Pyrimidine compounds as purine receptor antagonist

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C544S242000

Reexamination Certificate

active

07875600

ABSTRACT:
Compounds of formula (I); wherein R1is H or NHZ; R2is optionally substituted aryl or heteroaryl attached via a carbon atom; R3is H; optionally substituted C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, or C3C7cycloalkyl, halogen; OH or OR, or R4is H, optionally substituted C1-C6alkyl, C3C6alkenyl, C3-C6alkynyl, C3-C7cycloalkyl, aryl or heteroaryl, R5is H or optionally substituted C1-C6alkyl, C3-C6alkenyl, C3-C6alkynyl, or C3-C7cycloalkyl; or R4and R5together form a 5 or 6-membered heterocyclic ring; and R10is optionally substituted C1-C6alkyl; are purine receptor, particularly adenosine receptor antagonists, useful for treatment of, inter alia, movement disorders such as Parkinsons disease.

REFERENCES:
patent: WO 02/055084 (2002-07-01), None
patent: WO 2004/029204 (2004-04-01), None
patent: WO 2004/080979 (2004-09-01), None
Dorwald, F. ‘Side Reactions in Organic Synthesis: a Guide to Successful Synthesis Design’ Wiley-VCH, Preface, p. ix, 2005.
Jordan, V. ‘Tamoxifen: a most unlikely pioneering medicine’ Nature Reviews: Drug Discovery, vol. 2, pp. 205-213, 2003.
Takao, S. et al: Chem. Pharm. Bull., vol. 28, No. 2, 1980, pp. 571-577, XP001206934.
Sakamoto, T. et al.: Chem, Pharm. Bull., vol. 28, No. 1, 1980, pp. 202-207, XP001206935.
Obrecht D et al: “5. A Novel and Officient Approach for the Combinatorial Synthesis of Structurally Diverse Pyrimidines on Solid Support” Helvetica Chimica ACTA, Verlag Helvetica CH1MICA ACTA. Basel, CH, vol. 80, 1997, pp. 65-72. XP002915327 ISSN: 0018-019X.

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