benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate

Base Information

Chemical Name:benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate
CAS No.:1572928-47-2
Molecular Formula:C₂₃H₂₇N₃O₄S
Molecular Weight:441.551
Hs Code.:

Synonyms:benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate

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Chemical Property of benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate

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Technology Process of benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate

There total 6 articles about benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate 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:

: 1361224-50-1
benzyl 3-(propan-1-yn-1-yl)piperazine-1-carboxylate

: 1984-25-4
4-bromo-N-ethylbenzenesulfonamide

: 1572928-47-2
benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate

Guidance literature:: With chloro(2-dicyclohexylphosphino-2′,6′-di-i-propoxy-1,1′-biphenyl)(2′-amino-1,1′-biphenyl-2-yl)-palladium(II); sodium t-butanolate; ruphos; In toluene; at 20 - 80 ℃; for 10h; Inert atmosphere;

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 1572928-47-2
benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium carbonate / water; 1,4-dioxane / 2 h / 20 °C

2.1: triethylamine; dmap / dichloromethane / 1 h / 20 °C

3.1: tetrahydrofuran / 2 h / 0 °C

4.1: trifluoroacetic acid / dichloromethane / 0.25 h / -10 - 20 °C

4.2: 2 h

5.1: chloro(2-dicyclohexylphosphino-2′,6′-di-i-propoxy-1,1′-biphenyl)(2′-amino-1,1′-biphenyl-2-yl)-palladium(II); sodium t-butanolate; ruphos / toluene / 10 h / 20 - 80 °C / Inert atmosphere

With dmap; chloro(2-dicyclohexylphosphino-2′,6′-di-i-propoxy-1,1′-biphenyl)(2′-amino-1,1′-biphenyl-2-yl)-palladium(II); sodium carbonate; triethylamine; trifluoroacetic acid; sodium t-butanolate; ruphos; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; toluene;

Reference yield:

: 78818-15-2
4-benzyloxycarbonylpiperazin-2-one

: 1572928-47-2
benzyl 4-(4-(ethylsulfamoyl)phenyl)-3-(1-propyn-1-yl)-1-piperazinecarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine; dmap / dichloromethane / 1 h / 20 °C

2.1: tetrahydrofuran / 2 h / 0 °C

3.1: trifluoroacetic acid / dichloromethane / 0.25 h / -10 - 20 °C

3.2: 2 h

4.1: chloro(2-dicyclohexylphosphino-2′,6′-di-i-propoxy-1,1′-biphenyl)(2′-amino-1,1′-biphenyl-2-yl)-palladium(II); sodium t-butanolate; ruphos / toluene / 10 h / 20 - 80 °C / Inert atmosphere

With dmap; chloro(2-dicyclohexylphosphino-2′,6′-di-i-propoxy-1,1′-biphenyl)(2′-amino-1,1′-biphenyl-2-yl)-palladium(II); triethylamine; trifluoroacetic acid; sodium t-butanolate; ruphos; In tetrahydrofuran; dichloromethane; toluene;