2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

Base Information

Chemical Name:2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine
CAS No.:312934-46-6
Molecular Formula:C₃₁H₃₀FIN₂O₅
Molecular Weight:656.493
Hs Code.:

Synonyms:2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

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Technology Process of 2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

There total 7 articles about 2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 14470-28-1
mono-4-methoxytrityl chloride

: 312934-33-1
2',3'-dideoxy-2β-fluoro-3'-C-(iodomethyl)-5-methyluridine

: 312934-46-6
2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethyl acetate; at 20 ℃;
DOI:10.1021/jo001699u

Reference yield:

: 312934-28-4
5'-O-(tert-butydiphenylsilyl)-2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5-methyluridine

: 312934-46-6
2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / triethylamine trifluoride / tetrahydrofuran / 20 °C

2: 88 percent / diisopropylethylamine / ethyl acetate; tetrahydrofuran / 20 °C

With triethylamine trifluoride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jo001699u

Reference yield:

: 110497-15-9
1-[5-(tert-butyl-diphenyl-silanyloxymethyl)-3-fluoro-4-hydroxy-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

: 312934-46-6
2',3'-dideoxy-2'-β-fluoro-3'-C-(iodomethyl)-5'-O-(4-methoxytrityl)-5-methyluridine

Guidance literature:: Multi-step reaction with 7 steps

2.1: 57 percent / AIBN / benzene / 2 h / Heating

3.1: OsO₄; H₂O; N-methylmorpholine oxide / dioxane / 20 °C

3.2: NaIO₄ / H₂O; dioxane / 0 - 20 °C

4.1: 1.77 g / NaBH₄ / ethanol; H₂O / 2 h / 20 °C

5.1: 92 percent / methyl triphenoxyphosphonium iodide; 2,6-lutidine / dimethylformamide / 0 - 20 °C

6.1: 92 percent / triethylamine trifluoride / tetrahydrofuran / 20 °C

7.1: 88 percent / diisopropylethylamine / ethyl acetate; tetrahydrofuran / 20 °C

With 2,6-dimethylpyridine; sodium tetrahydroborate; osmium(VIII) oxide; 2,2'-azobis(isobutyronitrile); triethylamine trifluoride; methyltriphenoxyphosphonium iodide; water; 4-methylmorpholine N-oxide; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; water; ethyl acetate; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jo001699u