N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester

Base Information

Chemical Name:N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester
CAS No.:941311-29-1
Molecular Formula:C₂₇H₃₀N₂O₈S
Molecular Weight:542.61
Hs Code.:

Synonyms:N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester

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Chemical Property of N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester

Chemical Property:

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Technology Process of N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester

There total 4 articles about N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl 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:

: 941311-27-9
(2-benzyloxy-5-phenoxyphenylamino)acetic acid methyl ester

: 147000-89-3
N-tert-butyloxycarbonylsulfamoyl chloride

: 941311-29-1
N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 2-benzyloxy-5-phenoxyphenylamine

: 941311-29-1
N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 2.5 h / 60 °C

2: triethylamine / dichloromethane / 2 h / 20 °C

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

Reference yield:

: 145279-04-5
2-nitro-4-phenoxyphenol

: 941311-29-1
N-(t-butoxycarbonylsulfamoyl)-N-(2-benzyloxy-5-phenoxyphenyl)glycine methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

2: hydrogenchloride; indium / tetrahydrofuran / 2.5 h / 20 °C

3: potassium carbonate / N,N-dimethyl-formamide / 2.5 h / 60 °C

4: triethylamine / dichloromethane / 2 h / 20 °C

With hydrogenchloride; indium; potassium carbonate; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;