5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide

Base Information

Chemical Name:5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide
CAS No.:70230-68-1
Molecular Formula:C₃₁H₃₄N₄O₅
Molecular Weight:542.635
Hs Code.:

Synonyms:5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide

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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 5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide

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Technology Process of 5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide

There total 4 articles about 5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide 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: 98.0%

: 70230-67-0
2',3',5'-tri-O-benzyl-N,N,3-trimethyladenosine iodide

: 70230-68-1
5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide

Guidance literature:: With sodium hydroxide; In ethanol; for 3h; Heating;

Reference yield:

: 70230-66-9
2',3',5'-tri-O-benzyl-N,N-dimethyladenosine

: 70230-68-1
5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / N,N-dimethyl-acetamide / 144 h / 40 °C

2: 98 percent / 1N aq. NaOH / ethanol / 3 h / Heating

With sodium hydroxide; In ethanol; N,N-dimethyl acetamide;

Reference yield:

: 3181-38-2
2',3',5'-tri-O-acetylinosine

: 70230-68-1
5-(Methylamino)-1-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)imidazole-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

2: 91 percent / KOH / dioxane; benzene / 1.5 h / Heating

3: 81 percent / N,N-dimethyl-acetamide / 144 h / 40 °C

4: 98 percent / 1N aq. NaOH / ethanol / 3 h / Heating

With potassium hydroxide; sodium hydroxide; In 1,4-dioxane; ethanol; N,N-dimethyl acetamide; benzene;