Patent Application
20070265311
Sulfonyl ester prodrugs of proton pump inhibitors have been recently disclosed. For example, U.S. Pat. No. 6,897,227, expressly disclosed herein by reference, discloses such compounds. These compounds are designed to hydrolyze in vivo to yield the traditional proton pump inhibitors such as omeprazole, lansoprazole, pantoprazole, rabeprazole, or related compounds. However, the prodrugs are also susceptible to hydrolysis in vitro in aqueous solutions. The salt forms of the prodrugs have been prepared to facilitate formulation. Up to the conception of the presently disclosed invention, these compounds had been neutralized using weak bases and often organic cosolvents to avoid hydrolytic byproducts of the neutralization reaction. As a result, organic solvent impurities and weak acid impurities have been observed in the product salt.
Disclosed herein is a method of converting a carboxylic acid to a salt comprising,
In this method, the pH may also be maintained above about 3. Alternatively the pH may be above about 5. Alternatively, the pH may be above about 7. The pH is also maintained below about 10. Alternatively, the pH is maintained below about 9. Thus, although other pH ranges are possible, examples of pH ranges for the neutralization include from about 3 to about 10, from about 5 to about 9, and from about 7 to about 9.
An arylsulfonyl leaving group is —SO2Ar, where the sulfur atom of the arylsulfonyl attaches to the nitrogen of the proton pump inhibitor. Ar is an aryl group, including a heteroaryl group, which includes, but is not limited to phenyl, naphthyl, thienyl, pyridinyl, and the like. Ar has at least one substituent, and at least one of the substituents has a carboxylic acid moiety.
In one embodiment, the carboxylic acid consists of
In one embodiment, the carboxylic acid is
In another embodiment the salt is a sodium salt.
In another embodiment the salt is sodium {4-[5-Methoxy-2-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethanesulfinyl)-benzoimidazole-1-sulfonyl]-phenoxy}-acetate.
A carboxylic acid is a compound having a CO2H moiety. A carboxylic acid has two forms: 1) the acid or protonated form, and 2) the deprotonated, carboxylate ion, conjugate base, or anionic form.
A salt is an associated pair of ions. In converting a carboxylic acid form to a salt, the carboxylic acid is deprotonated by a base such that the carboxylate ion is formed. This ion is formally associated with a positively charged counterion, such as sodium, potassium, ammonium, or the like. But the salt may be dissolved and dissociated such that the counterion is not actually near the anionic CO2—. Thus, the corresponding salt form of a carboxylic acid is the salt that is formed when the carboxylic acid is deprotonated by a base.
A strong base has the meaning generally understood in the art. In other words, a strong base is a base which reacts essentially completely with water to form OH—, or alternatively, dissociates essentially completely in water to yield free OH—. Examples include, but are not limited to:
In one embodiment, the temperature is maintained below about 30° C. while the base is added. In another embodiment, the temperature is maintained below about 22° C. while the base is added. The temperature must be high enough for the aqueous solution to be liquid. The melting point of an aqueous liquid is at or below 0° C., depending upon the concentration of dissolved material in the water. The freezing point depression can be determined by a person of ordinary skill in the art, or the freezing point of a liquid can be determined experimentally, but aqueous liquids are often at least −20° C. In another embodiment, the temperature is at least −10° C. In another embodiment the temperature is at least −5° C. In another embodiment, the temperature is at least 0° C.
The salts shown below are useful products of the processes disclosed herein, and are useful in the compositions and dosage forms disclosed herein. The names of the salts depicted are given below the corresponding structure.
Sodium {4-[5-Methoxy-2-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethanesulfinyl)-benzoimidazole-1-sulfonyl]-phenoxy}-acetate
Sodium 4-methyl-3-{2-[3-methyl-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethanesulfinyl]-benzoimidazole-1-sulfonyl}-benzoate
Sodium {4-[5-Difluoromethoxy-2-(3,4-dimethoxy-pyridin-2-ylmethanesulfinyl)-benzoimidazole-1-sulfonyl]-phenoxy}-acetate
The present process facilitates neutralization of the carboxylic acid in greater quantities than was previously feasible. Thus, a composition consisting essentially of the carboxylic acid salt can be prepared, wherein the composition has a mass of from about 1 kg to about 10,000 kg. In other embodiments, the composition has a mass of from about 1 kg to about 1000 kg. In other embodiments, the composition has a mass of about 1 kg to 100 kg. In other embodiments, the composition has a mass of from about 7 kg to about 10,000 kg. In other embodiments, the composition has a mass of from about 7 kg to about 1000 kg. In other embodiments, the composition has a mass of about 7 kg to 100 kg. In other embodiments, the composition has a mass of from about 16 kg to about 10,000 kg. In other embodiments, the composition has a mass of from about 16 kg to about 1000 kg. In other embodiments, the composition has a mass of about 16 kg to 100 kg.
In one embodiment, greater than 1 kg of the carboxylic acid is used, neutralized, or converted in the described process. In another embodiment, greater than 7 kg of the carboxylic acid is used, neutralized, or converted in the described process. In another embodiment, greater than 16 kg of the carboxylic acid is used, neutralized, or converted in the described process.
In another embodiment, a further step in the process comprises spray drying an aqueous solution containing the salt form, the neutralized carboxylic acid, or the converted form of the carboxylic acid. In another embodiment, the aqueous solution that results from converting a carboxylic acid or neutralizing a carboxylic acid form is used directly in the spray drying process. In other words, no steps are taken on the solution between neutralizing or converting and spray drying.
In one embodiment, the carboxylic acid, which is obtained by the process described in U.S. Pat. No. 6,897,227, is dissolved or dispersed in water with vigorous stirring. A sodium hydroxide solution (0.34 M) is added slowly with continued stirring, such that the temperature is maintained between about 19° C. and 22° C., and the pH is maintained below about 10. When the pH exceeds about 10, addition of the sodium hydroxide is halted until the pH falls below about 10, when the addition is resumed. Addition is complete when the number of moles of sodium hydroxide added is equal to the number of moles of the carboxylic acid initially added to the mixture.
In another embodiment, the pH is maintained below about 9.
In one embodiment, no organic solvents are used during the process. Thus, compositions and dosage forms which are free of trace amounts of organic solvents are contemplated.
In another embodiment, no carbonate or bicarbonate is used in the process. Thus, compositions and dosage forms which are free of carbonate or bicarbonate are contemplated.
Another embodiment is a composition or dosage form containing less than 1% omeprazole on an active basis, i.e. less than 1% of the therapeutically active salt is omeprazole.
Unless otherwise indicated, % is intended to mean % w/w.
Another embodiment is a composition comprising a pharmaceutically acceptable salt of
wherein said composition is at least about 96% pure on an anhydrous basis.
Another embodiment is a composition consisting of an essentially pure pharmaceutically acceptable salt of
wherein said composition contains no ethyl hexanoic acid or acetonitrile.
Another composition consists essentially of pure
Another composition consists essentially of pure
Another composition consists essentially of pure
Another embodiment is a dosage form prepared by a process comprising
In another embodiment, the dosage form is prepared in a process which further comprises spray drying the aqueous mixture of the salt form.
Another embodiment is a dosage form comprising a salt form of a therapeutically active agent having a structure chosen from
wherein said dosage form contains less than 107 parts per million of acetonitrile.
In another embodiment, the dosage form contains no acetonitrile.
Another embodiment is a dosage form comprising a salt form of a therapeutically active agent having a structure chosen from
wherein said dosage form contains no ethyl hexanoic acid.
In another embodiment, the composition or dosage form contains no ethyl hexanoic acid.
In another embodiment, the composition or dosage form contains no acetonitrile.
In another embodiment, the composition or dosage form contains less than 107 parts per million of acetonitrile.
The methods disclosed herein may be useful in preparing dosage forms or compositions comprising a carboxylic acid salt which is free of one or more of the compounds shown below.
In Table 1 below, the impurity profile of a salt prepared by the process disclosed herein (G) is compared to the impurity profile of the same salt prepared using bicarbonate/carbonate or sodium ethyl hexanoate as the base and an organic solvent such as acetonitrile as a cosolvent (A-F). The structure of the salt is depicted below the Table.
NA Not available
Another embodiment is a method of converting a carboxylic acid to a salt comprising,
In another embodiment, the carboxylic acid is maintained at a temperature below about 30° C. while said base is added.
In another embodiment, wherein the carboxylic acid is maintained at a temperature below about 22° C. while said base is added.
In another embodiment, the carboxylic acid is
In another embodiment the salt is a sodium salt.
In another embodiment the salt is sodium {4-[5-Methoxy-2-(4-methoxy-3,5-dimethyl-pyridin-2-ylmethanesulfinyl)-benzoimidazole-1-sulfonyl]-phenoxy}-acetate.
In another embodiment greater than 1 kg of the carboxylic acid form is used.
Another embodiment is a composition consisting of an essentially pure pharmaceutically acceptable salt of
wherein said composition contains no ethyl hexanoic acid or acetonitrile.
Another embodiment is a composition consisting essentially of pure
Another embodiment is a composition consisting essentially of pure
Another embodiment is a composition consisting essentially of pure
Another embodiment is a dosage form prepared by a process comprising
In another embodiment said process further comprises spray drying said aqueous mixture of said salt form.
Another embodiment is a dosage form comprising a salt form of a therapeutically active agent having a structure chosen from
wherein said dosage form contains less than 107 parts per million of acetonitrile.
In another embodiment, the dosage form contains no acetonitrile.
Another embodiment is a dosage form comprising a salt form of a therapeutically active agent having a structure chosen from
wherein said dosage form contains no ethyl hexanoic acid.
In another embodiment, the dosage form contains no acetonitrile.
Another embodiment is a dosage form comprising a salt form of a therapeutically active agent having a structure chosen from
wherein the salt is greater than 96% pure on an anhydrous basis when it is used in the dosage form.
“On an anhydrous basis” means that the purity of a substance is what the purity of the substance is or would be when no water is present.
Another embodiment is a method of converting a carboxylic acid to a salt comprising,
Another embodiment is a composition, said composition having a mass of from about 1 kg to about 10,000 kg, wherein said composition consists essentially of
Although many specific embodiments are disclosed herein, they are merely examples, and none of these are intended to limit the scope of the invention in any way. The scope of the invention sought to be protected will be defined in the claims.
This application is based on, and claims priority under 35 U.S.C. § 120 to U.S. Provisional Patent Application No. 60/757,763 filed on Jan. 10, 2006, and which is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 60757763 | Jan 2006 | US |
