N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide

Base Information

Chemical Name:N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide
CAS No.:1447018-11-2
Molecular Formula:C₂₉H₂₂BrFIN₃O₃S
Molecular Weight:718.385
Hs Code.:

Synonyms:N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide

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Chemical Property of N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide

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Technology Process of N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide

There total 4 articles about N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide 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: 81.0%

: 186584-73-6
2-fluoro-5-iodobenzoyl chloride

: 1447017-93-7
2-amino-N-(3-(benzylthio)-2-(methylcarbamoyl)phenyl)-6-bromobenzamide

: 1447018-11-2
N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Cooling with ice;
DOI:10.1016/j.cclet.2013.04.047

Reference yield:

: 1447017-92-6
2-amino-6-bromo-N-(3-bromo-2-(methylcarbamoyl)phenyl)benzamide

: 1447018-11-2
N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 12 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

With potassium carbonate; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.cclet.2013.04.047

Reference yield:

: 124700-41-0
2-fluoro-5-iodobenzoic acid

: 1447018-11-2
N-(2-((3-(benzylthio)-2-(methylcarbamoyl)phenyl)carbamoyl)-3-bromophenyl)-2-fluoro-5-iodobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 2 h / Reflux

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 20 °C / Cooling with ice

With thionyl chloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1016/j.cclet.2013.04.047