N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide

Base Information

Chemical Name:N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide
CAS No.:1542226-08-3
Molecular Formula:C₂₃H₃₀BrN₃O₄
Molecular Weight:492.413
Hs Code.:

Synonyms:N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide

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Chemical Property of N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide

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Technology Process of N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide

There total 5 articles about N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide 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: 64.0%

: 1159689-74-3
C₁₁H₁₃BrO₃

: 91646-29-6
N-(2-(piperazin-1-yl)phenyl)acetamide

: 1542226-08-3
N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide

Guidance literature:: With ethanol; for 8h; Reflux;
DOI:10.1016/j.bmcl.2014.01.070

Reference yield:

: 34743-88-9
2-(4-bromophenoxy)ethanol

: 1542226-08-3
N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

1.2: 10 h / Inert atmosphere; Reflux

2.1: ethanol / 8 h / Reflux

With ethanol; sodium hydride; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2014.01.070

Reference yield:

: 106-41-2
4-bromo-phenol

: 1542226-08-3
N-(2-(4-(3-(2-(4-bromophenoxy)ethoxy)-2-hydroxypropyl)piperazin-1-yl)phenyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / water / 24 h / 20 °C / Inert atmosphere

2.1: sodium hydride / tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

2.2: 10 h / Inert atmosphere; Reflux

3.1: ethanol / 8 h / Reflux

With ethanol; sodium hydride; sodium hydroxide; In tetrahydrofuran; water;
DOI:10.1016/j.bmcl.2014.01.070