Method for the purification of lansoprazole

A METHOD FOR THE PURIFICATION OF LANSOPRAZOLE

FIELD OF THE INVENTION

The present invention relates to a method for preparing a substantially pure 2-(2pyridylmethyl) sulfinyl-lLf-benzimidazole (lansoprazole) that is free of sulfone and sulfide derivatives.

BACKGROUND OF THE INVENTION

Several substituted 2-(2-pyridylmethyl) sulfinyl-!//-benzimidazole derivatives are wellknown gastric proton pump inhibitors. These benzimidazole derivatives include lansoprazole, omeprazole, pantoprazole, and rabeprazole. This class of benzimidazole derivatives is generally represented by the following chemical formula A:

<img file="IL166985A_D0001.tif" />

U.S. Pat. No. 4,628,098 describes the generic lansoprazole compound. Lansoprazole has as its chemical name (2-[[[3-methyl-4-(2,2,2-trifluoro-ethoxy)-2-pyridinyl]methyl]sulfinyl]-l/fbenzimidazole), i.e., when R1 is methyl, R2 is trifluoroethoxy, R3 is hydrogen and R4 is hydrogen.

As a characteristic shared with other benzimidazole derivatives (e.g., ompeprazole and pantoprazole), lansoprazole can inhibit gastric acid secretion, and thus commonly used as an antiulcer agent.

Several methods for preparing lansoprazole are known. The majority of these methods involve the use of a lansoprazole precursor that contains a thioether group. The thioether group is oxidized in the last step of preparation to form the lansoprazole.

U.S. Pat. Nos. 4,628,098 and 5,578,732 (the ‘732 patent) describe the oxidation of the thioether group using m-chloro-perbenzoic acid as the oxidizing agent. However, the use of m-chloro-perbenzoic acid often results in a non-selective oxidation of the thioether group. The ‘732 patent further describes an oxidation method with hydrogen peroxide (HjO2) in the presence of a specific vanadium catalyst. Other patents such as ES 2105953, WO 0121617, ES 2063705, U.S. Pat No. 6,313,303, WO9947514, WO0168594 describe the use of other oxidation reagents and/or other catalysts. None of these oxidation methods result in selective oxidation of the thioether group.

In addition, the preparation of lansoprazole by conventional methods is always accompanied by the formation of small quantities of the corresponding sulfone derivative as an impurity. For example, U.S. Pat. No. 6,180,652 (the‘652 patent) describes the presence of sulfone derivative. Formation of sulfone derivative brings about the drawback of low yield of the desired sulfoxide.

Although attempts have been made to separate the sulfone derivative from lansoprazole, it is not a simple task, given their very similar structures and physicochemical properties. For this purpose, the ‘652 patent describes a method which permits separation of lansprazole from its sulfone derivative. An acetone complex of the lansoprazole salt is purified in this method.

Lansoprazole and other 2-(2-pyridylmethyl) sulfinyl-benzimidazole derivatives tend to lose stability and undergo decomposition when contaminated with traces of a solvent, particularly water, in their crystal structure. It is desirable that the benzimidazole crystals be solvent free (i.e., residual solvent should be reduced to a minimum).

The ’732 patent describes the crystallization of lansoprazole using a ethanol :water solvent system (vol:vol of ethanokwater is 9:1). U.S. Pat No. 6,002,011 (the ’011 patent) describes the crystallization of lansoprazole from the same ethanokwater system, containing traces of ammonia (0.03 mole NH4OH: 1 mole lansoprazole). The ’011 patent discloses a reslurry method in water, which permits to obtain more stable solvent free lansoprazole. The ’011 patent fails to disclose the level of purity for lansoprazole. In addition, the ethanol and water are difficult to eliminate. Even after intensive drying, lansoprazole still contains solvent and is unstable under storage.

There is continuing need to obtain 2-(2-pyridylmethyl) sulfinyl-1/Z-benzimidazoles (e.g., lansoprazole) that are free of contaminants including sulfone and sulfide derivatives. There has also been a long-felt need for a method to prepare 2-(2-pyridylmethyl) sulfinyl1/7-benzimidazoles (e.g., lansoprazole) having reduced water content (&lt;0.1% wt/wt water).

We discovered that solvent free lansoprazole can be obtained by the crystallization from different solvents. Lansoprazole obtained by this method of crystallization can be dried to &lt;0.1% water, as is required by the USP forum.

SUMMARY OF THE INVENTION

In one aspect, the present invention provides a method of purifying lansoprazole, especially to 0.20% impurities or less, which method includes the steps of: providing a solution of lansoprazole in a solvent selected from an organic solvent, especially an alcohol (especially ethanol), acetone, 2-butanone, dimethyl-formamide and tetrahydrofuran, or a mixture of organic solvent and water in the presence of an amine compound, especially ammonia, ammonium hydroxide, diethyl amine, triethyl amine, or methyl amine; combining the provided solution with an acid, especially acetic acid, formic acid, or hydrochloric acid; and isolating the purified lansoprazole, wherein the ratio of amine compound to lansoprazole is between 17:1 and 1:1 (mol/mol).

Preferably the process of the present invention provides lansoprazole having less than

0.20 wt־% impurities, especially when the water content is 0.1% by wt or less.

Preferably the process of the present invention provides lansoprazole having less than

0.20 wt-% combined sulfide and sulfone derivatives, especially when the water content is 0.1 wt-% or less.

Preferably the process of the present invention provides lansoprazole having less than 0.10% wt-% of either sulfone or sulfide derivative, especially in combination with a water content of 0.1 wt-% or less.

DETAILED DESCRIPTION OF THE INVENTION

As used herein LNPS refers to the sulfide-containing starting compound for lansoprazole preparation. The chemical name for LNPS is 2-[[3-methyl-4-(2,2,2-trifluoroethoxy)-2 pyridinyl]thio]-l//-benzimidazole. LNP refers to lansoprazole which has the chemical name of 2[[3-methyl-4-(2,2,2-trifluoroethoxy)-2- pyridinyl]methyl]sulfinyl-lE/-bensimidazole. The present invention provides a substantially pure lansoprazole ie. lansoprazole containing less than 0.2 wt-% impurities, preferably less than 0.2 wt-% combined sulfide and sulfone impurities. Substantially pure lansoprazole preferably contains less than about 0.10% (wt/wt) sulfone derivative and less than about 0.10% sulfide derivative.

Water is not considered an impurity per se, but its presence in lansoprazole is undesirable. The present invention also provides lansoprazole that contains less than about 0.1% (wt/wt) water, referred to as solvent free (i.e. desolvated) lansoprazole.

Unless otherwise stated, % and % (wt/wt) refer to percent on a weight basis.

As used herein in connection with a numerical quantity, &lt; refers to less than.

In accordance with the present invention, 2-[[3-methyl2,2,2)-4־-trifluoro ethoxy)-2pyridinyl]thio]־lZ/־benzimidazole (LNPS) is used as a starting material for preparation of 2-[[3methyl-4-(2,2,2-trifluoroethoxy)-2-pyridinyl]methyl]sulf1nyl-li/-benzimidazole and is dissolved in an organic solvent or a mixture of organic solvent with water. Any residue of the LNPS remaining in the final product is an impurity and difficult to remove.

Exemplary organic solvents suitable for use in the practice of the present invention include alcohols such as ethanol, methanol, n-propanol, i-propanol; ketones such as acetone and 2-butanone; dimethyl-formamide; tetrahydrofuran ; and the like. Preferably, the organic solvent is ethanol.

In particular embodiments, mixtures of an organine solvent listed above with water can be used. When mixtures of organic solvent and water are used, different volume ratios (vol/vol) of organic solvent and water can be used. The organic solvent/_water ratio can vary between about 0.2:1 to 3:1. Preferably, the solvent/water ratio is about 1.5:1. Use of larger solvent/water ratios may result in poor crystallization yields.

When mixtures of an organic solvent and water are used, the overall ratio, on a volume per weight basis, of solvent/water (i.e., organic solvent + water) to lansoprazole ratio can vary between about 17:1 toabout5:l (vol:wt). Preferably, the ratio of solvent/water to lansoprazole is about 11:1 (vol/wt).

Amine compounds are used in the practice of the present invention. The overall ratio, on a mole basis, of amine compound to lansoprazole (mol/mol) can vary between about 17:1 to about 1:1. Preferably, the amine compound to lansoprazole ratio is between 17:1 and 7:1 (mol/mol), or between 7:1 and 1:1 (mol/mol). Preferably, the amine compound :lansoprazole (mol/mol) ratio is about 7:1. Exemplary amine compounds useful in the practice of the present invention include ammonia, ammonium hydroxide, diethylamine, triethylamine, methylamine and the like. Preferably, the amine compound is ammonium hydroxide. Crystallization of lansoprazole under such conditions permits a good separation of lansoprazole from impurities, especially sulfone and/or sulfide derivatives.

In one embodiment, the present invention provides a crystallization purification method for purifying lansoprazole. Crystallization of lansoprazole from solution in an organic solvent or a mixture of organic solvent and water in the presence of an amine compound according to the crystallization purification method of the present invention results in substantially pure lansoprazole.

In the present invention, purification of lansoprazole by crystallization is achieved by acidifying (i.e. combining with acid) a solution of lansoprazole in an organic solvent or a mixture of organic solvent and water. The acid combined can neutralize the amine compound during the crystallization of lansoprazole.

Exemplary acids combined to crystallize lansoprazole include acetic acid, formic acid, hydrochloric acid (HC1) and the like. Preferably, the acid is acetic acid.

Although the purified lansoprazole obtained by the above-mentioned crystallization purification process is substantially pure and can be advantageous, it does not necessarily contain &lt;0.1% water in accordance with the USP forum. As mentioned previously, water can have a negative impact on the long-term stability of lansoprazole (U.S. Pat. No.6,002,011).

Thus, in another embodiment of the present invention, a method for reducing the water (i.e. desolvating) lansoprazole is provided. In this embodiment, the water content of substantially pure lansoprazole, can be reduced to &lt;0.1% water by crystallization from organic solvent.

Crystallizing organic solvents for obtaining lansoprazole having &lt;1%, wt/wt, water are methanol, dimethylcarbonate, diethyl-_carbonate, acetone, and 2-butanone. Preferably, such crystallizing organic solvents are methanol, dimethyl-carbonate and diethyl-_carbonate. Most preferably, such crystallizing organic solvent is acetone.

Crystallization of lansoprazole to obtain lansopraolze having &lt;0.1 % water can be and preferrably is carriedout in the presence of an amine compound. Exemplary amine compounds include ammonia, ammonium hydroxide, diethylamine, triethylamine, methylamine and the like. Preferably, the amine compound is ammonium hydroxide.

Preferably, in this embodiment the mole ratio of amine compound to lansopraozle (mole:mole or mole/mole) is about 0.05:1.

Preferably the lansoprazole to be desolvated is completely dissolved in the solvent before crystallization. The dissolution of lansoprazole can be promoted by the presence of small amounts of water. The presence of a small amount of water can be insured by using wet lansoprazole from the previously mentioned purification step or by adding &lt;20% (vol/vol) water to the solvent.

The dissolution of lansoprazole to be desolvated can be performed at the crystallization solvent reflux temperature. Preferred dissolution temperatures are lower than the reflux temperature, given the reported instability of lansoprazole at higher temperatures. Preferably, the dissolution temperature does not exceed 50°C.

The crystallization yield of lansopiazole can be improved by cooling or by removing solvent or water form the crystallization system. One skilled in the art would appreciate the techniques used to remove water from a mixture of organic solvent and water include, e.g., azeotropic distillation.

The present invention can be illustrated by the following nonlimiting examples.

Example 1

Preparation of Lansoprazole Crude

Into a flask IL ethanol was charged and cooled under stirring to 5°C. Under mixing 200 grams 2[[3-rnethyl-4-(2,2,4-trifluoroethoxy)-2-pyridinyl]thio]-l# benzimidazole (LNPS) and 3 grams vanadium acetyl acetonate were added. 110 grams tert-butyl-hydroperoxide solution were dropped slowly into the suspension. The suspension was maintained under mixing during 4 hours. 40 grams of Na₂SO₃ dissolved in 400 mL water were added. Separate solid phase by vacuum filtration and dry. 165 grams of LNP crude were obtained (yield 79 %).

Sulfone 0.3%

LNPS 0.3%

Chromatographic purity method of lansoprazole monograph in USP Forum Vol.

26(5) (Sept-Oct. 2000].

HPLC Condition:

<td> Column:</td><td> , C18</td>

<td> Mobile phase: Flow:</td><td> Gradient of triethyl amine in water with acetonitrile 0.8 mL/min</td>

<td> Detection:</td><td> 285 nm</td>

This chromatographic assay has the detection sensitivity of less than 0.1% impurities in LNP.

Example 1A

Preparation of Lansoprazole crude

Into a flask IL ethanol (95%) was charged and cooled under stirring to 5°C. Under mixing 200 grams 2-[[[3-methyl-4-(2,2_J2-trifluoroethoxy)-2-pyridmyl] thio]-lH benzimidazole (LNPS) and 3 grams vanadium acetyl acetonate were added. 110 grams tert-butyl-hydroperoxide solution were dropped slowly into the suspension. The suspension was maintained under mixing during 6 hours. 40 grams of Na2SO3 dissolved in 400 ml water were added.

IL of water (pH was about 8-8.5; the pH was adjusted by the addition of NH4OH) was added to the suspension and the suspension was further mixed for 17 hours at 25°C. The suspension was cooled to 5°C and the solid phase separated by vacuum filtration then dried. 178 grams of LNP crude were obtained (yield 85 %). Sulfone 0.15%.

Example 2

Purification of Lansoprazole

In a 0.25 L flask 67.5 mL ethanol 95%, 15 mL of ammonium hydroxide (NH4OH) 24% and 45 mL water were charged and cooled under stirring to 5°C. Under mixing 10 grams lansoprazole erode were added and heated to 52°C to dissolution. 1 gram of active carbon was added to the slightly turbid solution and maintained a short time at 49°C. The carbon was separated on a filter and the cake washed with a mixture of mL ethanol and 12 mL water. The solution was cooled and lansoprazole was precipitated by the addition of 3.75 mL acetic acid. The suspension was cooled to 10°C and filtered. The product was washed with water and ethanol and dryed. 8.7 grams of lansoprazole pure were obtained (yield: 89%). Sulfone 0.05%, LNPS under the detection limit.

The above-described procedure was applied in other examples where the solvent and/or the amine was different. The following table is illustrative for these examples:

<td> Example</td><td> Solvent</td><td> water</td><td> Amine</td><td> Yield</td><td> Sulfone</td><td> LNPS</td>

<td></td><td></td><td> yes/no</td><td></td><td> %</td><td> %</td><td> %</td>

<td> 3</td><td> i-propanol</td><td> no</td><td> NH4OH</td><td> 52.7</td><td> 0.03</td><td> 0.02</td>

<td> 4</td><td> Ethanol</td><td> no</td><td> NH4OH</td><td> 46.5</td><td> 0.07</td><td> &lt;DL*</td>

<td> 5</td><td> n-propanol</td><td> yes</td><td> NH4OH</td><td> 91.5</td><td> 0.08</td><td> 0.04</td>

<td> 6</td><td> i-propanol</td><td> yes</td><td> NH4OH</td><td> 90.8</td><td> 0.07</td><td> &lt;DL</td>

<td> 7</td><td> Ethanol</td><td> yes</td><td> Triethylamine</td><td> 87.6</td><td> 0.05</td><td> &lt;DL</td>

<td> 8</td><td> i-buthanol</td><td> yes</td><td> Triethylamine</td><td> 80.7</td><td> 0.06</td><td> &lt;DL</td>

¹ less than detection limit

Example 9

Preparation of Lansoprazole Containing &lt;0.1% (wt/wt) Water

In a 0.25L flask 29.8 grams wet LNP crystal and 30 mL acetone were charged. The suspension was heated to 52°C and 150 mL acetone was dropped until a clear solution was obtained. The solution was cooled to 10°C and concentrated until the weight of the reaction mass was 48.5 grams. The solid was separated by filtration and 20 washed with 20 mL cold acetone. After drying 18.58 grams product were obtained (yield: 91 %). Content of water according to Karl Fischer test 0.05%.

Similar to example 3, the following other examples were performed:

<td> Examples</td><td> Solvent</td><td> Yield</td><td> Water</td>

<td></td><td></td><td> %</td><td> %(KF‘)</td>

<td> 10</td><td> Dimethylcafbonatc</td><td> 87.5</td><td> 0.04</td>

<td> 11</td><td> 2-butanone</td><td> 88.5</td><td> 0.03</td>

<td> 12</td><td> Methanol</td><td> 72%</td><td> 0.06</td>

¹Karl Fisher method for Water determination is the USP method as written in USP Forum Vol. 26(5) [Sept.- Oct. 2000].

Example 13

Preparation of Lansoprazole Containing &lt;0.1% (wt/wt) Water

In a 0.1 L flask 4 grams dry LNP crystals and 60 mL acetone containing 15% water were charged. The solution was maintained under mixing at 25 °C for 17 hours. The solution was concentrated to 15 grams and filtered. After drying 3.4 grams product were obtained (yield: 84.7%). Content of water according to Karl Fischer test:

0.06%.

Example 14

Preparation of Lansoprazole Containing &lt;0.1% (wt/wt) Water

In a 50 mL flask 11.6 mL acetone, 3.1 mL water and 0.05 mL NH4OH were charged. The solution was heated to 45°C and under mixing 5.8 grams of LNP crystal were charged. The solution was heated to 61°C and immediately cooled to 510°־C. After filtration and drying 5.0 grams product was obtained (yield: 87%). Content of water according to Karl Fischer test: 0,03%.

Example 15

Lansoprazole (5.0 grams) was dissolved in 30 ml of acetone, containing 15 volume % of water, at heating at reflux. Water (30 ml) was added drop wise for 5 min to the clear solution. After cooling to room temperature the slurry was filtered, giving after 25 drying 4.5 grams of the product (yield: 90%). Content of the water according to Karl

Fischer test was 0.08%.

Example 16

Lansoprazole (5.0 grams) was dissolved in 30 ml of acetone, containing 15 30 volume % of water, at heating at reflux. Water (60 ml) was added dropwise for 5 min to the clear solution. After cooling to room temperature the slurry was filtered, giving after drying 4.6 grams of the product (yield: 92%). Content of the water according to Karl

Fischer test was 0.08%.

A number of embodiments of the present invention have been described. The present invention is not to be limited in scope by the specific embodiments described herein. It will be understood that various modifications may be made without departing from the spirit and scope of the invention. Various publications are cited herein, the disclosures of which are incorporated by reference in their entireties.