Organic compounds -- part of the class 532-570 series – Organic compounds – Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
2001-07-16
2004-12-21
Berch, Mark L. (Department: 1624)
Organic compounds -- part of the class 532-570 series
Organic compounds
Heterocyclic carbon compounds containing a hetero ring...
Reexamination Certificate
active
06833452
ABSTRACT:
FIELD OF THE INVENTION
The present invention relates to a process for the preparation of highly pure crystalline form of cefuroxime-1-acetoxyethyl ester (cefuroxime axetil) from cefuroxime in a single step.
BACKGROUND OF THE INVENTION
Cefuroxime is chemically (6R, 7R)-3-carbamoyloxymethyl-7-[(Z)-2-(fur-2-yl)-2-methoxy-iminoacetamido] ceph-3-em-4-carboxylic acid and has the structural Formula II:
Cefuroxime axetil having the structural Formula I:
is the 1-acetoxyethyl ester of cefuroxime, a cephalosporin antibiotic with a broad spectrum of activity against gram-positive and gram negative micro-organisms. This compound as well as many other esters of cefuroxime, are disclosed and claimed in U.S. Pat. No. 4,267,320. According to this patent, the presence of an appropriate esterifying group, such as the 1-acetoxyethyl group of cefuroxime axetil, enhances absorption of cefuroxime from the gastrointestinal tract, whereupon the esterifying group is hydrolyzed by enzymes present in the human body. Because of the presence of an asymmetric carbon atom at the 1-position of the 1-acetoxyethyl group, cefuroxime axetil can be produced as R and S diastereoisomers or as a racemic mixture of the R and S diastereoisomers. U.S. Pat. No. 4,267,320 discloses conventional methods for preparing a mixture of the R and S isomers in the crystalline form, as well as for separating the individual R and S diastereoisomers.
The difference in the activity of different polymorphic forms of a given drug has drawn the attention of many workers in recent years to undertake the study on polymorphism. Cefuroxime axetil is the classical example of amorphous form exhibiting higher bioavailability than the crystalline form.
U.S. Pat. No. 4,562,181 and the related U.S. Pat. Nos. 4,820,833; 4,994,567 and 5,013,833, disclose that cefuroxime axetil in amorphous form, essentially free from crystalline material and having a purity of at least 95% aside from residual solvents, has a higher bioavailability than the crystalline form while also having adequate chemical stability. These patents disclose that highly pure cefuroxime axetil can be recovered in substantially amorphous form from a solution containing cefuroxime axetil by spray drying, roller drying, or solvent precipitation. In each case, crystalline cefuroxime axetil is dissolved in an organic solvent and the cefuroxime axetil is recovered from the solution in a highly pure, substantially amorphous form.
Another U.S. Pat. No. 5,063,224 discloses that crystalline R-cefuroxime axetil which is substantially free of S-isomer is readily absorbed from the stomach and gastrointestinal tract of animals and is therefore ideally suited to oral therapy of bacterial infections. According to this patent, such selective administration of R-cefuroxime axetil results in surprisingly greater bioavailability ability of cefuroxime, and thus dramatically reduces the amount of unabsorbable cefuroxime remaining in the gut lumen, thereby diminishing adverse side effects attributable to cefuroxime.
British Patent Specification No. 2,145,409 discloses a process for obtaining pure crystalline cefuroxime axetil and is said to be an improvement over British Patent Specification No. 1,571,683. Sodium cefuroxime is used as the starting material in the disclosed specification, which in turn, is prepared from either 3-hydroxy cefuroxime or cefuroxime. Said process involves an additional step of preparing sodium cefuroxime, and therefore is not economical from commercial point of view.
SUMMARY OF THE INVENTION
It is the object of the present invention to provide an efficient process for the preparation of highly pure crystalline form of cefuroxime axetil. Such a product would not only be useful in being a highly pure form of the active compound but would also be highly useful as a starting material for the preparation of a highly pure, substantially amorphous form of cefuroxime axetil, which has high bioavailability upon oral administration. The present process uses conditions which are convenient to perform on a commercial scale, operationally safe and provides the product in pure form.
Accordingly, the present invention provides a process for the preparation of highly pure crystalline form of cefuroxime axetil of structural Formula I:
from cefuroxime of structural Formula II:
in a single step which comprises preparing an amine salt of cefuroxime followed by its reaction in situ with an esterifying reagent.
Amine salt is prepared by reacting cefuroxime with a suitable amine in the presence of an inert organic solvent, at a temperature from about −15 to about 25° C., the preferred range being −10 to 10° C. and the most preferred range being −10 to 5° C. Cefuroxime axetil is obtained from the amine salt after an esterification reaction and a suitable aqueous work-up. After work-up cefuroxime axetil is thus produced in a single step starting from cefuroxime.
The term “suitable amine” includes primary, secondary, tertiary and cyclic amines. Suitable amine for the preparation of amine salt is selected from ethylamine, diethylamine, diisopropylamine, dibutylamine, di-sec-butylamine, triethylamine, dicyclohexylamine, or didecylamine. Most preferably, dicyclohexylamine is used.
Organic solvent is selected from inert solvents such as N,N-dimethyl-acetamide, N,N-dimethylformamide, N-methylpyrrolidone, acetonitrile, or mixtures thereof. Most preferably, N, N-dimethylacetamide is used.
A preferred reagent for the esterification reaction is (R,S) 1-acetoxy-ethyl bromide and is prepared by the methods known in the literature.
The esterification reaction is generally carried out in the presence of another base. The base required in the esterification step is selected from carbonate or bicarbonate salts of sodium, potassium, calcium or magnesium. Most preferably, potassium carbonate is used.
Suitable aqueous work-up involves the adjustment of pH with mineral acids and extractions with organic solvents. Acids may include hydrochloric acid, sulfuric acid, and phosphoric acid. Hydrochloric acid being the preferred acid. Any organic solvent may be used for extraction and such solvents are known to a person of ordinary skill in the art and include: water-immiscible and partially miscible solvents, such as chloroform, dichloromethane, 1,2-dichloroethane, hexanes, cyclohexane, toluene, methyl acetate, ethyl acetate and the like.
The product may be obtained by reducing the volume of organic solvent containing cefuroxime axetil by evaporation, adding a miscible polar solvent and precipitating the desired product by addition of an anti-solvent or by adding a polar solvent to the solvent system containing cefuroxime axetil and precipitating by addition of anti-solvent. The addition of polar solvent greatly reduces the presence of impurities, specifically &Dgr;
2
isomer of cefuroxime axetil in the final product. Polar solvent may be selected from a group consisting of a lower alkanol, denatured spirit, isopropanol, and the like, ketones such as acetone, or esters such as methyl acetate or ethyl acetate and mixtures thereof. Precipitation may be effected by the addition of appropriate quantities of anti-solvent for the cefuroxime axetil. Suitable anti-solvents include water, alkanes, mixtures of alkanes, such as hexane, cyclohexane or cyclopentane, ethers such as isopropyl ether, or aromatic hydrocarbons, such as benzene or toluene. The polar solvent and an anti-solvent should be at least partially miscible and preferably completely miscible.
Methods known in the art may be used with the process of this invention to enhance any aspect of this process. For example, the solution may be seeded with the crystals of cefuroxime axetil prior to the initiation of product crystallization or the slurry may be cooled prior to filtration. The product obtained may further be purified by recrystallization from solvent(s) using similar conditions for precipitation as those described above which give cefuroxime axetil. This includes dissolving cefuroxime axetil in a solvent and precipitating it with an ant
Handa Vijay Kumar
Tyagi Om Dutt
Yadav Gyan Chand
Berch Mark L.
Deshmukh Esq. Jayadeep R.
Hare, Esq. William D.
Heibel Esq. George E.
Ranbaxy Laboratories Limited
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