(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol

Base Information

• Chemical Name: (1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol
• CAS No.: 180633-60-7
• Molecular Formula: C₃₃H₂₈IN₃O₅S
• Molecular Weight: 705.573
• Mol file: 180633-60-7.mol

Synonyms:(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol

Chemical Property of (1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol

There total 1 articles about (1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol 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: 74.0%

1-benzyloxymethyl-4,5-diiodo-1H-imidazole (134420-43-2) + 1-benzenesulfonyl-6-benzyloxy-1H-indole-3-carboxaldehyde (180633-56-1) → (1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol (180633-60-7)

Guidance literature:

1-benzyloxymethyl-4,5-diiodo-1H-imidazole; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.75h;

1-benzenesulfonyl-6-benzyloxy-1H-indole-3-carboxaldehyde; In tetrahydrofuran; at -78 - 0 ℃; Further stages.;

DOI:10.1016/j.tet.2008.04.045

Reference yield: 95.0%

(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol (180633-60-7) → (1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanone (180633-62-9)

Guidance literature:

With manganese(IV) oxide; In dichloromethane; for 5h; Ambient temperature;

DOI:10.1016/0040-4039(96)01148-3

Reference yield:

(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanol (180633-60-7) → (6-benzyloxy-1H-indol-3-yl)-[1-benzyloxymethyl-4-(1H-indol-3-yl)-1H-imidazol-2-yl]-methanone (180633-76-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 95 percent / MnO₂ / CH₂Cl₂ / 5 h / Ambient temperature

2: 81 percent / CuI / PdCl₂(PPh₃)2 / dimethylformamide / 2 h / 100 °C

3: 97 percent / 10 percent KOH / ethanol; tetrahydrofuran / 2 h / Heating

With manganese(IV) oxide; potassium hydroxide; copper(l) iodide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/0040-4039(96)01148-3

upstream raw materials:

1-benzyloxymethyl-4,5-diiodo-1H-imidazole

1-benzenesulfonyl-6-benzyloxy-1H-indole-3-carboxaldehyde

Downstream raw materials:

(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-(1-benzyloxymethyl-4-iodo-1H-imidazol-2-yl)-methanone

topsentin

(6-benzyloxy-1H-indol-3-yl)-[1-benzyloxymethyl-4-(1H-indol-3-yl)-1H-imidazol-2-yl]-methanone

(1-benzenesulfonyl-6-benzyloxy-1H-indol-3-yl)-[4-(1-benzenesulfonyl-1H-indol-3-yl)-1-benzyloxymethyl-1H-imidazol-2-yl]-methanone