methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate

Base Information

Chemical Name:methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate
CAS No.:1191069-82-5
Molecular Formula:C₂₂H₁₉ClFNO₄S
Molecular Weight:447.915
Hs Code.:

Synonyms:methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate

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Chemical Property of methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate

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Technology Process of methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate

There total 3 articles about methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate 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: 91.0%

: 446-48-0
o-fluorobenzyl bromide

: 1186212-02-1
methyl 4-(((4-chlorophenyl)sulfonamido)methyl)benzoate

: 1191069-82-5
methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate

Guidance literature:: methyl 4-(((4-chlorophenyl)sulfonamido)methyl)benzoate; With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; for 0.25h;

o-fluorobenzyl bromide; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

Reference yield:

: methyl 4-(((2-fluorobenzyl)amino)methyl)benzoate hydrochloride

: 98-60-2
4-chlorobenzenesulfonyl chloride

: 1191069-82-5
methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate

Guidance literature:: With triethylamine; In dichloromethane;
DOI:10.1016/j.bmcl.2010.04.113

Reference yield:

: 98-60-2
4-chlorobenzenesulfonyl chloride

: 1191069-82-5
methyl 4-{[[(4-chlorophenyl)sulfonyl](2-fluorobenzyl)amino]methyl}benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / dichloromethane / 0.17 h / 0 °C

2.1: potassium carbonate; potassium iodide / N,N-dimethyl-formamide / 0.25 h

2.2: 12 h / 20 °C

With potassium carbonate; triethylamine; potassium iodide; In dichloromethane; N,N-dimethyl-formamide;