5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide

Base Information

• Chemical Name: 5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide
• CAS No.: 100313-39-1
• Molecular Formula: C₂₀H₂₆N₆O₇
• Molecular Weight: 462.462
• Mol file: 100313-39-1.mol

Synonyms:5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide

Chemical Property of 5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide

There total 2 articles about 5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(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:

ethyl N-(benzylcarbamothioyl)carbamate (54035-70-0) → 5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide (100313-39-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 40 percent / Et₃N, phosgene / benzene / 1 h / Heating

2: 64 percent / N,N-dimethyl-acetamide / Ambient temperature

With phosgene; triethylamine; In N,N-dimethyl acetamide; benzene;

DOI:10.1021/jo00358a021

Reference yield:

benzylamine (100-46-9) → 5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide (100313-39-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 93 percent / diethyl ether / 0.5 h / Ambient temperature

2: 40 percent / Et₃N, phosgene / benzene / 1 h / Heating

3: 64 percent / N,N-dimethyl-acetamide / Ambient temperature

With phosgene; triethylamine; In diethyl ether; N,N-dimethyl acetamide; benzene;

DOI:10.1021/jo00358a021

Reference yield:

5-(3-benzyl-3'-(ethoxycarbonyl)-1-guanidino)-1-(β-D-ribofuranosyl)imidazole-4-carboxamide (100313-39-1) → G (118-00-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 73 percent / cyclohexene, PdO / ethanol / 48 h / Heating

2: 95 percent / concd. NH₄OH, pyridine / 48 h / 45 °C

With pyridine; ammonium hydroxide; cyclohexene; trimethyleneglycol; In ethanol;

DOI:10.1021/jo00358a021

upstream raw materials:

ethyl N-(benzylcarbamothioyl)carbamate

benzylamine

Downstream raw materials:

G

Refernces