4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile

Base Information

Chemical Name:4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile
CAS No.:855869-41-9
Molecular Formula:C₃₂H₂₄N₆O₇
Molecular Weight:604.579
Hs Code.:

Synonyms:4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile

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Chemical Property of 4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile

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Technology Process of 4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile

There total 6 articles about 4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile 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: 49.0%

: 855869-39-5
C₃₄H₂₄N₈O₇

: 4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrole-3,4-dicarbonitrile

: 855869-41-9
4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile

Guidance literature:: With ammonia; In 1,4-dioxane; acetonitrile; at 45 ℃; for 168h;
DOI:10.1021/jm0402014

Reference yield:

: 855869-34-0
2-nitro-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrole-3,4-dicarboxamide

: 855869-41-9
4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: 263 mg / H₂ / Pd/C / ethanol; tetrahydrofuran / 18 h / 2068.59 Torr

2.1: 71 percent / aq. NaNO₂; HCl / acetonitrile / -40 - 0 °C

3.1: POCl₃; Et₃N / acetonitrile / 1 h / 0 °C

3.2: 58 percent / acetonitrile / 1.5 h / 20 °C

4.1: 49 percent / NH₃ / dioxane; acetonitrile / 168 h / 45 °C

With hydrogenchloride; ammonia; hydrogen; triethylamine; sodium nitrite; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol; acetonitrile;
DOI:10.1021/jm0402014

Reference yield:

: 5991-01-5
2,3,5-(tri-O-benzoyl)-D-ribofuranosyl chloride

: 855869-41-9
4-amino-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)pyrrolo[2,3-d][1,2,3]triazine-5-carbonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: 263 mg / H₂ / Pd/C / ethanol; tetrahydrofuran / 18 h / 2068.59 Torr

2.1: 71 percent / aq. NaNO₂; HCl / acetonitrile / -40 - 0 °C

3.1: POCl₃; Et₃N / acetonitrile / 1 h / 0 °C

3.2: 58 percent / acetonitrile / 1.5 h / 20 °C

4.1: 49 percent / NH₃ / dioxane; acetonitrile / 168 h / 45 °C

With hydrogenchloride; ammonia; hydrogen; triethylamine; sodium nitrite; trichlorophosphate; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol; acetonitrile;
DOI:10.1021/jm0402014