Process for producing 2,6-dihalogenopurine

Organic compounds -- part of the class 532-570 series – Organic compounds – Pteroyl per se or having -c- – wherein x is chalcogen – bonded...

Reexamination Certificate

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C544S277000

Reexamination Certificate

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06936713

ABSTRACT:
A process for conveniently and efficiently preparing a 2,6-dihalogenopurine using an inexpensive starting material. A process for preparing a 2,6-dihalogenopurine, comprising treating a 2-amino-6-halogenopurine having a protective group at 7thposition or 9thposition with a diazotizating agent and a halogen source; and a process for preparing a 9-acyl-2-amino-6-halogenopurine, comprising treating a 2-amino-6-halogenopurine with an acylating agent in the presence of a base.

REFERENCES:
patent: 3314938 (1967-04-01), Kawashima et al.
patent: 6455696 (2002-09-01), Hayashi et al.
patent: 138683 (1985-04-01), None
patent: 1172365 (2002-01-01), None
Richard E. Austin, Tet. Letters 43 6169 (2002).
Vasu Nair, et al., “Modificaton of Nucleic Acid Bases via Radical Intermediates: Synthesis of Dihalogenated Purine Nucleosides,” Synthesis, vol. 8, 1982, pp. 670-672.
P. Francom, et al, “Nucleic Acid Related Compouds 116, Nonaqueous Diazotization of Aminopurine Nucleosides,” Journal of Organic Chemistry, vol. 67, No. 19, 2002, pp. 6788-6796.
Radiochimiya, vol. 23, No. 4, pp. 607-613; 1981, With English translation.
Michael R. Harnden et al.: “Analogues of the antiviral acyclonucleoside 9-(4-hydroxy-3-hydroxymethybutyl)guanine. Part 4. Substitution on the 2-amino group”, J. Chem. Soc., Perkins Trans. 1, pp. 2207-2213, 1989.
Anupma Dhanda et al.: “Facile conversion of 4-endo-hydroxy-2-oxabicyclo[3.3.0]oct-7-en-3-one into carbocyclic 2′-deoxyribonucleoside analogues”, J. Chem. Soc., Perkins Trans. 1, pp. 3469-3475, 1999.
Nathanael S. Gray et al.: “Combinational synthesis of 2, 9-substituted purines”, Tetrahedron Letters, vol. 38, No. 7, pp. 1161-1164, 1997.
J. Warren Beach et al.: “A highly stereoselective synthesis of anti-HIV 2′, 3′-dideoxy- and 2′, 3′-didehydro2′3′-dideoxynucleosides” J. Org. Chem., vol. 57, No. 14, pp. 3887-3894, 1992.
Suzanne E. Keeling et al.: “The discovery and synthesis of highly potent, A2areceptor agonists”, Bioorganic & Medicinal Chemistry Letters, vol. 10, pp. 403-406, 2000.
Kazunori Niiya et al.: “2-(N′-alkylidenehydrazino) adenosines: Potent and selective coronary vasodilators”, J. Med. Chem., vol. 35, No. 24, pp. 4557-4561, 1992.
B. Ha Seung et al.: “New base-altered adenosine analogues: synthesis and affinity at adenosine A1and A2Areceptors”, Bioorganic & Medicinal Chemistry Letters, vol. 7, No. 24, pp. 3085-3090, Jan. 16, 2002.
Elizabeth Dyer et al.: “Acylations of some 2-amino-6-halo- and 2-amino-6-alkylthiopurines”, J. Med. Chem., vol. 11, No. 6, pp. 1232-1234, 1968.

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