Organic compounds -- part of the class 532-570 series – Organic compounds – Unsubstituted hydrocarbyl chain between the ring and the -c-...
Patent
1997-11-24
1999-11-30
Berch, Mark L.
Organic compounds -- part of the class 532-570 series
Organic compounds
Unsubstituted hydrocarbyl chain between the ring and the -c-...
C07D50300, C12P 1718, C12N 102
Patent
active
059945346
DESCRIPTION:
BRIEF SUMMARY
BACKGROUND OF THE INVENTION
This invention relates to a process for preparation of pharmaceutically acceptable salts of clavulanic acid, particularly but not exclusively alkali salts especially potassium clavulanate.
Clavulanic acid is the common name for (2R,5R,Z)-30(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2 -carboxylic acid. Clavulanic acid and its alkali metal salts and esters are active as inhibitors of beta lactamase produced by some Gram positive as well as Gram negative micro-organisms. In addition to inhibition of beta lactamase, clavulanic acid and alkali metal salts thereof also have a synergistic action with penicillin and cephalosporin antibiotics. Clavulanic acid and its salts are used in pharmaceutical preparations to prevent the deactivation of beta lactam antibiotics. Commercial preparations contain potassium clavulanate in combination with amoxycillin trihydrate. Potassium clavulanate is more stable than the free acid or other salts.
Clavulanic acid is prepared by fermentation of a micro-organism such as strains of Streptomyces such as S. clavuligerus NRRL 3585, S. jimonjinensis NRRL 5741 and S. katsurahamanus IFO 13716 and Streptomyces sp. P5621 FERM P2804. The aqueous culture obtained after fermentation is purified and concentrated in accordance with conventional processes for example filtration and chromatographic purification as disclosed in GB 1508977, prior to extraction of the aqueous solution with an organic solvent to obtain a solution of impure clavulanic acid in the solvent.
GB 1508977 discloses preparation of clavulanate salts by filtration of the fermentation broth by passage through an anionic exchange resin. This process may achieve acceptable yields but sophisticated chromatographic purification methods are required and the use of resin columns involves substantial investment for manufacture on a commercial scale.
GB 1543563 discloses a fermentation process wherein the pH value of the medium is maintained in the range 6.3 to 6.7. Pharmaceutically acceptable salts such as potassium clavulanate are prepared by re-salting from lithium clavulanate. GB 1563103 discloses a process wherein crude clavulanic acid is obtained by primary isolation processes with a subsequent purification process being necessary.
EP-A-0026044 discloses use of the tertiary butylanine salt of clavulanic acid as an intermediate for purification of clavulanic acid. This salt was known from BE-862211 or DE 2733230 which disclosed that the salt was even more stable than the sodium or potassium clavulanate salts. Tertiary butylamine is a toxic compound and is also difficult to remove from waste water giving rise to serious pollution concerns.
EP-A-0312813 discloses a process for purification of clavulanic acid via the intermediate lithium salt.
EP-A-0562583 discloses use of salts of clavulanic acid with N,N'-monosubstituted symmetric ethylene diamines such as N,N'-diisopropyethylene diammonium diclavulanate as useful intermediates for isolation and preparation of pure clavulanic acid or alkaline metal clavulanate salts from ethyl acstate extract.
WO93/25557 discloses use of clavulanate salts with numerous amines as intermediates for preparation of clavulanic acid or pharmaceutically acceptable salts or esters.
EP-A-0594099 discloses use of tertiary octylamine with clavulanic acid as an intermediate in preparation of clavulanic acid or pharmaceutically acceptable salts.
WO94/21647 discloses use of N,N'-substituted diamines such as N,N'-diisopropylethylene diammonium diclavulanate as a useful intermediate for preparation of clavulanic acid and alkali salts.
WO94/22873 discloses use of novel tertiary diammonium salts of clavulanic acid such as N,N,N',N'-tetramethyl-1,2-diaminoethane clavulanate as a useful intermediate for preparation of clavulanic acid and salts thereof.
The aim of this invention is to prepare clavulanic acid and its pharmaceutically acceptable salts, such as potassium clavulanate in a new and simple manner, wherein the desired substance is obtained in a high yield and of h
REFERENCES:
patent: 4465693 (1984-08-01), Strauss
patent: 4886602 (1989-12-01), Kuehne et al.
patent: 4911847 (1990-03-01), Shmidt
patent: 5073263 (1991-12-01), Fagundas
patent: 5126053 (1992-06-01), Schneider
patent: 5130241 (1992-07-01), Woroniecki
patent: 5240600 (1993-08-01), Wang
patent: 5470356 (1995-11-01), Meszaros
patent: 5470481 (1995-11-01), Modell
patent: 5650101 (1997-07-01), Newkome
patent: 5691141 (1997-11-01), Koster
patent: 5780274 (1998-07-01), Capruder
patent: 5837365 (1998-11-01), Chung
patent: 5858892 (1999-01-01), Kinoshita
Belter, Ed, "Bioseparations" (Wiley and Sons, NY), pp. 13-17, 39-42, 237-238, 250-255, 1988.
Kent, ed, "Riegel's Handbook of Industrial Chemistry, Ninth Edition" (Van Nostrand Reinhold, NY) pp. 935, 937, 973-974, 1992.
Derwent, Abstract No. 92-395374/48 of JP-04295494, (1992).
Belter, et al., "Downstream Processing for Biotechnology", Bioseparations, Ch. 2, pp. 13-42, Ch. 9, pp. 237-255 (1988).
Noble, Richard D., "Principles and Applications," Membrane Separations Technology Series 2, pp. 354-413, (1995).
Notice of Opposition to a European Patent, pp. 1-22, (Jul. 22, 1998).
Rompp Chemie Lexikon, 9.sup.th edition, vol. 4 (1991), p. 2779.
Rompp Chemie Lexikon, 9.sup.th edition, vol. 6 (1992), p. 4798.
Michaels, et al., "Membranes in Biotechnology: State of the Art," Desalination, vol. 53, pp. 231-258, (1985).
Derwent for JP4-75596 (1992).
Derwent for JP60-70092 (1985).
Schweitzer, Philip A., "Membrane Filtration Section 2.1", Handbook of Separation Techniques for Chemical Engineers, Second Edition, 1988, pp. 2-4 through 2-103.
Berch Mark L.
Lek Pharmaceutical and Chemical Co. D.D
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