1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

Base Information

Chemical Name:1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione
CAS No.:1433812-81-7
Molecular Formula:C₂₀H₁₇N₃O₅
Molecular Weight:379.372
Hs Code.:

Synonyms:1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

Suppliers and Price of 1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

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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’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

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Technology Process of 1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

There total 6 articles about 1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione 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: 92.0%

: 1433812-41-9
1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

: 1433812-81-7
1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1021/ol400930s

Reference yield:

: 1433812-19-1
1’-(3’-O-tertbutyldimethylsilyl-5’-O-triisopropylsilyl-2’-deoxy-β-D-ribofuranoside)-6-bromoquinazoline- 2,4-(3H)-dione

: 1433812-81-7
1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

Guidance literature:: Multi-step reaction with 2 steps

1: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 18 h / 90 °C / Schlenk technique; Inert atmosphere

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; tetrabutyl ammonium fluoride; potassium acetate; In tetrahydrofuran; 1,4-dioxane; 1: |Suzuki-Miyaura Coupling;
DOI:10.1021/ol400930s

Reference yield:

: p-tolyl-3-O-acetyl-1-thio-5-O-triisopropylsilyl-2-deoxy-D-ribofuranoside

: 1433812-81-7
1’-(2’-deoxy-β-D-ribofuranoside)-6-(4-cyano)phenylquinazoline-2,4-(3H)-dione

Guidance literature:: Multi-step reaction with 5 steps

1.1: N,O-bis-(trimethylsilyl)-acetamide / dichloromethane / 2.08 h / 20 °C / Molecular sieve

1.2: 0.12 h / 0 °C

2.1: potassium carbonate / dichloromethane; methanol / 18 h / 20 °C

3.1: 1H-imidazole / N,N-dimethyl-formamide / 18 h / 20 °C

4.1: potassium acetate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 18 h / 90 °C / Schlenk technique; Inert atmosphere

5.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With 1H-imidazole; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; N,O-bis-(trimethylsilyl)-acetamide; tetrabutyl ammonium fluoride; potassium acetate; potassium carbonate; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; 4.1: |Suzuki-Miyaura Coupling;
DOI:10.1021/ol400930s