Method for the synthesis of...

Organic compounds -- part of the class 532-570 series – Organic compounds – Nitrogen attached directly or indirectly to the purine ring...

Reexamination Certificate

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Reexamination Certificate

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06927291

ABSTRACT:
An efficient synthetic route to antiviral 2′,3′-dideoxy-2′,3′-didehydro-nucleosides, such as 2′,3′-dideoxy and 2′- or 3′-deoxyribo-nucleoside analogs, from available precursors is disclosed, with the option of introducing functionality as needed. In one embodiment, a method for the preparation of β-D and β-L-2′,3′-dideoxy-2′,3′-didehydro-nucleosides is described that includes: activating a compound of structure (1)wherein B is a pyrimidine or purine base and Y is O, S or CH2with an acyl halide of the formula X—C(═O)R1, X—C(═O)C(R1)2OC(═O)R1or X—C(═O)OR1(wherein X is a halogen, and each R1is independently hydrogen, lower alkyl, alkyl, aryl or phenyl); reducing the resulting compound with a reducing agent to form a 2′,3′-dideoxy-2′,3′-didehydro-nucleoside; and optionally deprotecting the nucleoside. The haloacylation of the first step can form the 2′-acyl-3′-halonucleoside, the 3′-acyl-2′-halonucleoside, or a mixture thereof.

REFERENCES:
patent: 3817982 (1974-06-01), Verheyden et al.
patent: 4594339 (1986-06-01), Lopez et al.
patent: 4847366 (1989-07-01), Yamamoto et al.
patent: 4900828 (1990-02-01), Belica et al.
patent: 4904770 (1990-02-01), Starrett, Jr. et al.
patent: 4987224 (1991-01-01), Chu
patent: 5130421 (1992-07-01), Starrett, Jr. et al.
patent: 5175267 (1992-12-01), Chu
patent: 5200514 (1993-04-01), Chu
patent: 5212298 (1993-05-01), Radamacher et al.
patent: 5384396 (1995-01-01), Chu et al.
patent: 5455339 (1995-10-01), Chu
patent: 5539099 (1996-07-01), Skonezny et al.
patent: 5561120 (1996-10-01), Lin et al.
patent: 5625057 (1997-04-01), Shiragami et al.
patent: 5703058 (1997-12-01), Schinazi et al.
patent: 5905070 (1999-05-01), Schinazi et al.
patent: 6232300 (2001-05-01), Schinazi et al.
patent: 0 334 368 (1989-09-01), None
patent: 0 409 227 (1990-07-01), None
patent: 8 901 258 (1990-12-01), None
patent: WO 96/22778 (1996-08-01), None
patent: WO 99/43691 (1999-09-01), None
Abdel-Medied, A. W.-S., et al.,Synthesis, 1991, 313.
Chen S., et al. “Synthesis and Biological Evaluation of a Series of 2′-Fluorinated-2′,3′-Didehydro-(L)-Nucleosides.”Biorganic&Medicinal Chemistry Letters. 8:3245-3250, 1998.
Chen, S., et al. “Stereoselective Synthesis of β-L-FD4C and β-L-FddC.”J. Org. Chem.62(11):3449-3452, 1997.
Cheng, Y., et al.,J. Med. Chem. 1996, 62, 1757-1759.
Horwitz, J. P., et al. “Nucleosides. IX. The Formation of 2′,3′-Unsaturated Pyrimidine Nucleosidesviaa Novel β-Elimination Reaction.”J. Org. Chem. 31:205-211, Jan. 1966.
Horwitz, J. P., et al. “Nucleosides. VI. The Introduction of Unsaturation into the Carbohydrate of a Pyrimidine Nucleosideviaa 2,3′-Anhydro Bond.”J. Am. Chem. Soc. 86:1896-1897, May 5, 1964.
Horwitz, J. P., et al. “Nucleosides. XI. 2′,3′-Dideoxycytidine.”J. Org. Chem. 32:817-818, Mar. 1967.
Jain, T.C., et al. “Reactions of 2-Acyloxyisobutyryl Halides with Nucleosides. IV. A Facile Synthesis of 2′,3′-Unsaturated Nucleosides Using Chromous Acetate.”J. Org. Chem. 39(1):30-38, 1974.
Manchand et al. “Syntheses of the Anti-AIDS Drug 2′,3′-Dideoxycytidine from Cytidine.”J. Org. Chem. 57(12):3473-3478, 1992.
Morikawa, T., et al.,Chem. Pharm Bull., 1992, 40, 3189.
Patrick, T.B., et al. “New Fluorobutenolide Templates for Synthesis.”J. Org. Chem. 59(5):1210-1212, 1994.
Robins, M. J., et al.,Tetrahedron Letters1984, 25, 367.
Russell, A. F., et al.,J. Am. Chem. Soc. 1973, 95, 4025.
Shi, et al. “Synthesis and Biological Evaluation of 2′,3′-Didehydro-2′,3′-dideoxy-5-fluorocytidine (D4FC) Analogues: Discovery of Carbocyclic Nucleoside Triphosphates with Potent Inhibitory Activity against HIV-1 Reverse Transcriptase.”J. Med. Chem. 42:859-867, 1999.
Sujino, K., et al. “Facile Synthesis of 2′,3′-Unsaturated Nucleosides from 2-Deoxyribose.”Tetrahedron Letters. 37(34):6133-6136, 1996.
Thenappan, A., et al. “Reduction-Olefination of Esters: A New and Efficient Synthesis of α,β-Unsaturated Esters.”J. Org. Chem. 55(15):4639-4612, 1990.
Verheyden, J.P., et al “2′,3′-Unsaturated nucleosides.”Chem. Abstr. 81:508(63942), 1974.
Coe, et al.,Journal of Flourine Chemistry, Elsevier Sequoia, Lausanne, CH, vol. 69, No. 1, pp. 19-24, 1994.
Classon, B. et al.,ACTA Chem. Scand., Ser. B., B36(4), 251-3, 1982.
Mansuri, M M et al.,J. of Organic Chemistry, American Chemical Society, vol. 54, No. 20, Sep. 29, 1989, 1780-4785.
Ozaki, S. et al.,Bull. Chem. Soc. Jpn., 50(8), 2197-8, 1977.
Ozaki, S. et al.,Nucleic Acids Symp. Ser., 9-1, 12, p. 11, table 1, 1983.
Watanabe, K.A. et al.,J. Med. Chem, 23(10), 1088-94, 1980.
Van Aerschot, A. et al.,j. MED Chem, 33(6), 1833-9, 1990.

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