Synthons for oligonucleotide synthesis

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

536 2533, 536 2534, C07H 1904, C07H 1920

Patent

active

061179930

ABSTRACT:
The invention provides new reagents and processes for synthesizing oligonucleotides, including stereoselective oligonucleotide synthesis. In a first aspect, the invention provides novel monomer synthons for the synthesis of oligonucleotides. Monomer synthons according to this aspect of the invention are useful in the synthesis of oligonucleotides and can be used in place of the well known beta-cyanoethyl phosphoramidite monomer synthon in the phosphoramidite synthesis procedure. Certain monomer synthons according to this aspect of the invention are useful in this procedure for producing oligonucleotides having defined stereochemistry.
In a second aspect, the invention provides processes for synthesizing monomer synthons according to the invention, including diastereomerically enriched or purified monomer synthons. In the processes according to this aspect of the invention, the chemical reactions are stereoretentive so that the products of each reaction retain the same stereoconfiguration as their precursor reagent.
In a third aspect, the invention provides processes for synthesizing oligonucleotides using the well known phosphoramidite approach. In the processes according to this aspect of the invention, any of the monomer synthons according to the invention is used in place of the conventional beta-cyanoethyl phosphoramidite.

REFERENCES:
patent: 4689320 (1987-08-01), Kaji et al.
patent: 4806463 (1989-02-01), Goodchild et al.
patent: 5107065 (1992-04-01), Shewmaker et al.
patent: 5149798 (1992-09-01), Agrawal et al.
patent: 5194428 (1993-03-01), Agrawal et al.
patent: 5359052 (1994-10-01), Stec et al.
patent: 5506212 (1996-04-01), Hoke et al.
patent: 5512668 (1996-04-01), Stec et al.
patent: 5614622 (1997-03-01), Iyer et al.
patent: 5646267 (1997-07-01), Stec et al.
patent: 5750674 (1998-05-01), Iyer et al.
Zon, "Oligonucleotide Analogues as Potential Chemotherapeutic Agents," Pharmaceutical Research, 5(9), 539-549 (1988).
Farquhar et al., "Synthesis and Biological Evaluation of Neutral Derivatives of 5-Fluoro-2-'deoxyurdine 5'-Phosphate," J. Medicinal Chem., 26(8), 1153-1158 (Aug. 1983).
Iyer et al.,"A Novel Nucleoside Phosphoramidite Synthon Derived From 1 R, 2 S-Ephredrine," Tetrahedron: Asymmetry, 6(5), 1051-1054 (May 1995).
Wang et al., "A Stereoselective Synthesis of Dinucleotide Phosphonothioate Triesters Through a Chiral Indol-oxazaphosphorine Intermediate," Tetrahedron Letters, 38(5), 705-708 (Feb. 3, 1997).
Krazewski et al., "Studies on Reactions of Nucleoside H-Phosphanates with Bifunctional Reagents. Part 1. Reactions with Amino Alcohols," J. Chem. Soc., Perkin Trans. 1, (No. 14), 1699-1704 (Jul. 21, 1993).
Jones et al., "Synthesis of Some Nucleoside Cyclic Phosphoramidates and Related Compounds Via Phosphoramidites," J. Chem. Soc., Perkin Trans. 1, (No. 2), 199-202 (Feb. 1985).
Kant et al., "Studies toward Structure-Activity Relationships of Taxol.RTM.: Synthesis and Cytotoxicity of Taxol.RTM. Analogues with C-2' Modified Phenylisoserine Side Chains," Bioorganic and Medicinal Chem. Letters, 3(11), 2471-2474 (1993).
Zamecnik et al., Proc. Natl. Acad. Sci. USA 75, 280-284 (1978).
Agrawal, Trends In Biotech., 10, 152 (1992).
Chang and Pettitt, Proc. Biophys. Molec. Biol., 58, 225 (1992).
Uhlmann and Peyman, Chem. Rev., 90, 543 (1990).
Stein and Cheng, Science, 261, 1004 (1993).
Agrawal and Tang, Antisense Res. And Dev., 2, 261 (1992).
Bayever et al., Antisense Res. And Dev., 3, 383 (1993).
Stec and Wilk, Angew-Chem. Int. Ed. Engl., 33, 709 (1994).
Lesnikowski, J. Bioorg. Chem., 21, 127 (1993).
Stec et al., J. Am. Chem. Soc. 106, 6077 (1984).
Iyer et al., J. Am. Chem. Soc., 112, 1253 (1990).
Iyer et al., J. Am. Chem. Soc., 55, 4693 (1990).
Storey et al., Nucleic Acids Res., 19, 4109 (1991).
Robertson et al., J. Virology, 54, 651 (1985).
Harris et al., J. Virology, 36, 659 (1980).
Rice et al., Science, 229, 726 (1985).
Davison and Scott, J. Gen. Virology 67, 2279 (1986).
Richards et al., Virology, 89, 395 (1978).
Miller and Purcell, Proc. Natl. Acad. Sci., 87, 2057 (1990).
Simmonds et al., J. Gen. Virol., 74 661-668 (1993).
Campbell et al., Nature, 311 350 (1984).
Zurita et al., Proc. Natl. Acad. Sci., 2340 (1987).
Stahl and Prusiner, FASEB J., 5, 2799 (1991).
Sum et al., J. Am. Chem. Soc. Perkin Trans. I, p. 3183 (1994).
Cary et al., J. Am. Chem. Soc. Perkin Trans I, p. 831 (1993).
Beaucage and Iyer, Tetrahedron Lett., 48 2223 (1992).
Bentrude et al., J. Am. Chem. Soc., 111 3981 (1989).
Iyer et al., Bioorg. Med. Chem. Lett. 4, 2471 (1994).
Agrawal and Sarin, Advanced Drug Delivery Rev., 6, 251 (1991).
Beaucage, Methods In Molecular Biology, 20, 33-61 (1993).
Khorana et al., J. Molec. Biol., 72, 209 (1972).
Reese, Tetrahedron Lett., 34, 3143-3179 (1978).
Beaucage et al., Tetrahedron Lett., 22, 1859-1862 (1981).
Agrawal et al., Tetrahedron Lett., 28, 3539-3542 (1987).
Connolly et al., Biochemistry, 23, 3443 (1984).
Jager et al., Biochemistry, 27, 7237 (1988).
Agrawal et al., Proc. Antl. Acad. Sci. 85, 7079-7083 (1988).
Padmapriya et al., Antisense Res. Dev., 4, 185 (1994).
Ravikumar et al., Tetrahedron, 50, 9255 (1994).
Theisen et al., Nucleosides & Nucleotides, 12, 43 (1994).
Iyer et al., Nucleosides & Nucleosides, 14, 1349 (1995).
Kuijpers et al., Nucl. Acids Res., 18, 5197 (1990).
Reddy et al., Tetrahedron Lett., 35, 4311 (1994).
Tang et al., Nucleosides & Nucleosides, 14, 958 (1995).
Koziolkiewicz et al., J. Antisense Nucl. Acid Drug Dev., 7, 43 (1997).
Wang et al., Tetrahedron Lett., 38, 3797 (1997).
Iyer et al., J. Org. Chem. 60, 5388 (1995).
Iyer et al., J. Org. Chem., 55, 4693 (1990).
Zon, Methods In Molecular Biology, vol. 20, pp. 465 (1993).
Agrawal and Iyer, Curr. Op. In Biotech, 6, 12 (1995).
Zon and Stec, Oligonucleotides and Analogues: A Practical Approach, pp. 87-108 (1991).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Synthons for oligonucleotide synthesis does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Synthons for oligonucleotide synthesis, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Synthons for oligonucleotide synthesis will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-97438

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.