ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate

Base Information

Chemical Name:ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate
CAS No.:1430476-05-3
Molecular Formula:C₂₃H₂₇N₃O₆S
Molecular Weight:473.55
Hs Code.:

Synonyms:ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate

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Chemical Property of ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate

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Technology Process of ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate

There total 4 articles about ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate 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:

: 1042628-75-0
2-(N-(tert-butyl)sulfamoyl)acetic acid

: 1430476-05-3
ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate

Guidance literature:: Multi-step reaction with 4 steps

1: Lawessons reagent / 1 h / 150 °C / Sealed tube

2: chloro-trimethyl-silane / N,N-dimethyl-formamide / 2 h / 135 °C / Sealed tube

3: palladium on activated charcoal; hydrogen / methanol / 16 h / 20 °C / High pressure

4: dmap / dichloromethane / 8 h / 0 - 20 °C

With Lawessons reagent; dmap; chloro-trimethyl-silane; palladium on activated charcoal; hydrogen; In methanol; dichloromethane; N,N-dimethyl-formamide; 2: |Knoevenagel Condensation;
DOI:10.1016/j.bmcl.2013.02.109

Reference yield:

: 1430476-02-0
1-(benzo[d]oxazol-2-yl)-N-(tert-butyl)methanesulfonamide

: 1430476-05-3
ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate

Guidance literature:: Multi-step reaction with 3 steps

1: chloro-trimethyl-silane / N,N-dimethyl-formamide / 2 h / 135 °C / Sealed tube

2: palladium on activated charcoal; hydrogen / methanol / 16 h / 20 °C / High pressure

3: dmap / dichloromethane / 8 h / 0 - 20 °C

With dmap; chloro-trimethyl-silane; palladium on activated charcoal; hydrogen; In methanol; dichloromethane; N,N-dimethyl-formamide; 1: |Knoevenagel Condensation;
DOI:10.1016/j.bmcl.2013.02.109

Reference yield:

: 67541-92-8
ethyl 2-(tert-butylaminosulfonyl)acetate

: 1430476-05-3
ethyl 2-((4-(2-(benzo[d]oxazol-2-yl)-2-(N-(tert-butyl)sulfamoyl)ethyl)phenyl)amino)-2-oxoacetate

Guidance literature:: Multi-step reaction with 5 steps

1: potassium hydroxide / water; tetrahydrofuran / 6 h / 0 - 20 °C

2: Lawessons reagent / 1 h / 150 °C / Sealed tube

3: chloro-trimethyl-silane / N,N-dimethyl-formamide / 2 h / 135 °C / Sealed tube

4: palladium on activated charcoal; hydrogen / methanol / 16 h / 20 °C / High pressure

5: dmap / dichloromethane / 8 h / 0 - 20 °C

With Lawessons reagent; dmap; chloro-trimethyl-silane; palladium on activated charcoal; hydrogen; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 3: |Knoevenagel Condensation;
DOI:10.1016/j.bmcl.2013.02.109