1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

Base Information

Chemical Name:1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil
CAS No.:1453217-82-7
Molecular Formula:C₄₃H₄₈N₂O₁₀SSi
Molecular Weight:813.013
Hs Code.:

1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

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Chemical Property of 1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

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Technology Process of 1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

There total 7 articles about 1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil 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:

: 956485-08-8
((3aR,5R,6S,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol

: 1453217-82-7
1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

Guidance literature:: Multi-step reaction with 8 steps

1.1: pyridinium chlorochromate / dichloromethane / 13 h / 40 °C / Inert atmosphere

2.1: boron trifluoride diethyl etherate / dichloromethane / 0.08 h / -41 °C / Inert atmosphere

2.2: 2 h / -41 °C / Inert atmosphere

3.1: pyridine / 24 h / 110 °C / Inert atmosphere

4.1: acetic acid; water / 3 h / 90 °C

5.1: pyridine / 12 h / 23 °C / Inert atmosphere

6.1: N,O-bis-(trimethylsilyl)-acetamide / acetonitrile / 1 h / 90 °C / Inert atmosphere

6.2: 16 h / 0 - 50 °C / Inert atmosphere

7.1: potassium carbonate / methanol / 1 h / 23 °C / Inert atmosphere

8.1: pyridine / 2 h / 23 °C / Inert atmosphere

With pyridine; N,O-bis-(trimethylsilyl)-acetamide; boron trifluoride diethyl etherate; water; potassium carbonate; acetic acid; pyridinium chlorochromate; In methanol; dichloromethane; acetonitrile; 2.1: |Sakurai Allylation / 6.1: |Vorbrueggen Nucleoside Synthesis / 6.2: |Vorbrueggen Nucleoside Synthesis;
DOI:10.1021/jo401170y

Reference yield:

: 1453217-80-5
1-(2,5-O-diacetyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

: 1453217-82-7
1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / methanol / 1 h / 23 °C / Inert atmosphere

2: pyridine / 2 h / 23 °C / Inert atmosphere

With pyridine; potassium carbonate; In methanol;
DOI:10.1021/jo401170y

Reference yield:

(3aR,5R,6S,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[2,3-d][1,3]dioxole-5-carbaldehyde: (3aR,5R,6S,6aR)-5-(((tert-butyldiphenylsilyl)oxy)methyl)-2,2-dimethyl-6-(naphthalen-2-ylmethoxy)tetrahydrofuro[2,3-d][1,3]dioxole-5-carbaldehyde

: 1453217-82-7
1-(2-O-methanesulfonyl-3-O-(2-naphthylmethyl)-4-C-(tert-butyldiphenylsilyl)oxymethyl-5-O-acetyl-6-deoxy-6-C-vinyl-α-L-mannofuranosyl)uracil

Guidance literature:: Multi-step reaction with 7 steps

1.1: boron trifluoride diethyl etherate / dichloromethane / 0.08 h / -41 °C / Inert atmosphere

1.2: 2 h / -41 °C / Inert atmosphere

2.1: pyridine / 24 h / 110 °C / Inert atmosphere

3.1: acetic acid; water / 3 h / 90 °C

4.1: pyridine / 12 h / 23 °C / Inert atmosphere

5.1: N,O-bis-(trimethylsilyl)-acetamide / acetonitrile / 1 h / 90 °C / Inert atmosphere

5.2: 16 h / 0 - 50 °C / Inert atmosphere

6.1: potassium carbonate / methanol / 1 h / 23 °C / Inert atmosphere

7.1: pyridine / 2 h / 23 °C / Inert atmosphere

With pyridine; N,O-bis-(trimethylsilyl)-acetamide; boron trifluoride diethyl etherate; water; potassium carbonate; acetic acid; In methanol; dichloromethane; acetonitrile; 1.1: |Sakurai Allylation / 5.1: |Vorbrueggen Nucleoside Synthesis / 5.2: |Vorbrueggen Nucleoside Synthesis;
DOI:10.1021/jo401170y