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Synthesis of 2', 3'-dideoxynucleosides for automated DNA synthesis and pyrophosphorolysis activated polymerization

a technology of dna and synthesis method, applied in the field of synthesis of various 2′, 3′-dideoxynucleoside supports, can solve the problems of inability to commercially synthesize dda, ddg, dt, and all such synthetic methods are labor-intensive and costly, and no adequate method for making dna containing dt has been described

Inactive Publication Date: 2017-10-26
LIFE TECH CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent text describes methods for synthesizing various 2',3'-dideoxynucleoside supports, such as 2',3'-dideoxyguanosine, 2',3'-dideoxyadenosine, and 3'-deoxythymidine. These methods involve reacting the nucleoside with specific intermediates and then cleaving off the protecting group to create the final support structure. The methods can be used in automated DNA synthesis methods and can also be used to detect nucleic acids. The technical effects of the patent text include improved methods for synthesizing these nucleoside supports and improved methods for detecting nucleic acids.

Problems solved by technology

While PAP is undoubtedly a very attractive technique, it has certain deficiencies and drawbacks.
One difficulty lies in the process of obtaining a suitable oligonucleotide P. For instance, such products as ddA, ddG, and dT are not available commercially and have to be synthesized.
All such synthetic methods are labor intensive and costly.
Likewise, no adequate method for making a DNA containing dT has been described, other than expensive 5′-to-3′ reverse synthesis.
This is likely due to the fact that there is a lack of convenient exocyclic functional group for covalent linkage on the thymine base.

Method used

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  • Synthesis of 2', 3'-dideoxynucleosides for automated DNA synthesis and pyrophosphorolysis activated polymerization
  • Synthesis of 2', 3'-dideoxynucleosides for automated DNA synthesis and pyrophosphorolysis activated polymerization
  • Synthesis of 2', 3'-dideoxynucleosides for automated DNA synthesis and pyrophosphorolysis activated polymerization

Examples

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Effect test

example 1

Preparation of A 2′,3′-Dideoxyadenosine Support Structure

[0098]

[0099]9-(5-((tris(4-methoxyphenyl)methoxy)methyl)tetrahydrofuran-2-yl)-9-purin-6-amine (product 12 in Reaction Scheme H, above) was synthesized first according to the reaction shown by Reaction Scheme H. To obtain this compound, 2′,3′-dideoxyadenosine (500 mg, 2.13 mmol) was dried three times by co-evaporation with pyridine, and suspended in about 10 mL of dry pyridine, were added DMTC1 (1.084 g, 3.2 mmol), triethylamine (0.45 mL, 3.2 mmol) and DMAP 6.48 mg, 0.053 mmol) were added. This reaction mixture was stirred at room temperature for about 4 hours, and then about 10 mL of 5% NaHCO3 were added.

[0100]The mixture was then extracted with two ˜30 mL portions of ethyl acetate, followed by combining the organic layers and by evaporation to dryness. The residue was purified by flash chromatography on silica gel (CH2Cl2 / CH3OH=10 / 1), to create product 12, i.e., 9-(5-((tris(4-methoxyphenyl)methoxy)methyl)tetrahydrofuran-2-yl)-...

example 2

Preparation of A 2′,3′-Dideoxyguanosine Support Structure

[0104]

[0105]9-(5-(hydroxymethyl)tetrahydrofuran-2-yl)-6-oxo-6,9-dihydropurin-2-yl)-N,N-dimethylformimidamide amine (product 3 in Reaction Scheme A, above) was synthesized first according to the reaction shown by Reaction Scheme A. To obtain this compound, 2′,3′-dideoxyguanosine (about 947 mg, 3.77 mmol) was dissolved in 20 mL of methanol and N,N-dimethylformamide dimethyl acetal (about 1.06 mL, 7.98 mmol) was added. The mixture was stirred overnight at room temperature followed by adding another portion of N,N-dimethylformamide dimethyl acetal (about 0.5 mL, 3.9 mmol). The mixture was again stirred for about 2 hours at room temperature. The solvent was evaporated to yield the product, (compound 3 in Reaction Scheme A, above) as a white solid.

[0106]Next, compound 3 as shown in reaction scheme A was used to obtain N,N-dimethyl-N′-(6-oxo-9-(5-((tris(4-methoxyphenyl) methoxy)methyl)tetrahydrofuran-2-yl)-6,9-dihydropurin-2-yl) form...

example 3

Preparation of N-(9-(5-(1-(4-methoxyphenyl)-1-phenylethoxy)methyl) tetrahydrofuran-2-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide

[0111]

[0112]Compound 5A shown in Reaction Schemes E and F, above, can be used for preparing compound 6 shown in Reaction Schemes C and F, instead of compound 5 discussed in Example 2, above. The synthesis was carried out according to the reaction showin by Reaction Scheme D. 2′,3′-dideoxyguanosine was co-evaporated with anhydrous pyridine three times before it was suspended in about 20 mL of dry pyridine. Trimethylchlorosilane (about 1.6 mL, 12.4 mmol) was added and the reaction mixture was stirred at room temperature for about 15 minutes, followed by adding about 2.6 mL (15.5 mmol) isobutyric anhydride. The reaction mixture was kept overnight at room temperature, followed by cooling in an ice bath and adding about 4 mL of water after about 5 minutes. Then, about 4 mL of about 29% aqueous ammonia was added and the reaction was stirred for about 15 min...

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Abstract

Methods for preparation of 2′,3′-dideoxynucleotides support structures, such as 2′,3′-dideoxyguanosine, 2′,3′-dideoxyadenosine, and 3′-deoxythymidine support structures are disclosed. Various methods of using such structures are also provided, such as their use for automated DNA synthesis and pyrophosphorolysis activated polymerization.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a divisional application of U.S. patent application Ser. No. 13 / 117,029, filed May 26, 2011 which claims the benefit of priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application Nos. 61 / 349,791, filed May 28, 2010 and 61 / 352,197, filed Jun. 7, 2010, which are herein incorporated by reference in their entirety.FIELD[0002]This invention relates generally to the field of nucleic acid polymerization and amplification. More specifically, this invention relates to methods of synthesis of various 2′,3′-dideoxynucleoside supports, such as 2′,3′-dideoxyguanosine, 2′,3′-dideoxyadenosine, 3′-deoxythymidine and 2′,3′-dideoxyuridine supports, and to their use.BACKGROUND[0003]Pyrophosphorolysis-activated polymerization (PAP) is a technique useful for nucleic acid polymerization and amplification. PAP is an allele-specific amplification method, the essence of which is that 3′-dideoxynucleotide-terminated primers (also d...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07H19/16C07H21/04C07H21/02C07H19/06C07D239/54C07D473/34C07D473/18C07D405/04C12Q1/68C07H21/00
CPCC07H21/02C07H19/06C07H21/00C12Q1/6806C07D405/04C07H21/04C07D473/18C07D239/54C07D473/34C07H19/16
Inventor MA, ZHAOCHUNMULLAH, KHAIRUZZAMAN BASHAREASON, ROBERT G.
Owner LIFE TECH CORP
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