methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate

Base Information

Chemical Name:methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate
CAS No.:1370229-14-3
Molecular Formula:C₂₂H₂₇N₃O₆S
Molecular Weight:461.539
Hs Code.:

Synonyms:methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate

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Chemical Property of methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate

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Technology Process of methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate

There total 3 articles about methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate 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: 46.0%

: 2971-79-1
isonipecotic acid methyl ester

: 1370228-86-6
2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetic acid

: 1370229-14-3
methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate

Guidance literature:: 2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetic acid; With 1,1'-carbonyldiimidazole; In tetrahydrofuran; at 20 ℃; for 0.333333h;

isonipecotic acid methyl ester; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.bmc.2012.01.030

Reference yield:

: 1370228-77-5
methyl 2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)amino)acetate

: 1370229-14-3
methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

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

1.2: pH Ca_. 2

2.1: trifluoroacetic acid / 0.5 h / 20 °C

3.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 0.33 h / 20 °C

3.2: 20 °C

With 1,1'-carbonyldiimidazole; trifluoroacetic acid; lithium hydroxide; In tetrahydrofuran; water;
DOI:10.1016/j.bmc.2012.01.030

Reference yield:

: 1370228-82-2
2-((N-(tert-butoxycarbonyl)-N-(3-phenoxybenzyl)sulfamoyl)amino)acetic acid

: 1370229-14-3
methyl 1-(2-((N-(3-phenoxybenzyl)sulfamoyl)amino)acetyl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: trifluoroacetic acid / 0.5 h / 20 °C

2.1: 1,1'-carbonyldiimidazole / tetrahydrofuran / 0.33 h / 20 °C

2.2: 20 °C

With 1,1'-carbonyldiimidazole; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1016/j.bmc.2012.01.030