Process for production of ceftiofur

Details Process for production of ceftiofur Process for production of ceftiofur

2001-11-20

2003-01-07

Berch, Mark L. (Department: 1624)

Organic compounds -- part of the class 532-570 series

Organic compounds

Heterocyclic carbon compounds containing a hetero ring...

C540S220000

Reexamination Certificate

active

06504026

ABSTRACT:

This application claims the benefit of provisional application No. 60/252,707 filed Nov. 22, 2000.
The present invention relates to organic compounds, such as cephalosporins, more specifically to ceftiofur of formula
which is {6R-[6&agr;,7&bgr;(Z)]}-7-{[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino}-3-{[(2-furanylcarbonyl)-thio]methyl }-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, e.g. described in The Merck Index, 12th edition, item 1999. Ceftiofur is known as a pharmaceutically active compound, e.g. useful as an antibiotic, such as an antibacterial agent, e.g. used in veterinary medicine, e.g. in the form of a salt with sodium and in the form of a salt with hydrochloric acid. Processes for the production of ceftiofur in free form, in the form of a salt with hydrochloric acid or hydrobromic acid or in the form of a sodium salt are known. Ceftiofur in the form of a sodium salt is chemically not very stable and is difficult to purify. E.g. for purification ceftiofur may be converted into a crystalline salt with hydrochloric acid or hydrobromic acid which may be used as a starting material for the production of ceftiofur in the form of a sodium salt. E.g. a known production process of ceftiofur in the form of a sodium salt comprises the following steps
a) treating ceftiofur in the form of a salt with hydrochloric or hydrobromic acid in aqueous organic solvent with polyvinylpyridine, which polyvinylpyridine is activated by treatment with aqueous hydrochloric acid, rinsing with water, treatment with 10% sodium hydroxide solution, rinsing with water and tetrahydrofurane and drying, to obtain a solution comprising ceftiofur,
b) filtering the solution obtained in step a) to remove the polyvinylpyrrolidone;
c) treating the filtrate obtained in step b) with 2-ethydhexanoic acid in the form of a sodium salt to obtain ceftiofur in the form of a sodium salt, and
d) isolating ceftiofur in the form of a sodium salt by precipitation from an aqueous organic solvent.
Ceftiofur in the form of a sodium salt may be obtained in amorphous form.
We have now surprisingly found a process for the production of pure ceftiofur in the form of a sodium salt starting from ceftiofur in the form of a salt with hydrochloric acid or hydrobromic acid, wherein the use of activated polyvinylpyrrolidone may be avoided.
In one aspect the present invention provides a process for the production of ceftiofur of formula I in the form of a sodium salt comprising the steps
a) treating a compound of formula I in the form of a salt with hydrochloric acid or hydrobromic acid with a basic sodium source, erg. sodium hydroxide, sodium carbonate, sodium bicarbonate; in aqueous solvent; e.g. in water; to obtain a compound of formula I in the form of a sodium salt beside sodium chloride or sodium bromide in aqueous solvent, e.g. water;
b) separating a compound of formula I in the form of a sodium salt from sodium chloride or sodium bromide in aqueous solvent obtained in step a) by use of an appropriate membrane separation system e.g. comprising a membrane which is appropriate for separation of sodium chloride or sodium bromide from a compound of formula I in the form of a sodium salt in aqueous solution, e.g. selected from a polyamide thinfilm composite on a polysulfone carrier or a ceramic membrane; and comprising means for removal of a solution of sodium chloride or sodium bromide from the system and for adding fresh water to the system; and
c) isolating a compound of formula I in the form of a sodium salt obtained in step b), e.g. by lyophilisation or spray drying, e.g. optionally after concentration of the solution obtained in step b).
A process according to the present invention may be carried out as follows: A compound of formula I in the form of a salt with hydrochloric acid or hydrobromic acid may be suspended or dissolved in aqueous solvent, e.g. including water or a mixture of water and an appropriate organic solvent, preferably water. It is one advantage of the present invention that organic solvent may be avoided. The mixture obtained is treated with an appropriate basic sodium source, e.g. including sodium hydroxide, sodium carbonate, sodium bicarbonate. The basic sodium source may be in solid form or in solution, e.g. in aqueous solution. A pH of 5 to 9, preferably of 5 to 7.5, is adjusted in the mixture obtained. Treatment with the basic sodium source is carried out at appropriate temperatures, e.g. including temperatures of 0° C. to about 30° C., preferably of 0° C. to 5° C. A solution is obtained comprising a compound of formula I in the form of a sodium salt beside sodium chloride or sodium bromide, which optionally may be treated with charcoal and/or an adsorber resin, e.g. for de-colorizing or clear filtration. The solution obtained is subjected to a membrane separation system comprising a membrane which is appropriate for separation of sodium chloride or sodium bromide from a compound of formula I in the form of a sodium salt in aqueous solution and comprising means for removal of a solution of sodium chloride or sodium bromide from the system and for adding fresh water to the system. Appropriate membranes include nanofiltration membranes having a cutoff of ca. 100 to 500 Dalton, a retention of MgSO4 of over 90%; e.g. and a retention of sodium chloride of below 80%. Such membranes are known and commercially available, e.g. a including polyamide thinfilm composite on a polysulfone carrier, such as the membranes Nanomax 50® of the firm Millipore, NF 45® or NF 70® of the firm Danish Separation Systems, SR-1®, SR-2® or MPF44® of the firm Koch, or other comparable membranes of the firms Celgard, Nitto Denko or PCI; and including ceramic membranes, e.g. ceramic membranes comprising separating layers from titanium or zirconium oxides and an aluminium oxide carrier material. The membrane separation system is run as appropriate, e.g. a separated solution of sodium chloride or sodium bromide is removed from the system and fresh water is added. Separation is run at appropriate temperatures e.g. including temperatures of 0° C. to about 30° C., preferably of 0° C. to 5° C. The concentration of the solution of a compound of formula I and sodium chloride or sodium bromide is not critical but separation is faster in a high concentrated solution compared with a low concentrated solution. Convenient concentrations include concentrations of a compound of formula I in the form of a sodium salt and of sodium chloride or bromide in water of 1% to 30%, preferably of 10% to 15%. A solution of a compound of formula I in the form of a sodium salt is obtained which is substantially free of sodium chloride or sodium bromide. A compound of formula I in the form of a sodium salt may be isolated from the solution obtained as appropriate, e.g. according to a method as conventional, e.g. including direct lyophilisation or spray drying, or, the solution obtained may be concentrated as appropriate e.g. according to a method as conventional, e.g. including solvent evaporation, reversed osmosis, and the concentrated solution may be subjected to lyophilisation or spray drying.
Before isolation of a compound of formula I in the form of a sodium salt a buffer may be added to the solution, e.g. including primary or tertiary sodium or potassium phosphate-buffers.
A compound of formula I in the form of a sodium salt in solid, amorphous form may be obtained, substantially free of sodium chloride or sodium bromide, e.g. containing 0.05% and less of sodium chloride or sodium bromide.
A compound of formula I in the form of a sodium salt in solid, amorphous form obtained according to the present invention is useful in the production of pharmaceutical compositions comprising ceftiofur as a pharmaceutically active compound beside pharmaceutically acceptable excipients, e.g. in sterile or non-sterile form.
In another aspect the present invention provides the use of a compound of formula I in the form of a sodium salt, e.g. in solid, amorphous form, obtained according to t

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