5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one

Base Information

Chemical Name:5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one
CAS No.:1354031-65-4
Molecular Formula:C₂₁H₂₄Cl₂N₄O₂
Molecular Weight:435.353
Hs Code.:

Synonyms:5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one

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Chemical Property of 5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one

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Technology Process of 5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one

There total 8 articles about 5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one 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: 32.0%

: 119532-26-2,864512-47-0
1-(2,3-dichlorophenyl)-piperazine hydrochloride

: 1354030-53-7
C₁₁H₁₃BrN₂O₂

: 1354031-65-4
5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: C₁₁H₁₃BrN₂O₂; With sodium iodide; In acetonitrile; for 0.5h; Reflux;

1-(2,3-dichlorophenyl)-piperazine hydrochloride; With potassium carbonate; In acetonitrile; Reflux;

Reference yield:

: 56961-77-4
1-bromo-2,3-dichlorobenzene

: 1354031-65-4
5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium t-butanolate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; 1,8-diazabicyclo[5.4.0]undec-7-ene / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / toluene / 60 - 70 °C / Inert atmosphere

1.2: 20 °C

2.1: hydrogenchloride / ethyl acetate / 1.5 h / 20 °C

3.1: sodium iodide / acetonitrile / 0.5 h / Reflux

3.2: Reflux

With hydrogenchloride; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; 1,8-diazabicyclo[5.4.0]undec-7-ene; sodium iodide; sodium t-butanolate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In ethyl acetate; toluene; acetonitrile;

Reference yield:

: 39513-24-1
5-hydroxybenzimidazol-2(3H)-one

: 1354031-65-4
5-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-1H-benzo[d]imidazol-2(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: potassium carbonate / ethanol / Reflux

2.1: sodium iodide / acetonitrile / 0.5 h / Reflux

2.2: Reflux

With potassium carbonate; sodium iodide; In ethanol; acetonitrile;