N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine

Base Information

Chemical Name:N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine
CAS No.:479035-82-0
Molecular Formula:C₂₃H₁₉F₂N₃O₅
Molecular Weight:455.418
Hs Code.:

N<sup>4</sup>-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine

Synonyms:N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine

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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 N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine

Chemical Property:

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Technology Process of N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine

There total 2 articles about N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine 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:

: 85743-99-3
N-(2-Trimethylsilanyloxy-pyrimidin-4-yl)-benzamide

: 479035-81-9
1-acetyl-5-O-benzoyl-2,3-dideoxy-3,3-difluoro-D-ribofuranose

: 479035-82-0
N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine

: 698391-73-0
N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-α-D-ribofuranosyl)cytosine

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In acetonitrile; at 20 ℃; for 3h;
DOI:10.1021/jm040027j

Reference yield:

: Benzoic acid (R)-3,3-difluoro-5-hydroxy-tetrahydro-furan-2-ylmethyl ester

: 479035-82-0
N⁴-benzoyl-1-(5-O-benzoyl-2,3-dideoxy-3,3-difluoro-β-D-ribofuranosyl)cytosine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.5 g / AcOH; H₂SO₄ / 0.5 h / 20 °C

2: trimethlysilyltrifluoromethane sulfonate / acetonitrile / 3 h / 20 °C

With trimethylsilyl trifluoromethanesulfonate; sulfuric acid; acetic acid; In acetonitrile;
DOI:10.1021/jm040027j