Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester

Base Information

• Chemical Name: Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester
• CAS No.: 184229-71-8
• Molecular Formula: C₃₃H₂₇N₅O₆S
• Molecular Weight: 621.673
• Mol file: 184229-71-8.mol

Synonyms:Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester

Chemical Property of Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester

There total 2 articles about Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester 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: 92.0%

benzoyl chloride (98-88-4) + Thioacetic acid S-[(2S,3S,5R)-5-(6-amino-purin-9-yl)-3-hydroxy-tetrahydro-furan-2-ylmethyl] ester (184229-70-7) → Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester (184229-71-8)

Guidance literature:

With pyridine; for 12h; Ambient temperature;

DOI:10.1021/ja961788h

Reference yield:

2'-deoxy-D-adenosine (958-09-8,7005-15-4) → Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester (184229-71-8)

Guidance literature:

Multi-step reaction with 2 steps

1: 88 percent / Ph₃P, diethyl azodicarboxylate / tetrahydrofuran / 1 h / Ambient temperature

2: 92 percent / pyridine / 12 h / Ambient temperature

With pyridine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran;

DOI:10.1021/ja961788h

Reference yield: 90.0%

Benzoic acid (2S,3S,5R)-2-acetylsulfanylmethyl-5-(6-dibenzoylamino-purin-9-yl)-tetrahydro-furan-3-yl ester (184229-71-8) → N-[9-((2R,4S,5S)-4-Hydroxy-5-mercaptomethyl-tetrahydro-furan-2-yl)-9H-purin-6-yl]-benzamide (184229-72-9)

Guidance literature:

With sodium hydroxide; In pyridine; ethanol; for 0.116667h; Ambient temperature;

DOI:10.1021/ja961788h

upstream raw materials:

benzoyl chloride

Thioacetic acid S-[(2S,3S,5R)-5-(6-amino-purin-9-yl)-3-hydroxy-tetrahydro-furan-2-ylmethyl] ester

2'-deoxy-D-adenosine

Downstream raw materials:

N-[9-((2R,4S,5S)-4-Hydroxy-5-mercaptomethyl-tetrahydro-furan-2-yl)-9H-purin-6-yl]-benzamide

N-(9-{(2R,4S,5S)-5-[Bis-(4-methoxy-phenyl)-phenyl-methylsulfanylmethyl]-4-hydroxy-tetrahydro-furan-2-yl}-9H-purin-6-yl)-benzamide

Diisopropyl-phosphoramidous acid (2S,3S,5R)-5-(6-benzoylamino-purin-9-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methylsulfanylmethyl]-tetrahydro-furan-3-yl ester 2-cyano-ethyl ester