N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

Base Information

Chemical Name:N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine
CAS No.:119139-11-6
Molecular Formula:C₂₃H₃₃N₅O₈
Molecular Weight:507.544
Hs Code.:

N'-benzyloxy-5-<N-(2,2-diethoxyethyl)formamido>-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

Synonyms:

Suppliers and Price of N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

There total 1 articles about N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine 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:

: 50507-48-7
N'-benzyloxy-5-formamido-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

: 51806-20-3
1,1-diethoxy-2-iodoethane

: 119139-11-6
N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

Guidance literature:: With 18-crown-6 ether; potassium carbonate; Yield given. Multistep reaction; 1.) DMF, RT, 1 h, 2.) DMF, from 16 deg C to 19 deg C, 93 h;
DOI:10.1248/cpb.42.1231

Reference yield:

: 119139-11-6
N'-benzyloxy-5--1-β-D-ribofuranosyl-1H-imidazole-4-carboxamidine

: 115173-45-0
3-β-D-ribofuranosylazepinomycin

Guidance literature:: Multi-step reaction with 4 steps

1: 339 mg / 1N aq. NaOH / 2 h / Ambient temperature

2: H₂, HCl / Raney Ni W-2 / H₂O / 6 h / Ambient temperature

3: 1N aq. NaOH / 0.5 h / Heating

4: 94 percent / 1N aq. HCl / 1 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; Raney Ni W-2; In water;
DOI:10.1248/cpb.42.1231