Stable amorphous form of sacubitril valsartan trisodium complex and processes for preparation thereof

Patent metadata

Field	Value
Publication number	US-11318116-B2
Application number	US-202017028495-A
Country	US
Kind code	B2
Filing date	Sep 22, 2020
Priority date	Oct 10, 2016
Publication date	May 3, 2022
Grant date	May 3, 2022

Abstract

The present invention relates to stable amorphous form of sacubitril valsartan trisodium complex and its solid dispersion compounds, processes for their preparation and pharmaceutical composition comprising the same. The present invention also relates to an improved process for the preparation of sacubitril sodium and its use in the preparation of sacubitril valsartan trisodium complex.

First claim

We claim:

1. A process for preparation of sacubitril sodium salt of Formula II,

comprising:
a) reacting a compound of Formula III with a suitable halogen source in presence of ethanol and a suitable non-polar solvent to obtain a compound of Formula IV or its acid addition salt thereof,

b) treating the compound of Formula IV or its acid addition salt with succinic anhydride in presence of a base to obtain sacubitril of Formula V,

and
c) treating the sacubitril of Formula V with a suitable sodium source to obtain the sacubitril sodium of Formula II.

2. The process of claim 1 , wherein the suitable halogen source is selected from the group consisting of thionyl chloride, oxalyl chloride, phosgene or acetyl chloride.

3. The process of claim 1 , wherein the suitable non-polar solvent is selected from the group consisting of cyclohexane, heptane, hexane, dichloromethane, toluene; and mixtures thereof.

4. The process of claim 1 , wherein the step a) reaction is carried out with thionyl chloride in presence of ethanol and cyclohexane.

5. The process of claim 1 , wherein base is selected from the group consisting of diethylamine, triethylamine, diisopropylamine, diisopropylethylamine, pyridine, piperidine, morpholine or DBU.

6. The process of claim 1 , wherein the base is added in a lot wise manner.

7. The process of claim 1 , wherein the step b) is carried out in a solvent selected from the group consisting of dichloromethane, dimethylformamide, dimethylacetamide, dimethylsulfoxide, N-methylpyrrolidone, acetonitrile, tetrahydrofuran or 2-methyltetrahydrofuran.

8. The process of claim 1 , wherein the sodium source is selected from the group consisting of sodium carbonate, sodium bicarbonate or sodium 2-ethyl hexanoate.

9. The process of claim 1 , further comprising:
d) purifying the sacubitril sodium of Formula II obtained in step c), comprising:
i) dissolving sacubitril sodium salt of Formula II in one or more solvents;
ii) optionally adding an antisolvent to the step i) reaction mixture or vice-versa; and
iii) isolating the pure sacubitril sodium salt of Formula II.

10. The process of claim 9 , wherein the one or more solvents are selected from ketones, esters, halogenated hydrocarbons and mixtures thereof.

11. The process of claim 10 , wherein the one or more solvents are selected from the group consisting of acetone, methyl isobutyl ketone, methyl ethyl ketone, methyl acetate, ethyl acetate, isopropyl acetate, n-propyl acetate, n-butyl acetate, t-butyl acetate, dichloromethane, dichloroethane, chloroform and mixtures thereof.

12. The process of claim 9 , further comprises adding an antisolvent to the step i) solution selected from the group consisting of toluene, xylene, n-hexane, n-heptane, cyclohexane, cycloheptane, tetrahydrofuran, dimethyl ether, diisopropyl ether, methyl tertiary butyl ether, 1,4-dioxane and mixtures thereof.

13. The process of claim 9 , wherein the solvent of step i) is methyl ethyl ketone and the anti solvent of step ii) is n-heptane.

14. The process of claim 1 , further comprising:
preparing a pharmaceutical composition by combining the sacubitril sodium of Formula II with at least one pharmaceutically acceptable excipient.

Assignees

• Laurus Labs Ltd

Inventors

• Bollu Ravindra Babu
• Thaimattam Ram
• Challagonda Venkateswar Rao
• Yasam Sivarami Reddy
• Seethamraju Pavan Kumar
• Vasireddi Uma Maheswar Rao

Classifications

• C07B2200/13

  Crystalline forms, e.g. polymorphs · CPC title

• A61K31/41 Primary

  having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole · CPC title

• A61K31/216 Primary

  of acids having aromatic rings, e.g. benactizyne, clofibrate · CPC title

• C07C233/47

  having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton · CPC title

• A61K47/38

  Cellulose; Derivatives thereof · CPC title