ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate

Base Information

Chemical Name:ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate
CAS No.:1357271-67-0
Molecular Formula:C₃₁H₃₄N₄O₅S
Molecular Weight:574.701
Hs Code.:

Synonyms:ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate

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Chemical Property of ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate

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Technology Process of ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate

There total 6 articles about ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate 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:

: 1357278-93-3
(1r,1r)-4-(3,4-diaminophenylsulfonamido)-N-((R)-1-phenylethyl)cyclohexanecarboxamide

: 33745-47-0
3-formyl-benzoic acid ethyl ester

: 1357271-67-0
ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate

Guidance literature:: iron(III) chloride; In dimethyl sulfoxide; at 20 ℃; for 24h;

Reference yield:

: 1310478-72-8
(1r,4r)-4-amino-N-((R)-1-phenylethyl)cyclohexanecarboxamide

: 1357271-67-0
ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 1 h / 20 °C

2: tetrahydrofuran / 80 °C

3: ammonium cerium (IV) nitrate / acetonitrile; water / 0.5 h

4: ammonium formate / palladium 10% on activated carbon / methanol / 2 h / Inert atmosphere

5: iron(III) chloride / dimethyl sulfoxide / 24 h / 20 °C

With ammonium cerium (IV) nitrate; ammonium formate; triethylamine; iron(III) chloride; palladium 10% on activated carbon; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 1357278-90-0
(1r,1r)-4-(4-chloro-3-nitrophenylsulfonamido)-N-((R)-1-phenylethyl)cyclohexanecarboxamide

: 1357271-67-0
ethyl 3-(6-(N-((1r,1r)-4-((R)-1phenylethylcarbamoyl)cyclohexyl)sulfamoyl)-1H-benzo[d]imidazol-2-yl)benzoate

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 80 °C

2: ammonium cerium (IV) nitrate / acetonitrile; water / 0.5 h

3: ammonium formate / palladium 10% on activated carbon / methanol / 2 h / Inert atmosphere

4: iron(III) chloride / dimethyl sulfoxide / 24 h / 20 °C

With ammonium cerium (IV) nitrate; ammonium formate; iron(III) chloride; palladium 10% on activated carbon; In tetrahydrofuran; methanol; water; dimethyl sulfoxide; acetonitrile;