2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide

Base Information

Chemical Name:2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide
CAS No.:1383485-22-0
Molecular Formula:C₂₃H₂₄F₃N₅O
Molecular Weight:443.472
Hs Code.:

Synonyms:2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide

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Chemical Property of 2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide

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Technology Process of 2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide

There total 5 articles about 2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide 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: 50.0%

: 1383485-14-0
1-cyclohexyl-2-(4-trifluoromethylphenyl)-5-acetyl-1H-benzimidazole

: 563-41-7
semicarbazide hydrochloride

: 1383485-22-0
2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide

Guidance literature:: With sodium acetate; In ethanol; water; for 5h; Reflux;
DOI:10.1016/j.ejmech.2012.03.038

Reference yield:

: 1368615-59-1
1-(3-amino-4-(cyclohexylamino)phenyl)ethanone

: 1383485-22-0
2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: Oxone / water; N,N-dimethyl-formamide / 1 h / 20 °C

2: sodium acetate / ethanol; water / 5 h / Reflux

With Oxone; sodium acetate; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.03.038

Reference yield:

: 18640-58-9
3-nitro-4-bromoacetophenone

: 1383485-22-0
2-(1-(1-cyclohexyl-2-(4-(trifluoromethyl)phenyl)-1H-benzimidazol-5-yl)ethylidene)hydrazinecarboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: dimethyl sulfoxide / 3 h / 70 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 2 h / 20 °C

3: Oxone / water; N,N-dimethyl-formamide / 1 h / 20 °C

4: sodium acetate / ethanol; water / 5 h / Reflux

With Oxone; palladium 10% on activated carbon; hydrogen; sodium acetate; In ethanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.03.038