NZ533859A - Improved process for preparation of gabapentin - Google Patents

Abstract

Disclosed is a process of producing gabapentin, comprising: (i) providing an aqueous alkaline solution of gabapentin hydrochloride salt and reacting with sulphuric acid followed by neutralising with inorganic bases, (ii) filtration of inorganic salts and distillation to obtain a resultant solid, (iii) dissolving the resultant solid of (ii) above in a protic solvent, filtering to removing traces of inorganic salts followed by distillation of the resulting solvent to obtain a residue, (iv) adding another solvent to the residue and isolating gabapentin therefrom by filtration.

Description

New Zealand Paient Spedficaiion for Paient Number 533859 533 859 1 IMPROVED PROCESS FOR PREPARATION OF GABAPENTIN FIELD OF THE INVENTION The present invention relates to a process for producing Gabapentin, l-(aminomethyl)-l-cyclohexaneacetic acid from Gabapentin hydrochloride salt. The process is directed to improvement in the manufacture of Gabapentin which would be industrially feasible and 5 facilitate simple and cost-effective manufacture of Gabapentin. Gabapentin obtained following the process of the invention is suitable as a drug especially in the treatment of cerebral diseases such as epilepsy.

BACKGROUND OF THE INVENTION Gabapentin, l-(aminomethyl)-l-cyclohexaneacetic acid is known to have the chemical structure as hereunder: Gabapentin is used in the treatment of cerebral diseases such as epilepsy. There are various methods presently known for preparing Gabapentin from a variety of starting materials. U.S. Patent 4,024,175 describes at least three methods of preparing Gabapentin from cyclohexyl- 1,1-diacetic acid. Each of these methods results in the formation of Gabapentin hydrochloride salt, which may be converted to l-(aminomethyl)- 1-cyclohexaneacetic acid by treatment with a basic ion exchanger and then crystallized from a solvent such as ethanol/ether.

U.S. Patent 4,894,476 specifically discloses an improved method for converting the hydrochloride salt into the free amino acid. This involves pouring a deionized water solution of the salt over an ion exchange column, eluting with deionized water, producing a slurry Fig-1 WO 2004/04608-1 2 from the elute, adding an alcohol to the slurry, centrifiiging and drying the slurry to obtain the free amino acid.

Alternative methods for preparing Gabapentin have been described that do not proceed via 5 the hydrochloride or any other mineral acid salt. Such methods include those described in U.S. Patent Nos. 5,132,451, 5,095,148, 5,068,413. Each of these methods involve a cyanic intermediate which is hydrogenated under severe conditions to produce the free amino acid.

These methods are industrially impractical. Those methods comprising ion exchange 10 columns require the use of large amounts of ion exchanger for lengthy periods of time to lower the level of chloride ions to the desired level. The alternative methods involve further more demanding steps.

WO 98/28255 describes the preparation of Gabapentin from Gabapentin hydrochloride 15 through optional pre-treatment to remove inorganic salts and then by treating suitable organic amines like triethylamine, tributylamine, tripropylamine, trihexylamine, diethylamine, ethanolamine and benzylamine. Preferably the amine is tributylamine.

OBJECTS OF THE INVENTION It is thus the basic object of the present invention to provide a process of producing Gabapentin which would be simple and avoid the aforediscussed problems of the known art.

Another object of the present invention is directed to a process for the manufacture of Gabapentin from Gabapentin hydrochloride salt which would avoid severe conditions and/or 25 complexities and can be readily adopted for industrial application.

Yet further object of the present invention is directed to provide a method of manufacture of Gabapentin which would have good yield and not involve lengthy extended process steps.

Yet another object of the present invention is to provide a method of manufacture of Gabapentin which would be cost-effective and can be carried out involving simple and readily available ingredients starting material.

WO 2004/046084 PCT/IN2002/000221 SUMMARY OF THE INVENTION Thus according to the present invention there is provided a process of producing Gabapentin comprising: i) providing an aqueous alkaline solution of Gabapentin Hydrochloride salt and 5 reacting with Sulfuric acid followed by neutralizing with inorganic base; ii) filtration of inorganic salts and distillation to obtain a resultant solid ; iii) dissolving the said resultant solid of (ii) above in an protic solvent, filtering to remove further inorganic salts followed by distillation of the resulting solvent to obtained a residue; iv) adding another solvent to said residue and isolating Gabapentin therefrom by filtration.

In the above process the inorganic bases can be selected from metal hydroxide or carbonate of Ha of periodic table preferably barium hydroxide.

The alkali used in the process can be selected from such as Sodium hydroxide, Potassium hydroxide, Calcium hydroxide and alkali metal hydroxides, carbonates.

The first solvents employed can be selected from Methanol, Acetonitrile, Isopropyl alcohol, 20 acetone.

The 'sccond' solvent can be selected from Isopropanol, acetone, Methanol, Acetonitrile, Dimethylformamide, Ethyl Acetate, Diisopropylether, Methylene choride.

The above process of the present invention provide an improved, industrially feasible method for preparing Gabapentin from Gabapentin hydrochloride. The process avoids the disadvantages associated with prior art methods and selectively employs the inorganic bases to convert Gabapentin hydrochloride to Gabapentin. Gabapentin hydrochloride used in the process can be prepared by the method known in prior art such as US Patent No. 4152326 30 (1979). 4 DETAILED DESCRIPTION OF THE INVENTION : In accordance with a preferred aspect the process of the invention comprises: (1) mixing aqueous solution of the Gabapentin hydrochloride with alkali; (2) filtration to separate solid and heating with dil. Sulfuric acid followed by pH 5 adjustment to neutral with inorganic bases at 30 - 80°C. (3) filtration of inorganic salts in particular sulfate and concentration of filtrate under vacuum. (4) redissolving the resultant solid in protic solvent (first solvent). (5) filtration of traces of inorganic salt in particular sulfate salts if any. 10 (6) concentration of protic solvent to dryness. (7) addition of second solvent and isolation of Gabapentin by filtration.

Thus the initial critical stages of the process of the present invention comprises of mixing of an aqueous solution of Gabapentin hydrochloride with alkali metal hydroxide or carbonate 15 solutions. Filtration of separated solids and reacting with dil. Sulfuric acid and then adjusting pH to neutral with inorganic base.

The subsequent critical steps of the process is the removal of water by distillation from the filtrate after filtration of corresponding sulfate salt. The water may be distilled off at 20 atmospheric pressure or under vacuum. The next step involves the addition of protic solvent (first solvent) to dissolve Gabapentin and filtration of traces of, if any, corresponding sulfate salt. In the next step the solvent from the filtrate is removed and addition of 'second' solvent and filtration of Gabapentin. The solvent may be distilled at atmospheric pressure or under vacuum.

Preferably, the Gabapentin hydrochloride salt is used as a solution in water in concentration ranging from 10 to 40%, more preferably 33%.

The inorganic bases are preferably used as solid and/or as aqueous solution of concentration 30 5 to 15% more preferably 10%.

The temperature of neutralization is selected from RT 30°C to 80°C preferably 40°C. the final pH of the neutralization is about 5 to 8 preferably 7.

The process of the invention, its objects and advantages are explained hereunder in greater 5 detail by way of the non-limiting exemplary illustrations of the process as discussed hereunder: Example 1 : Gabapentin hydrochloride (10 g.) was dissolved in water 30 ml. and heated to 40-60°C. To this solution was added Sodium hydroxide to pH 9.0 to 14.0 and the reaction mixture heated 10 at 40-60°C for 3 to 6 hrs. The reaction mass is cooled to 5-10°C and maintained at this temperature for 6 hrs. The separated solid is filtered and added to dil. Sulfuric acid 30 ml. (5 ml. Sulfuric acid diluted to 30 ml. with water).

The reaction mixture heated under reflux for 12 hrs. and then cooled to 30°C. The pH of the 15 solution was adjusted to 7.0 to 7.5 with barium hydroxide suspension in water. The separated barium sulfate is filtered off and wash with water 10 ml. The filtrate is concentrated to dryness under vacuum. Methanol (120 ml.) added to the residue and then clear solution is filtered through Celite. Methanol is recovered under vacuum at below 50°C. The product remained was treated with Iso-propanol (50 ml.), stirred of 30 min. at RT and 20 filtered off. The product obtained is dried till content weight of 6.7 g.

Examples 2-9 : The method of Example 1 was followed using different solvents shown in Tablel alongwith percentage yield (w/w) TABLE -1 Example No.

First Solvent Second Solvent Yield (w/w) % 2 Methanol Methanol 55 3 Methanol IPA 67 4 Methanol Acetone 65 Methanol Acetonitrile 52 6 Acetonitrile Methanol 53 7 Acetonitrile IPA 64 8 Acetonitrile Acetone 65 9 Acetonitrile Acetonitrile 51

Claims (18)

WO 2004/046084 PCT/IN2002/000221 6 Importantly, the various options of the first and second solvents tried as above in accordance with the process of the invention have demonstrated good yield by way of a simple and cost effective process. The above exemplary illustrations also demonstrate the simplicity on the process and the possible avoiding of complexity involved in manufacture of Gabapentin from Gabapentin hydrochloride salt. The process is industrially viable and should serve in wide-scale manufacture of Gabapentin especially for its drug/medicinal applications/end uses. 7 CLAIMS

1. A process of producing gabapentin comprising : i) providing an aqueous alkaline solution of gabapentin hydrochloride salt and reacting with sulfuric acid followed by neutralizing with inorganic bases; ii) filtration of inorganic salts and distillation to obtain a resultant solid ; iii) dissolving the said resultant solid of (ii) above in a protic solvent, filtering to removing traces of inorganic salts followed by distillation of the resulting solvent to obtained a residue ; iv) adding another solvent to said residue and isolating gabapentin therefrom by filtration.

2. A process as claimed in claim 1 comprising : (1) mixing aqueous solution of the gabapentin hydrochloride with alkali. (2) filtration to separate solid and heating with dilute sulfuric acid followed by pH adjustment to neutral with inorganic bases at 30 - 80°C. (3) filtration of inorganic salts in particular sulfate and concentration of filtrate under vacuum. (4) redissolving the resultant solid in a protic solvent. (5) filtration of traces of inorganic salt in particular sulfate salt, if any. (6) concentration of protic solvent to dryness. (7) addition of a second sol vent and isolation of gabapentin by filtration.

3. A process as claimed in claim 1 or 2 wherein said alkali used is selected from such as sodium hydroxide, potassium hydroxide, calcium hydroxide and alkali metal hydroxides, carbonates.

4. A process as claimed in anyone of claims 1 to 3 wherein the inorganic bases are selected from metal hydroxide or carbonate of Ha of periodic table. 8

5. A process as claimed in anyone of claims 1 to 4 wherein the gabapentin salts are used as a solution in water in concentration ranging from 10 to 40%.

6. A process as claimed in claim 5 wherein the concentration of the aqueous solution is 33%.

7. The process as claimed in anyone of claims 1 to 6 wherein the inorganic base used is preferably barium hydroxide.

8. The process as claimed in anyone of claims 1 to 7 wherein the inorganic bases axe used as solid and/or as aqueous solutions of concentration 5 to 15%.

9. The process as claimed in claim 8 wherein the inorganic bases are used as solid and/or as aqueous solution of concentration of the solution of inorganic base is 10%.

10. The process as claimed in anyone of claims 1 to 9 wherein the temperature of neutralization is maintained between 30°C to 80°C.

11. The process as claimed in claim 10 wherein the temperature of neutralisation is maintained at 40°C.

12. The process as claimed in anyone of claims 1 to 11 wherein the final pH of the neutralisation is 5 to 8.

13. The process as claimed in claim 12 wherein the final pH of the neutralisation is 7.

14. The process as claimed in anyone of claims 1 to 13 wherein the protic solvent is selected from the group consisting of methanol, acetonitrile, isopropyl alcohol, ac etone.

15. The process as claimed in claim 14 wherein the protic solvent is methanol. Intellectual Property Office of NZ :: 2004 9

16. The process as claimed in anyone of claims 1 to 15, wherein the second solvent is selected from the group consisting of isopropanol, acetone, methanol, acetonitrile. dimethylformamide, ethyl acetate, diisopropylether, methylene chloride.

17. The process as claimed in claim 16, wherein the second solvent is preferably isopropanol.

18. A process of producing gabapentin substantially as herein described and illustrated with reference to the accompanying examples.