5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide

Base Information

Chemical Name:5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide
CAS No.:181272-12-8
Molecular Formula:C₁₉H₂₃ClN₂O₆S
Molecular Weight:442.92
Hs Code.:

Synonyms:5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide

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Chemical Property of 5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide

Chemical Property:

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Technology Process of 5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide

There total 6 articles about 5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide 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:

: 3438-16-2
5-chloro-2-methoxybenzoic acid

: 2-(4-methoxyethoxy-3-sulfamoylphenyl)ethylamine hydrochloride

: 181272-12-8
5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide

Guidance literature:: With TEA; 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 20 ℃; for 12h;
DOI:10.1021/jm000985v

Reference yield:

: 125960-59-0
2-Methoxy-5-(2-(2,2,2-trifluoroacetamido)ethyl)benzenesulfonamide

: 181272-12-8
5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 5 steps

1: 85 percent / dimethylformamide / 3 h

2: 95 percent / BBr₃ / CH₂Cl₂ / 5 h / 20 °C

3: K₂CO₃ / dimethylformamide / 3 h / 80 °C

4: 5.5N aq. HCl / methanol / 8 h / Heating

5: N,N'-carbonyldiimidazole; TEA / tetrahydrofuran / 12 h / 20 °C

With hydrogenchloride; TEA; boron tribromide; potassium carbonate; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm000985v

Reference yield:

: (E)-N-(3-(N-((dimethylamino)methylene)sulfamoyl)-4-methoxyphenethyl)-2,2,2-trifluoroacetamide

: 181272-12-8
5-(2-(5-chloro-2-methoxybenzamido)ethyl)-2-(2-methoxyethoxy)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / BBr₃ / CH₂Cl₂ / 5 h / 20 °C

2: K₂CO₃ / dimethylformamide / 3 h / 80 °C

3: 5.5N aq. HCl / methanol / 8 h / Heating

4: N,N'-carbonyldiimidazole; TEA / tetrahydrofuran / 12 h / 20 °C

With hydrogenchloride; TEA; boron tribromide; potassium carbonate; 1,1'-carbonyldiimidazole; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm000985v