methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate

Base Information

Chemical Name:methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate
CAS No.:1357465-01-0
Molecular Formula:C₂₈H₃₃N₃O₅S
Molecular Weight:523.653
Hs Code.:

Synonyms:methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate

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Chemical Property of methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate

Chemical Property:

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Technology Process of methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate

There total 3 articles about methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate 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:

: 62243-48-5
3-butylamino-5-(dimethylaminomethylene-sulfamoyl)-4-phenoxy-benzoic acid methyl ester

: 100-39-0
benzyl bromide

: 1357465-01-0
methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate

Guidance literature:: With potassium carbonate; In acetonitrile; Reflux;

Reference yield:

: 28395-03-1
Bumetanide

: 1357465-01-0
methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate

Guidance literature:: Multi-step reaction with 3 steps

1: thionyl chloride / 50 °C

2: acetonitrile / 20 °C

3: potassium carbonate / acetonitrile / Reflux

With thionyl chloride; potassium carbonate; In acetonitrile;

Reference yield:

: 28510-66-9
methyl 3-(butylamino)-4-phenoxy-5-sulfamoylbenzoate

: 1357465-01-0
methyl 3-(benzyl(butyl)amino)-5-(N-((dimethylamino)methylene)sulfamoyl)-4-phenoxybenzoate

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 20 °C

2: potassium carbonate / acetonitrile / Reflux

With potassium carbonate; In acetonitrile;