(2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol

Base Information

• Chemical Name: (2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol
• CAS No.: 338800-85-4
• Molecular Formula: C₃₇H₃₆N₂O₅
• Molecular Weight: 588.703
• Mol file: 338800-85-4.mol

Synonyms:(2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol

Chemical Property of (2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol

There total 5 articles about (2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol 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: 32.0%

4,4'-dimethoxytrityl chloride (40615-36-9) + (2R,3S)-5-[2,2']Bipyridinyl-5-ylmethyl-2-hydroxymethyl-tetrahydro-furan-3-ol (340130-36-1) → (2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol (338800-85-4) + (2R,3S,5S)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol (340130-37-2)

Guidance literature:

With pyridine; dmap; at 20 ℃; for 1h;

DOI:10.1021/ja005785n

Reference yield:

3,5-di-O-benzyl-2-deoxy-D-ribofuranose (6160-50-5) → (2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol (338800-85-4)

Guidance literature:

Multi-step reaction with 4 steps

1.1: LDA / tetrahydrofuran; heptane / 0.5 h / -78 - -15 °C

1.2: 72 percent / tetrahydrofuran; heptane / -78 - 20 °C

2.1: 87 percent / diethylazodicarboxylate; Ph₃P / tetrahydrofuran / 20 °C

3.1: 58 percent / BCl₃ / CH₂Cl₂ / 1.5 h / -78 °C

4.1: 32 percent / DMAP; Py / 1 h / 20 °C

With pyridine; dmap; boron trichloride; triphenylphosphine; lithium diisopropyl amide; diethylazodicarboxylate; In tetrahydrofuran; n-heptane; dichloromethane; 2.1: Mitsunobu reaction;

DOI:10.1021/ja005785n

Reference yield:

5-methyl-2,2'-bipyridine (56100-20-0) → (2R,3S,5R)-5-[2,2']Bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-ol (338800-85-4)

Guidance literature:

Multi-step reaction with 4 steps

1.1: LDA / tetrahydrofuran; heptane / 0.5 h / -78 - -15 °C

1.2: 72 percent / tetrahydrofuran; heptane / -78 - 20 °C

2.1: 87 percent / diethylazodicarboxylate; Ph₃P / tetrahydrofuran / 20 °C

3.1: 58 percent / BCl₃ / CH₂Cl₂ / 1.5 h / -78 °C

4.1: 32 percent / DMAP; Py / 1 h / 20 °C

With pyridine; dmap; boron trichloride; triphenylphosphine; lithium diisopropyl amide; diethylazodicarboxylate; In tetrahydrofuran; n-heptane; dichloromethane; 2.1: Mitsunobu reaction;

DOI:10.1021/ja005785n

upstream raw materials:

4,4'-dimethoxytrityl chloride

(2R,3S)-5-[2,2']Bipyridinyl-5-ylmethyl-2-hydroxymethyl-tetrahydro-furan-3-ol

3,5-di-O-benzyl-2-deoxy-D-ribofuranose

5-methyl-2,2'-bipyridine

Downstream raw materials:

Acetic acid (2R,3S,5R)-5-[2,2']bipyridinyl-5-ylmethyl-2-[{(2R,3S,5R)-5-[2,2']bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yloxy}-(2-cyano-ethoxy)-phosphoryloxymethyl]-tetrahydro-furan-3-yl ester

Diisopropyl-phosphoramidous acid (2R,3S,5R)-5-[2,2']bipyridinyl-5-ylmethyl-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 2-cyano-ethyl ester