N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide

Base Information

Chemical Name:N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide
CAS No.:1295584-90-5
Molecular Formula:C₂₈H₃₀ClN₃O₂
Molecular Weight:476.018
Hs Code.:

Synonyms:N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide

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Chemical Property of N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide

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Technology Process of N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide

There total 3 articles about N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide 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: 58.0%

: 64262-23-3,5308-27-0
1-n-propylpiperazine dihydrobromide

: N-(2-benzoyl-4-chloro-phenyl)-2-chloro-2-phenyl-acetamide

: 1295584-90-5
N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide

Guidance literature:: With sodium hydrogencarbonate; In acetonitrile; Reflux;
DOI:10.1016/j.ejmech.2011.01.056

Reference yield:

: 719-59-5
5-chloro-2-aminobenzophenone

: 1295584-90-5
N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: oxalyl dichloride / dichloromethane / 2 h

1.2: 2 h / Reflux

2.1: sodium hydrogencarbonate / acetonitrile / Reflux

With oxalyl dichloride; sodium hydrogencarbonate; In dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2011.01.056

Reference yield:

: 4755-72-0,39266-56-3
Chloro-phenyl-acetic acid

: 1295584-90-5
N-(2-benzoyl-4-chlorophenyl)-2-(4-propyl-1-piperazinyl)-2-phenylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: oxalyl dichloride / dichloromethane / 2 h

1.2: 2 h / Reflux

2.1: sodium hydrogencarbonate / acetonitrile / Reflux

With oxalyl dichloride; sodium hydrogencarbonate; In dichloromethane; acetonitrile;
DOI:10.1016/j.ejmech.2011.01.056