N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide

Base Information

Chemical Name:N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide
CAS No.:1448524-17-1
Molecular Formula:C₁₇H₁₅Br₂FN₂O₃
Molecular Weight:474.124
Hs Code.:

Synonyms:N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide

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Chemical Property of N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide

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Technology Process of N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide

There total 6 articles about N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)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: 85.0%

: 1448524-17-1
N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide

Guidance literature:: With 1,1'-carbonyldiimidazole; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere;

In dichloromethane; at 20 ℃; Inert atmosphere;

Reference yield:

: 1509574-25-7
C₉H₁₀BrFN₂O

: 110009-65-9
C₁₁H₉BrN₂O₂

: 1448524-17-1
N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide

Guidance literature:: In dichloromethane; at 20 ℃; for 24h;
DOI:10.1016/j.bmcl.2014.07.003

Reference yield:

: 4841-23-0
(4-bromophenoxy)acetic acid methyl ester

: 1448524-17-1
N-[(4-bromo-2-fluorobenzylcarbamoyl)methyl]-2-(4-bromophenoxy)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: lithium hydroxide monohydrate / methanol; water / 2 h / Reflux

2: dichloromethane / 1 h / 20 °C

3: dichloromethane / 24 h / 20 °C

With lithium hydroxide monohydrate; In methanol; dichloromethane; water;
DOI:10.1016/j.bmcl.2014.07.003