Quinoline derivatives

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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Details

C546S167000

Reexamination Certificate

active

06894062

ABSTRACT:
The present invention relates to compounds of Formula I,wherein R1, R2, R3, R4, and n are as defined, and to pharmaceutically acceptable salts of said compounds. Compounds of Formula I have activity in agonizing 5HT7 receptors and are useful in treating, for example, disorders that can be treated by modulating circadian rhythms.

REFERENCES:
patent: 0173585 (1985-03-01), None
patent: 812911 (1951-09-01), None
Diaz de Arce, Humberto; “Some Derivatives of 8-Bromo-6-methylquinoline”, J. American Chemical Society, vol. 72, 1950, pp. 2971-2974; XP002273437.
Manabe, Kel; “Receptors for Oxo Acids: Effects of Intra-Ion Pair Hydrogen Bonding on Acid-Base Equilibria”, J. Org. Chem., vol. 58, 1993, pp. 6692-6700 XP-002273436.
Steck, Edgar A.; “Quinolines. III. The Synthesis of 5- and 7-Chloro- and Bromo-3-methyl-4-dialkylaminoalkylaminoquinolines”, J. American Chemical Society, vol. 68, 1946, pp. 380-383, XP-002273436.
Alabaster, C. T., 2(1H)-Quinolinones with Cardiac Stimulant Activity. 1. Synthesis and Biological Activities of (Six-Membered Heteroaryl)-Substituted Derivatives. J. Med. Chem., vol. 31, 1988, pp. 2048-2056, XP-002273434.
Davis, Steven E., 2,4-Diamino-5-benzylpyrimidines and Analogues as Antibacterial Agents. 11.Quinolylmethyl Analogues with Basic Substituents Conveying Specificity, J. Med. Chem, vol. 32, 1989, pp. 1936-1942, XP-002273433.
Jacobs, Christopher, “1-Imidazolyl(alkyl)-Substituted Di-and Tetrahydroquinolines and Analogues Syntheses and Evaluation of Dual Inhibitors of Thromboxane A2 Synthase and Aromatase” J. Med. Chem. vol. 43, 2000, pp. 1841-1851, XP-002273432.

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