2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide

Base Information

Chemical Name:2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide
CAS No.:1436405-84-3
Molecular Formula:C₂₈H₃₁ClFN₅O₃
Molecular Weight:540.037
Hs Code.:

Synonyms:2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide

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Chemical Property of 2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide

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Technology Process of 2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide

There total 8 articles about 2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)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: 85.0%

: 1436405-83-2
N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)-2-nitrobenzamide

: 1436405-84-3
2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide

Guidance literature:: With calcium chloride; zinc; In ethanol; water; for 10h; Reflux;
DOI:10.1016/j.bmc.2013.03.053

Reference yield:

: 91004-38-5
3-acetamido-4-hydroxybenzoic acid

: 1436405-84-3
2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C

2: acetic acid; nitric acid / 6 h / 25 - 35 °C

3: thionyl chloride / dichloromethane / 1 h / Reflux

4: dichloromethane / 0.5 h / 0 °C

5: potassium carbonate / tetrahydrofuran; methanol / 3 h / 20 °C

6: pyridine / 4 h / 0 °C

7: zinc; calcium chloride / water; ethanol / 10 h / Reflux

With pyridine; thionyl chloride; nitric acid; potassium carbonate; acetic acid; calcium chloride; zinc; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.03.053

Reference yield:

: 1356916-92-1
3-acetamido-4-ethoxybenzoic acid

: 1436405-84-3
2-amino-N-(3-chloro-4-fluorophenyl)-4-ethoxy-5-(4-((4-methylpiperazin-1-yl)methyl)benzamido)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: acetic acid; nitric acid / 6 h / 25 - 35 °C

2: thionyl chloride / dichloromethane / 1 h / Reflux

3: dichloromethane / 0.5 h / 0 °C

4: potassium carbonate / tetrahydrofuran; methanol / 3 h / 20 °C

5: pyridine / 4 h / 0 °C

6: zinc; calcium chloride / water; ethanol / 10 h / Reflux

With pyridine; thionyl chloride; nitric acid; potassium carbonate; acetic acid; calcium chloride; zinc; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;
DOI:10.1016/j.bmc.2013.03.053