Method for producing 3-amidinophenylalanine derivatives
View Patent ↗The present invention describes a method for the synthesis of enantiomerically pure 3-amidinophenylalanine derivatives, which are used as pharmaceutically effective urokinase inhibitors, by starting from 3-cyanophenylalanine derivatives. The methods of manufacture comprising only one synthesis step lead to new intermediates, namely 3-hydroxyamidino- and 3-amidrazonophenylalanine derivatives. These intermediates or their acetyl derivatives can be reduced into the desired 3-amidinophenylalanine derivatives under gentle conditions (H 2 or ammonium formiate, Pd/C (approx. 10%), ethanol/water, room temperature, normal pressure or also H 2 , Pd/C, AcOH or HOI/ethanol, 1–3 bar) in excellent yields and in an enantiomeric excess of up to 99.9%.
1. A method of synthesizing 3-hydroxyamidino-phenylalanine derivatives of formula (IIa)
which are present as:
L- or D-enantiomers,
(E)- or (Z)-isomers,
or (E/Z)-mixtures
and as free bases or salts thereof formed with acids, wherein R 1 is:
(a) a group of formula
wherein R 3 is selected from the group consisting of methoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, dimethylaminocarbonyl, acetyl, and propionyl,
comprising the reaction of a nitrile of general formula (III)
wherein R 1 is as defined above,
with hydroxylamine hydrochloride in the presence of sodium carbonate in alcoholic-aqueous solution at reflux temperature.
2. The method of claim 1 , wherein the reaction of the nitrile of general formula III occurs at room temperature with hydroxylamine hydrochloride in the presence of triethylamine in alcoholic solution, said alcoholic solution optionally containing an additional organic solvent.
3. The method of claim 2 , wherein the additional organic solvent is methylene chloride.
4. The method of claim 1 , wherein a one to 5-fold excess of hydroxylamine hydrochloride is used and the quantity of sodium carbonate amounts to 0.5 to 0.6 mol equivalents relative to the hydroxylamine hydrochloride.
5. The method of claim 1 , wherein the reaction occurs in ethanolic-aqueous solution under reflux.
6. A compound of the formula (IIa)
as (L)- or (D)-enantiomers, and as (E)- or (Z)-isomers or (E/Z)-mixtures, and as free bases or as salts thereof formed with acids, wherein R 1 is a group of formula
wherein R 3 is selected from the group consisting of methoxycarbonyl, ethoxycarbonyl, benzyloxycarbonyl, dimethylaminocarbonyl, acetyl, and propionyl.
7. A compound of formula (IV)
as (L)- or (D)-enantiomers, and as (E)- or (Z)-isomers or (E/Z)-mixtures, and as free bases or as salts thereof formed with acids.