Quinolone carboxylic acids, derivatives thereof, and methods...

Organic compounds -- part of the class 532-570 series – Organic compounds – Unsubstituted hydrocarbyl chain between the ring and the -c-...

Reexamination Certificate

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Reexamination Certificate

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07632944

ABSTRACT:
A process of preparing a quinolone carboxylic acid or its derivatives having Formula I, Ia, or IV, as shown herein, comprises using a starting quinolone that already has one or more desired substituents at one or more particular positions on the quinolone ring and preserving the orientation of such substituents throughout the synthesis. The present process comprises fewer steps than prior-art processes. The present process also can include a simple separation of a desired enantiomer of the quinolone carboxylic acid or its derivatives from the enantiomeric mixture. Pharmaceutical compositions comprising fluoroquinolones prepared by the present process can be used effectively against a variety of microbial pathogens.

REFERENCES:
patent: 5385900 (1995-01-01), Konno et al.
patent: 5447926 (1995-09-01), Konno et al.
patent: 6685958 (2004-02-01), Roy et al.
patent: 6699492 (2004-03-01), Roy et al.
patent: 0230946 (1987-08-01), None
patent: 0493608 (1992-07-01), None
patent: 0601197 (1994-06-01), None
patent: 2706459 (1994-12-01), None
patent: 63132885 (1988-06-01), None
patent: 63196579 (1988-08-01), None
patent: 63196580 (1988-08-01), None
patent: WO 94/15933 (1994-07-01), None
Araki et al., “Quinolone antimicrobial agents substituted with morpholines at the 7-position. Syntheses and structure—activity relationships,” J Med Chem, 1993, (vol. 36), (p. 1356-1363).
Takei et al., “Target Preference of 15 Quinolones AgainstStaphylococcus aureus, Based on Antibacterial Activities and Target Inhibition,” Antimicrobial Agents and Chemotherapy, Dec. 2001, vol. 45 ( No. 12), p. 3544-3547.
Oizumi et al., “Relationship Between Mutations in the DNA Gyrase and Topoisomerase IV Genes and Nadifloxacin Resistance in Clinically Isolated Quinolone-ResistantStaphylococcus aureus,” J. Infect. Chemother., 2001, p. 191-194.
Adamson, “The Anhydrides of Basic Amino-acids,” Dyson Perrins Laboratory, Oxford University, p. 39-40, (Nov. 17, 1942).
Pellegata et al., “An Improved Synthesis of y-,o-, and e-Lactams,” Communications, 1978, Georg Theime Publishers, p. 614-616.
Saburi et al., “Stereochemical Properties of Copper (II) Complexes of (X)-3-Aminohexahydroazepine, Crystal and Molecular Structure of Bromobis[(S)-3-aminohexahydroazepine]copper(II) Perchlorate [CuBr(S-ahaz)2]C1O4,” Bull. Chem. Soc. of Japan, Jan. 1987, p. 141-148.
Chong et al., “Stereoselective and Regioselective Synthesis of Azepane and Azepine Derivatives via Piperidine Ring Expansion,” J. Chem. Soc., Perkin Trans., 2002, p. 2080-2086.
Barluenga, “Fischer Carbene Complexes. A New Tool for Heterocyclic Synthesis,” Pure Appl. Chem., 2002, vol. 74 ( No. 8), p. 1317-1325.
Naito et al., “A Novel and Chiral Synthesis of Both Enantiomers of Trans-3-Amino-4-Hydroxyhexahydroazepine, a Key Intermediate fo the Synthesis of Balanol,” Kobe Pharm. University, www.ch.ic.ac.uk/ectoc/echet96/papers/054/index.htm, 2006.

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