N⁴-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine

Base Information

• Chemical Name: N⁴-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine
• CAS No.: 181423-22-3
• Molecular Formula: C₄₂H₃₇N₃O₁₂
• Molecular Weight: 775.769

Synonyms:N⁴-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine

Chemical Property of N⁴-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

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Technology Process of N⁴-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine

There total 3 articles about N⁴-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-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: 89.0%

N4-benzoyl-1-[5-O-tert-butyldiphenylsilyl-3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine (181423-12-1) → N4-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine (181423-22-3)

Guidance literature:

With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 0.75h;

DOI:10.1080/07328319608002433

Reference yield:

N-(1-((2R,4S,5R)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)benzamide (139244-40-9) → N4-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine (181423-22-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 71 percent / SnCl₄ / 1,2-dichloro-ethane / 0.67 h / 0 °C

2: 89 percent / Bu₄NF*3H₂O / tetrahydrofuran / 0.75 h / 20 °C

With tetrabutyl ammonium fluoride; tin(IV) chloride; In tetrahydrofuran; 1,2-dichloro-ethane;

DOI:10.1080/07328319608002433

Reference yield:

N4-benzoyl-2'-deoxycytidine (4836-13-9) → N4-benzoyl-1-[3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine (181423-22-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 80 percent / imidazole / pyridine / 5 h / 20 °C

2: 71 percent / SnCl₄ / 1,2-dichloro-ethane / 0.67 h / 0 °C

3: 89 percent / Bu₄NF*3H₂O / tetrahydrofuran / 0.75 h / 20 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; tin(IV) chloride; In tetrahydrofuran; pyridine; 1,2-dichloro-ethane;

DOI:10.1080/07328319608002433

upstream raw materials:

N⁴-benzoyl-1-[5-O-tert-butyldiphenylsilyl-3-O-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2-deoxy-β-D-ribofuranosyl]-cytosine

N-(1-((2R,4S,5R)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-4-hydroxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)benzamide

N₄-benzoyl-2'-deoxycytidine

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