Substituted thieno[2,3-d]pyrimidin-2,4-dione compounds and...

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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C544S278000

Reexamination Certificate

active

08058280

ABSTRACT:
The present invention provides a compound represented by the formula:wherein R1is a C1-4alkyl; R2is (1) a 5- to 7-membered nitrogen-containing heterocyclic group which may have a substituent selected from the group consisting of (1′) a halogen, (2′) a hydroxy group, (3′) a C1-4alkyl and (4′) a C1-4alkoxy, (2) a phenyl which may have a substituent selected from the group consisting of (1′) a halogen, (2′) a C1-4alkoxy-C1-4alkyl, (3′) a mono-C1-4alkyl-carbamoyl-C1-4alkyl, (4′) a C1-4alkoxy and (5′) a mono-C1-4alkylcarbamoyl-C1-4alkoxy, or the like; R3is a C1-4alkyl; R4is a C1-4alkoxy, or the like; n is an integer of 1 to 4; or a salt thereof, as a thienopyrimidine compound having gonadotropin-releasing hormone antagonistic activity.

REFERENCES:
patent: 6048863 (2000-04-01), Furuya et al.
patent: 6297379 (2001-10-01), Furuya et al.
patent: 6340686 (2002-01-01), Furuya et al.
patent: 2003/0004172 (2003-01-01), Harter et al.
patent: 2003/0055269 (2003-03-01), Fukuoka et al.
patent: 2003/0134863 (2003-07-01), Furuya et al.
patent: 2004/0023987 (2004-02-01), Hata et al.
patent: 2004/0034039 (2004-02-01), Nakano et al.
patent: 1297850 (2003-04-01), None
patent: 2001-278884 (2001-10-01), None
patent: 2001-316391 (2001-11-01), None
patent: 2001-354588 (2001-12-01), None
patent: 2002-68982 (2002-03-01), None
patent: 2002-80397 (2002-03-01), None
patent: 2002-167327 (2002-06-01), None
patent: 2003-292492 (2003-10-01), None
patent: 2004-2321 (2004-01-01), None
patent: 2004-2377 (2004-01-01), None
patent: 96/24597 (1996-08-01), None
patent: 00/56739 (2000-09-01), None
patent: 02/43766 (2002-06-01), None
patent: 02/47722 (2002-06-01), None
patent: 02/064598 (2002-08-01), None
patent: 03/064429 (2003-08-01), None
patent: 03/075958 (2003-09-01), None
patent: 03/086464 (2003-10-01), None
Wolff, Manfred E. “Burger's Medicinal Chemistry, 5ed, Part I”, John Wiley & Sons, 1995, pp. 975-977.
Banker, G.S. et al, “Modern Pharmaceutics, 3ed.”, Marcel Dekker, New York, 1996, pp. 451 and 596.
Guo, Z. et al.; “Synthesis and structure-activity relationships of thieno (2, 3-d) pyrimidine-2, 4-dione derivatives as potent GnRH receptor agnagonists”; Bioorg. Med. Chem. Lett., Oct. 20, 2003; vol. 13; No. 20; pp. 3617 to 3622 full test; p. 3619,. compound 18.
Hara, T. et al.; “Suppression of a pituitary-ovarian axis by chronic oral administration of a novel nonpeptide gonadotrop in-releasing hormone antagonist, TAK-013, in cynomolgus monkesy”; J. Clin. Endocrinol. Metab.; (Apr. 2003); vol. 88; No. 4; pp. 1697 to 1704; full text.
Sasaki, S. et al.; “Discovery of a thieno (2, 3-d) pyrimidine-2, 4-dione bearing a p-methoxyureido phenyl moiety at the 6-poswition; a highlypotent and orally bioavailable non-peptide antagonist for the human luteinizing hormone-releasing hormone receptor:”; J. Med. Chem.; Jan. 2, 2003; vol. 46; No. 1; pp. 113 to 124; full text; p. 115, compound 9k-9m, p. 117, table 2.

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