compound in a buffered aqueous solution containing sodium hypophosphite as a hydrogenating agent, in the presence of a Raney-Nickel catalyst to obtain the substituted 3-indolepyruvic acid of formula I.
Dependencies are inferred from the claim text.