5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide

Base Information

Chemical Name:5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide
CAS No.:1420290-85-2
Molecular Formula:C₂₀H₂₂Cl₂N₄O₄
Molecular Weight:453.325
Hs Code.:

Synonyms:5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide

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Technology Process of 5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide

There total 3 articles about 5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide 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: 55.0%

: 109-01-3
1-methyl-piperazine

: 1046321-35-0
2-(2-bromoethoxy)-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide

: 1420290-85-2
5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide

Guidance literature:: With potassium carbonate; potassium iodide; In acetone; at 0 - 75 ℃; for 18h; Inert atmosphere;
DOI:10.1021/ml3003082

Reference yield:

: 5464-12-0
2-(4-methylpiperazinyl)ethanol

: 50-65-7
Niclosamide

: 1420290-85-2
5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃;
DOI:10.1016/j.bmcl.2019.03.032

Reference yield:

: 50-65-7
Niclosamide

: 1420290-85-2
5-chloro-N-(2-chloro-4-nitrophenyl)-2-[2-(4-methylpiperazin-1-yl)-ethoxy]benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 16 h / 20 °C / Inert atmosphere

2: potassium iodide; potassium carbonate / acetone / 18 h / 0 - 75 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; potassium iodide; In tetrahydrofuran; acetone; 1: |Mitsunobu Displacement;
DOI:10.1021/ml3003082