N⁶,N⁶-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine

Base Information

• Chemical Name: N⁶,N⁶-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine
• CAS No.: 80541-27-1
• Molecular Formula: C₄₅H₄₃N₅O₄
• Molecular Weight: 717.868
• Mol file: 80541-27-1.mol

Synonyms:N⁶,N⁶-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine

Chemical Property of N⁶,N⁶-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N⁶,N⁶-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine

There total 1 articles about N⁶,N⁶-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine 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:

benzyl chloride (100-44-7) + adenosine (58-61-7) → N6,N6-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine (80541-27-1)

Guidance literature:

With sodium hydride; In N,N-dimethyl-formamide; benzene; at 80 ℃;

DOI:10.1246/cl.1981.1541

Reference yield: 69.0%

N6,N6-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine (80541-27-1) → (2R,3R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-2-(6-dibenzylamino-purin-9-yl)-tetrahydro-furan-3-ol (80541-28-2)

Guidance literature:

With tert-butylmagnesium bromide; In diethyl ether; benzene; at 80 ℃; for 2.45h;

DOI:10.1246/cl.1981.1541

Reference yield:

N6,N6-dibenzyl-9-(2,3,5-tri-O-benzyl-β-D-ribofuranosyl)adenine (80541-27-1) → Acetic acid (2R,3R,4R,5R)-4-benzyloxy-5-benzyloxymethyl-2-(6-dibenzylamino-purin-9-yl)-tetrahydro-furan-3-yl ester (80541-29-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 69 percent / t-BuMgBr / diethyl ether; benzene / 2.45 h / 80 °C

With tert-butylmagnesium bromide; In diethyl ether; benzene;

DOI:10.1246/cl.1981.1541

upstream raw materials:

benzyl chloride

adenosine

Downstream raw materials:

(2R,3R,4S,5R)-4-Benzyloxy-5-benzyloxymethyl-2-(6-dibenzylamino-purin-9-yl)-tetrahydro-furan-3-ol

Acetic acid (2R,3R,4R,5R)-4-benzyloxy-5-benzyloxymethyl-2-(6-dibenzylamino-purin-9-yl)-tetrahydro-furan-3-yl ester