Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...
Reexamination Certificate
2006-09-12
2006-09-12
Morris, Patricia L. (Department: 1625)
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Having -c-, wherein x is chalcogen, bonded directly to...
C546S271400
Reexamination Certificate
active
07105547
ABSTRACT:
The present invention provides antibacterial agents of formula I,or a pharmaceutically acceptable salt thereof.
REFERENCES:
patent: 5668286 (1997-09-01), Yamada et al.
patent: WO 93/23384 (1993-11-01), None
patent: WO 98/54161 (1998-12-01), None
patent: WO 99/41244 (1999-08-01), None
patent: WO 00/10566 (2000-03-01), None
patent: WO 03/066631 (2003-08-01), None
patent: WO 03/072553 (2003-09-01), None
Approved Standard. Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically,3rded., published 1993 by the National Committee for Clinical Laboratory Standards, Villanova, Pennsylvania, USA.
Blache, et al.,Heterocycles, Application of the Mercuric Acetate-Edetic Acid Oxidation Method to the Synthesis of 11-Aza-1,2,3,4,5,6,7,12b-Octahydroindolo[2,3-α]Quinolizines, 1997, 45(1):57-69.
Brickner, S.J.,Current Pharmaceutical Design, Betham Science Publishers, Schiphol, NL, Oxazolidinone Antibacterial Agents, 1996, vol. 2, 175-194. XP001007528.
Brickner, et al,J. Med. Chem., Synthesis and Antibacterial Activity of U-100592 and U-100766, Two Oxazolidinone Antibacterial Agents for the Potential Treatment of Multidrug-Resistant Gram-Positive Bacterial Infections, 1996, 39:673-679.
Comins, et al.,Heterocycles, Regio- and Stereoselective Addition of Nucleophiles to 1-Phenoxycarbonyl-2,3-Dihydropyridinium Salts, 1994, 37(2):1121-1140.
Comins, et al.,Tetrahedron Lett., Preparation of 2,6-Disubstituted 2,3-Dihydro-4-pyridones: Dehydrogenation of Trimethylsilyl Enol Ethers with Palladium(II) Acetate., 1995, 36(52):9449-9452.
Dehmlow, et al.,Heterocycles, Studies Towards 3,4-Dimethoxy-1-Methyl-1,2-Dihydroxpyridine, So-Called Arecolidine, or its Tautomers, 1994, 37(1):355-366.
Diez, et al.,Heterocycles, Preparation of a New Chiral 5,6-Dihydropyridinium Synthon, 1990, 31(3):485-492.
Dodd, et al.,Tetrahedron Lett., Efficient Route to the Synthesis of C-2, C-3 Substituted 4-Piperidones, 1991, 32(30):3643-3646.
Evans, et al., Tetrahedron Lett., Regioselective Preparation of α,β—Unsaturated Ketones via the Direct Dehydrogenation of Triisopropylsilyl Enol Ethers, 1995, 36(23):3985-3988.
Guerry and Neier, Chimia, Photochemical Cycloadditions to 5,6-Dihydro-4-pyridones, Oct. 1987, 41(10), 341-342.
Guerry, et al.,Synthesis, Reduktion von 4-Pyridinonen, 1984, 485-488.
Haider, et al.,Helv. Chim. Acta, Synthesis of 4-Oxo-1,2,3,4-tetrahydropyridine (2,3-Dihydro-4(1H)pyridinone), 1975, 58(5):1287-1292.
Ishii, et al.,Tetrahedron Lett., Rhodium-Catalyzed Reaction of N-Acylpiperazines with CO and Ethylene. Carbonylation at a C-H Bond Directed by an Amido Group, 1997, 38(43):7565-7568.
Kirschbaum and Waldmann,J. Org. Chem., Three-Step Access to the Tricyclic Benzo[a]quinolizine Ring System, 1998, 63:4936-4946.
Kirschbaum and Waldmann,Tetrahedron Lett., Construction of the Tricyclic Benzoquinolizine Ring System by Combination of a Tandem Mannich-Michael Reaction with a Heck Reaction, 1997, 38(16):2829-2832.
Livermore, D.M.,Journal of Antimicrobial Chemotherapy, Linezolid in vitro: mechanism and antibacterial spectrum, 2003, 51(S2):119-1116. XP002267748.
Lock and Waldmann,Chem. Eur. J., Enantioselective Construction of Highly Functionalized Indoloquinolizines-Congeners to Polycyclic Indole Alkaloids, 1997, 3(1):143-151.
Lock and Waldmann,Tetrahedron Lett., Asymmetric Synthesis of Highly Functionalized Tetracyclic Indole Bases Embodying the Basic Skeleton of Yohimbine- and Reserpine Type Alkaloids, 1996, 37(16):2753-2756.
Stutz and Stadler,Tetrahedron Lett., A Novel Approach to Cyclic β-Carbonyl-EnaminesΔ7,8-Lysergic Acid Derivatives via the Polonovski Reaction, 1973, 51:5095-5098.
Waldmann, et al.,Tetrahedron, Asymmetric Synthesis of Indolo[2,3-α]quinolizidin-2-ones-Congeners to Yohimbine-Type Alkaloids, 1993, 49(2):397-416.
Gordeev Mikhail Fedor
May Paul Dennis
Patel Dinesh Vinoobhai
Singh Upinder
Morris Patricia L.
Pharmacia and Upjohn Company
Yang Lucy X.
LandOfFree
Antimicrobial 1-aryl dihydropyridone compounds does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Antimicrobial 1-aryl dihydropyridone compounds, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Antimicrobial 1-aryl dihydropyridone compounds will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3596182