3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide

Base Information

• Chemical Name: 3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide
• CAS No.: 1086423-48-4
• Molecular Formula: C₂₀H₂₂F₃N₃O₂
• Molecular Weight: 393.409
• Mol file: 1086423-48-4.mol

Synonyms:3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide

Chemical Property of 3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide

There total 7 articles about 3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)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:

4-methyl-3-nitrobenzoic acid (96-98-0) → 3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide (1086423-48-4)

Guidance literature:

Multi-step reaction with 3 steps

1: oxalyl dichloride / N,N-dimethyl-formamide; dichloromethane / 2 h / 20 °C

2: triethylamine / dichloromethane / 5 h / 20 °C

3: iron; ammonium chloride / ethanol / 2 h / Reflux

With oxalyl dichloride; iron; ammonium chloride; triethylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1016/j.ejmech.2017.02.041

Reference yield:

4-methyl-3-nitrobenzoyl chloride (10397-30-5) → 3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide (1086423-48-4)

Guidance literature:

Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 5 h / 20 °C

2: iron; ammonium chloride / ethanol / 2 h / Reflux

With iron; ammonium chloride; triethylamine; In ethanol; dichloromethane;

DOI:10.1016/j.ejmech.2017.02.041

Reference yield:

1-methyl-4-nitro-2-(trifluoromethyl) benzene (89976-12-5) → 3-amino-4-methyl-N-(4-(morpholinomethyl)-3-(trifluoromethyl) phenyl)benzamide (1086423-48-4)

Guidance literature:

Multi-step reaction with 5 steps

1: N-Bromosuccinimide / 1,2-dichloro-ethane / 5 h / Reflux

2: triethylamine / tetrahydrofuran / 2 h / Reflux

3: iron; ammonium chloride / ethanol / 2 h / Reflux

4: triethylamine / dichloromethane / 5 h / 20 °C

5: iron; ammonium chloride / ethanol / 2 h / Reflux

With N-Bromosuccinimide; iron; ammonium chloride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; 1,2-dichloro-ethane;

DOI:10.1016/j.ejmech.2017.02.041

upstream raw materials:

4-methyl-3-nitrobenzoic acid

4-methyl-3-nitrobenzoyl chloride

1-methyl-4-nitro-2-(trifluoromethyl) benzene

4-(morpholin-4-ylmethyl)-3-(trifluoro-methyl)aniline

Downstream raw materials:

1H-pyrrolo[2,3-b]pyridine-5-carboxylic acid [2-methyl-5-(4-morpholin-4-ylmethyl-3-trifluoromethyl-phenylcarbamoyl)-phenyl]-amide