1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil

Base Information

Chemical Name:1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil
CAS No.:1332457-21-2
Molecular Formula:C₂₈H₂₅N₃O₆
Molecular Weight:499.523
Hs Code.:

Synonyms:1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil

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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 1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil

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Technology Process of 1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil

There total 9 articles about 1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]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: 85.0%

: 1332456-99-1
1-[3-C-phenylethynyl-3-O-(2-propynyl)-β-D-ribo-pentofuranosyl]uracil

: 54060-30-9
3-acetylenephenylamine

: 1332457-21-2
1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil

Guidance literature:: With (cyclooctadienyl)(cyclopentadienyl)ruthenium chloride; In 1,2-dichloro-ethane; at 20 ℃; regioselective reaction; Inert atmosphere;
DOI:10.1016/j.tetlet.2011.06.100

Reference yield: 85.0%

: 1332457-21-2
1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil

Guidance literature:

Reference yield:

: C₂₁H₂₄O₆

: 1332457-21-2
1-[3-C,3-O-{o-(2-phenyl-(3-aminophenyl))phenylenemethylene}-β-D-ribofuranosyl]uracil

Guidance literature:: Multi-step reaction with 4 steps

1: dmap; triethylamine / dichloromethane / 1 h / 20 °C

2: N,O-bis-(trimethylsilyl)-acetamide; trimethylsilyl trifluoromethanesulfonate / acetonitrile / 2 h / 50 °C

3: methanol; sodium methylate / 0.33 h / 20 °C

4: (cyclooctadienyl)(cyclopentadienyl)ruthenium chloride / 1,2-dichloro-ethane / 20 °C / Inert atmosphere

With methanol; dmap; N,O-bis-(trimethylsilyl)-acetamide; (cyclooctadienyl)(cyclopentadienyl)ruthenium chloride; trimethylsilyl trifluoromethanesulfonate; sodium methylate; triethylamine; In dichloromethane; 1,2-dichloro-ethane; acetonitrile; 3: Zemplen deacetylation;
DOI:10.1016/j.tetlet.2011.06.100