Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2001-04-20
2004-01-06
Rotman, Alan L. (Department: 1625)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
06673936
ABSTRACT:
BACKGROUND OF THE INVENTION
Until recently, omeprazole, the active ingredient in AstraZeneca's proton pump inhibitor commercially sold in the United States under the brand name Prilosec®), was chemically believed to be 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, in the solid state, represented by formula (1b):
However, Whittle, R. R., et al. disclosed in POT patent application WO 01/14367 that omeprazole, as a free base or as a salt, hydrate, or combination thereof, is actually two positional isomers co-crystallizing in a single crystalline lattice: the above-referenced 5-methoxy omeprazole represented by the formula (1b), and its preferred 6-methoxy isomer: 6-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, represented by formula (1a):
Whittle, et al. further disclosed that the stability of omeprazole is affected by the ratio of 6-methoxy omeprazole to 5-methoxy omeprazole, with omeprazole being more favorably stable as the percentage of 6-methoxy omeprazole is increased. However, the processes presently available for preparing a higher percentage of the more preferred isomer, 6-methoxy omeprazole, and reduction in the 5-methoxy omeprazole percentage of the less preferred require controlling the rate of recrystallization, the solvent used, and other environmental factors. An alternative to the expensive and time-consuming method for increasing the percentage of 6-methoxy omeprazole in the crystalline lattice from an amount of 5(6)-methoxy omeprazole, would be technically and commercially beneficial.
SUMMARY OF INVENTION
Accordingly, the present invention provides methods for increasing the solid state percentage of 6-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, or a pharmaceutically acceptable salt, hydrate or combination thereof, from an amount of 5(6)-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, or a pharmaceutically acceptable salt, hydrate or combination thereof and, thus, also decreasing the percentage of 5-methoxy omeprazole proportionately.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The present invention is described herein below in greater detail with reference to its preferred embodiments. These embodiments, however, are set forth to illustrate the invention and are not to be construed as a limitation thereof, the invention being defined by the claims.
It has been reported and further substantiated, that omeprazole API having higher percentages of 6-methoxy omeprazole compound relative to the respective 5(6)-methoxy omeprazole starting material typically provides greater stability, resulting in better commercial viability. Improved stability may also provide an improved safety profile via the minimization of degradants over time.
Accordingly, one aspect of the present invention provides processes for increasing, in the solid state, the percentage of a compound of formula (1a) compared to the percentage of such compound in co-crystallized (1a) and (1b) starting material (also known as omeprazole active pharmaceutical ingredient or “API”; and also referred to herein as 5(6)-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, or 5(6)-methoxy omeprazole or pharmaceutically acceptable salts, hydrates, or combinations thereof). As used herein, the compound represented by formula (1a) is also referred to as 6-methoxy omeprazole and the compound represented by formula (1b) is also referred to as 5-methoxy omeprazole.
As such, the starting material for the processes of the present invention is 5(6)-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, or pharmaceutically acceptable salts, hydrates, or combinations thereof. 5(6) methoxy omeprazole is prepared via various known methods including, for example, the methods described in PCT publication WO 01/14367 and U.S. Pat. No. 4,255,431.
In one embodiment, an amount of 5(6)-methoxy omeprazole is placed in a suitable container or, preferably, a Büchner funnel, to which is added an aliquot of short carbon chain (C
1
-C
4
) alcohol solvent including, for example, methanol, ethanol, and isopropyl alcohol, or a furan-based solvent such as, for example tetrahydrofuran (“THF”). THF has solvent properties similar to such short carbon chain alcohol solvents. Sufficient solvent is added to substantially cover and wet the starting material with gentle and thorough stirring. The solvent is then removed via methods known in the art, preferably under vacuum. As used herein, this process is referred to as “rinsing” the 5(6)-methoxy omeprazole API.
The amount of time required for such rinsing will typically be proportionate to the size of the starting material sample. In addition, the length of time the wetted material is stirred, as well as the percentage of 5-methoxy omeprazole in the starting material, can affect the final yield with longer wetting/stirring times providing potentially lower yields. As such, it may be better to minimize such wetting/stirring time, vacuum off the solvent, then re-rinse the starting material one or more times using the same procedure until the desired ratio of 6-methoxy omeprazole to 5-methoxy omeprazole is obtained.
Typically, this rinsing process is carried out at ambient temperature.
Unexpectedly, it was discovered that of the organic solvents examined, only THF and the short carbon chain alcohol solvents used in the processes of the present invention were capable of substantially selectively solubilizing the 5-methoxy omeprazole in the starting material, leaving a higher percentage of 6-methoxy omeprazole in the resulting product. Other solvents tested included, for example, ethyl acetate, isopropyl ether, acetone, acetonitrile, and water. Furthermore, it was discovered that the effectiveness of the rinsing process was directly related to the length of the carbon chain of such solvent, with the shorter chain alcohol solvents being preferred and methanol being especially preferred.
Accordingly, the rinsing portion of the instant process can last from about 5 seconds to about 30 seconds and more typically from about 10 seconds to about 20 seconds for small, test batches, and considerably longer as batch size increases.
The second step of the present process is drying the product from the rinse step. Generally, drying can be accomplished by a multitude of methods known to the ordinarily skilled artisan provided, if heat is used, the amount of heat used is insufficient to degrade or modify the product from the first step.
Typically, the product is placed in an appropriate, inert vessel, which is placed in a vacuum oven. Preferably, the oven is set at about 0 mm Hg and ambient temperature (about 25° C.) until the product is dry, although other conditions may possibly be employed. For small test samples, product is dried for about 24 hours, with drying time being increased for larger amounts of such product.
Preferably, the processes of the present invention provide 5(6)-methoxy omeprazole (or 6-methoxy omeprazole essentially devoid of 5-methoxy omeprazole) having a 5-methoxy percentage not greater than about ten percent of the sum of the total percentage of 5-methoxy omeprazole and 6-methoxy omeprazole. However, incremental reduction in the amount of 5-methoxy omeprazole compared to the respective starting material typically can provide improved stability attributes. As such, relative stability of the final product of the present processes increases as the percent of 5-methoxy omeprazole decreases, for example, from about 30% to about 25% to about 20% to about 15% to about 10% to about 5% to about 0%. Typically, the processes of the present invention are most effective at reducing the 5-methoxy omeprazole percentage to a range from about 6% to about 9%. Thus, processes of the present invention are most effective for reducing the level of 5-methoxy omeprazole in an amoun
Stowell Grayson Walker
Whittall Linda B.
Whittle Robert R.
Myers Bigel & Sibley Sajovec, PA
Robinson Binta
Rotman Alan L.
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