5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole

Base Information

• Chemical Name: 5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole
• CAS No.: 1025906-94-8
• Molecular Formula: C₂₄H₂₂ClNO₅S₂
• Molecular Weight: 504.027
• Mol file: 1025906-94-8.mol

Synonyms:5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole

Chemical Property of 5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole

There total 3 articles about 5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole 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: 30.0%

p-toluenesulfonyl chloride (98-59-9) + 2-(5-chloro-1H-indol-3-yl)ethanol (61220-51-7) → 5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole (1025906-94-8)

Guidance literature:

2-(5-chloro-1H-indol-3-yl)ethanol; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 1h;

p-toluenesulfonyl chloride; In tetrahydrofuran; at 20 ℃; Further stages.;

DOI:10.1021/jm061278q

Reference yield: 30.0%

→ 5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole (1025906-94-8)

Guidance literature:

Reference yield:

4-chlorophenylhydrazine hydrochloride (1073-70-7) → 5-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole (1025906-94-8)

Guidance literature:

Multi-step reaction with 2 steps

1.1: aq. ethanol / Heating

2.1: sodium hydride / tetrahydrofuran / 1 h / 0 °C

2.2: 30 percent / tetrahydrofuran / 20 °C

With sodium hydride; In tetrahydrofuran; ethanol; 1.1: Fisher indole ring cyclization;

DOI:10.1021/jm061278q

upstream raw materials:

p-toluenesulfonyl chloride

2-(5-chloro-1H-indol-3-yl)ethanol

4-chlorophenylhydrazine hydrochloride

Downstream raw materials:

5-chloro-3-(2-iodoethyl)-1-(p-toluenesulfonyl)indole

2-(3-(5-chloro-1-(p-toluenesulfonyl)indolyl)ethyloxy)adenosine

6-chloro-2-(3''-(5''-chloro-1''-(p-toluenesulfonyl)indolyl)ethyloxy)-3',4',5'-triacetyladenosine