N⁶-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine

Base Information

• Chemical Name: N⁶-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine
• CAS No.: 912567-50-1
• Molecular Formula: C₅₇H₆₅N₅O₁₂
• Molecular Weight: 1012.17

Synonyms:N⁶-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine

Chemical Property of N⁶-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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Useful:

Technology Process of N⁶-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine

There total 9 articles about N⁶-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-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: 60.0%

5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-1,2-di-O-isobutyryl-5-phenethyl-D-ribofuranose (912567-48-7) + N-benzoyladenine (4005-49-6) → N6-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine (912567-50-1)

Guidance literature:

N-benzoyladenine; With pyridine; 1,1,1,3,3,3-hexamethyl-disilazane;

5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-1,2-di-O-isobutyryl-5-phenethyl-D-ribofuranose; With tin(IV) chloride; In acetonitrile; at 20 ℃;

DOI:10.1021/jm060310d

Reference yield:

2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-1-phenylsulfinyl-β-D-glucopyranoside (518332-41-7) → N6-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine (912567-50-1)

Guidance literature:

Multi-step reaction with 8 steps

1.1: 78 percent / 2,6-di-tert-butyl-4-methylpyridine / diethyl ether / 8 h / -78 °C

2.1: 82 percent / TBAF / tetrahydrofuran / 20 °C

3.1: 118 mg / tetrahydrofuran / 20 °C

4.1: PhOCSCl; DMAP / acetonitrile / 20 °C

4.2: 64 percent / Bu₃SnH; AIBN / toluene / Heating

5.1: aq. TFA / 20 °C

6.1: Et₃N; DMAP / acetonitrile / 20 °C

7.1: hexamethyldisilazane; pyridine

7.2: 60 percent / SnCl₄ / acetonitrile / 20 °C

With pyridine; dmap; 2,6-di-tert-butyl-4-methylpyridine; tetrabutyl ammonium fluoride; triethylamine; 1,1,1,3,3,3-hexamethyl-disilazane; trifluoroacetic acid; phenylcarbonochloridothioate; In tetrahydrofuran; diethyl ether; acetonitrile; 3.1: Moffatt oxidation / 5.2: Barton deoxygenation / 8.2: Vorbrueggen glycosylation;

DOI:10.1021/jm060310d

Reference yield:

1,2-O-isopropylidene-5-O-(tert-butyl)dimethylsilyl-α-D-ribofuranoside (196868-07-2) → N6-benzoyl-9-[5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-2-O-isobutyryl-5-phenethyl-β-D-ribofuranosyl]adenine (912567-50-1)

Guidance literature:

Multi-step reaction with 8 steps

1.1: 78 percent / 2,6-di-tert-butyl-4-methylpyridine / diethyl ether / 8 h / -78 °C

2.1: 82 percent / TBAF / tetrahydrofuran / 20 °C

3.1: 118 mg / tetrahydrofuran / 20 °C

4.1: PhOCSCl; DMAP / acetonitrile / 20 °C

4.2: 64 percent / Bu₃SnH; AIBN / toluene / Heating

5.1: aq. TFA / 20 °C

6.1: Et₃N; DMAP / acetonitrile / 20 °C

7.1: hexamethyldisilazane; pyridine

7.2: 60 percent / SnCl₄ / acetonitrile / 20 °C

With pyridine; dmap; 2,6-di-tert-butyl-4-methylpyridine; tetrabutyl ammonium fluoride; triethylamine; 1,1,1,3,3,3-hexamethyl-disilazane; trifluoroacetic acid; phenylcarbonochloridothioate; In tetrahydrofuran; diethyl ether; acetonitrile; 3.1: Moffatt oxidation / 5.2: Barton deoxygenation / 8.2: Vorbrueggen glycosylation;

DOI:10.1021/jm060310d

upstream raw materials:

5-deoxy-3-O-(2,6-di-O-benzyl-3,4-di-O-isobutyryl-α-D-glucopyranosyl)-1,2-di-O-isobutyryl-5-phenethyl-D-ribofuranose

N-benzoyladenine

2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-1-phenylsulfinyl-β-D-glucopyranoside

5-O-tert-butyldimethylsilyl-3-O-[2,6-di-O-benzyl-3,4-O-[(2S,3S)-2,3-dimethoxybutan-2,3-yl]-α-D-glucopyranosyl]-1,2-O-isopropylidene-α-D-ribofuranose

Downstream raw materials:

C₆₂H₆₄N₅O₁₇P₃

9-[5-deoxy-3-O-(2,6-di-O-benzyl-α-D-glucopyranosyl)-5-phenethyl-β-D-ribofuranosyl]adenine

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