Pyrimidine compounds

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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Details

C514S235800, C514S252140, C514S269000, C514S275000, C544S320000, C544S324000, C544S336000, C544S059000, C544S111000

Reexamination Certificate

active

06958332

ABSTRACT:
This invention features pyrimidine compounds of formula (I):each of R2and R4is H; R3is H, alkyl, aryl, heteroaryl, cyclyl, heterocyclyl, or alkylcarbonyl; R5is H or alkyl; n is 0, 1, 2, 3, 4, 5, or 6; X is NRc; Y is covalent bond, CH2, C(O), C═N—Rc, C═N—ORc, C═N—SRc, O, S, S(O), S(O2), or NRc; Z is N or CH; one of U and V is N, and the other is CRc; and W is O, S, S(O), S(O2), NRc, or NC(O)Rc; in which each of Raand Rb, independently, is H, alkyl, aryl, heteroaryl; and Rcis H, alkyl, aryl, heteroaryl, cyclyl, heterocyclyl, or alkylcarbonyl.

REFERENCES:
patent: 6384032 (2002-05-01), Ono et al.
patent: WO 00/62778 (2000-10-01), None
Trincheri, Current Opinion In Hematology 4: 59-66, 1997.
Arvanitis, et al.Non-Peptide Corticotropin-Releasing Hormone Antagonists: Syntheses and Structure—Activity Relationships of 2-Anilinopyrimidines and -triazines. J. med. Chem, vol. 42, 1999, pp. 805-818.
Mylari, et al.Sorbitol Dehydrogenase Inhibitors(SDIs): A New Potent, Enantiomeric SDI,4-[2-1-R-Hydroxy-ethyl)-pyrimidin-4-yl]-piperazine-I-sulfonic Acid Dimethylamide. J. Med Chem, vol. 44, 2001, pp. 2695-2700.
International Search Report dated Jun. 12, 2003.
Nishigaki, et al., “Synthesis of Iminodipyrimidines,” Tetrahedron Letters 7:539-542 (1969).
Copy of European Search Report dated Feb. 7, 2005.
Trinchieri, G. “Function and Clinical Use of Interleukin-12”, Current Opinion in Hematology 4: 59-66 (1997).

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