2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Base Information

Chemical Name:2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)benzo[d][1,2]selenazol-3(2H)-one
CAS No.:1567327-14-3
Molecular Formula:C₂₀H₂₂N₂O₂Se
Molecular Weight:401.367
Hs Code.:

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

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

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

There total 6 articles about 2-(4-(2-(piperidin-1-yl)ethoxy)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:

: 38948-27-5
4-(2-(piperidin-1-yl)ethoxy)aniline

: 1441-85-6
2-(chloroseleno)benzoyl chloride

: 1567327-14-3
2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; for 5.25h;
DOI:10.1016/j.bmc.2013.12.066

Reference yield:

: 100-02-7,78813-13-5,89830-32-0
4-nitro-phenol

: 1567327-14-3
2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 80 °C

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

3: 10% Pt/activated carbon; hydrogen / methanol / 6 h / 15514.9 Torr

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

With 10% Pt/activated carbon; hydrogen; potassium carbonate; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.12.066

Reference yield:

: 6512-83-0
2,2'-diselanediyl-di-benzoic acid

: 1567327-14-3
2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)benzo[d][1,2]selenazol-3(2H)-one

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