N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide

Base Information

Chemical Name:N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide
CAS No.:873659-40-6
Molecular Formula:C₂₆H₂₇ClN₄O₂
Molecular Weight:462.979
Hs Code.:

Synonyms:N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide

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Chemical Property of N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide

Chemical Property:

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Technology Process of N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide

There total 6 articles about N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide 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:

: N-(2-benzoyl-4-nitro-phenyl)-2-(4-chloro-phenyl)-2-(4-methyl-piperazin-1-yl)-acetamide

: 873659-40-6
N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide

Guidance literature:: With tin(ll) chloride; In ethyl acetate; for 2h; Heating;
DOI:10.1021/jm050456x

Reference yield:

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

: 873659-40-6
N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 24 h / Heating

2: SnCl₂ / ethyl acetate / 2 h / Heating

With tin(ll) chloride; In ethyl acetate; acetonitrile;
DOI:10.1002/anie.200351169

Reference yield:

: 52574-79-5
α-bromo-p-chlorophenylacetic acid chloride

: 873659-40-6
N-(4-amino-2-benzoylphenyl)-2-(4-chlorophenyl)-2-(4-methyl-1-piperazinyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: toluene; dioxane / 2 h / Heating

2: acetonitrile / 24 h / Heating

3: SnCl₂ / ethyl acetate / 2 h / Heating

With tin(ll) chloride; In 1,4-dioxane; ethyl acetate; toluene; acetonitrile;
DOI:10.1002/anie.200351169