N⁴-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]cytosine

Base Information

• Chemical Name: N⁴-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]cytosine
• CAS No.: 635293-04-8
• Molecular Formula: C₄₂H₄₀N₆O₁₅
• Molecular Weight: 868.811

Synonyms:N⁴-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]cytosine

Chemical Property of N⁴-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]cytosine

Chemical Property:

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Technology Process of N⁴-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]cytosine

There total 2 articles about N⁴-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]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: 79.7%

4-benzoylamino-1-(O2,O3-dibenzoyl-β-D-arabinofuranosyl)-1H-pyrimidin-2-one (15585-06-5) + 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-β-D-mannopyranose (635292-85-2) → N4-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]cytosine (635293-04-8)

Guidance literature:

With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃;

DOI:10.1002/hlca.200390163

Reference yield:

D-glucal triacetate (2873-29-2) → N4-benzoyl-1-[2,3-di-O-benzoyl-5-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl)-β-D-arabinofuranosyl]cytosine (635293-04-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: cerium(IV) ammonium nitrate; NaN₃ / acetonitrile / 24 h / 20 °C

1.2: 26.6 percent / AcOH / 2 h / 100 °C

2.1: 79.7 percent / BF₃*OEt₂ / CH₂Cl₂ / 20 °C

With sodium azide; ammonium cerium(IV) nitrate; boron trifluoride diethyl etherate; In dichloromethane; acetonitrile;

DOI:10.1002/hlca.200390163

upstream raw materials:

4-benzoylamino-1-(O²,O³-dibenzoyl-β-D-arabinofuranosyl)-1H-pyrimidin-2-one

1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-β-D-mannopyranose

D-glucal triacetate

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