{ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester

Base Information

Chemical Name:{ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester
CAS No.:796113-62-7
Molecular Formula:C₂₃H₂₉N₃O₇S
Molecular Weight:491.565
Hs Code.:

Synonyms:{ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester

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Chemical Property of {ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester

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Technology Process of {ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester

There total 4 articles about {ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester 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: 77.0%

: 138-37-4
mafenide hydrochloride

: 807315-22-6
4-[(bis-ethoxycarbonylmethyl-amino)-methyl]-benzoic acid

: 796113-62-7
{ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In chloroform; N,N-dimethyl-formamide; at 20 ℃; for 12h;
DOI:10.1021/ja047271k

Reference yield:

: 6290-05-7
Diethyl iminodiacetate

: 796113-62-7
{ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / K₂CO₃ / acetonitrile / 12 h / Heating

2: 83 percent / TFA / CH₂Cl₂ / 5 h / 20 °C

3: 77 percent / BOP; Et₃N / CHCl₃; dimethylformamide / 12 h / 20 °C

With potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; trifluoroacetic acid; In dichloromethane; chloroform; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/ja047271k

Reference yield:

: 108052-76-2
4-(bromomethyl)benzoic acid 1,1-dimethylethyl ester

: 796113-62-7
{ethoxycarbonylmethyl-[4-(4-sulfamoyl-benzylcarbamoyl)-benzyl]-amino}-acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 77 percent / K₂CO₃ / acetonitrile / 12 h / Heating

2: 83 percent / TFA / CH₂Cl₂ / 5 h / 20 °C

3: 77 percent / BOP; Et₃N / CHCl₃; dimethylformamide / 12 h / 20 °C

With potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; trifluoroacetic acid; In dichloromethane; chloroform; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/ja047271k