Process for the synthesis of amphetamine derivatives
View Patent ↗The invention relates to processes for preparing acylated amphetamine, methamphetamine and dexamphetamine derivatives by reacting the parent amine with the to be-coupled acid or a salt of the to-be coupled acid which acid is optionally protected, in the presence of an alkylphosphonic acid anhydride as coupling agent and, if the acid was protected then cleaving the protecting group(s), in a one-pot reaction or in two or more separate steps.
1. A process for preparing acylated amphetamine, methamphetamine and dexamphetamine derivatives (V4 or V4a) or its salt comprising reacting
a parent amine (V1) with
a to be coupled acid (V2) or a salt of the to be coupled acid (V2), said acid (V2) further being optionally protected by protecting group(s)
in the presence of an alkylphosphonic acid anhydride (V3) as coupling agent and
cleaving the protecting group(s) if the acid (V2) was protected,
said process being performed in a one-pot reaction or in two or more separate steps according to the following equation 1:
wherein n and the radicals R1 to R5 have the following meaning:
R1 is benzyl, mono-, di-, tri-lower-alkyl-substituted phenylmethyl, mono-, di- or tri-lower-alkoxy-substituted phenylmethyl,
R2 is lower alkyl
R3 is H or lower alkyl
R4 is an amino acid radical or an amino acid radical wherein at least one amino group is protected with a protecting group, or is a substituted alkyl group different from the amino acid radical
R5 is C1-C8-alkyl
n is a number ranging from either 3 to 5 if (V3) is a cyclic anhydride or 3 to 1000 if (V3) is an open-chain oligomer, including if (V3) is a mixtures of different open-chain and/or cyclic anhydrides.
2. The process as claimed in claim 1 , wherein the alkylphosphonic acid anhydride (V3) is a cyclic trimer of iso- and/or n-propylphosphonic acid anhydride or is an open-chain oligo- or polymer or is a mixture of cyclic and open-chain compounds.
3. The process as claimed in claim 1 , wherein the alkylphosphonic acid anhydride (V3) is a cyclic trimer of n-propylphosphonic acid.
4. The process as claimed in claim 1 , wherein the alkylphosphonic acid anhydride is optionally added in solution in a non-reactive solvent.
5. The process as claimed in claim 1 , wherein said process is performed in a one-pot reaction.
6. The process as claimed in claim 1 , wherein said process is performed in two or more separate steps.
7. The process as claimed in claim 1 , said process further comprising performing the reaction at temperatures in the range of −20° C. to +80° C.
8. The process as claimed in claim 1 , said process further comprising performing the reaction in the presence of a base.
9. The process as claimed in claim 1 , wherein said process has a yield of >90%.
10. The process as claimed in claim 1 , wherein (V4) or (V4a) has a purity of >98.0%.
11. The process as claimed in claim 1 , wherein said process has an ee loss of <1.0%.
12. The process as claimed in claim 1 , wherein (V4) or (V4a) is Lisdexamphetamine or a salt of Lisdexamphetamine, (V2) is N-protected Lysine and (V1) is Dexamphetamine.