3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide

Base Information

• Chemical Name: 3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide
• CAS No.: 1168138-81-5
• Molecular Formula: C₂₃H₂₃Cl₂N₃O
• Molecular Weight: 428.361
• Mol file: 1168138-81-5.mol

Synonyms:3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide

Chemical Property of 3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide

There total 5 articles about 3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]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-fluoro-3-nitro-N-[(1R)-1-phenylpropyl]benzamide (1168138-38-2) → 3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide (1168138-81-5)

Guidance literature:

Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 17 h / Reflux

2: tin(II) chloride dihdyrate / ethyl acetate / 2 h / Reflux

With tin(II) chloride dihdyrate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethyl acetate;

DOI:10.1016/j.bmcl.2011.06.088

Reference yield:

4-{[(3,4-dichlorophenyl)methyl]amino}-3-nitro-N-[(1R)-1-phenylpropyl]benzamide (1168138-64-4) → 3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide (1168138-81-5)

Guidance literature:

With tin(II) chloride dihdyrate; In ethyl acetate; for 2h; Reflux;

DOI:10.1016/j.bmcl.2011.06.088

Reference yield:

3-nitro-4-fluorobenzoic acid (453-71-4) → 3-amino-4-{[(3,4-dichlorophenyl)methyl]amino}-N-[(1R)-1-phenylpropyl]benzamide (1168138-81-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran; dichloromethane / 21 h / 0 - 20 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 17 h / Reflux

3: tin(II) chloride dihdyrate / ethyl acetate / 2 h / Reflux

With tin(II) chloride dihdyrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; ethyl acetate;

DOI:10.1016/j.bmcl.2011.06.088

upstream raw materials:

4-fluoro-3-nitro-N-[(1R)-1-phenylpropyl]benzamide

4-{[(3,4-dichlorophenyl)methyl]amino}-3-nitro-N-[(1R)-1-phenylpropyl]benzamide

3-nitro-4-fluorobenzoic acid

1-phenylpropylamine

Downstream raw materials:

1-[(3,4-dichlorophenyl)methyl]-N-[(1R)-1-phenylpropyl]-1H-benzimidazole-5-carboxamide