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

Base Information

Chemical Name:2-(4-(2-(pyrrolidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one
CAS No.:1567327-13-2
Molecular Formula:C₁₉H₂₀N₂OSe
Molecular Weight:371.341
Hs Code.:

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

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

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

There total 6 articles about 2-(4-(2-(pyrrolidin-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:

: 168897-20-9
4-(2-pyrrolidin-1-yl-ethyl)phenylamine

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

: 1567327-13-2
2-(4-(2-(pyrrolidin-1-yl)ethyl)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:

: 103-63-9
1-phenyl-2-bromoethane

: 1567327-13-2
2-(4-(2-(pyrrolidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: nitric acid; sulfuric acid / dichloromethane / 4 h / 0 - 20 °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 sulfuric acid; 10% Pt/activated carbon; hydrogen; nitric acid; potassium carbonate; triethylamine; In methanol; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/j.bmc.2013.12.066

Reference yield:

: 168897-19-6
4-(2-(1-pyrrolidinyl)ethyl)nitrobenzene

: 1567327-13-2
2-(4-(2-(pyrrolidin-1-yl)ethyl)phenyl)benzo[d][1,2]selenazol-3(2H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: 10% Pt/activated carbon; hydrogen / methanol / 6 h / 15514.9 Torr

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

With 10% Pt/activated carbon; hydrogen; triethylamine; In methanol; dichloromethane;
DOI:10.1016/j.bmc.2013.12.066