Process for preparing ethyl (S)-2-ethoxy-4-[N-[1-(2-piperidinophenyl)-3-methyl-1-butyl]aminocarbonyl methyl]benzoate and use thereof for the preparation of Repaglinide
Described herein is an improved, commercially viable and industrially advantageous process for the preparation of Repaglinide intermediate, ethyl (S)-2-ethoxy-4-[N-(1-(2-piperidino-phenyl)-3-methyl-1-butyl)-aminocarbonylmethyl]-benzoate. The process provides the Repaglinide intermediate in higher yield and purity compared to the previously disclosed processes, thereby providing for production of Repaglinide and its pharmaceutically acceptable salts in high purity and in high yield.
1. A process for preparation of Repaglinide intermediate of formula I:
or an acid addition salt thereof, wherein the R is a protecting group, comprising:
reacting (S)-3-methyl-1-(2-piperidinophenyl)-1-butylamine of formula II:
or a salt thereof with a protected carboxylic acid of formula III:
in the presence of a dehydrating agent and a suitable solvent to produce the compound of formula I;
and optionally converting the compound of formula I into its acid addition salts thereof;
wherein the dehydrating agent is an aryl or a substituted aryl boronic acid; and
wherein R is a protecting group.
2. The process of claim 1 , wherein the aryl or substituted aryl boronic acid is selected from the group consisting of phenylboronic acid, 2-chlorophenylboronic acid, 2-nitrophenyl boronic acid, 3-nitrophenylboronic acid, 4-nitrophenylboronic acid, 2-carboxyphenyl boronic acid, 2-chloro-4-carboxyphenylboronic acid, 2-chloro-5-carboxyphenylboronic acid, 3-chloro-4-carboxyphenylboronic acid, 2-chloro4-fluorophenylboronic acid, 4-chloro-2-fluorophenylboronic acid, 2-chloro-4-methylphenylboronic acid, 2-chloro-5-methylphenylboronic acid, 2-chloro-3-methylpyridine-5-boronic acid, and naphthyl boronic acid.
3. The process of claim 1 , wherein the solvent is selected from the group consisting of toluene, benzene, xylene, acetone, methyl isobutyl ketone, tetrahydrofuran, dioxane, acetonitrile, hexane, heptane, cyclohexane, methylene chloride, dimethylformamide, and mixtures thereof.
4. The process of claim 3 , wherein the solvent is toluene, methylene chloride, tetrahydrofuran, acetonitrile, or dimethylformamide.
5. The process of claim 4 , wherein the solvent is toluene.
6. The process of claim 1 , wherein the protecting group R is methyl, ethyl, tert-butyl, benzyl, p-nitrobenzyl, or p-methoxybenzyl.
7. The process of claim 6 , wherein the protecting group R is ethyl.
8. The process of claim 1 , wherein the reaction is carried out at a temperature of −25° C. to a reflux temperature of the solvent.
9. The process of claim 1 , wherein the dehydrating agent is used in a molar ratio of 0.005 to 1.0 moles relative to 1 mole of the (S)-3-methyl-1-(2-piperidinophenyl)-1-butylamine of formula II.
10. The process of claim 9 , wherein the dehydrating agent is used in a molar ratio of 0.1 to 0.2 moles relative to 1 mole of (S)-3-methyl-1-(2-piperidinophenyl)-1-butylamine of formula II.
11. The process of claim 1 , wherein the compound of formula I obtained has a purity of greater than 99% as measured by HPLC.
12. The process of claim 11 , wherein the compound of formula I obtained has a purity of greater than 99.9% as measured by HPLC.