2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid

Base Information

• Chemical Name: 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid
• CAS No.: 1370228-99-1
• Molecular Formula: C₂₁H₂₆N₂O₇S
• Molecular Weight: 450.513
• Mol file: 1370228-99-1.mol

Synonyms:2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid

Chemical Property of 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid

There total 2 articles about 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid 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: 64.0%

methyl 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetate (1370228-97-9) → 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid (1370228-99-1)

Guidance literature:

methyl 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetate; With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 1.5h;

With hydrogenchloride; In water; pH=Ca. 2;

DOI:10.1016/j.bmc.2012.01.030

Reference yield:

methyl -glycinate (174466-48-9) → 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid (1370228-99-1)

Guidance literature:

Multi-step reaction with 3 steps

1.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 0 °C

2.1: sodium hydride / acetonitrile / 0.5 h / Cooling

2.2: Cooling; Reflux

3.1: lithium hydroxide / tetrahydrofuran; water / 1.5 h / 20 °C

3.2: pH Ca_. 2

With di-isopropyl azodicarboxylate; sodium hydride; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; water; acetonitrile; 1.1: Mitsunobu reaction;

DOI:10.1016/j.bmc.2012.01.030

Reference yield: 95.0%

2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetic acid (1370228-99-1) → 2-(methyl(N-(3-phenoxybenzyl)sulfamoyl)amino)acetic acid (1370229-01-8)

Guidance literature:

With trifluoroacetic acid; at 20 ℃; for 0.333333h;

DOI:10.1016/j.bmc.2012.01.030

upstream raw materials:

methyl 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)(methyl)amino)acetate

methyl -glycinate

Downstream raw materials:

2-(methyl(N-(3-phenoxybenzyl)sulfamoyl)amino)acetic acid

2-(methyl(N-(3-phenoxybenzyl)sulfamoyl)amino)-N-(2-morpholinoethyl)acetamide

2-(methyl(N-(3-phenoxybenzyl)sulfamoyl)amino)-N-(2-morpholinoethyl)acetamide hydrochloride