5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Base Information

• Chemical Name: 5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one
• CAS No.: 1567327-20-1
• Molecular Formula: C₂₂H₂₆N₂O₃Se
• Molecular Weight: 445.42
• Mol file: 1567327-20-1.mol

Synonyms:5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Chemical Property of 5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one

There total 6 articles about 5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one 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:

4-(2-piperidin-1-yl-ethyl)-phenylamine (168897-21-0) + C9H8Cl2O3Se → 5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one (1567327-20-1)

Guidance literature:

With triethylamine; In dichloromethane; at 0 - 20 ℃; for 5.25h;

DOI:10.1016/j.bmc.2013.12.066

Reference yield:

diselenodi(4,5-dimethoxybenzoic acid) → 5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one (1567327-20-1)

Guidance literature:

Multi-step reaction with 2 steps

1: thionyl chloride; N,N-dimethyl-formamide / 3 h / 85 °C

2: triethylamine / dichloromethane / 5.25 h / 0 - 20 °C

With thionyl chloride; triethylamine; N,N-dimethyl-formamide; In dichloromethane;

DOI:10.1016/j.bmc.2013.12.066

Reference yield:

(4-nitrophenyl)ethyl bromide (5339-26-4) → 5,6-dimethoxy-2-(4-(2-(piperidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one (1567327-20-1)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / dimethyl sulfoxide / 3 h / 90 °C

2: 10% Pt/activated carbon; hydrogen / methanol / 6 h / 15514.9 Torr

3: triethylamine / dichloromethane / 5.25 h / 0 - 20 °C

With 10% Pt/activated carbon; hydrogen; potassium carbonate; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide;

DOI:10.1016/j.bmc.2013.12.066

upstream raw materials:

2-Amino-4,5-dimethoxybenzoic acid

4-(2-piperidin-1-yl-ethyl)-phenylamine

1-phenyl-2-bromoethane

(4-nitrophenyl)ethyl bromide